FWBD Mop 2019
FWBD Mop 2019
FWBD Mop 2019
Manual of
Procedures
Table of Contents
Foreword........................................................................................................................................................ i
Acronyms ...................................................................................................................................................... ii
Glossary ......................................................................................................................................................... v
1.0 Introduction ...................................................................................................................................... 2
1.1 Purpose and Scope of the Manual................................................................................................... 2
1.2 Users of the Manual .......................................................................................................................... 2
1.3 Food and Water-borne Diseases ...................................................................................................... 3
1.3.1. What is food and water-borne disease?....................................................................................... 3
1.3.2. Why food and water-borne diseases are of global concern ....................................................... 3
1.3.3. Epidemiology of food and water-borne diseases ....................................................................... 4
1.4 Food and Water-borne Diseases Prevention and Control Program .............................................. 5
1.4.1. Policy Background: ....................................................................................................................... 5
1.4.2. Structure: ...................................................................................................................................... 7
1.4.3. Milestones ..................................................................................................................................... 9
1.4.4. National Strategic Plan 2019-2023 ........................................................................................... 10
2.0 Implementation Arrangement....................................................................................................... 15
2.1. Implementation Framework ............................................................................................................ 15
2.2. Multi-sectoral Collaboration ............................................................................................................ 17
2.3. Roles and Responsibilities ................................................................................................................. 19
2.3.1 Department of Health Central Office ........................................................................................ 19
2.3.2 Department of Health Central Office – Center for Health Development ............................... 23
2.3.3 Other Government Agencies ..................................................................................................... 26
3.0 Case Management and Prevention ..................................................................................................... 31
3.1 Detecting Diarrhea Case ................................................................................................................... 31
3.2 Assessment of Dehydration ............................................................................................................... 32
3.3 Management of Diarrhea Case ........................................................................................................ 34
3.3.1 Fluid Replacement Therapy ....................................................................................................... 34
3.3.2 Anti-microbials and Other Adjunctive Therapy ....................................................................... 36
3.3 Preventive Measures ......................................................................................................................... 39
3.3.1 Personal Hygiene ........................................................................................................................ 39
3.3.2 Safe, clean water ........................................................................................................................ 39
3.3.3 Proper Food Handling ............................................................................................................... 40
3.3.4 Vaccination ................................................................................................................................. 42
3.3.5 Health Promotion activities ....................................................................................................... 42
4.0 Laboratory Management .................................................................................................................... 44
4.1 Clinical Laboratory ............................................................................................................................ 44
4.1.1 Role of clinical laboratory ............................................................................................................ 44
4.1.2 Structure...................................................................................................................................... 45
4.1.3 Services ........................................................................................................................................ 47
4.1.3 Referral Flow During Outbreaks ................................................................................................ 61
4.2 Food Laboratory............................................................................................................................... 68
4.2.1 Food and Drug Administration .................................................................................................. 68
4.2.2 Bureau of Quarantine ............................................................................................................... 68
4.2.3 National Meat Inspection Service .............................................................................................. 69
4.2.4 Bureau of Fisheries and Aquatic Resources .............................................................................. 69
5.0 Surveillance and Outbreak Response .................................................................................................. 71
5.1 Surveillance of Human Cases ............................................................................................................ 71
5.1.1. Definition ..................................................................................................................................... 71
5.1.2. Importance of surveillance in food and waterborne diseases ................................................... 71
5.1.3. Uses of surveillance and response to FWBD .............................................................................. 72
5.1.4 Policies ......................................................................................................................................... 72
5.1.5 Structure...................................................................................................................................... 73
5.1.6. Detection, Reporting, Analysis and Interpretation of FWBD data .......................................... 74
5.2. Other Surveillance System Related to FWBD ................................................................................ 82
5.2.1. Water Quality Surveillance....................................................................................................... 82
5.2.2. Surveillance in Unprocessed Food (Veterinary Surveillance) .................................................. 82
5.2 Outbreak response............................................................................................................................ 83
5.2.1 What is the role of FWBD-PCP in the outbreak response for FWBD outbreak? ..................... 83
5.2.2 Detection of a food and water-borne outbreak ...................................................................... 83
5.2.3 Food and water-borne outbreak investigation ........................................................................ 85
5.2.4 Control of the Outbreak ............................................................................................................ 94
5.2.4.1 Controlling the source .............................................................................................................. 94
5.2.4.2 Controlling the transmission .................................................................................................... 95
.2.5 Declaring that the outbreak is over ............................................................................................ 95
5.2.6 Communicate the Findings ........................................................................................................ 95
6.0 Health Promotion and Communication ............................................................................................. 97
6.1 General Guidelines............................................................................................................................. 97
6.2 Understanding Basic Concepts ......................................................................................................... 98
6.2.1 Health promotion ....................................................................................................................... 98
6.2.2 Health communication .............................................................................................................. 98
6.2.3 Behavior Change Communication ............................................................................................ 99
6.3 Risk Communication ....................................................................................................................... 101
6.3.1 Analysis of the Situation ........................................................................................................... 102
6.3.2 Steps in Developing Effective Messages During Outbreaks: ................................................... 103
6.4 Communication Plan ..................................................................................................................... 104
6.5 Other Advocacy materials.............................................................................................................. 111
6.5.1 Public Health Advisory ............................................................................................................. 111
6.5.2 Program Briefer ....................................................................................................................... 112
6.5.3. Program Reports ..................................................................................................................... 112
6.5.4 Short videos .............................................................................................................................. 112
7.0 Other Programmatic Functions ......................................................................................................... 114
7.1 Policy Development ........................................................................................................................ 114
7.2 Capacity Building ........................................................................................................................... 114
7.3 Monitoring and Evaluation, Research ............................................................................................ 114
References: ............................................................................................................................................... 115
Annexes ..................................................................................................................................................... 117
Annex A: Policies and Guidelines For the National Control of Diarrheal Diseases ............................ 118
Annex B: DOH Organizational Structure of Disease Prevention and Control Bureau ....................... 119
Annex C: Findings of the Assessment .................................................................................................. 120
Annex D: DPO on the Creation of Technical Working Group, Expert Panel and Steering Committee
For the FWBD-PCP ................................................................................................................................ 122
Annex E: IHR Provision Stating the conditions for Reporting FWBD cases/events ........................... 127
Annex F: Guidelines on Rotavirus and cholera vaccination ................................................................ 129
Annex G: Summary of Roles and Responsibilities of Laboratories at Different Levels of Service
Capability .............................................................................................................................................. 135
Annex H: General Guidelines on Specimen Collection ....................................................................... 137
Annex I: List of International Laws for Transporting Dangerous Goods ............................................ 139
Annex J: List of Microorganisms Considered Under Category A Infectious Substance ..................... 140
Annex K: UN Number and Proper Shipping Name .............................................................................. 141
Annex L: Example of Hazard and Handling Labels .............................................................................. 142
Annex M: Forms for Communicating Laboratory Results of Specimen in an Outbreak Response ... 144
Annex N: Laboratory Referral Form for Outbreak Testing ................................................................. 147
Annex O: Flow of Weekly PIDSR reports ............................................................................................. 148
Annex P: Description of FWBD Diseases on Surveillance ................................................................... 149
Annex Q: PIDSR reporting Forms ......................................................................................................... 152
Annex R: Conditions of National and International Concern ............................................................. 157
Annex S: Core Function of EICT ............................................................................................................ 158
Annex T: National Health Promotion and Communication Plan ........................................................ 159
Annex U: National Health Advisory (Sample) ..................................................................................... 164
Foreword
Food and water-borne diseases (FWBD) are conditions caused by intake of contaminated food
and water. Globally, people are at risk of developing a food and water-borne disease daily
because food and water can be contaminated at any point of its production. Diarrhea is the
most common manifestation of food and water-borne diseases. In the Philippines, a total of
41,220 cases and 91 deaths due to diarrhea (caused by infectious organisms) were reported in
2017.
The Department of Health recognizes the magnitude of the problem caused by food and water-
borne diseases. It also acknowledges that a successful prevention and control program involves
the coordination and collaboration with other DOH and non-DOH agencies. Thus in 1997
through the Administrative Order 29-A, the FWBD Prevention and Control Program was
established.
After more than a decade, the program has achieved important milestones in its’
implementation such as Clinical Practice Guidelines (CPG) for Management of Acute Diarrhea
and a National Strategic Plan for FWBD-PCP 2019-2023. Thus, in support and to facilitate the
operationalization of the National Strategic Plan, this Manual of Procedures was developed.
The manual provides the reader an account of the program’s development and current
implementation framework wherein the responsibility of the various agencies involved in the
implementation of the program are clearly defined. The manual was developed with the health
workers and supervisors as the main users. Thus, in certain sections, basic principles are
included to provide further information or the rationale for certain processes. The manual was
developed through concerted efforts of the various agencies involved in the effective
implementation of the program.
I would like to enjoin our program managers and frontline health workers in health care
facilities involved in preventing, detecting and managing cases at the local government units to
partake in the achievement of the FWBD program’s vision. It may not be easy, but with
everyone doing its roles as stipulated in this MOP, I believe we can achieve.
i
Acronyms
AO Administrative Order
BQ Bureau of Quarantine
DA Department of Agriculture
DC Department Circular
EB Epidemiology Bureau
ii
FDA Food and Drug Administration
RA Republic Act
iii
RDT Rapid Diagnostic Test
iv
Glossary
Is the passage of three or more loose stools from an
Acute Diarrhea immunocompetent person’s normal baseline in a 24 hour
period with a duration of less than 14 days. (CPG)
is suspected if a patient presents with passage of 3 or more
loose, watery or bloody stools within 24 hours that may be
Acute Infectious Diarrhea accompanied by any of the following symptoms: nausea,
vomiting, abdominal pain, and fever. (CPG)
Acute Bloody Diarrhea Is a diarrheal disease with visible blood in the stool
v
Case, confirmed Is a case verified by laboratory analysis
Case Fatality Ratio The proportion of all cases that die because of the disease
vi
Refers to the occurrence in the community or region of
cases of an illness, specific health related behavior or
other health related events clearly in excess of normal
expectancy. The number of cases indicating the presence
Epidemic
of epidemic varies according to the agent, size and type of
population exposed; previous experience or lack of
exposure to the disease, and time and place of
occurrence.
Food and water-borne Any disease of an infectious or toxic nature caused by the
disease consumption of contaminated food or water
Food and water-borne The occurrence of two or more cases resulting from the
diseases outbreak ingestion of the same food or drink
vii
Refers to the international legal instrument that binds all
WHO Member States to implement a set of international
standards with the aim to prevent, protect against,
International Health control and provide public health response to the
Regulation international spread of disease in ways that are
commensurate with and restricted to public health risks,
and which avoid unnecessary interference with
international traffic and trade
viii
MANUAL OF PROCEDURES
1
1.0 Introduction
This manual covers the present scope of the program; which focuses on food or water-
borne diseases caused by bacteria, viruses and foodborne helminths. Toxins and
biochemicals are not included even if they cause a food or water-borne event or
disease. Discussion on specific FWBD is limited to the syndromic manifestations (bloody
and watery diarrhea). However, some infectious FWBD such as Cholera, Hepatitis A,
Typhoid Fever and Rotavirus are also discussed because of their public health
importance that such diseases are included in the national disease surveillance system
as mandated by the law.
The manual is intended for use primarily by the health workers (doctors, nurses,
midwives, sanitary inspectors and barangay health workers) in health care facilities
involved in detecting, managing cases and implementing preventive measures at the
local government units. Thus, the manual contains principles and processes. It also has
boxes and annexes that provide additional information or illustrations.
Other users of the manual may include but not be limited to:
Program supervisors at the regional health and provincial health offices
who are involved in addressing food and water-borne diseases including
health emergencies situations;
Members of the epidemic investigation and control team;
Program managers of other government agencies at the provincial,
regional and national level
2
1.3 Food and Water-borne Diseases
Food and water-borne diseases are conditions caused by intake of contaminated food
and water. Across the different stages of food production pathway, conditions or
factors may be present. These conditions posed a risk for the growth of bacteria/viruses
or introduction of food-borne helminths in food/water causing a disease in humans
(Figure 1)
3
1.3.3. Epidemiology of food and water-borne diseases
Yearly, billions of people are at risk of developing food and water-borne diseases
(FWBDs) and millions will have the disease. Diarrhea is the most common manifestation
of food and water-borne diseases. Globally, infectious agents that caused diarrheal
diseases accounted for the majority of the 600M cases of illness caused by food-borne
hazards (WHO, 2015). According to the Global Health Observatory (GHO) data, diarrhea
accounts for 9% (525, 000 each year) of the total deaths among children below 5 years
old.
The South-East Asian Region has the second highest burden of FWBDs after the African
Region, with more than 150 million cases and 175 000 deaths annually (WHO, 2016. In
South East Asia three out of 10 under-five children suffer from diarrhea and the region
contributes one third of the global deaths due to diarrhea in the under-five children
(WHO, 2016). Figure 2 shows the common pathogens that caused food-borne diseases
in children under-five years of age in the Southeast Asian Region.
4
In the Philippines, a total of 143 food and water-borne health events were verified by
the Event-Based Surveillance (ESR) from 2012-2016; with 17, 246 cases and 115 deaths.
There are five (5) infectious FWBDs that are under surveillance in the Philippines. These
are acute bloody diarrhea, cholera, rotavirus, hepatitis A and typhoid. As compared to
2016, there is an increase in the number of cases of acute bloody diarrhea and cholera
in 2017 with 30.45% and 9.24%, respectively (Table 1). Cholera has the highest case
fatality rate at 0.77%.
Although the program was established in 1997, the Presidential Decree 856, also known
as, Sanitation Code of the Philippines was signed in 1975 by the incumbent President
and was given the force of law. The ultimate objective of the Sanitation Code is
directing public health services towards the protection and promotion of health of the
people (PD 856). The Code covers the general sanitation policies on water supply; food
establishments; markets and abattoirs; school sanitation and health services; port,
airports, vessel and aircraft sanitation; vermin control; sewage collection and disposal
and excreta disposal and drainage; refuse disposal etc. All the provisions of the Code
when strictly implemented will prevent/reduce the food and water-borne diseases.
5
In November 1993, the Department Circular No. 179 was signed and approved by DOH
Undersecretary Galvez Tan. The DC 179 refers to the Policies and Guidelines for the
National Control of Diarrheal Diseases (Annex A). CDD program was focused on
management, treatment and prevention of diarrhea among under-five children and was
later on integrated in the Integrated Management of Childhood Illnesses (IMCI). DC 179
was followed by DC 110: Intensifying the Program on Food Handlers and Water Quality
Surveillance to curb outbreaks from water and sanitation related diseases.
Finally, Administrative Order 29-A established the food and water-borne diseases
prevention and control program in 1997 under the Communicable Disease Control
Service. The AO 29-A stated the five program objectives and defines the six program
components. After the creation of the FWBD-PCP, more policies were passed to
support the implementation of the program (Box 1).
1997. DOH Designation of Ad Hoc Committee for the formulation of plans, policies
DO No. 99-H and standards for the FWBD-PCP
PhilHealth Strict Compliance to Republic Act – the Law on Reporting
Circular No. Communicable Diseases
030s-2000
2001. DOH Revised of List of Notifiable or Reportable Diseases
DC No. 176
2005. AO No. Development of Guidelines for FWBD Surveillance
0012
2007 AO No. Issuance of the Philippine National Standards for Drinking Water
0012
2010 AO No Issuance of Diagnosis and Treatment Guidelines for Paragonimiasis
2010-0037
2012. RA Food Safety Act
10611
2014 Manual of Procedures for the Surveillance, Outbreak Investigation and
Response to Microbial Agents of Food and Water-borne Diseases
supported by WHO and Research Institute for Tropical Medicine (RITM)
AO No. 2015- Designation of the Research Institute for Tropical Medicine as the
0050 National Reference Laboratory for Rotaviruses and Other Enteric
Viruses
DPO No. Creation of the Technical Task Force, Expert Panel and Steering
2017-3642 Committee for the Development of Clinical Practice Guidelines on
Selected Food and Water-borne Diseases
DPO No. Creation of the TWG, Expert Panel and Steering Committee for the Food
2017-5438 and Waterborne Disease Prevention and Control Program
6
1.4.2. Structure:
Executive Order No. 366 lists the different health divisions under the Disease Prevention
and Control Bureau (DPCB) wherein the Infectious Diseases for Prevention and Control
Division (IDPCD) is included (Fig. 3). The FWBD-PCP is one of the programs under the
said Division. To achieve its goal of reducing morbidity and mortality of food and water-
borne diseases, the program will be working with the Environmental Related Diseases
Division which is under the same Bureau.
The program is also working with the other Bureaus and Services within the Department of
Health such as the Epidemiology Bureau, Health Emergency and Management Bureau, Health
Promotion and Communication Services, Procurement Services, Food and Drug Administration,
Bureau of Quarantine, and Research Institute for Tropical Medicine (Annex B) and San Lazaro
Hospital. The program is also working with the Academe (UP), other multi-specialty societies,
WHO and other development partners and other agencies working on food and safety
(DA/FDA/NMIS/BAI).
7
The FWBD-PC Program is managed by a Program Manager at the Central DOH. Its
mandates and activities are implemented and supervised by the Program and the
Regional FWBD Coordinators (Fig. 4). The Regional FWBD coordinator will work with the
Regional Surveillance Unit, Family Health Cluster, Environmental and Occupational
Health Unit, Health Education and Promotion Unit, Provincial DOH Office, and supervise
the implementation of the program at the Local Government Units. At the LGU level,
there are designated FWBD coordinator.
8
1.4.3. Milestones
9
1.4.4. National Strategic Plan 2019-2023
1) establish FWBD-PCP performance level against the goals and targets set in the
2011-2016 DOH-National Objectives for Health (NOH);
2) determine the extent by which the FWBD’s key strategies were operationalized and
implemented;
3) identify the factors that influenced the performance levels and implementation status
of the FWBD-PCP components;
4) summarize the gaps and challenges and come up with recommendations to address
them.
Service absence of CPGs on the diagnosis and management of FWBDs resulting to varying
Delivery standards and protocols practiced by the different hospitals
ORT corners no longer found operational in health facilities
a. Supply inadequate knowledge of service providers on diarrhea management
lack of trained staff on IMCI in the health facility
non-availability of vaccines for all cases of diarrhea
service delivery network for FWBDs unclear
negative attitude of health workers
10
Reform Area Gaps and Challenges
b. Demand poor health seeking behaviors of patients due to varying reasons (e.g. cultural beliefs)
community not aware of disease consequences due to lack of IEC resulting from
inappropriate messages and ineffective information dissemination
No KAP survey conducted
Lack of trust in government health facilities
Leadership low priority on FWBD program in some LGUs
lack of support from some LCEs
lack of ownership of the program
wrong perception of devolution particularly political will on health matters
political problems/intervention/ interest among departments
lack of good governance and ethical leadership
Organizational management of FWBD-PCP has been transferred from one DOH unit to another (from
Support IDO to EH and back to IDO); management within IDO also transferred from NTD cluster
Structure to the other IDO unit
National and Regional FWBD-PCP Coordinators only recently designated; all regional
coordinators are handling other programs
overall management of FWBD-PCP remains unclear at the local level; no overall
coordinator assigned; in some areas, the program is placed either under the Sanitation
Unit or the municipal/city surveillance and epidemiology unit, but none has been
designated to coordinate diagnosis, management and treatment including governance
component
Regional and local FWBD-PCP Coordinators not trained
fast turn-over of coordinators
no clear-cut coordination among DOH offices involved in the program
scope and limitation of FWBD-PCP vis-à-vis other programs not clearly streamlined
Policies/ FWBD-PCP lacks overall program framework; hence implementation of components
Guidelines remains fragmented
and Plans absence of strategic plan to guide implementation
no manual of operations to provide standards to be followed
compliance/adherence to national policies and laws not monitored
management of other FWBDs (e.g. Hepatitis A, amoebiasis dysentery, etc.) still without
CPGs
program not cascaded and institutionalized at regional and local levels; unaware of
policies including roles and functions
lack of orientation on FWBD-PCP; preventive vis-à-vis curative not clear to all
stakeholders
Health Human limited number of sanitary inspectors at the local level (e.g. Tanay, Rizal with > 100,000
Resource population has only 1 SI
some SIs are under contractual/job order employment; no plantilla position for SIs
most nurses and midwives lack training on IMCI while some are still not oriented on IYCF
no specific training on FWBD diagnosis, management, treatment
11
Reform Area Gaps and Challenges
12
Fig.5 National Strategic Plan 2019-2023 Framework
13
Section II:
Implementation
Arrangement
This section discusses the:
Implementation Framework
Multi-sectoral Collaboration
Roles and Responsibilities of
government agencies involved in the
prevention and control of FWBD
14
2.0 Implementation Arrangement
The over-all goal of the program is to reduce disease, disability and death caused by
food and water-borne diseases (focusing on bacteria, virus, and foodborne helminths).
In achieving this goal, the FWBD-PCP implementation framework (Figure 6) aligns with
the five objectives of the NSP (2019-2023) that addresses governance, financing, service
delivery, regulation and performance accountability. The nine program components, as
stated in the Guidelines on the Implementation of the Food and Water-borne Diseases
Prevention and Control program, will help achieve the five objectives. Each component
may involve two or more agencies working together to achieve the desired change in
reducing morbidity and mortality from food and water-borne diseases
15
These components are the following:
1. Case Management focuses on the treatment and management of cases.
2. Laboratory Diagnosis refers to the to the collection, submission and processing of
specimen for confirming the etiologic agent of the food and water-borne disease.
3. Surveillance refers to the reporting of human cases and animal health conditions that
may also cause the disease in man.
4. Policy development focuses in the development and implementation of
policies/guidelines that will help in the achievement of the program objectives.
5. Capacity building provides the necessary knowledge and skills to health worker to
provide the necessary services of the program and proper reporting.
6. Health Promotion and disease prevention refers to program activities that advocate
for support (policies and resources) and adapting preventive behavior.
7. Logistic Management refers to the availability of drugs and supplies needed routinely
by the program and during outbreaks and other health emergency situations.
8. Monitoring and Evaluation (includes research) pertains to tracking of program
activities and indicators which will indicate the achievement of program objectives.
9. Intra and inter-agency collaboration focuses on the interaction and collaboration of
the different agencies within and outside the Department of Health to achieve the
program objectives.
Components 4-8 (policy development, capacity building, health promotion, logistic
management and monitoring and evaluation) supports across case management,
laboratory diagnosis and surveillance. On the other hand, changes in technology,
treatment regimen, trends and emergence of new diseases affects or will redefine
components 4-8.
Intra and inter-agency collaboration is the ground for the interplay of the other
components wherein various agencies need to work together to be able to achieve the
program goal.
Also, the nine components work across the different structure of the government from
the devolved local government units (City/Municipality, Provinces) to the National level.
16
Moreover, the program deals with diseases covered by international health regulation.
Thus, the program output both covers commitment to national and international
community.
17
Office provides policies and guidelines on the integration of FWBD policies and activities
in maternal and child care.
2. Laboratory Diagnosis involves hospital laboratories (regional) and National
Reference Laboratories (RITM) and FDA. Agencies working on animal Health (BAI, NMIS,
BFAR, etc.) perform laboratory testing on food and food products.
3. Surveillance and outbreak response function is the mandate of the
Epidemiology Bureau. However, the reporting process involves the LGU, and Provincial
Health Office, Regional Health. Other agencies such as the Bureau of Quarantine, RITM
and other National Referral Laboratories perform laboratory testing related to
surveillance activities. Agencies working on animal surveillance (Department of
Agriculture, BFAR) complete the whole surveillance process. Any positive findings shall
be reported to Epidemiology Bureau (EB) which is also the focal office for International
Health Regulation.
The Health Emergency Management Bureau (HEMB) collaborates with the
program during human-crisis situations (disasters, siege) wherein food and water-borne
diseases become a health problem in such situations.
4. National agencies develop policies in relation to the prevention and control
food and water-borne diseases. However, devolved health offices and facilities may
develop internal guidelines that will strengthen implementation of program activities
such as referral process of patients from community, integrated logistics management,
infection control guidelines.
5. Capacity building pertains to formal training wherein training modules are
developed by national technical experts; but the regional and provincial offices conduct
the actual training.
6. Health Promotion and disease prevention: development of posters and
training guide involves national DOH (FWBD-PCP and HPCS). However, promotion of
personal hygiene practices may include the Department of Education and DSWD.
Regional, Provincial and local health offices may also be involved in health promotion
activities.
7. Logistic Management involves the different health structure from the national
to the local units.
8. Monitoring and Evaluation, research involves regional and national health
offices.
DPO No. 2017-5438 provided the mechanism by which the multi-sectoral collaboration
can function effectively. The DPO also states the creation of a Steering committee,
18
Expert Panel and Technical Working Group for FWBD (Annex D). The composition and
functions are stated in the DPO. The Steering committee provides the over-all oversight
of the FWBD-PCP and recommends to the Secretary of Health the approval of all
technical outputs.
The Expert Panel reviews policy issuances and strategies and all technical products of
the program.
The FWBD Technical Working Group was created and becomes the arm for the program
collaborative function. The TWG will be chaired by the Program Manager. The co-
chairman may rotate among the different partner agencies. The TWG will meet on the
2nd week of each quarter (coinciding with the quarterly reporting period of the
department). During the meeting each agency will present accomplishments (in terms
of planned activities and specific indicators) and updates on new technology; findings
during supervisory visits; and issues that need the decision of the TWG in relation to
FWBD. The TWG shall also be the venue to discuss any policy, financing and regulation
agenda of the program. It will be a venue to discuss programmatic issues and be
resolved as a group. The chair may convene special meetings if there are urgent issues
requiring decision from the group.
Clear delineation of functions and responsibilities will lessen tasks not being
implemented or encroaching on each other function resulting to duplication of tasks.
The roles and responsibilities stated in this MOP was taken from the new AO: Guidelines
on the Implementation of the Food and Water-borne Disease Prevention and Control
program.
The DOH-DPCB shall be responsible for the overall execution of the policy and
guidelines.
19
a. Overall management and coordination of the FWBD-CP. It takes the lead in
setting the overall direction and focus of the Program.
b. Formulate and disseminate national policies and guidelines governing the
management and implementation of the FWBD-PCP;
c. Develop strategic plans and cascade these to the CHDs for adoption;
d. Ensure the provision/delivery of quality diagnosis, management and treatment
services of FWBDs;
e. Design and facilitate the conduct of training on various components of the
program;
f. Manage the logistics requirements of the Program and secure logistics support;
g. Establish partnership with other national government agencies and other
partners in the private sector;
h. Maintain and regularly update a directory of FWBD focal persons from DOH-
CHDs, provinces, municipalities/cities as well as partner agencies; strengthen
coordination and linkages with RO focal persons
i. Coordinate with related offices/agencies on any outbreak due to FWBDs such as
EB for surveillance and monitoring, HEMB for logistic augmentation,
Environmental Related Disease Division for immediate action on water and
sanitation, DA for diseases that may be attributed to contamination of animals
and plants and BFAR for contamination of seafood products;
j. Coordinate with other DOH offices in promoting WASH practices and key
messages on prevention and control of FWBDs;
k. Undertake monitoring and evaluation of the status and performance of the
FWBD-PCP
a. Provide technical assistance to the regions and LGUs to comply with the
provisions and requirements of the Sanitation Code of the Philippines;
b. Formulate and promote policies and guidelines in promoting increased access to
safe water and sanitation services;
c. Design strategic approaches to achieve zero open defecation areas nationwide;
d. Augment logistics for water testing facilities;
e. Coordinate with the Department of Environment and Natural Resources (DENR)
and Department of Agriculture (DA) for interventions that will support the
prevention and control of FWBDs.
20
2.3.1.3 Family Health Office (FHO) Women and Men’s Health
Development Division and Children’s Health Development Division
21
c. Support in the augmentation of logistics to FWBD to respond to emergencies,
disaster and outbreaks.
a. Perform confirmatory laboratory testing for human samples referred for the
FWBD surveillance and outbreak investigation (e.g. stool, sputum, blood, urine);
b. Provide technical support for collection, transport and storage of specimen for
the disease reporting unit;
c. Provide training on lab diagnosis of FWBD pathogens and quality assurance to
the regional laboratories;
d. Provide line-list of laboratory results to EB and RESU, and individual laboratory
results to the RESU, in the form of transmittals (for distribution to the DRUs);
e. Perform further studies to determine other etiologies of FWBD;
f. Conduct laboratory surveillance for the FWB pathogens;
g. Conduct RDT validation for the FWBD.
22
2.3.1.9 Food and Drug Administration (FDA)
23
2.3.2.2. Regional Laboratories
a. Regions to receive and collate data base reports from the LGUs and
hospitals; they should ensure completeness and timeliness of reports
from the LGUs and hospitals;
b. Provide technical assistance to LGUs (ESUs) in the conduct of outbreak
investigation;
c. Coordinate and facilitate submission of samples;
d. Conduct weekly analysis of FWBD data and submit weekly report to EB
on notifiable diseases;
e. Immediate reporting through ESR if there is an outbreak or clustering of
cases
f. Notify EB as the International Health Regulations (IHR) National Focal
Point Office when the assessment of an event indicates a food or
waterborne disease event that is notifiable pursuant to paragraph 1 of
Article 6 and Annex 2 and to inform WHO as required pursuant to Article
7 and paragraph 2 of Article 9 of IHR.
24
2.3.2.4 Family Health Cluster [WMDD and CHDD]
25
2.3.2.6 Health Education and Promotion Unit
26
2.3.3.2 Department of Education
27
2.3.3.5 Department of Environment and Natural Resources
The LGUs are primarily responsible for the delivery of quality FWBD diagnosis,
management and treatment and conduct of preventive and control interventions
at the local level. Specifically, the LGUs shall:
28
i) Fill-up laboratory request forms and submit appropriately labeled
specimens from patients and samples of suspected food/water
vehicle to the appropriate DOH or DA laboratory for microbial tests;
j) Collate and submit epidemiologic data on the occurrence of
Salmonellosis and other food/water-borne infection to EB;
k) Submit monthly reports of FWBD to RESU;
l) Notify RESU when the assessment of an event indicates a food or
waterborne disease event that is notifiable pursuant to paragraph 1
of Article 6 and Annex 2 and to inform WHO as required pursuant to
Article 7 and paragraph 2 of Article 9 of IHR;
29
Section III: Case
Management
This section provides the guide on:
Detecting diarrhea case
Assessing the dehydration level
Management of cases
Preventive measures
30
3.0 Case Management and Prevention
The most common symptom of food and water-borne diseases is diarrhea. And the most
threatening consequence of diarrhea is dehydration. Diarrhea causes loss of water and
electrolytes in the body which can lead to complications and death. Thus, it is important for
health workers to be able to detect diarrhea cases early and provide appropriate actions.
A diarrhea case may be detected in the community/facility by a barangay health worker
(BHW). During the initial encounter, basic information obtained, such as when the condition
started, the characteristic of the stool (watery or bloody), from the patient and the assessment
of the patient’s physical condition. The barangay health worker (BHW) should also be able to
assess the level of dehydration, provide advice and refer the patient to the facility for further
evaluation.
Figure 7 provides a guide for health worker on how to proceed when a diarrhea case is seen
whether in the community or health facility.
YES
Rehydrate and refer to the next
Moderate - Severe higher facility
Note: For watery diarrhea and a high suspicion of cholera, RDT (Rapid diagnostic test) can be
done (if available) and/or C&S testing of the stool specimen.
31
3.2 Assessment of Dehydration
Always assess the level of dehydration of the patient as part of the physical examination. Keep
in mind that the clinical manifestations of dehydration for children is different from adults.
A trained BHW should be able to assess the level of dehydration of children with diarrhea seen
at the community using parameters 2,3, 4,5. Any sign of Moderate to Severe dehydration
should be referred for further evaluation and management to a health facility. Table 3 provides
a summary of clinical manifestations for children.
(Source: Philippine Clinical Practice Guidelines on the Management of Acute Infectious Diarrhea).
32
Level of dehydration for adult patients should also be assessed early on the course of the
disease to prevent complications or death. Table 4 provides a guide in assessing the level of
dehydration of adult patients.
Table 4. Clinical Manifestation of Diarrhea in Adults According to the Level of Dehydration
Fatigue +/- + +
Thirst +/- + +
Sunken eyes - + +
Blood pressure Normal Orthostatic Shock
Hypertension
Other parameters for assessing dehydration in adults is listed in the CPG manual.
33
3.3 Management of Diarrhea Case
34
3.3.1.2 Fluid Replacement in Adult
According to CPG, if the following conditions are present in an adult patient,
referral for hospital admission is highly recommended:
Inability to tolerate oral rehydration;
Moderate to severe dehydration;
Acute Kidney injury;
Presence of electrolyte abnormalities;
Co-morbid conditions such as uncontrolled diabetes, congestive heart
failure, coronary artery disease, chronic kidney disease, chronic liver
disease, immunocompromised conditions;
Weak or elderly patients (>60 years old);
Poor nutritional status;
In the FWBD CPG Reference Manual provides the guide for fluid replacement in
adults is shown in Table 6. The recommended fluid for hydration and
resuscitation of diarrhea patients is Plain Lactated Ringer’s Solution (PLRS), a
chloride restricted intravenous fluid. If this is not available, plain normal saline
solution may be used.
Table 6. Recommended Rehydration Guide For Adults According to the Level of Dehydration
35
Mild dehydration Moderate dehydration Severe dehydration
1.5-2 ml/kg/hour PLRS for 1.5-2 ml/kg/hour PLRS for
patients with actual or patients with actual or
estimated body weight of >50 estimated body weight of>
kg; 50 kg.
Use ideal body weight for Use ideal body weight for
overweight or obese patients; overweight or obese
Replace ongoing losses volume patients.
per volume with PLRS boluses or
ORS (if tolerated). Replace ongoing losses volume
per volume with PLRS boluses.
ORS is not recommended since
patients with severe
dehydration may have
compromised mental status and
therefore have high risk for
aspiration.
Note: Sport drinks and sodas are not recommended to replace fluid losses. Elderly patients and
those at risks of fluid over load (patients with heart failure or kidney disease) should be referred to
a specialist for individualized fluid management.
Antibiotic treatment should not be given routinely in children. Table 7 provides the recommended
treatment.
36
The FWBD CPG Reference Manual provides the following position for adjunctive therapy:
Zinc supplementation is given for acute infectious diarrhea in children more than 6 months old
at a dosage of 20 mg/day for 10-14 days. This adjunctive therapy shortens the duration of
diarrhea and decreases the frequency of stool. Zinc supplementation is not routinely given to
children less than 6 months of age.
Probiotics is recommended adjunctive therapy because it reduces the severity of the symptoms
and duration of diarrhea. Probiotics are given within the duration of diarrhea and may extend
for another 7 days after the completion of the antibiotics. Specific probiotics are listed in the
FWBD CPG Reference Manual.
Doxycycline (use only for > 8 years old): 2mg/kg single dose (max dose: 100 mg/dose)
37
3.3.2.2 Treatment for Adults
Empiric microbial treatment refers to the giving of antibiotic treatment without
identifying the etiologic cause of the acute infectious diarrhea. The decision is based
on clinical experience. The CPG manual recommends empiric microbial treatment
for adults with acute diarrhea and concomitant moderate to severe dehydration plus
the following clinical manifestation: fever alone, fever and bloody stools, or
symptoms persisting for more than 3 days. The recommended microbials are:
Azithromycin 1-gram single dose, or
Ciprofloxacin 500 mgs. twice daily for 3-5 days;
The above microbial treatment will be modified upon confirmation of the suspected
microorganism according to the recommended antibiotics in Table 8.
Racecadotril (100 mg three times a day) may be given to decrease the frequency and duration of
diarrhea.
38
Note: Complications of acute infectious diarrhea in adults (acute kidney injury, hyponatremia or
hypernatremia, hypokalemia or hyperkalemia) can be life threatening and immediately refer the
patient to a specialist. Hospitalization and close monitoring are needed.
When food and water-borne diseases occur, it reflects a failure to lower the risks in the
food production pathway. Thus, the achievement of program goal lies in the
implementation of preventive measures. However, most of the preventive measures
are the under the mandate of other government agencies. Strict application of these
standards lies in the local government unit. However, the Regional Office
Environmental and Occupational Health Unit provides the technical guidance and
capacitation to local government units for proper implementation of the guidelines
Thus, a strong multi-sectoral collaboration of the FWBD PCP is a key in achieving the
goal and objectives of the program.
Strong promotional and advocacy campaign for personal hygiene and proper
handwashing should be done in the community, health care facility, schools, day care
centers, offices and food establishments including resettlements/evacuation sites
during health emergencies. Providing logistical support (clean water for handwashing,
availability of soap and clean communal toilet facilities) for effective implementation
create a supportive environment that encourages and sustains a change in behavior.
Administrative Order No. 2017-0010 provides the Philippine Standards for Drinking
Water. It defines drinking water as water intended for direct human consumption or for
use in food preparation and related processes. According to the manual, drinking water
must be clear and does not have objectionable taste, odor and color. It should be free
from all harmful organisms, chemical substances and radionuclides in amounts that
could be hazardous to humans. To ensure the safety of drinking water, the manual
provides guidelines on the following:
39
a. Water sampling and examination of all types of water sources that includes the
frequency sampling for physical, chemical, microbiological examination.
b. Drinking water from refilling stations, vending machines, mobile tanks and bulk
water supply for the required initial and periodic examinations for
microbiological, physical, chemical and radiological quality.
c. Standard values of mandatory parameters that will be considered safe for
human consumption.
d. Evaluation and interpretation of results
e. Emergency drinking water parameters
Simple boiling of water for 3-5 minutes may remove physical and microbiological impurities.
Chapter III of the Sanitation Code of the Philippines (PD 856) provides the full details on
the rules and regulation for food establishments to ensure food are safe from
contamination. Presently, the local government unit has the responsibility to implement
these rules and regulations. Regional (Environmental Health Staff) and Provincial staff
(Sanitary Engineer and Inspector) should monitor the implementation of these rules and
regulation. Food establishments include eating and drinking places where food and drinks
are processed, manufactured, served or stored. These can be classified as follows:
a. Food Eating and Drinking Establishments
b. Food Processing
c. Food Retailing
d. Street Food Trade
e. Market and Slaughterhouse
40
Some of the regulations from Chapter III of PD 856 are as follows:
a. No food establishment operates for public patronage without a Sanitary Permit.
The permit is renewable yearly and should be posted in a conspicuous area.
b. No person shall be employed in any food establishment without a health
certificate issued by the city/municipal health officer. This certificate shall be
issued only after the required physical and mental examinations and
immunizations.
c. Requirements for food handlers:
1. Food preparation:
2. Food storage
41
3. Food serving
Food and food materials are properly displayed and protected from all
possible contamination.
Food are served with clean and sanitized utensils.
Maintenance of proper temperature
Separate utensils are used for each kind of food.
Left-over foods are never used.
All contaminated foods of those of doubtful quality are condemned.
3.3.4 Vaccination
Killed oral cholera vaccine may be given to children and adults living in endemic
areas to prevent outbreaks caused by cholera;
However, cholera vaccine is not meant to replace the provision for clean
water and sanitation and hygiene (WASH), which are the core strategy
for prevention of cholera.
Rotavirus is an important cause of diarrheal disease particularly in children under
5 years. Rotavirus vaccines are effective in preventing rotavirus diarrhea and
immunization of infants with rotavirus vaccine is recommended.
Health promotional and education materials (posters, leaflets and flip charts) shall be
developed by the program (FWBD-PCP) at the national level. Prototype e-copy will be
distributed to the regional health office for additional reproduction if needed. Regional,
provincial and hospital health promotion officers are encouraged to develop their health
promotion and communication plan. A more detailed discussion on these can be found
in Section VI.
42
Section IV:
Laboratory
Management
This section discusses the:
Clinical laboratory role, its structure
and services;
Specimen Collection, Handling
and storage;
Specimen Packaging and
Transport;
Referral of Specimen
Food laboratory role and agencies
providing the services.
RITM as the National Reference Laboratory
provides the policy and guidelines for clinical
laboratory services. Currently RITM is
revising its MOP. Any changes in policies in
the revised MOP (RITM) will take
precedence over what is stated in this
section. The FWBD-PCP will provide the
necessary addendum.
43
4.0 Laboratory Management
Laboratory services for FWBD-PCP involves clinical and food laboratories within the different
government agencies. Policies and guidelines are developed by specific agencies and
disseminated through the Technical Working Group especially those related to the food and
water-borne diseases.
44
4.1.2 Structure
Peripheral Laboratory
45
In order to maximize the efficient use of these existing laboratories during disease outbreaks,
the NRL defined their relationship in a Laboratory Referral System. From the lower level
(example: peripheral laboratory), specimen and isolates are referred to the next level (a
qualified tertiary laboratory or qualified regional laboratory) who had the capacity to perform
the required confirmatory test. The higher-level-laboratories (reference laboratories) provide
technical guidance, capacity building and quality assurance checking to the peripheral
laboratories. There is sharing of data and expertise at each level (Figure 8). Each level has its
own roles and responsibilities. A summary of these roles and responsibilities in each level is
Annex G.
Figure 8: Laboratories Level of Service Capability and their Technical Relationships(in terms of
referral of specimen, sharing of information, capacity and expertise)
RITM, 2013
Source: Guidelines for Specimen Collection, Transport and Referral For Infectious Diseases
Outbreak Response; Manual For Clinical Specimen, RITM 2013
During FWBD outbreaks and other conditions of international concern when there is a
need to urgently confirm the diagnosis and to save the quality of the specimen, clinical
specimens from the LGU are transported directly to the National Reference Laboratory.
46
4.1.3 Services
4.1.3.1 Specimen Collection, Handling and Storage
Based on the clinical symptoms and data gathered, the initial impression will
determine the possible etiologic agent and the kind of specimen to be collected.
Table 10 provides a summary guide for specimen collection for specific illness
that are currently under surveillance. There are general guidelines on specimen
collection to ensure the integrity of the specimen (Annex H).
During outbreaks, the Philippine Integrated Disease and Response (PIDSR) MOP
states that the Regional Epidemiology Unit shall identify and coordinate with the
laboratories within the region. It is important to identify and contact the
laboratory with appropriate capabilities at the onset of the investigation to
obtain instructions on the type of specimen, proper specimen collection,
handling, storage and transport of specimen including the special media and
other logistics.
47
Table 10: Summary Guide For Specimen Collection
RITM, 2013
Disease Etiologic Tests Appropriate Time of Quantity Container/ Storage Transport/ Is the test Turn- Testing
Agent Specimen Collection Transport Condition Time Confirmatory/ around Centers
Medium Prior to conditions Rapid/ Time
Transport Presumptive
Test
Acute Shigella Culture Fresh stool As soon 2-5 ml Clean, dry, Cary Blair at Cold Pac/k Confirmatory 3-5 days RITM or
Bloody spp. as liquid or wide room within 3-6 any
Diarrhea possible 5 grams mouthed, temperature hours qualified
Salmonella
after solid leak-proof or 4 degrees (within 24 tertiary
spp.
onset of (pea container Celsius up to hours) laboratory
illness size) 24 hours
preferably Room
during temperature
active within 24
diarrhea hours
Sero- Pure isolate Nutrient Refrigerated Cold pack as Confirmatory 1-2 hours
grouping/ Agar butt/ temperature soon as except for
Sero- slant in possible Salmonell
typing disposable a H-typing
plastic (minimum
leak-proof of 5 days)
tube
48
Disease Etiologic Tests Appropriate Time of Quantity Container/ Storage Transport/ Is the test Turn- Testing
Agent Specimen Collection Transport Condition Time Confirmatory/ around Centers
Medium Prior to conditions Rapid/ Time
Transport Presumptive
Test
Cholera Cholera Culture Fresh stool As soon 2-5 ml Clean, dry, Cary Blair at Cold Pac/k Confirmatory 3-5 RITM or any
vibrio as liquid or wide room within 3-6 days qualified
possible 5 grams mouthed, temperature hours tertiary
after solid leak-proof or 4 degrees (within 24 laboratory/
onset of (pea container Celsius up to hours) regional/
illness size) or Cary 24 hours reference
preferably Blair Room laboratory
during temperature
active within 24
diarrhea hours
49
Disease Etiologic Tests Appropriate Time of Quantity Container/ Storage Transport/ Is the test Turn- Testing
Agent Specimen Collection Transport Condition Time Confirmatory/ around Centers
Medium Prior to conditions Rapid/ Time
Transport Presumptive
Test
Typhoid Salmonella Culture Fresh stool 2nd to 3rd 5 grams Clean, dry, Room Confirmatory Minimum RITM or
typhi week solid wide temperature of 5 days any
after (pea mouthed, within 1-2 qualified
onset of size) leak-proof hours tertiary
Salmonella illness container laboratory
or Cary Cold packs/
Paratyphi
Blair Room
A
temperature
(within 24
hours)
Salmonella within3-6
spp. hours
In a holding Room
medium at temperature
room or 4 degrees
temperature Celsius/
or 4 degrees within 24
Celsius for hours
up to 24
hours
50
Disease Etiologic Tests Appropriate Time of Quantity Container/ Storage Transport/ Time Is the test Turn- Testing
Agent Specimen Collection Transport Condition conditions Confirmatory/ around Centers
Medium Prior to Rapid/ Time
Transport Presumptive
Test
Typhoid Salmonella Culture Rectal swab 2nd to 3rd 2 swabs Cary Blair Room Room Confirmatory 3-5 days RITM or
typhi week Transport temperature temperature or 4 any
after Medium in up to 24 degrees qualified
onset of screw hours Centigrade/within tertiary
Salmonella illness capped a week laboratory
Paratyphi tube
A
Blood 1st week Adult: Blood Incubate at Room 7 days
after Culture 35-37 temperature/
1:5 to 1:10
onset of Broth Degrees within 3 after
Salmonella ratio with
illness Celsius or collection
spp. BCB
store at
room
temperature
Infant/Child: until ready
for
1:10 to 1:20
transport
ratio with
BCB
51
Disease Etiologic Tests Appropriate Time of Quantity Container/ Storage Transport/ Is the test Turn- Testing
Agent Specimen Collection Transport Condition Time Confirmatory/ around Centers
Medium Prior to conditions Rapid/ Time
Transport Presumptive
Test
Acute Rotavirus ELISA Stool Upon first 5-10 ml Sterile Refrigerated In ice within Presumptive 5-7 RITM
Watery contact leak-proof prior to 72 hours days
Diarrhea with the screw transport
patient capped
type
container
Hepatitis Hepatitis HAV Serum 1 Onset of At least 1- Screw 4 degrees In ice Presumptive 24
A IgM sample only illness 2 ml capped Centigrade hours
cryotube Celsius
Source: Guidelines For Specimen Collection, Transport and Referral For Infectious Diseases Outbreak Response; Manual For Clinical Specimen,
RITM 2013
52
4.1.3.2 Specimen Packaging and Transport
53
Clinical laboratories are at various level of service capability; hence clinical
specimens are being transported from the local government unit (Municipality/ city/
province) to regional or reference laboratory. Currently, postal or airline industry
act as courier of the clinical specimen. Thus, there are regulatory requirements in
packaging and shipping conditions to preserve the integrity of the specimen and
prompt arrival to the testing laboratory. The National Reference Laboratory – RITM
developed the guidelines for packaging and transporting these clinical specimens
with the following objectives:
Ensure that specimens are packaged and transported using safe and
standardized techniques and methods;
Prevent the loss of vital laboratory information due to deterioration or
loss of specimen (improper packaging, poor transport arrangement)
Ensure safety of health workers during packaging and transporting of
specimens;
Ensure timely arrival of the specimen to testing laboratory
The FWBD-PCP will collaborate with RITM and EB to define the arrangement of
transporting specimen including budgetary concerns of the LGU (routine testing and
outbreak investigation).
54
Markings
Clinical specimen packages are marked to provide information about the contents of
the package, the nature of the hazard, and the packaging standards applied. All
marks on the package shall be placed in a way that it is clearly visible and not
covered by other labels or mark. Each package shall display the following
information on the outer packaging:
The shipper’s name and address;
The name and contact number of a responsible person, knowledgeable
about the shipment;
The receiver’s name and address; the UN number and followed by the Proper
shipping name (UN 2814 “INFECTIOUS SUBSTANCE AFFECTING HUMAN);
Note: Temperature storage requirement is optional. When dry ice or liquid nitrogen
is used – the name of the refrigerant, the appropriate UN number and the net
quantity should be indicated.
Labelling
There are two types of label: a) Hazard label: in the form of a square set at angle of
45 degrees (diamond shape) are required for most dangerous goods in all classes; b)
handling labels: in various shapes are required either alone or in addition to hazard
labels. Annex L provides an illustration of these labels.
General Guidelines
1) The testing laboratory prepares the following documents using the standard
forms (Annex M):
Line list of official laboratory results for outbreak/ special pathogen
which is released to EB, CHD and concerned RESU only;
Individualized Official Laboratory Result;
55
Cover letter to CHD Regional Director through the RESU Head copy
furnished EB
2) Official Laboratory result may only be released to authorized personnel. It
may also be sent electronically through authorized fax number and official e-
mail address. Official Laboratory Result may not be released over the
phone or through SMS text messages. In releasing the result, the testing
laboratory staff shall document the time and date, the mode of transmittal
and to whom it was released.
3) EB shall provide the DOH-Central, DOH Infectious Disease Office, WHO
Philippine Country Office, and other relevant stakeholders with a summary of
the surveillance/outbreak reports for appropriate actions at the national
level. RESU is responsible in providing the concerned PESU/CESU/MESU or
the referring institution with the results for appropriate action at their level.
4) The flow of laboratory information (results of the diagnostic testing) from the
testing laboratory to the referring institution is in Figure 8.
56
Figure 8: Flow of Laboratory Information from the Testing Laboratory to the
Referring Institution
Laboratory
Testing Facility
WHO Country
and Regional EB RESU
Office IHR Focal Point Office
Flow of information
Flow of reports
Source: Guidelines for Specimen Collection, Transport and Referral For Infectious Disease Outbreak
Response. Manual for Clinical Specimens, RITM 2013
57
4.1.3.3 Interpreting of Results
A quick guide in interpreting the laboratory result is given in Table 11.
Acute Diarrhea (with Salmonella spp. Culture and Serology Positive for Salmonella spp., A sensitivity result is
or without blood) Salmonella spp. isolated by culture included according to
and sero typed by the latest CLSI
serology
Positive for Shigella
Shigella spp. Shigella spp., isolated
spp.
by culture and
confirmed by
serology
No important entero-
pathogen isolated Negative for Shigella
Cholera Vibrio cholera 01 Culture and serology Positive for Vibrio Vibrio cholera O1- A sensitivity result is
cholera O1 Ogawa El Tor isolated included according to
by culture and the latest CLSI
Ogawa El Tor
confirmed by
Classical
serology
58
Clinical Impression Etiologic Agent Test Performed Result Interpretation Remark
Cholera Vibrio Cholera 01 Culture and serology Positive for Vibrio Vibrio cholera O1- A sensitivity result is
cholera O1 Hikojima El Tor included according to
isolated by culture the latest CLSI
Hikojima El Tor
and confirmed by
Classical
serology
59
Clinical Impression Etiologic Agent Test Performed Result Interpretation Remark
Typhoid/Paratyphoid Salmonella Typhi, S. Culture and serology Positive for Salmonella isolated A sensitivity result is
Fever/Non Typhoidal paratyphi, and other Salmonella by culture and included according
Fever Salmonella spp. confirmed by to the latest CLSI
serology
Source: Guidelines For Specimen Collection, Transport and Referral For Infectious Diseases Outbreak Response; Manual For Clinical Specimen,
RITM 2013
60
4.1.3 Referral Flow During Outbreaks
In a disease outbreak investigation, microbiological testing of clinical samples is
important in isolating and identifying the causal agent. A functional referral system
for specimen starts with the facility/point where the specimens are collected,
handled, packed, documented and until it is transported to the appropriate
laboratory for testing. A good referral system ensures that the integrity of the
specimens is maintained until it is properly processed and prevents loss of
specimens. The referral flow is illustrated in Figure 9.
Source: Guidelines For Specimen Collection, Transport and Referral For Infectious Diseases Outbreak Response;
Manual For Clinical Specimen, RITM 2013
Note: RITM Manual is currently being revised. The above flow chart may change accordingly.
61
4.1.3.1 Requirements for Referral
RITM “Manual for Clinical Specimen”, set the following requirements for
specimen referral. The three categories of requirements should be complied by
the referring facility.
Category 1: Specimen Requirement
This category refers to requirements in specimen collection wherein efforts are
exerted to maintain the integrity of the specimen.
Specimen Quality Ideally the specimen should be freshly and aseptically collected;
Should be collected before administration of antimicrobial therapy;
The specimen should be in an appropriate transport media;
Specimen Storage The temperature inside the specimen container depends on the type of
test that will be performed and the sensitivity of the organism to
extreme of temperature;
If the type of test requires a viable organism in the specimen, then the
temperature during storage should be ideal for the growth of the
organism;
Appropriate transport media should be used if a viable organism is
required by the test procedure
62
Box 3: Requirements for Proper Specimen Packing
Specimen Label The specimen should be properly labeled with the following information
b) Age/Sex;
c) Specimen Type;
The tables were taken from the Guidelines for Specimen Collection, Transport and Referral For
Infectious Disease Outbreak Response. Manual for Clinical Specimens, RITM 2013
The above picture is taken from the Guidance on Regulations for the Transport of Infectious
Substance 2017-2018. Geneva Switzerland, WHO;2017 License: CC-BY-NC-SA 3.0 IGO
63
Category 2: Document Requirement
All clinical specimens should come with the corresponding documents to provide
identification and minimize specimen loss. Box 3 provides the proper required
documents for specimen during outbreak investigation.
The tables and picture were taken from the Guidelines for Specimen Collection, Transport and
Referral For Infectious Disease Outbreak Response. Manual for Clinical Specimens, RITM 2013
Reminder:
64
Category 3: Communication/Coordination Requirement
Notification of Testing Inform the testing laboratory of patient and sample details through
Laboratory of Shipment the required accompanying documents for referred specimens
Acknowledgement of Ensure that the testing laboratory acknowledges the receipt of the
Receipt of Samples by parcel
Testing Laboratory
Acknowledgement of Ensure results are received on the expected date of release of results,
Receipt of Results by which would be based on the turn-around time of the requested test
Referring Institution
Source: Guidelines for Specimen Collection, Transport and Referral For Infectious Disease Outbreak
Response. Manual for Clinical Specimens, RITM 2013
65
4.1.3.2 Criteria for Rejection of an Outbreak Specimen
Source: Guidelines for Specimen Collection, Transport and Referral For Infectious Disease Outbreak
Response. Manual for Clinical Specimens, RITM 2013
66
Criterion 2: Non-Compliance with Documents Requirements
This happens when the submitted documents are incomplete or the information
in the document are incomplete. If this happens, the staff of the testing
laboratory shall withhold the release of the results until the missing information
is completed or clarified by the referring institution. The laboratory staff shall
also communicate to the referring institution that it may lead to delays in the
results due to incomplete specimen information.
67
4.2 Food Laboratory
68
4.2.3 National Meat Inspection Service
NMIS performs microbiological tests on suspected fresh, chilled, frozen, local
and imported meat and meat products as food vehicles for FWBD. Any positive
findings should be reported to EB.
69
Section V:
Surveillance
and Outbreak
Response
This section discusses the:
Surveillance
Outbreak Response
Detecting the Outbreak
Outbreak Investigation.
EB is currently revising its MOP for PIDSR.
Reporting forms and processes may change
after the approval and dissemination of this
MOP. The revised guidelines from EB will
take precedence over those currently
included in this MOP.
70
5.0 Surveillance and Outbreak Response
5.1 Surveillance of Human Cases
5.1.1. Definition
Surveillance is a core public health function. It is the continuous and systematic
collection, analysis, and interpretation of health-related data needed for planning,
implementation and evaluation of public health practices.
71
5.1.3. Uses of surveillance and response to FWBD
1. Monitor trends of syndromes that might indicate foodborne illnesses;
2. Detect and respond to foodborne events to allow rapid implementation of
control measures;
3. Establish a culture of systematically collecting information from foodborne
event investigation to begin to identify high risk food items and hazards;
4. Guide to policy development and for monitoring and evaluation
5.1.4 Policies
Food and water-borne diseases should be detected and notified because under
the International Health Regulation (IHR) 2005, these are considered
international public health threats. Under the Philippine law (Republic Act
3573), some food and waterborne diseases are included in the list of
communicable diseases that should be reported by all individuals and health
facilities.
72
5.1.5 Structure
Disease surveillance for food and water-borne diseases is included in the
existing Philippine Integrated Disease Surveillance System and Response
(PIDSR). PIDSR is under the Public Health Surveillance and Informatics Division
of Epidemiology Bureau.
Food-borne events can also be detected through the Event Based Surveillance
(ESR). Event-based surveillance is the organized, unstructured capture of
information on new events that are not included in the indicator-based
surveillance; events that occur in populations which do not access health care
through formal channels; rare, unusual or unexpected events. ESR describes
illnesses and deaths occurring in individuals or clusters or those related to
potential exposures that threaten public health. ESR is on the Applied
Epidemiology Health Management Division of Epidemiology Bureau.
The program is concerned with cluster of diseases or syndromes captured by ESR
wherein the symptoms occur after the intake of food and water contaminated
by microorganisms (bacteria, viruses, protozoans and foodborne helminths).
Food and water-borne diseases are also reported through the PIDSR wherein
aggregated data of food and water-borne diseases or syndromes are reported on
a weekly basis. The diseases or syndromes are reported through structured
channels and follows criteria (case definition) in order for such diseases to be
counted.
73
5.1.6. Detection, Reporting, Analysis and Interpretation of FWBD
data
What is the role of FWBD-PCP in surveillance activity?
The importance of surveillance to the FWBD-PCP has been clearly stated in
section 5.1.3 (page 74). Thus, a reliable, timely and quality surveillance data is
needed. The FWBD-PCP should facilitate/assist in the timely collection of PIDSR
reports. Regional FWBD coordinators can work with RESU/PESU/CESU/MESU
in the collection of surveillance reports during their supervisory visits. The flow
of surveillance report as stated in the PIDSR MOP is shown in Annex O. The
algorithm of the surveillance report flow is shown in this manual for the FWBD
Regional coordinator be familiarize with the flow and type of reports to be
collected.
5.1.6.1 Detection
Each disease under surveillance has a standard case definition to allow data
consistency across all reporting units and ensure accurate tracking of a disease
or syndrome. Case definition is a set of criteria that is used to determine if a
person has a disease, syndrome or condition and if a case should be included in
reporting and investigation (MOP, PIDSR). Cases are further classified into a
suspect case, probable case and confirmed case. A suspected case is a case
presenting indicative clinical picture without being a confirmed or probable case.
Probable case is a case with clear clinical picture or linked epidemiologically with
a confirmed case. A confirmed case is a case verified by laboratory analysis
(MOP, PIDSR).
Food and water-borne diseases that are included in the national surveillance
system are described in Annex P. This information can be useful for health
facilities in analyzing their data and in investigating food and water-borne
outbreaks in their locality.
Cases can be detected in the community, health facilities (barangay health
stations, Rural health unit, city health office, hospitals, private health providers
and school clinics). Cases are detected from the clinical manifestations of the
patients and good history taking.
Laboratory testing is needed in confirming specific etiologic agent of a food and
water-borne disease. Ideally laboratory confirmation for a food and water-borne
disease should be done (depending in availability of resource) routinely.
However, this is dependent on the capacity of
74
the laboratory in the area. Based on the clinical diagnosis, the appropriate
specimen should be collected. Refer to Section 4.1.3.1 (pages 48-52) under
Laboratory services, the Summary guide for specimen collection.
5.1.6.2 Reporting
Like in case detection, surveillance data reports come from the DRUs (BHS,
RHUs). There are two source documents for food and water-borne diseases are
the weekly notifiable disease reporting and the case report form (Annex Q):
1. Weekly Notifiable Diseases Report Summary Page – It serves as the summary
table for the weekly reporting of notifiable diseases. It also shows the category
and frequency of reporting of all the notifiable disease included in the PIDSR;
2. Case Report form – It is a disease specific report form that should be filled up
by the DSC for diseases/syndromes under Category II)
The following section provides practical steps for health facility staff in processing
their surveillance data. Surveillance data is useful if it is processed and use for
decision making. The main user of surveillance data is the facility where the data
emanates. Thus, health facility should be able to process their own data.
5.1.6.3 Analysis
For the disease surveillance system to monitor trends of a disease and detect
clustering of cases, surveillance data should be analyzed regularly. Ideally each of
the data reporting unit should analyze their data. Whether the basic analysis will
be done manually or through a data base program, DRU should check on the
completeness, accuracy and consistency in the data collected. Analyze the data
in terms of time, person and place.
75
a. Analyze Data by Time
Presenting no. of cases reported by specific time period (by weeks; by months;
or by years (Figure 10)
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b. Analyze Data by Person
77
Box 6 How to calculate annual notification rate
1. Extract the number of diarrhea notification each year over the past
five years from your surveillance data.
2. Obtain the population estimate each year over the past five years.
3. Put the data in a table and ensure there is a title in each column as shown below.
Note: The numbers above do not pertain to an actual data of a particular locality.
The numbers are used to illustrate calculation of notification rate.
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c. Analyze Data by Place
Place analysis is examining the data by place where the disease condition
occurred. Maps are commonly used to graphically represent the data and
provide other important information obtained by analyzing data by place:
1. Areas with highest rates of the disease being described are easily identified
which can facilitate in finding the causes and instituting intervention;
2. Characterize the population involved in terms of density and distribution;
3. Existence of health facilities (hospitals, clinics, BHS, RHUs) that can be used
for management and treatment of cases; emergencies; or evacuations;
4. Presence of environmental resources (rivers, lakes, dams, streams, land
forms and vegetation) that maybe useful in the analysis of the disease
condition.
A spot map should show all important structures such as school, resorts,
food establishments. Figure 12 below demonstrates a spot map of showing
the distribution of diarrhea cases and deaths across the geographical area.
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5.1.6.4 Interpretation
In interpreting the data, compare the present data with previous weeks,
months or years and note if the number of notified cases or deaths of a
specific food and water borne disease or syndrome shows an increasing,
decreasing or stable trend. Then determine if the threshold for action
has been reached for a certain disease or syndrome. Thresholds are
indicator when something should happen or change and serves as a
decision guide as to when and what actions to be taken
Alert threshold refers to the level of a disease occurrence that serves as
an early warning for epidemics. An increase in the number of cases above
the alert threshold warrants an investigation, check epidemic
preparedness, and implement appropriate prevention and control
measures. Calculation of alert threshold is shown in Box 7.
In summary, the responsibility of surveillance (for human health)
activities can be shared across different agencies as shown below.
Office/Person Tasks
EB Consolidates report
Provides weekly report to FWBD Program Manager
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81
5.2. Other Surveillance System Related to FWBD
Animal Health surveillance and water quality surveillance are also important component of
FWBD-PCP. The systems are lodged in their respective agencies, but any positive findings shall
be reported to EB or to their respective RESU/PESU/CESU.
Administrative Order No. 2017-0100 (Philippine National Standards for Drinking Water
of 2017) provides the standards and procedures on drinking water quality to protect
public health. The policy covers all drinking water service providers including
government and private developers and operators. Only laboratories accredited by
DOH shall perform quality examination for drinking water. The East Avenue Medical
Center is the National Reference Laboratory for water quality surveillance.
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5.2 Outbreak response
The FWBD-PCP Regional program coordinator should be part of the EICT during an
outbreak investigation and response activity. The Regional Coordinator should mobilize
the provincial designated FWBD coordinator and assist in the investigation and
institution of control measures. The Regional FWBD Coordinator should coordinate with
the National FWBD Program Manager for any logistical needs (rehydration fluids and
drugs) during the outbreak. He/She should follow-up the provincial FWBD coordinator
on the actions taken regarding the recommendations to prevent similar outbreaks.
The FWBD Program Manager provides logistical support (antibiotics, rehydration fluids,
IEC materials) during the outbreak response. He/She should facilitate mobilization of
resources through coordination with other national agencies if needed. He/She should
ensure the FWBD Regional Coordinator is actively providing support during outbreak
response. Using the learnings from outbreak response reports, he/she should lead the
discussion in the Technical Working Group of problems/issues encountered during
outbreak response and agrees on actions for stronger collaboration at the local level.
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Who confirms and how to confirm an outbreak?
The physician or the nurse in the health facility should investigate to confirm the
existence of an outbreak through:
Compare the current number of cases with the previous weeks, months or year
to determine if the alert threshold has been surpassed;
Mapping of cases and observe whether there is clustering in certain
sitios/villages or barangay;
Determine the magnitude of the illness. Check with the Provincial Health office
and nearby hospitals or clinics for similar cases or number of deaths reported
from possible waterborne or foodborne related events;
Check for other events prior to sudden increase of diarrhea cases such as big
events (weddings, burials), flooding
Check laboratory results of suspected cases for confirmation of diagnosis
The Local Chief Executive can declare an outbreak as mandated by the Local
Government Code of 1991. The declaration of an outbreak should be supported by
surveillance data and the above steps for confirming the outbreak has been done
thoroughly.
However, PIDSR MOP states the provision of the DOH Rules and Regulations
Implementing the Local Government Code of 1991 (DOH RRILGC of 1991), Chapter
11, Section 44 c, as follows the Department of Health has the final decision regarding
the presence of epidemic, pestilence, or other widespread public health danger in a
particular area or region. In compliance to this rule, the Secretary of Health shall
have the sole authority to affirm or reverse any declaration of an epidemic
EB as the IHR focal office shall take the lead in the investigation of epidemics of
national and international importance, in coordination with the CHD, local
government unit, and other concerned agencies. The Secretary of Health shall have
the sole authority to declare epidemics of national and/or international concerns.
Annex R enumerates conditions of national or international concern.
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5.2.3 Food and water-borne outbreak investigation
Decrease the number of people affected and prevents death by limiting the
further spread of the illness/disease;
Determine the cause and institute measures to mitigate the risk of recurrence;
Information obtained from identifying the cause and risk factors are crucial in
improving the existing preventive and control measures for all partners
involved in the program;
Outbreak experience and information obtained during actual investigation
activities will be helpful in preparing similar outbreaks in the future;
85
Fig. 13 Flow of Investigation, Reporting and Response to a
Suspect/Reported FWBD Outbreak
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5.2.3.1 Determining Authority and Responsibility
In a FWBD outbreak (local), the authority resides in the Local Chief Executive
(LCE) as mandated by the Local Government Code of 1991. The LCE appoints the
MHO/CHO, as the head of the health unit in the area, to lead a team (local staff
and experts) in the investigation. He has the authority to mobilize resources,
coordinate with other local agencies during the investigation and
implementation of control measures. He/She is also responsible in
communicating with the CHD, EB in relation to the said outbreak. The
MHO/CHO is also accountable to carry out the directives of the Local Chief
Executive regarding outbreak.
The Epidemiology Bureau (through the RESU/PESU/CESU), Food and Waterborne
National Program Manager(role) or the Regional FWBD Coordinator, RESU or the
Provincial Health Office should provide assistance to the local government unit
during outbreak investigation and response. The assistance can be in three
forms: a) Logistics (supplies, equipment, IEC materials etc); b) Technical advice
(verbal or written guidance); c) technical assistance (investigation team, experts
or consultants who will go to the field and assist in the investigation or with the
control measures); and d) laboratory back-up.
However, EB will lead the outbreak investigation in cases wherein the outbreak is
of national and international concern. Likewise, HEMB will be
notified/mobilized in situation of human crisis/emergencies.
87
Personnel from agencies working on animal health such as meat
inspectors/DA/BFAR staff);
Sanitary officers/inspectors/engineers;
The EICT members should have a clear understanding of their roles during the
epidemic investigation and response. Reporting lines should be set prior to
actual field investigation. As stated in the PIDSR, the core function of the EICT is
listed in Annex S.
5.2.3.3 Communication
After the declaration of the epidemic and until the epidemic has been declared
as over; stakeholders, media, health workers and other people with interest on
the epidemic should be informed on the progress of the investigation, interim
results and actions taken to control the epidemic. Thus, it is important during
the preparation phase to discuss the communication process. Any
communication on the outbreak should be cleared by the Team leader
(MHO/CHO) to ensure information are accurate and consistent. The MHO/CHO
may designate the Nurse (PHN) as the point person for any update or report for
consistency and mitigating the risk of miscommunication or conflicting
information. Table 13 provides the purpose and methods of communication
across the different audience groups
Audience
Purpose of Communication Method of Communication
Group
Health To ensure accurate case finding Established communication channels-such
Authorities and as regular meetings, briefer or reports
other To facilitate the implementation of
government control measures
stakeholders
To inform partners in other
administrative areas who may benefit
from the information about the
epidemic and may be able to provide
additional information about similar
outbreaks
To ensure government officials are
updated about the status and progress
of the investigation
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Health Care To ensure accurate case finding Regular meetings
Providers
To facilitate the implementation of
control measures
People directly To respond to concerns Method of communication will depend on
affected by the the local situation, but may include
outbreak To provide advice on personal hygiene contacting those affected by:
measures to reduce the risk of person- - phone, mail
to-person spread - face-to-face meetings
The public To provide accurate information about Method of communication will depend on
the epidemic the local situation, but may include:
- regular press releases via newspapers
To provide accurate information on - radio or television announcements
implicated food and how they should be - leaflets delivered to households and
handled public gathering places
- face-to face advice in clinics
To provide advice on personal hygiene - messages displayed on notice boards
measures to reduce the risk of person- and shared with consumer groups
to-person spread
To inform the public about avoidance of Arrange a specific time to meet with the
risk factors for illness and about media. This may involve daily briefings.
appropriate preventive measures
Ensure that information provided is timely,
To maintain public and political support accurate and consistent
for disease investigation and control
Ensure that information released to the
To minimize the appearance of media has been authorized by the EICT
conflicting information from different
authorities (which may undermine their
credibility)
Source: Strengthening Surveillance of and Response to Foodborne Diseases: A Practical Manual. Stage 1:
Investigating Foodborne Disease Outbreak; WHO 2017,
89
5.2.3.3 Logistics
All logistic requirements should be prepared which includes: a) transportation of
the team to conduct environmental investigation and interview of patients and
collection of specimens; b) transportation of specimen to the laboratory; c)
packing boxes for specimens; d) material for specimen collection and water
collection for water analysis; e) ORESOL and other rehydrating fluids; f) IEC
materials; g) antibiotics for treatment of patients.
The FWBD-PCP Program Manager through the FWBD Regional Coordinator will
provide the rehydrating fluids (ORESOL), antibiotics (if needed) and IEC
materials. The transportation cost of EICT members from the regional/national
staff will be charged under their sending agencies as include in the AO. The LGU
may provide other logistics in the implementation of control measures such as
transportation costs in the chlorination of water sources.
All records on the investigation of the FWBD outbreak will follow the provision of
the data privacy law. The following are some suggested documentation records:
90
5.2.3.5 Identifying the point of contamination
a) Identify the source and distribution of foods so that the public is alerted and
the removal of the contaminated production from the market place (product
recall;
b) Compare the distribution of illnesses and of the product in order to
strengthen a suspected epidemiological association;
c) Determine the potential route or source of contamination by evaluating
common distribution sites, processors, growers
91
Food trace back process requires coordination of many investigators from
different agencies and organizations. It entails a detailed review of dates,
quantities, source and conditions of food received, information on lot
number, facilities involved and production dates.
92
An assessment of the toilet facilities and sewage disposal system;
Measurement of temperatures in refrigerators or food and pH and water
activity of food using appropriate equipment
A) Food samples:
The sampling of food for laboratory analysis of microbial agent should be
guided by the epidemiologic and environmental investigations. However,
if an implicated food has not been identified, several sample foods
maybe collected and stored for future laboratory testing after more
information becomes available. Food samples that may be appropriate
for sampling and testing includes (in order of importance):
Leftover food from the suspected meal;
Ingredients that were used in the implicated food;
Food from the menu that was associated with the outbreak
epidemiologically;
Food that is associated with suspected pathogen;
Food in the environment that may have nurtured the growth or
survival of the pathogen
93
If a packaged food is implicated as the culprit in an outbreak, it is
essential to collect unopened package (ideally from the same batch). It
may help determine the time of contamination (if before or after the
preparation period). Also collect samples of the ingredients or raw
materials.
The EICT should closely coordinate with the laboratory for appropriate
sample size; collection process; storage and transportation.
B) Environmental samples:
Environmental samples are collected to trace the source and evaluate the
extent of contamination that led to the outbreak. Environmental
samples should be taken from work surfaces; food contact surfaces of
equipment, containers and other surfaces such (refrigerators, door
handles); and water used for food processing.
94
5.2.4.2 Controlling the transmission
After the outbreak, there should be a structured review with all the people
involved in the outbreak response. A debriefing should be done to a) ensure the
control measures instituted were effective; b) identify resource needs, structural
changes, needed improvement in the outbreak response for future outbreaks; c)
identify factors that compromised the investigation and discuss solutions; d)
discuss legal issues that arisen; e) update current guidelines if needed.
95
Section VI:
Health
Promotion and
Communication
The content of this section:
General Guidelines
Basic Concepts
Risk Communication
Communication plan
Other advocacy materials
96
6.0 Health Promotion and Communication
6.1 General Guidelines
97
6.2 Understanding Basic Concepts
6.2.1 Health promotion
It is important element of disease prevention
program as it empowers individuals and Health promotion the process of enabling
communities to make better choices and people to increase control over and
reduce their risk of developing the disease or improve their health focusing not only in
a disability. Health promotion and disease the individual behavior but also the social
prevention programs often deals with the and environmental interventions
social determinants of health which influence Source: WHO
changeable risk behavior (RHI Hub).
Social determinants of health are the circumstances in which people are born, grow up,
live, work and age and the systems put in place to deal with illnesses. These
circumstances are in turn shaped by a wider set of forces: economics, social, policies
and politics (WHO). As these social determinants had been with individuals throughout
their life, it had influenced their habits and practices which to some extent became
barriers to health.
98
Figure.15 Communication Approach Through IEC
Thus, it did not translate to change in behavior; because long term behavior change
involves several stages. This is the core principle of Behavior Change Communication.
99
According to BCC, people and communities maybe in the different stages of change when they
received or hear the information and these affects how people respond to it. For change in
behavior to occur, the health worker needs to understand the various barriers and addressed
them. Understanding the different stages of change (Fig. 16) will help us understand our
audience so we can tailor the message and determine the right time to deliver the message. It is
important to remember that change is slow process.
100
A person may enter and leave these five stages anytime. For some individuals, it will take time
to get in the maintenance stage. For people to maintain their new health behavior, there should
be:
a) Supportive environment:
Supporting change at the individual level – developing the skills of the person so
they can adapt the new healthy behavior (informing the mother the array of
health services available in the facility). It is important for the health worker to
understand that there are certain factors that is beyond the person’s control
and may affect his decision to make the change. Thus, it will be helpful to still
provide support and consistent follow-up until the person’s condition improves.
Supporting change at the community level – looking at the total social and
community environment (presence of community volunteers and community
meetings;
Promoting change at the government level (policies, resources that enable and
encourage behavior change (accessibility of services even in the far-flung sitios
101
Reassure the audience (reduce anxiety and manage outrage);
Improve relationships (build trusts, cooperation and networks);
Involve actors in decision making;
Enable mutual dialogue and understanding
These goals should be monitored and assessed the changes in knowledge, behavior,
and practice. Unmonitored outcome leads to ineffective risk communication
messages; consumes and waste resources and create a false sense of achievement.
Identify affected or potentially affected population (the target audience for the
messages): The population most vulnerable to the suspected disease for the
outbreak.
Identify behavior factors that might place the person at risks: Observe or conduct
one-on-one/group dialogue to identify existing behavior that put persons at risk
(buying from street food vendors, drinking water from doubtful sources).
Identify partners that can help in reaching affected persons or populations: These
can be community volunteers, community leaders, faith-based organizations. Also
identify the appropriate time to engage and orient them.
102
Identify perceptions in the community that might affect communications in an
outbreak situation: Engage in a dialogue and understand how the local authorities,
affected people and community leaders perceived the current situation. Listen to
the concern and fears of the community. Consider the language, culture and socio-
economic factors in the community in making the messages. Tailor
recommendations in plain language that can be easily adhered to by the affected
population.
6.3.2.2. Identify and explain the public health threat – the disease: Provide
information about the disease/cause of the event; who is at risk and factors that put
a person at risk. Provide advice on actions to be taken to lessen their risk of getting
the disease or where to go when a family member shows signs of the illness. Provide
facts.
6.3.2.3. Explain what is currently known and unknown: Provide details of what
specific information is available. Acknowledge if information is not yet available but
provide specific timeline for providing updated information.
6.3.2.4 Explain what health actions are being taken and why: Describe in brief but
clear terms the agencies involve in the response, their roles and actions that are
taken.
103
Figure.17 Risk Communication During the Different Phases of an
Outbreak
104
105
MANUAL OF PROCEDURES
This information can be obtained from reviewing records and reports as well as through
interviews, community consultations. To be able to formulate your behavioral
objectives, you need to identify the vulnerability and risk in your community.
Vulnerability is about a person not having the power or ability to make choices or to act
on them. This can often be because of a person’s situation within the community – the
social environment. Families in rural communities whose source of drinking water are
open deep wells or hand pump that are usually submerged in floods during rainy season
are examples of vulnerabilities. Or families with no sanitary toilets and practicing open
defecation. Risk is an attitude or behavior that put a person at risk of a specific disease
such as students buying from street food vendors or not practicing proper handwashing.
:
Box 9: Activity 1 for Communication Plan Development
1. Start listing any vulnerable groups in your community such as school children,
out of school children, IPs, resettlement sites, urban poor communities;
2. List also the existing behavioral factors in your communities that put people at
risks for FWBD (poor personal hygiene, open defecation, rampant small-scale
food vendors -street foods);
3. List of existing environmental factors such as:
- Type of drinking water source in the community (point source,
communal faucet system, waterworks system0;
- Presence of small-scale food vendors/markets
MANUAL OF PROCEDURES
With your situational analysis, identify your target audience. An audience is the group of
people you are trying to reach with your communication plan. Breaking down all possible
target audience and the existing risks and opportunities may help you define a more concrete
communication objective. There are two types of target audience: a) Primary are people you
would like to reach and change their attitudes and behaviors; b) secondary are people who
may/can influence the primary audience. Activity 2 may guide you on how to do this.
You may need to gather more information about your audience to identify the barriers and
opportunities. You can gather this information by interviewing health workers (who know the
profile of the community); visiting and interviewing teachers and school administrators;
Interviewing community leaders; and conducting focus group discussions. Sometimes you may
need to segregate your target audience (Children: school children and out of school children;
mothers: working mothers and housewife). This information may also influence your strategy,
Secondary audience is important because they provide support and influence to the
primary audience. They are sometimes called “gatekeepers” of primary audience
as they provide leadership, shape opinions and impact on access to services and
resources. (Pacific BCC Manual).
Continuing from your listing your different target audience, their risk/barriers and
opportunities. You can then identify the priority target audience and what behavior of
your target group you need to change. It is important to keep in my mind that it is
better to focus on a few audience than trying to address all as it may be difficult for you
to track it later.
Your communication plan should align with the goal of the national program – reducing
the morbidity and mortality due to food and water-borne diseases. However, your
communication plan objective should address the problem you have identified in your
situational analysis. Achieving your objective will then lead in reducing cases and death
due to food and water-borne diseases in your locality.
Appropriate: Are your objectives relevant to the program goals? Can the issue or
problem actually be addressed by communication?
Realistic: Is it possible to achieve your objective? Can you actually reach your
target audience? Do you have enough manpower and funding to
reach the number of people within the given timeline?
Timebound: For how long do you expect to implement your plan? Is this period of
time realistic to achieve your objectives?
Source: Pacific BCC Manual
a) Building Healthy Public Policy: are intended for local government officials (policy
makers). It may require advocacy strategy and activity that will lead to the
development and issuance of policy instruments (local issuances, ordinances,
administrative order, memorandum of agreement) that will support implementation
of preventive measures for food and water-borne diseases.
b) Creating a supportive environment: can be both physical (making services more
accessible) or organizational (creation of networks, inter-agency committees and
alliances to multiply the number of people promoting particular health actions. Your
audience needs to be linked with products and services that will reinforce their
change in behavior and practices.
MANUAL OF PROCEDURES
Annex T is the FWBD communication plan at the national level. This may serve as a
guide for you in developing your local communication plan.
6.5 Other Advocacy materials
In public health, we need to advocate either to the local decision-makers for support in
resources or the issuance of local policy or ordinances that will strengthen the
implementation of the program. We may also advocate to other funding institutions or
community leaders. Most of the time, we advocate by meeting with these people of
influence. However, it will be helpful if we have materials that can help bring our
message to the table and influence decision makers.
111
MANUAL OF PROCEDURES
Section VII:
Other
Programmatic
Functions
Under this section are other programmatic functions such:
Policy Development
Capacity Building
Monitoring and Evaluation, Research
MANUAL OF PROCEDURES
Abbigail J., Tumpy D. and Glen N.; Communicating During an Outbreak or Public Health
Investigation; Field Epidemiology Manual, CDC
Advocacy Reference Manual, Asia Pacific Executive Matrix
Burden of Food-borne Diseases in the South East Asia Region, WHO Regional Office for SEA;
2016
Creating an effective Communication Project in the Pacific Region for HIV/STI and Other Sexual
and Reproductive Health Projects, Secretariat of the Pacific Community 2008
Communicable Disease Epidemiologic Profile, WHO, Geneva, Switzerland 2009
2017 Food and Water-borne Diseases; Morbidity Week (MW1-MW48); Epidemiology Bureau
Gaya Ganhewage, An Introduction to Risk Communication, 2014
Georg Kaperrud, Outbreak of Food and Water-borne Diseases: Guidelines for Investigation and
response, September 2018.
Guidance on the regulations for the Transport of Infectious Substance 2017-2018. Geneva
Switzerland; WHO, 2017 Lic. CC-BY-NC-SA 3.0 IGO
Guidelines for Specimen Collection, Transport, and Referral for Infectious Disease Outbreak
Response, Manual for Clinical Specimen. RITM 2013
Guidelines for the Collection of Clinical Specimen During Field Investigation of Outbreaks, WHO,
Department of Communicable Disease Surveillance and Response
Health Promotion, National Malaria Program: Manual of Operation, Department of Health,
Philippines
Managing Epidemics: Key facts about major deadly diseases, Geneva: WHO 2018, CC BY-NC-SA
3.0 IGO
Manual of Procedures for the Philippine Integrated Disease Surveillance and Response;
Epidemiology Bureau, Department of Health 2007.
Manual of Procedures For The Surveillance, Outbreak Investigation and Response to Microbial
Agents of Food and Water-borne Diseases, Research Institute of Tropical Medicine, Department
of Health; 2007
National Strategic Plan 2017-2020, Food and Water-borne Disease Program
Philippine National Standards for Drinking Water, Department of Health
115
Philippine National Aedes-borne Viral Diseases Prevention and Control Program, Manual of
Procedures, Volume 5: Health Promotion
Strengthening Surveillance of and Response to Food-borne Diseases: A Practical Manual.
Introductory Module. Geneva: World Health Organization; 2017 Lic.CC BY-NC-SA 3.0 ICD
Strengthening Surveillance of and Response to Foodborne Diseases: A Practical Manual.
Strengthening Indicator-Based Surveillance Module. Geneva: World Health Organization; 2017
Lic.CC BY-NC-SA 3.0 ICD
Strengthening Surveillance of and Response to Foodborne Diseases: A Practical Manual.
Investigating Foodborne Disease Outbreak Module. Geneva: World Health Organization; 2017
Lic.CC BY-NC-SA 3.0 ICD
WHO Estimates of the Global Burden of Food-borne Diseases, WHO 2015.
WHO Fact Sheets For Cholera, Hepatitis A, Typhoid Fever and Rotavirus
Https://www.ruralhealthinfo.org/toolkits/health-promotion
116
Annexes
117
Annex A: Policies and Guidelines For the National Control of Diarrheal Diseases
118
Annex B: DOH Organizational Structure of Disease Prevention and Control Bureau
119
Annex C: Findings of the Assessment
Strategy 1. Regulate and monitor food and water sanitation practices at the local level through enforcement of national and
local legislations, application of appropriate technical standards and participation of non-government agencies.
Implementation There is a robust set of laws and policies that support food and water sanitation practices in the country.
Status 2012. RA 10611 on Food Safety Act to strengthen the food safety regulatory system in the country
to protect consumer health and facilitate market access of local foods and food product
2000 RA Act 9003. providing for an ecological solid waste management program, creating the
necessary institutional mechanisms and incentives declaring certain acts prohibited and providing
penalties, appropriating funds therefore and for other purpose
1975 PD No. 856 Code of Sanitation of the Philippines
o Due to the absence of data (full scale policy review) relative to the implementation of the above
policies, the extent of compliance and adherence to these laws and policies cannot be fully
ascertained.
Strategy 2. Sustain inter-agency collaboration to fast-track sanitation infrastructure development in poor urban areas and in
rural areas with low access to safe water and sanitation facilities.
Implementation Established Interagency Committee on Environmental Health with sub-task forces on Water, Solid
Status Waste, Toxic Chemicals and Occupational Health
Strategy 3. Promote personal hygiene, food and water sanitation practices and the principles of environmental health.
Implementation 90% of HHs have access to safe water (2015)
Status 86.7% of HHs with sanitary toilets (2015)
No data available to establish extent of personal hygiene practices
Strategy 4. Promote the use of ORS in the management of diarrhea to prevent dehydration, especially among infants and
children.
Implementation ORS continues to be the primary intervention of children with diarrhea as shown by the 2015 FHSIS
Status Reports that 100% of diarrhea cases were given ORS.
However, facilities visited are already without ORT Corners
Likewise, some health facilities have inadequate supply of zinc
120
Strategy 5. Promote breastfeeding and other good feeding practices for infants and children.
Implementation The 2013 NDHS showed that bottle-feeding is relatively still common in the Philippines with 27% of infants
Status under age two months being fed using a bottle with a nipple.
Strategy 6. Continue training of health personnel in the early diagnosis and treatment of food-borne and water-borne
diseases.
Implementation No training has been conducted on the early diagnosis and treatment of FWBDs; the clinic practice
Status guidelines are still currently being finalized which will be packaged into a Training Module for both hospital
and public health facility staff
Strategy 7. Continue nationwide information campaign for the prevention and control of food-borne and water-borne
diseases.
Implementation No nationwide information campaign has been designed and mounted on the prevention and
Status control of FWBDs in the past 6 years
121
Annex D: DPO on the Creation of Technical Working Group, Expert Panel and Steering
Committee For the FWBD-PCP
122
123
124
125
126
Annex E: IHR Provision Stating the conditions for Reporting FWBD cases/events
127
128
Annex F: Guidelines on Rotavirus and cholera vaccination
129
130
131
132
133
134
Annex G: Summary of Roles and Responsibilities of Laboratories at Different Levels of Service Capability
135
136
Annex H: General Guidelines on Specimen Collection
Safety and decontamination measures protects the specimen collector, laboratory staff and the
patients from risk associated with specimen collection. Universal safety precaution requires
health personnel to handle all clinical specimens as infectious. Thus, the use of basic protective
equipment such as gloves, masks and eye protection. Safety work practices, such as
handwashing before and after specimen collection; wearing of protective clothing at work
places; disinfection of work areas and decontamination of blood spills and other bodily fluids,
should be followed to reduce exposure to potentially infective material
General provisions for specimen quality and quantity has been described in B.1.1 Specimen
Requirements for Referral of outbreak specimen.
If possible, all specimens should be in appropriate transport medium (e.g., VTM for viruses and
Cary and Blair TM for bacteria causing diarrhea). Specimen should be placed aseptically in a
sterile and/or appropriate container. The outside of the specimen container should always be
cleaned and decontaminated. The type of container to be used is based on the clinical
specimen as follows:
Liquids should be contained in a leak-proof, screw capped container with a
capacity of less than 1 liter;
Solids must be stored in a sift-proof container weighing less than four
kilograms;
In order to preserve the bacterial viability or viral integrity of microorganisms in specimen for
culture or inoculation, specimens should be placed in appropriate transport media and stored
at recommended temperatures. These conditions should also take into consideration the
transportation time of the specimen. Other factors should also be taken into consideration
137
such as the type of specimen, the pathogen, and the sensitivity of the pathogen to desiccation,
nutrient and ph.
Clinical specimens for viral isolation are acceptable for culture even after two days if it is stored
in a specific media at 4-8 degrees Celsius. For longer period, preserved at -70 degrees Celsius.
For bacterial culture, specimen should be kept in appropriate transport medium at
recommended temperature. Except for urine and sputum, most specimens maybe kept at
room temperature if processed within 24 hours. For longer periods, store it at 4-8 degrees
Celsius is advised except for cold sensitive organisms such as shigella.
138
Annex I: List of International Laws for Transporting Dangerous Goods
Air The Technical Instructions for the Safe Transport of Dangerous Goods by Air
published by the International Civil Aviation Organization (ICAO).
The International Air Transport Association (IATA) publishes Dangerous
Goods Regulation (DGR) that incorporates the ICAO provisions. The ICAO
rules apply on all international flights.
For national flights (within one country), the national civil aviation authorities
apply national legislation.
Road The European Agreement concerning the International Carriage of Dangerous
Goods by Road (ADR) applies to 49 countries. Modified versions of the
convention are being used in South America and South East Asia
Post Letter Post Manual published by the Universal Postal Union reflects the
United Nations Recommendations using the ICAO provisions as the basis for
shipment
Source: Guidance on the Regulation for the Transport of Infectious Substance 2017-2018. Geneva,
Switzerland, WHO;2017
139
Annex J: List of Microorganisms Considered Under Category A Infectious Substance
140
Annex K: UN Number and Proper Shipping Name
Assignment to UN2814 or UN 2900 shall be based on the known medical history and
symptoms of the source human or animal, endemic local conditions, or professional
judgement concerning individual circumstances of the source human or animal.
Source: Guidelines for Specimen Collection, Transport and Referral For Infectious Disease
Outbreak Response. Manual for Clinical Specimens, RITM 2013
141
Annex L: Example of Hazard and Handling Labels
Source: Guidance on the Regulation for the Transport of Infectious Substance 2017-2018. Geneva,
Switzerland, WHO;2017
Hazard label for liquid nitrogen; substances packed using liquid nitrogen
142
Box 3: Example of Handling Labels (Annex)
Orientation label to indicate position of closures on the primary receptacles; for the air
transport of quantities of liquid infectious substance in Category A that exceeds 50 ml per
primary receptacle, this label shall be affixed to two opposite sides of the package with the
arrows pointing to the right direction
Cargo Aircraft (CAO) is used on packages that may only be transported on a cargo aircraft
143
Annex M: Forms for Communicating Laboratory Results of Specimen in an Outbreak Response
144
145
Laboratory Result Cover Letter Template
146
Annex N: Laboratory Referral Form for Outbreak Testing
Source: Guidelines For Specimen Collection, Transport and Referral For Infectious Diseases Outbreak Response; Manual For Clinical Specimen, RITM 2013
147
Annex O: Flow of Weekly PIDSR reports
Cases from
the
Community
Cases from
Regional level 3 and
Epidemiology and retained
Surveillance Units hospitals,
(RESU) ports, airports
Cases from
referral National
hospitals, Epidemiology
laboratories, Center
ports, airports
148
Annex P: Description of FWBD Diseases on Surveillance
Features Cholera Hepatitis A Rotavirus Typhoid and Paratyphoid
Etiologic Vibrio cholerae serogroup O1 Hepatitis A virus Rotavirus a double stranded Salmonella typhi
Agent and O139; biotypes Classical RNA virus which cause more
Salmonella paratyphi
and El Tor than 90% infections in
humans
Epidemiology Around 1.3-4 M estimated Globally, it is estimated that Rota virus are the most It is estimated that 11-20
cholera cases yearly with 1.4 M people are infected with common cause of severe M people get sick from
deaths ranging from 21,000 to Hepatitis A very year (WHO, diarrhea diseases in young typhoid fever and
143,000 worldwide. In 2016, 2014). And Hepatitis A caused children. In 2013, WHO between 128,000 to
the number of notified cases approximately 11,000 deaths estimates about 215,000 of 161,00 died from it (WHO
and deaths from 38 countries in 2015 accounting for 0.8% of under-five children die each Fact Sheet).
were 132,121 and 2,420 mortality from viral hepatitis year from rotavirus.
respectively (WHO Fact sheet) (WHO Global Health Report on Majority of these children In 2017, the country’s
Hepatitis). live in low income countries surveillance system
(WHO -Immunization, received a total of 21,653
In the Philippines, a total of Vaccines and Biologicals). typhoid cases and 40
3,653 cases of cholera was In country, a total of 422 deaths. This is 28% lower
notified in 2017 (January- Hepatitis A cases notified in than the cases notified in
December 2); with 27 deaths 2017; with one death In the Philippines, 3,512 2016 (29, 984). However,
(CFR=0.74). Out of the 3653 reported. This is 35% lower as cases were notified in 2017; the culture confirmed
cholera cases notified, 370 compared to the total notified with 27 deaths (CFR=0.77%). cases (345) is still 11%
(10%) submitted samples for cases in 2016. All regions have This is lower than the 2016 higher than the 2016 data
confirmation. Thirty-five notified cases of Hepatitis A. notified cases (4,718). Of reported
percent (130/370) were However, most of the cases the 3,512 cases notified,
laboratory confirmed cholera. came from Region VII 1,247 (36%) were laboratory
contributing 25% (109/422). confirmed.
All reported cases were tested
for Hepatitis A. And all
showed reactive for IgM anti-
HAV.
149
Features Cholera Hepatitis A Rotavirus Typhoid and Paratyphoid
Incubation Period Few hours to 5 days 15-50 days (average: 28-30 1-3 days Typhoid fever: 3-60 days (ranges
days) from 8-14 days)
Period of From onset of illness until recovery 1-2 weeks before and at least First 2-5 days From one week until the
communicability one week after onset of individual has recovered
illness
Case Definition: Suspected Case: Under the PIDSR, there is Suspected Case: A person with
case definition for Hepatitis. an illness characterized by
- A person aged 5 years or more insidious onset of sustained
with severe dehydration or Suspected Case: A person fever, headache, malaise,
who died from acute watery with an acute illness anorexia, relative bradycardia,
constipation or diarrhea, and
diarrhea (If diseases is characterized by acute non-productive cough.
unknown in the area); jaundice, dark urine, loss of
- For endemic area: A person appetite, body weakness, Probable Case: A suspected case
that is epidemiologically linked to
aged 5 years or more with extreme fatigue and high
a confirmed case in an outbreak.
acute watery diarrhea with or upper quadrant tenderness
without vomiting; Confirmed Case: A suspected or
Probable case: not probable case that is laboratory
- In area where there is cholera,
applicable confirmed through isolation of
a person with acute watery Salmonella enterica from blood,
diarrhea with or without Confirmed case: a suspected stool and other clinical
vomiting case confirmed by positive
specimen
Probable Case: Not applicable result for IgM anti-HAV
Confirmed Case: A suspected case
that is laboratory-confirmed
through isolation of Vibrio
Cholerae from the stool of the
patient.
150
Clinical Presentation 90% of cases mild to Abrupt onset of fever; malaise; Fever; vomiting; and Characterized by
moderate diarrhea anorexia; nausea and watery non-bloody insidious onset of
vomiting; abdominal diarrhea sustained fever; severe
discomfort; dark urine and headache; malaise;
5%-10% of cases pale stool followed by icteric anorexia; a non-
manifest as sudden phase (development of productive cough and
onset of profuse, jaundice). Icteric phase hepatosplenomegaly in
painless, watery stools usually begins 10 days after 50% of cases
with nausea and onset of symptoms.
vomiting. Stools are It can also manifest as
colorless with flecks of In children 5 years and below, non-specific symptoms
mucous – “rice water only 30% shows any of chills, diaphoresis;
diarrhea”. symptoms. dizziness; muscle pain;
weakness that usually
occurs before the onset
of fever
151
Annex Q: PIDSR reporting Forms
152
153
154
155
156
Annex R: Conditions of National and International Concern
157
Annex S: Core Function of EICT
158
Annex T: National Health Promotion and Communication Plan
II. Rationale:
- Parent’s knowledge on the signs and symptoms of food and water-borne diseases are very limited.
- Food and Water-borne Diseases Prevention and Control Program aimed at reducing the morbidity and mortality rate due to diarrhea
Food and Waterborne Diseases (FWBD) including outbreaks
- This Health Promotion and Communication Plan is developed to support the (FWBD) program in achieving its objectives.
By end of 2022
90% of parents are able to detect early signs and symptoms of Food and Water-borne Diseases and submit patient to the nearest health
facility
90% 0f parents with diarrheal cases in the family are able to give Oral Rehydration Theraphy as first aid
100% of Health workers are providing correct and appropriate treatment to FWBDs patients
90% LGUs fully support the FWBD program by providing financial human resources.
159
IV. Communication Matrix
IEC
TARGET COMMUNICATION CURRENT TARGET GAPS/
KEY MESSAGES STRATEGIES MATERIA
AUDIENCE OBJECTIVES BEHAVIOR BEHAVIOR ISSUES
LS
Parents To create awareness Parents takes Parents are Lack of FWBD if not treated may IEC AVP, TV and
category (CDE) of parents on the for granted able to knowledge lead to death development Radio
signs and symptoms diarrhea detect early on FWBD and commercial
of the different because they signs of disease and dissemination
FWBD diseases. are not aware symptoms risk Signs and Symptoms and
that it might of FWBD. prevention of FWBD Poster
be a sign of (Infectious Bloody, Inter—Personal
FWBD. Diarrhea, Typhoid Fever, Communication
Parents Cholera, Amoebaiasis, (IPC)with Advisories/flye
with Rotavirus ans Salmonella) parents during rs
diarrheal mothers class
cases in the
family Preparation of Oral
should be Rehydration Theraphy in
able to give case there is no available
Oral ORESOL.
Rehydratio
n Therapy
at home. Go to the nearest health
center if signs and
symptoms occurs.
Continue breastfeeding
160
Health To educate health No focus on Health Multitasking Correct and Orientation/Re Flip chart
Workers workers on the specific workers are appropriate orientation
different FWBDs program able to management of HW on
signs, symptoms provide Lack of FWBDs. Guidelines on
FWBD Program
and management. correct and resources diarrhea
Reactive appropriate management
response to treatment Referral system for
cases to FWBDs Lack of difficult cases
patients manpower FAQs
Lack of Fan
incentives
Lack of
guidelines
LGU/stakehold To encourage LGUs LGUs do not LGUs No funding Brief Overview of Advocacy Advocacy Kit
ers to support the allocate support the FWBD Program Meeting
FWBD Program by budget for FWBD
providing financial FWBD program by Not priority AVP
and human because of providing Importance of
resources. other financial LGU/stakeholders
priorities and human No support to the
resources knowledge of program.
WFBD
program and
it’s the risk of
the diseases
to the
community
161
v. Strategies/ Activities/ Timeline
TARGET
TOTAL TOTAL COST
STRATEGIES ACTIVITIES 1ST 2ND 3RD 4TH
TARGET RESPONSIBLE PERSON
QTR QTR QTR QTR c/o FWBD
Budget
I. Building Healthy
Public Policy
A. Development of policies
B. Review of policies
b.1 Review of AO
b.2 review of AO
II. Creating
Supportive
Environment
III. Developing
Personal Skills
a.1 Training on Regional Coordinators and / 150,000.00 Program & HPCS (CMMD)
HEPOs
D. Harmonize Awarding
163
Annex U: National Health Advisory (Sample)
164
Annex V: Epidemic Intelligence
165