CHN - M3
CHN - M3
CHN - M3
UNDATION
Angeles City
College of Nursing
MODULE OVERVIEW
Introduction
A key role of the CHN is the prevention and treatment of communicable
diseases. This module describes the language of communicable disease and discusses
the goals nurses use in evaluating the success of disease prevention programs. It also
examines common communicable diseases that community health nurses are likely to
encounter in their practices.
Key Points to Review
Communicable disease - a disease or illness in a susceptible host, caused by a
potentially harmful infectious organism or its toxic byproducts. Communicable disease
spreads due to contact between an infectious agent and a susceptible host.
Infectious disease - a disease or illness caused by an infectious agent entering the body
of a susceptible host and then developing or growing.
Host - a person or other living being that can be infected by an organism
Infectious agent - an organism that causes infectious disease. Agents can be bacteria,
fungi, viruses, metazoa, or protozoa.
Agent - something that must be present in the environment for a disease to occur in a
susceptible host.
Endemic - when an infectious agent or disease has a constant presence within a
defined geographic area.
Epidemic - occurrences of an infectious agent or disease that clearly exceed the usual
expected frequency of the disease in a particular population--for example, an influenza
epidemic, when a large number of elderly people in a city get the flu.
Pandemic - when an epidemic outbreak occurs worldwide.
Tuberculosis
Vulnerable populations:
- Children
- persons with HIV infection
- persons in congregate living such as prisons, shelters, long-term care facilities,
and dormitories
- Poor, homeless people without access to health care or follow-up
- Immigrants from countries where TB is endemic
- People with HIV infection and compromised immune systems
- Anyone with poor access to health care for follow-up
Primary prevention strategies include:
- Health promotion and education
- Education on behaviors to reduce risk of transmission from infected persons
- Education about environmental factors (sunlight, ventilation) that can reduce
transmission
- educating the public about the need to complete the entire course of drug
treatment
Secondary prevention strategies include:
- Screening high-risk populations
- Early diagnosis and treatment
- minimizing the disease’s ability to spread throughout the community;
- preventing treatment failures from individuals with poor compliance with the
lengthy, potentially complicated therapy program
Tertiary prevention strategies include:
- Monitoring long-term health status
- Direct observation of therapy to ensure compliance with treatment
Treatment: multidrug regimen with direct observation therapy to ensure compliance.
Community health nurses have a key role in tuberculosis prevention and treatment.
They can identify people at risk, initiate testing programs, do follow-up for compliance
and provide education.
TB situation in the Philippines
The incidence of TB is considered very high, and an increase in the prevalence
of multidrug-resistant TB (MDR-TB) and Human Immunodeficiency Virus (HIV) makes the
disease difficult to control. The country ranks 4th in the burden of TB worldwide with an
estimated 22,000 deaths in 2017 and particularly drug-resistant (DR) has cost a
projected loss of 0.31 billion USD in the country’s Gross Domestic Product (GDP).
You may get the global tuberculosis report data in your
mobile phones. You can get current statistics and
trends, compare countries and regions.
Recent findings about TB
https://doi.org/10.1038/s41598-019-45566-5
Points to know from the study
- The country has a high incidence of tuberculosis disease.
- The increasing prevalence of multidrug-resistant Mycobacterium tuberculosis
(MDR-TB) strains makes it difficult to control.
- M. tuberculosis “Manila” ancient lineage 1 strain-type
- Majority of the isolates (80.3%, 143/178) belonged to the lineage 1 Manila clade
- Minority belonged to lineages 4 (European-American, 18.5%) and 2 (East Asian,
1.1%)
- A high proportion of the isolates (19.1%) were found to be MDR
The National Tuberculosis Control Program
What is Tuberculosis?
Vision: A country where TB is no longer a public health problem
Mission: Ensure that TB DOTS services are available, accessible, and affordable to the
communities in collaboration with the LGU’s and other partners
Objectives:
A. Improve access to and quality of services provided to TB patients, TB
symptomatic, and communities by health care institutions and providers.
B. Enhance the health-seeking behavior on TB by communities, especially the TB
symptomatic.
C. Increases and sustain support and financing for TB control activities
D. Strengthen management of TB control services at all levels.
RA 10767
AN ACT ESTABLISHING A COMPREHENSIVE PHILIPPINE PLAN OF ACTION TO ELIMINATE
TUBERCULOSIS AS A PUBLIC HEALTH PROBLEM AND APPROPRIATING FUND THEREFOR
Points to know about its legal basis:
A. Comprehensive Philippine Plan of Action to Eliminate Tuberculosis. – The
Secretary of the Department of Health (DOH) shall establish a Comprehensive
Philippine Plan of Action to Eliminate Tuberculosis in consultation with
appropriate public and private entities. The Philippine Plan of Action shall consist
of the following:
(a) The country’s targets and strategies in addressing the disease;
(b) The prevention, diagnosis, treatment, care and support, and other
components of the country’s response;
(c) The development and application of appropriate technologies to
diagnose and treat the disease;
(d) The strengthening of linkages with local and international organizations
for possible partnership in education, advocacy, research and funding
assistance;
(e) The establishment of a review and monitoring system to gather data
and monitor the progress made in the elimination of tuberculosis; and
(f) The immediate mobilization of anti-TB services during and after natural
and man-made disasters through collaborative efforts of national and
local governments and other entities.
B. Strengthening of the Regional Centers for Health Development in the Provision of
Health Services to Eliminate TB. – The Secretary of Health shall strengthen the
Regional Centers for Health Development in the provision of health services to
eliminate TB by undertaking the following activities:
(a) Provide free laboratory services through the DOH retained hospitals;
(b) Provide reliable supply of drugs to patients for free by ensuring that
local health centers, through coordination with local government units
(LGUs) concerned, have sufficient supply of medicines for the
communities they serve;
(c) Undertake public information and education programs to train the
public on basic ways and means to prevent the spread of tuberculosis;
(d) Train and enhance the capability of health providers in both public
and private hospitals;
(e) Ensure the proper monitoring of tuberculosis cases in the country; and
(f) Ensure that monitoring services are extended as far as practicable, at
the lowest local level health unit.
C. Education Programs. – The Secretary of Health, in coordination with the
Commission on Higher Education (CHED), shall encourage the faculty of schools
of medicine, nursing or medical technology and allied health institutions, to
intensify information and education programs, including the development of
curricula, to significantly increase the opportunities for students and for
practicing providers to learn the principles and practices of preventing,
detecting, managing, and controlling tuberculosis.
D. Inclusion in Basic Education. – The Secretary of Health, in coordination with the
Secretary of the Department of Education (DepED), shall work for the inclusion of
modules on the principles and practices of preventing, detecting, managing
and controlling tuberculosis in the health curriculum of every public and private
elementary and high school.
E. Media Campaign. – The Secretary of Health, in coordination with the Philippine
Information Agency (PIA), shall encourage local media outlets to launch a
media campaign on tuberculosis control, treatment and management, using all
forms of multimedia and other electronic means of communication.
The media campaign shall include materials that would discourage the
general public from spitting in public places and exhibiting unhygienic behavior
that tend to undermine the overall effort of preventing the spread of the disease.
F. Regulation on Sale and Use of TB Drugs. – The Food and Drug Administration
(FDA) shall strengthen its implementation of the “No prescription, No anti-TB
drugs” to regulate the sale and use of anti-TB drugs in the market. It shall also
ensure the quality of TB drugs distributed in the market.
G. Notification on TB Cases. – All public and private health centers, hospitals and
facilities shall observe the national protocol on TB management arid shall notify
the DOH of all TB cases as prescribed under the Manual of Procedures of the
National TB Program and the Philippine Plan of Action on Tuberculosis Control.
H. PhilHealth TB Package. – The Philippine Health Insurance Corporation, otherwise
known as the PhilHealth, shall, as far as practicable, expand its benefit package
for TB patients to include new, relapse and return-after-default cases, and
extension of treatment.
The PhilHealth shall enhance its present outpatient Directly Observed
Treatment Short Course (DOTS) package to make it more responsive to patients’
needs. It shall likewise increase the number of accredited DOTS facilities to widen
target beneficiaries who may avail of reimbursements.
Comprehensive Philippine Plan of Action to Eliminate Tuberculosis
I. Vision = TB -free Philippines
II. Mission:
- To reduce TB burden (TB incidence and TB mortality)
- To achieve catastrophic cost of TB-affected households
- To responsively deliver TB service
III. Program Components
● Health Promotion
● Financing and Policy
● Human Resource
● Information System
● Regulation
● Service Delivery
● Governance
IV. Target Population / Client = Presumptive TB and TB affected households
V. Area of Coverage = Nationwide
VI. Partner Institutions
● Department of Health : Food and Drug Administration, Bureau of Quarantine
● Other Government: DepEd, DSWD, DILG (BJMP), DOJ (BuCor)
● Non Government Organizations: PhilCAT, PBSP
● International Organizations: WHO, USAID, GFATM, ICRC, HIVOS-KNCV
VII. Policies and Laws = RA 10767 : Comprehensive TB Elimination Plan Act of 2016
VIII. Strategies, Action Points and Timeline
2017-2022 Philippine Strategic TB Elimination Plan
❏ Activate communities and patient groups to promptly access quality TB
services
❏ Collaborate with other government agencies to reduce out-of-pocket
expenses and expand social protection programs
❏ Harmonize local and national efforts mobilize adequate and competent
human resources
❏ Innovate TB information generation and utilization for decision making
❏ Enforce standards on TB care and prevention and use of quality products
❏ Value clients and patients through integrated patient-centered TB
services
❏ Engage national, regional and local government units/ agencies on
multi-sectoral implementation of TB elimination plan
Definition of Terms
Active TB disease – a presumptive TB case that is either bacteriologically confirmed or
clinically diagnosed by the attending physician.
Pulmonary TB (PTB) – refers to a case of tuberculosis involving the lung parenchyma.
A patient with both pulmonary and extrapulmonary tuberculosis should be classified as
a case of pulmonary TB.
Extrapulmonary TB (EPTB) – refers to a case of tuberculosis involving organs other than
the lungs (e.g. larynx, pleura, lymph nodes, abdomen, genito-urinary tract, skin, joints
and bones, meninges).
Bacteriologically confirmed TB (BCTB) – refers to a patient from whom a biological
specimen, either sputum or non-sputum sample, is positive for TB by smear
microscopy, culture or rapid diagnostic tests (such as Xpert MTB/RIF, line probe assay
for TB, TB LAMP).
Clinically diagnosed TB (CDTB) – refers to a patient for which the criterion for
bacteriological confirmation is not fulfilled but diagnosis is made by the attending
physicians on the basis of clinical findings, X-ray abnormalities, suggestive histology
and/or other biochemistry or imaging tests.
New – refers to a patient who has never had treatment for TB or who has taken anti-TB
drugs for less than one month. Preventive treatment is not considered as previous TB
treatment.
Previously treated for TB – refers to a patient who had received one month or more of
anti- TB drugs in the past. Also referred to as Retreatment.
High risk for multidrug-resistant tuberculosis (MDR-TB) – previously treated for TB, new
TB cases that are contacts of confirmed DR-TB (drug resistant TB) cases or
non-converter among patients on DS-TB (drug sensitive TB) regimens.
Rifampicin-resistant TB (RR-TB) – resistance to rifampicin detected using phenotypic or
genotypic methods, with or without resistance to other anti-TB drugs. It includes any
resistance to rifampicin, whether monoresistance, multidrug resistance, polydrug
resistance or extensive drug resistance.
Turnaround time (TAT) – the time from collection of first sputum sample to initiation of
treatment for TB. The desired turnaround time is five working days (also referred to as
Program TAT).
Systematic screening for pulmonary PTB in adults ≥ 15 years old with unknown HIV
infection status in health facilities
Systemic screening in health facilities (intensified case finding)
Systematic screening in facilities shall be done for all clients visiting the facility
regardless of reason for consultation. If the patient consults due to any of the four
cardinal signs/symptoms (i.e. at least two weeks of cough, unexplained fever,
unexplained weight loss and night sweats)
The following steps are involved in screening for pulmonary TB (PTB) in adults ≥ 15 years
old:
1.1 Record the patient’s demographic and contact information in a register of consults.
1.2 Ask all patients consulting the health facility, if they have the following cardinal signs
and symptoms that are lasting for ≥2 weeks:
a. cough
b. unexplained fever
c. unexplained weight loss
d. night sweats.
1.3 If any of the above signs/symptoms are present for at least two weeks, identify as a
presumptive TB.
1.4 For those who do not have any of the cardinal signs/symptoms above or
experienced it for less than two weeks, offer chest X-ray screening if one has not been
conducted in the past year.
A chest X-ray posteroanterior (PA) upright view should be requested and
previous chest X-rays should be brought for comparison. For pregnant women, a written
consent shall be taken and an abdominal protective shield shall be used by the X-ray
facility. The National TB Prevalence Survey in 2016 showed that “screening for TB cases
using symptoms alone would have missed one-third to two-thirds of bacteriologically
confirmed pulmonary TB cases.”
If resources are limited, you have the option to prioritize those with TB risk factors
as primary clients for chest X-ray screening.
Risk factors include:
a. contacts of TB patients;
b. those ever treated for TB (i.e. with history of previous TB treatment);
c. people living with HIV (PLHIV);
d. elderly (> 60 years old);
e. diabetics;
f. smokers;
g. health-care workers;
h. urban and rural poor (indigents); and
i. those with other immune-suppressive medical conditions (silicosis, solid organ
transplant, connective tissue or autoimmune disorder, end-stage renal disease,
chronic corticosteroid use, alcohol or substance abuse, chemotherapy or other
forms of medical treatment for cancer).
NOTE: If a chest X-ray is not available and these high-risk patients have signs and
symptoms lasting less than two weeks, the physician may decide whether to consider
the patient a presumptive TB case.
Diagnosis and clinical application of Xpert/MTB RIF
The following steps are involved in the screening for pulmonary TB (PTB) in children < 15
years old:
DIAGNOSIS OF TUBERCULOSIS DISEASE
Smear Microscopy
➢ Sputum smear microscopy allows a rapid and reliable identification of patients
with pulmonary tuberculosis (PTB) where there are more than 5000 bacilli/ml of
sputum.
➢ If the sputum has less than 5000 bacilli/ml, smear microscopy is highly unlikely to
diagnose PTB.
TB lamp
➢ is a manual assay that requires less than one hour to perform and can be read
with the naked eye under ultra violet light.
➢ Following review of the latest evidence, WHO recommends that TB-LAMP can be
used as a replacement for microscopy for the diagnosis of pulmonary TB in adults
with signs and symptoms of TB.
➢ It can also be considered as a follow-on test to microscopy in adults with signs
and symptoms of pulmonary TB, especially when further testing of sputum
smear-negative specimens is necessary.
Collection of Sputum
➔ Prepare a sputum cup or 50 ml conical tube and accomplish Form 2a.
Laboratory Request and Result Form.
➔ Instruct patient to expectorate one sputum sample on the spot for diagnostic
testing with Xpert (if not available, SM or TB LAMP). Collect 1ml for Xpert MTB/RIF
and TB LAMP and 3–5 ml for SM.
➔ Collect specimen in a well-ventilated designated sputum collection area, or
outside the health facility.
➔ Instruct the patient on how to expectorate:
a. clean mouth by thoroughly rinsing with water
b. breathe deeply, hold breath for a second or two, and then exhale
slowly. Repeat the entire sequence two more times;
c. cough strongly after inhaling deeply for the third time and try to bring
up sputum from deep within the lungs; and
d. expectorate the sputum in the sputum cup or conical tube.
➔ Sputum induction for individuals unable to expectorate should be done only in
facilities where the staff is trained, supplies and equipment are available, and
infection control measures are in place.
➔ If the child cannot expectorate (especially < 5 years old), nasopharyngeal
aspirate or gastric lavage may be performed in facilities where trained staff,
supply and equipment are available.
➔ Label the body of the sputum cup/conical tube, indicating patient’s complete
name and indicating the specimen for Xpert (or SM/TB LAMP).
➔ Check quality of the sputum.
➔ For Xpert, testing should be performed on any collected spot sputum sample (i.e.
a coughed-out sample) regardless whether it is sputum or saliva.
➔ For SM, examine the specimen to see that it is not just saliva. Mucus from the
nose and throat, and saliva from the mouth are not good specimens. Repeat the
process if necessary.
➔ For SM, instruct to collect a second sample one hour later or an early-morning
sputum sample the following day. Follow-up within three days if patient fails to
submit a second specimen unless the first specimen already tests positive for
acid-fast bacillus (AFB) in which case the second specimen will not be
necessary.
➔ Seal the sputum cup or conical tube and transport it to an Xpert site, TB
microscopy laboratory or TB LAMP site together with the completed Form 2a.
Laboratory Request and Result Form.
➔ If the laboratory is in another facility, use the triple packaging system.
(Reference: Manual on Collection, Storage and Transport of Specimens for TB
testing, http://bit.ly/CSTSManual)7.1 Place the primary container in individual
plastic bags.
➔ Place each in a durable, leak-proof, water-tight and properly sealed container
(i.e. biological bottles or plastic jars as secondary containers).
➔ Enclose in the sputum transport box (tertiary container).
➔ Transport at cold temperature by placing cold packs inside the tertiary
container.
➔ Accomplish a dispatch list.
➔ Specimens for SM can also be smeared immediately by trained volunteers and
then stored appropriately before transport to the TB microscopy laboratory.
➔ For diagnosis of EPTB, facilities with the necessary capability can collect body
fluid samples or tissue biopsy sample from the suspicious site. Refer if necessary.
PROCEDURES
Initiation of treatment Inform the patient that they have TB disease. Provide key
messages for TB patients and families: Basic information about TB disease covering:
cause, transmission, clinical signs and symptoms; how TB is diagnosed; and how to
prevent TB
“TUTOK GAMUTAN”