Cam02a Information Paper
Cam02a Information Paper
Cam02a Information Paper
March 2015
Publication Details
Publication title: NHMRC Information Paper: Evidence on the effectiveness of homeopathy for treating
healthconditions
Published:
March 2015
Publisher:
CAM02A
Online version:
www.nhmrc.gov.au/guidelines-publications/cam02
ISBN Online:
978-1-925129-29-8
Suggested citation: National Health and Medical Research Council. 2015. NHMRC Information Paper: Evidence on the
effectiveness of homeopathy for treating healthconditions. Canberra: National Health and Medical
Research Council; 2015
Copyright
Commonwealth of Australia 2015
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or call (02) 6217 9000
Contents
About NHMRC
Executive summary
Homeopathy 5
Methods 5
Findings 6
Conclusions 6
Introduction 7
Purpose 7
Scope 7
What is homeopathy?
7
Why did NHMRC conduct an assessment of homeopathy?
8
9
11
11
14
15
16
Overview 16
Information provided by homeopathy interest groups and individuals
21
Overall findings based on the evidence
24
25
27
28
30
Explanatory notes
30
31
33
33
33
References 39
About NHMRC
NHMRC is Australias peak body for supporting health and medical research by funding the best
research, selected through a competitive peer review process. NHMRC also develops health advice
for the Australian community, health professionals and governments in the form of public health
and clinical practice guidelines, Statements, Information Papers and evidence reviews. NHMRC also
provides advice on ethical behaviour in health care and in the conduct of health and medical research.
The work of NHMRC is guided by its Strategic Plan, and defined by the National Health and Medical
Research Council (NHMRC) Act 1992. The Strategic Plan covers a three year period and is submitted
to the Health Minster for approval, prior to being tabled in Parliament. The NHMRC Strategic Plan
20132015[1] has identified claiming benefit for human health not based on evidence as a major health
issue for consideration.
This Information Paper is an example of NHMRCs function to advise the community under section
7(1)(a) of the NHMRC Act 1992. Published research on a topic of interest has been identified,
analysed and synthesised into a summary of the evidence for the Australian community, health
professionals and policy makers. This information can then be utilised to assist people in making
healthcare choices, guide clinical practice or influence policy and perhaps new funding approaches,
all of which lead to improvements in health and health care delivery.
Within our health system, there are practices which are currently not based on sturdy evidence.
Health and medical research is the means by which we test the value of procedures, processes,
systems and products offered to patients, or proposed as preventive means by the health system
andits policy and decision makers.
NHMRC is a strong advocate for the development and use of evidence to inform policy and practice
and in recent years, NHMRC and other health research funding bodies have increased funding for
such research.
NHMRC is of the view that when offering treatments for illness, all registered health practitioners must
give consideration to the evidence for the effectiveness of such treatments. This consideration should
be reflected in their professional ethics and clinical practices.
Executive summary
Homeopathy
Homeopathy is a type of complementary and alternative medicine that is commonly used in Australia
and around the world. It is based on two premises:
that substances that may cause illness or symptoms in a healthy person can, in very small doses,
treat those symptoms in a person who is unwell, and
that highly diluted preparations retain a memory of the original substance. Homeopathic
medicines are prepared by taking a substance (e.g. plant, animal material, or chemical), diluting
itin water or alcohol, then forcefully hitting the container against a hand or a surface. This process
is repeated several times.
Homeopathic medicines include pellets placed under the tongue, tablets, liquids, ointments,
spraysand creams.
Methods
The National Health and Medical Research Council (NHMRC) undertook an assessment of the
evidence of the effectiveness of homeopathy. This assessment was based on:
an overview of published systematic reviews by an independent contractor[2],
an independent evaluation of information provided by homeopathy interest groups and the
public[3, 4], and
consideration of clinical practice guidelines and government reports on homeopathy published
inother countries.
The assessment of the evidence used standardised, accepted methods for assessing the quality
andreliability of evidence for whether or not a therapy is effective for treating health conditions.
This work was overseen by the Homeopathy Working Committee established by the NHMRC.
Given their collective expertise in evidence-based medicine, study design, and complementary and
alternative medicine research, the Homeopathy Working Committee also provided advice on how the
evidence should be interpreted in developing an Information Paper. An approach, similar to that of a
Health Technology Assessment, was used to consider the outcomes of the assessment of the evidence.
This means that for a treatment to be considered effective, it must result in health improvements that
cannot be explained by the placebo effect, and these health improvements must be meaningful for
a persons overall health. There must be evidence that the health improvements in people taking the
treatment are unlikely to be due to chance and the result must be seen consistently in several studies.
Evidence on homeopathy was collected by identifying systematic reviews which evaluated the
effectiveness of homeopathy in treating health conditions in humans. In total, 57 systematic reviews
were identified that contained 176 individual studies. Studies were only considered by NHMRC if
they compared a group of people who were given homeopathic treatment with a similar group of
people who were not given homeopathic treatment (controlled studies). For each health condition,
the evidence reviewers assessed the quality of the systematic reviews using a standard, internationally
accepted method, and recorded the number and type of studies that were included in the systematic
reviews. Using the information provided by the systematic reviews, the reviewers also assessed the
quality of each individual study and its number of participants, taking into account factors that could
bias the results in favour of homeopathy, placebo or another treatment.
Additional information was submitted to NHMRC, for consideration as part of its review of
homeopathy, by homeopathy interest groups and the public on two occasions: before the
commissioned overview of evidence (preliminary submitted literature) and during the review of
the draft Information Paper (public consultation submitted literature). The preliminary and public
consultation submitted literature was assessed using a similar method to that applied in the overview.
Where a clinical condition had already been considered in the overview, the results from the
submitted literature were compared to the conclusions of the overview to examine the consistency
of results against the body of evidence. Where a clinical condition had not been considered in the
overview, the results of the submitted literature were assessed with regards to their study design, size
and different kinds of bias to see if any comment on the effectiveness of homeopathy could be made.
Findings
There was no reliable evidence from research in humans that homeopathy was effective for
treating the range of health conditions considered: no good-quality, well-designed studies with
enough participants for a meaningful result reported either that homeopathy caused greater health
improvements than placebo, or caused health improvements equal to those of another treatment.
For some health conditions, studies reported that homeopathy was not more effective than placebo.
For other health conditions, there were poor-quality studies that reported homeopathy was more
effective than placebo, or as effective as another treatment. However, based on their limitations, those
studies were not reliable for making conclusions about whether homeopathy was effective. For the
remaining health conditions it was not possible to make any conclusion about whether homeopathy
was effective or not, because there was not enough evidence.
Conclusions
Based on the assessment of the evidence of effectiveness of homeopathy, NHMRC concludes that
there are no health conditions for which there is reliable evidence that homeopathy is effective.
Homeopathy should not be used to treat health conditions that are chronic, serious, or could become
serious. People who choose homeopathy may put their health at risk if they reject or delay treatments
for which there is good evidence for safety and effectiveness. People who are considering whether
to use homeopathy should first get advice from a registered health practitioner. Those who use
homeopathy should tell their health practitioner and should keep taking any prescribed treatments.
Introduction
Purpose
This Information Paper provides a summary of evidence from research on the effectiveness of
homeopathy in treating health conditions in humans.
Scope
NHMRC assessed the evidence on homeopathy to answer this question: Is homeopathy an effective
treatment for health conditions, compared with no homeopathy, or compared to other treatments?
NHMRC did not consider any of these types of evidence:
laboratory studies;
studies in animals;
studies in humans without a specific health condition, including:
studies investigating whether or not homeopathy is effective for preventing health conditions;
evidence about homeopathic vaccines; and
whether homeopathy is good for general health and wellbeing.
The focus of the assessment of the evidence was on the effectiveness of homeopathic medicines,
nottheir safety.
What is homeopathy?
Homeopathy is a type of complementary and alternative medicine. It is based on two premises:
that substances that may cause illness or symptoms in a healthy person can, in very small doses,
treat those symptoms in a person who is unwell (like cures like); and
that highly diluted preparations retain a memory of the original substance.
Homeopathic medicines are prepared by taking a substance (e.g. plant, animal material, or chemical)
and repeatedly diluting it in water or alcohol. The container holding the preparation is then forcefully
hit against a hand or a surface in a process known as potentiation or dynamisation. Homeopathic
medicines can include pellets placed under the tongue, tablets, liquids, ointments, sprays and creams.
Homeopaths provide either individualised homeopathy or clinical homeopathy. In individualised
homeopathy, the homeopath matches all the persons symptoms to a single homeopathic medicine,
rather than treating the person for a particular health condition using one or more homeopathic
medicines. In clinical homeopathy, the homeopath chooses one or more homeopathic medicines
totreat a particular health condition.
Homeopathy is commonly used around the world, however, there are no reliable estimates of
Australians current use of homeopathic medicines. A 2009 WorldHealthOrganisation review on the
safety of homeopathy reported that each year, Australians spend an estimated US $7.3 million on
homeopathic medicines.[5]
When assessing the effectiveness of treatments for health conditions, not all evidence has equal value.
It is not possible to tell whether a health treatment is effective or not simply by considering
individuals experiences or healthcare practitioners beliefs. One reason personal testimonials are
not reliable is that people may experience health benefits because they believe that a treatment is
effective. This is known as the placebo effect. Another reason is that healthcare practitioners cannot
always tell whether changes in a persons health condition are due to the treatment or some other
reason. For these reasons, medicines must be tested in a planned, structured scientific research project
designed to prevent these kinds of experiences giving the false impression that a medicine is more or
less effective than it really is.
Some types of studies provide stronger evidence than others because of how they are designed. If
studies are poorly designed, there is a risk that results may be biased; that is, the results may under or
over-estimate the real effect of the treatment being tested. Researchers have developed particular ways
of designing studies that aim to minimise the potential for such bias. Reliable information about whether
a particular medicine is effective for treating a health condition or not, comes from studies in which:
the medicine is compared with a substance that has no effect (placebo) in a group of people
with the health condition (placebo-controlled trial), or the medicine is compared with an effective
standard treatment (controlled trial);
each participant is given either the medicine or the placebo/other treatment at random
(randomisedtrial);
participants do not know whether they are taking the medicine or the placebo/other treatment,
andresearchers to not know which participants are taking each treatment, until the study is
finished (double-blinded trial);
there are enough participants to be reasonably confident that, if there is a bigger change in the
health condition in one group compared to another, this is not just due to chance; and
the correct statistical methods are used to analyse the results.
When treatments are intended to be adjusted for the individual patient (e.g. different doses or
combinations of medicines), it is still necessary to test whether the medicine is effective or not. It is
possible to design high-quality studies to assess treatment approaches that involve individualisation,
such as homeopathy.
Even where researchers take care to design studies in a way that minimises bias, there is a chance
that the results will show a statistically significant difference in favour of a treatment, when there
is actually no effect. Therefore, the results of individual studies need to be repeated in other
independent studies, to make sure the effects seen were not just due to chance. The most reliable
information comes from research that combines the results of all available similar studies and analyses
the results together (systematic reviews).
When evaluating health evidence and drafting health advice, NHMRC uses a rigorous approach that
has been developed by Australian experts in research methods.[6] Under the NHMRC system, there
are different levels of evidence, ranging from level one (highest level, strongest evidence) to level
four (lowest level, weakest evidence).[7] Further detail about this hierarchy is provided at AppendixA.
Thelevel of evidence assigned to each study design is based on the extent to which each study
design is expected to minimise bias. The level of evidence is used to decide how much a studys
results should be relied upon, when judging the overall evidence.
A treatment is considered effective for treating a health condition if it meets all of these key criteria:
the treatment causes health improvements that cannot be explained by the placebo effect;
health improvements that occur in people taking the treatment are unlikely to be due to chance;
the health improvements caused by the treatment are meaningful for a persons overall health; and
the health improvement occurs consistently in several studies.
10
Sources of information
The NHMRC assessment of the evidence used a combination of three main sources of information
about the effectiveness of homeopathy (Figure 1):
an evidence review (the overview of systematic reviews), comprising a systematic review
ofpublished systematic reviews (summarised in the Overview report)[2];
evidence provided by homeopathy interest groups and the public at the beginning of the process,
before the commissioned overview of evidence (preliminary submitted literature) and during
review of the draft Information Paper (public consultation submitted literature).[3, 4]
evidence-based clinical practice guidelines, government reports on homeopathy published in other
countries, and other reports.
The NHMRCs assessment was guided by a committee of experts in evidence evaluation,
theHomeopathy Working Committee, appointed in April2012 (Appendix B).
11
additional literature for consideration in the development of this Information Paper (public
consultation submitted literature).
All submitted literature was assessed by independent contractors to identify evidence within the
scopeof NHMRCs assessment. Only the types of studies that were included in the overview
(prospective, controlled studies) were assessed in detail. For each study included, the independent
contractors assessed the quality and reliability of the results and summarised the findings in a
reviewof submitted literature.[3, 4]
This evidence was considered when preparing this Information Paper.
12
EVIDENCE ASSESSMENT
Overview report
Preliminary submitted literature
Other government reports and guidelines
Independent methodological
review of Overview report
NHMRC Statement
13
14
in the overview, the quality of each study was evaluated using a standardised, internationally
acceptedmethod.
A full description of the methods used are provided in the Effectiveness of homeopathy for any clinical
condition: evaluation of the evidenceReview of submitted literature[3] and Effectiveness of homeopathy
for clinical conditions: evaluation of the evidenceReview of literature from public submissions.[4]
For more information on NHMRCs processes for reviewing evidence, see About the NHMRC
assessment of the evidence.
Expert review
NHMRC commissioned an independent organisation with expertise in research methodology (The
Australasian Cochrane Centre) to review the methods used in the overview and ensure that processes
for identifying and assessing the evidence were scientifically rigorous, consistently applied, and clearly
documented. All the reviewers comments and suggestions were considered in consultation with the
Homeopathy Working Committee and the report amended accordingly.
NHMRC invited three national and international reviewers, with expertise in complementary
medicines research, to comment on the draft Information Paper to ensure that the evidence had
been accurately interpreted. All comments received were considered by the Homeopathy Working
Committee and the draft Information Paper was amended accordingly. A summary of the expert
reviewerscomments and the considerations of the Homeopathy Working Committee is available
atwww.nhmrc.gov.au/guidelines-publications/cam02.
Public consultation
A public consultation process was undertaken on the draft Information Paper. Public consultation
ensured that relevant studies, examining the effectiveness of homeopathy that occurred outside of the
search dates of the systematic reviews included in the overview, could be considered. Consultation
also provided the opportunity for comment on the clarity of the process by which the Homeopathy
Working Committee translated the research findings into advice.
All comments received from public consultation were collated and considered by the Homeopathy
Working Committee. A report outlining the common themes raised during public consultation, the
Homeopathy Working Committee consideration of those themes and the subsequent changes to the
Information Paper is available at www.nhmrc.gov.au/guidelines-publications/cam02.
NHMRC INFORMATION PAPER
EVIDENCE ON THE EFFECTIVENESS OF HOMEOPATHY FOR TREATING HEALTH CONDITIONS
15
Overview
The overview[2] considered 57 systematic reviews that assessed the effectiveness of homeopathy
(individualised homeopathy or clinical homeopathy) compared to placebo or other treatment, for
treating health conditions.
These systematic reviews searched for published research on homeopathy for 68 health conditions
and found published research on 61 of these conditions. No published research was found for the
remaining seven conditions.
The systematic reviews included 176 individual studies. The overview assessed the quality and
considered the findings of each study using the information provided in the systematic reviews.
A list of all included studies is available at www.nhmrc.gov.au/guidelines-publications/cam02.
Based on all the evidence considered, there were no health conditions for which there was
reliable evidence that homeopathy was effective. No good-quality, well-designed studies with
enough participants for a meaningful result reported either that homeopathy caused greater health
improvements than placebo, or caused health improvements equal to those of another treatment.
16
17
Homeopathy is not more effective than placebo for the treatment of these health conditions:
adenoid vegetation in children (abnormal growth of adenoid tonsils behind the nose)
asthma
anxiety or stress-related conditions
diarrhoea in childrencombined homeopathy tablet (clinical homeopathy)
headache and migraine
muscle soreness (delayed onset)
labour (inducing or shortening labour)
pain due to dental work
pain due to orthopaedic surgery
postoperative ileus (abnormally slow movement of bowel after surgery)
premenstrual syndrome
upper respiratory tract infections (e.g. colds)
warts.
There is no reliable evidence that homeopathy is more effective than placebo for the
treatment of these health conditions:
allergic rhinitis
attention deficit/hyperactivity disorder (ADHD) in children
bruising
chronic fatigue syndrome
diarrhoea in childrenindividualised homeopathy
fibromyalgia
18
Conclusions
acne vulgaris
acute otitis media (inflammation of the middle ear) in children
acute ankle sprain
acute trauma in orthopaedic patients
amoebiasis and giardiasis (gastrointestinal conditions caused by parasites)
ankylosing spondylitis
boils and pyoderma (types of skin infections)
Brocas aphasia in people who have had a stroke
bronchitis
cholera
cough
chronic polyarthritis
dystocia (difficult labour)
eczema
heroin addiction
knee joint haematoma (bruising)
lower back pain
nausea and vomiting associated with chemotherapy
oral lichen planus
osteoarthritis
proctocolitis
postoperative pain-agitation syndrome
radiodermatitis (skin damage caused by radiotherapy) in women with breast cancer
seborrhoeic dermatitis
suppression of lactation after childbirth in women who elect not to breastfeed
stroke
traumatic brain injury (mild)
uraemic pruritis
vein problems due to cannulas in people receiving chemotherapy.
There is no reliable evidence that homeopathy is as effective as the other therapies for the
treatment of these health conditions:
acute otitis media or otitis media with effusion (inflammation of the middle ear) in
children (compared with antibiotics, mucolytic medicines, secretolytic medicines,
antipyretic medicines, nasal sprays, or monitoring the condition but not providing
treatment [watchful waiting])
allergic rhinitis (compared with antihistamines, cortisone or intranasal cromolyn sodium)
anxiety or stress-related conditions (compared with lorazepam, diazepam or cognitive
behavioural therapy)
depression (compared with fluoxetine or diazepam)
eczema (compared with corticosteroids, antihistamines, or other unspecified therapies)
non-allergic rhinitis (compared with aspirin, xylometazoline or other therapies)
osteoarthritis (compared with paracetamol or various nonsteroidal anti-inflammatory
drugs)
upper respiratory tract infection (compared with anti-inflammatory drugs, antibiotics or
other therapies).
19
Conclusions
Systematic reviews included in the overview searched for, but did not find, studies assessing homeopathy in people with these conditions:
borderline personality disorder, dementia, constipation in children, glaucoma, nocturnal enuresis (bedwetting), lower urinary tract symptoms in
men, and chronic facial pain.
Systematic reviews included in the overview searched for, but did not find, studies that compared homeopathy with placebo in people with these
conditions: burns (second and third degree), depression, irritable bowel syndrome, lower back pain, malaria, non-allergic rhinitis, and vulvovaginal
candidiasis. For these conditions, systematic reviews found only studies that compared homeopathy with other treatments.
20
21
The included studies investigated homeopathy for the treatment of 14 health conditions (16studies)
that were covered by systematic reviews included in the overview: rheumatoid arthritis, influenza-like
illness, hot flushes, rhinosinusitis, ankle sprain, oral dryness, psychophysiological-onset insomnia,
stress, dermatological reactions to radiotherapy, warts, osteoarthritis of the knee, chronic low back
pain, upper respiratory tract infection and otitis media.
Most studies were assessed to have a moderate, moderate-to-high or high risk of bias. Many of these
studies were poorly designed, poorly conducted or poorly reported. In addition, the studies had too
few participants to be able to detect differences in health outcomes between the treatment groups.
The findings of these studies did not alter the overall conclusions of the NHMRC review. Although
one small study with a low risk of bias favoured homeopathy for the treatment of cough in upper
respiratory tract infections, this study did not have enough participants to outweigh the wider body
of evidence considered in the overview, which found that homeopathy was not more effective than
placebo overall (Table 1).
Health conditions not already covered by the NHMRC overview
The submissions also included published studies on 21 clinical conditions (24 studies) that were not
covered by systematic reviews included in the overview:
coffee-related insomnia;
arsenic toxicity;
anal fissures;
haemorrhoids;
pulmonary tuberculosis;
plantar fasciitis;
mental fatigue;
acute febrile infections;
varicose veins;
vertigo;
chronic periodontitis;
cat allergy;
diaper dermatitis;
diabetic polyneuropathy;
pain after tonsillectomy;
essential hypertension;
end-stage renal failure;
subcutaneous mechanical injury in athletes;
mucositis during stem cell therapy;
post-rhinoplasty ecchymosis and oedema;
malnourishment.
22
The majority of these studies reported results in favour of homeopathy. However, they were generally
poor quality. Only one study[20] was assessed as having a low risk of bias, and evaluated the effect
of homeopathy, compared with placebo, on self-reported mental fatigue in 86 university staff and
students. This study reported no difference between treatment groups, however it had too few
participants to give a meaningful result.
For all other studies, the risk of bias ranged from moderate to high. Many of these studies were
poorly designed, poorly conducted or poorly reported. Many of the studies had too few participants
to be able to detect differences in health outcomes between the treatment groups.
The findings of studies on health conditions not already considered by the overview did not alter
the overall conclusions of the NHMRC review. Although some studies reported results favouring
homeopathy, none were high-quality studies judged to be at low risk of bias. In addition, these were
only selected examples of studies on those health conditions.
23
24
The studies of homeopathy were generally poor quality. For some health conditions, this meant that
no conclusion could be made on whether or not homeopathy was effective. For other conditions,
thismeant that NHMRC could not be confident that the results reported by studies were reliable.
The overview was based on finding systematic reviews of homeopathy, rather than searching for all
individual published studies of homeopathy. The advantage of this strategy was to make use of the
large amount of work that had already been done by researchers around the world in finding and
assessing studies and to provide an overarching picture of the whole body of evidence. However,
there were also some disadvantages:
As the overview only included systematic reviews, some individual studies of homeopathy may not
have been considered (particularly recent studies published since the latest systematic reviews).
This risk was offset by inviting homeopathy interest groups and the public to provide extra
evidence at two stages of the review: before the overview and at public consultation on the draft
of this Information Paper. From this process an additional 42 studies were considered as part of the
assessment of the evidence. These studies did not alter the overall findings of the assessment of the
evidence.
To assess the quality of individual studies, the research group had to rely on the way that these
were reported by systematic reviews. Details of study design (e.g. the outcomes measured and the
length of follow up), the statistical significance of the results and the clinical importance of any
reported health benefits were not always available. Also, the description of an individual study
was sometimes inconsistent between systematic reviews. In these instances, the findings of the
systematic review which was assessed to be of a higher quality was considered.
It was not possible to separate the evidence for clinical homeopathy (in which the homeopath
chooses one or more homeopathic medicines to treat a particular health condition) and
individualised homeopathy (in which the homeopath matches all the persons symptoms to a single
homeopathic medicine), because most of the systematic reviews did not analyse these separately.
Most of the studies used clinical homeopathy.
It was not possible to make conclusions about the effects of homeopathy on each of the specific
health outcomes (e.g. pain, mobility) relevant to a particular health condition (e.g. arthritis),
because of the large number of outcomes and the different reporting of outcomes between the
different systematic reviews. Instead, outcomes were aggregated for each health condition and
asingle conclusion made.
It was often difficult in studies to find the details of other treatments with which homeopathy
was compared. To interpret the studies that compared homeopathy with another treatment, it
is necessary to understand whether the other treatment is an effective standard treatment. This
information was often not available from the systematic reviews.
It is also likely that some studies assessing homeopathic treatments have never been published.
Searching of clinical trials registries can identify unpublished studies and enable researchers to
obtain and analyse the results, but cannot identify studies that have not been registered. The
overview identified only 10 systematic reviews that reported having considered publication bias,
and only two of these made a comprehensive, systematic search for missing studies.
25
One of these systematic reviews reported significant publication bias, which the authors suggested
was primarily due to under-reporting of studies with statistically non-significant effects and with
negative effects.[2] Clinical trial registries (included the World Health Organisation Clinical Trials
Registry, the US governments ClinicalTrials.gov and the Australian New Zealand Clinical Trials
Registry) were searched but did not identify any extra studies.
Despite the above limitations, it is unlikely that a review of primary studies (rather than of systematic
reviews) would have altered the findings. This is because the studies on homeopathy identified
through this process were generally small and of poor quality (either poorly designed or poorly
done). Due to the poor quality of the evidence base, the Homeopathy Working Committee had to
apply caution when considering the results reported by studies. For some health conditions, this
meant that no conclusion could be made on whether or not homeopathy was effective. For other
conditions, this meant that NHMRC could not be confident that the results reported by studies
werereliable.
26
Based on the overall findings of the assessment of the evidence of effectiveness of homeopathy,
NHMRC has reached these conclusions:
There is no reliable evidence that homeopathy is effective for treating health conditions.
Homeopathy should not be used to treat health conditions that are chronic, serious, or could
become serious.
People who choose homeopathy may put their health at risk if they reject or delay treatments for
which there is good evidence for safety and effectiveness.
People who are considering whether to use homeopathy should first get advice from a registered
health practitioner. Those who use homeopathy should tell their health practitioner, and should
keep taking any prescribed treatments.
27
Body of evidence
The range of health care practices, therapies, procedures and devices that
are not currently considered to be part of conventional medicine.
A study in which the treatment being evaluated was compared with either
another treatment, or placebo (a treatment or substance known to have no
health benefits), in similar groups of people with the health condition.
Effectiveness
(of a treatment for a health condition)
The extent to which a treatment works or not when used to treat health
conditions in patients.
Evidence
(medical evidence or clinical evidence)
Homeopathy
Placebo effect
A study that measures effects as they occur over time, beginning from
an agreed time point (not by using records made in the past). The health
outcomes to be measured are defined in advance, the way to measure the
effects of treatment on these outcomes is planned in advance, and the
results are then measured at specified times.
28
Statistically significant
Systematic review
A type of research that involves searching for all the published evidence
(e.g. studies) to answer a particular question, such as whether a particular
treatment is more effective than no treatment or as effective as another
treatment for treating a specified health condition in a certain group of
patients (e.g. children, adults). There are internationally accepted standards
for good quality systematic reviews.
29
I2
II
III-1
III-2
III-3
IV
Explanatory notes
1. Definitions of these study designs are provided on pages 78 of How to use the evidence: assessment and application of scientific evidence
(NHMRC 2000).
2. A systematic review will only be assigned a level of evidence as high as the studies it contains, excepting where those studies are of level
II evidence. Systematic reviews of level II evidence provide more data than the individual studies and any meta-analyses will increase the
precision of the overall results, reducing the likelihood that the results are affected by chance. Systematic reviews of lower level evidence
present results of likely poor internal validity and thus are rated on the likelihood that the results have been affected by bias, rather than
whether the systematic review itself is of good quality. Systematic review quality should be assessed separately. A systematic review should
consist of at least two studies. In systematic reviews that include different study designs, the overall level of evidence should relate to each
individual outcome/result, as different studies (and study designs) might contribute to each different outcome.
30
The Homeopathy Working Committee was made up of experts in evidence-based medicine, study
design, and complementary medicines research. The Committees roles were:
to guide an independent review of the evidence on the effectiveness of homeopathy. This included
providing advice on methods of evaluating and interpreting relevant information.
to guide NHMRC to produce a document that summarises current evidence on whether
homeopathy is effective for health conditions, and give Australians information to help them make
decisions about using homeopathy as part of their health care.
Homeopathy Working Committee members are listed in Table 2. Information about individual
committee members credentials and declarations of interest are available at www.nhmrc.gov.au/yourhealth/complementary-medicines/membership-homeopathy-working-committee.
Table 2. The Homeopathy Working Committee
Name and qualifications
Chair
General practitioner
Rheumatologist
Director of the Australian Health Workforce Institute, University of
Melbourne, Victoria (to September 2013)
Executive Director Research, Northern Hospital, Epping, Victoria
Former board member, Australian Centre for Complementary Medicine
Education and Research, University of Queensland
Neuroscientist
Consumer
31
Pharmacist
Discipline head for complementary medicine teaching and research, School
of Pharmacy and Griffith Health Institute, Griffith University, Gold Coast,
Queensland
Member, Clinical Trials Coordinating Centre, Griffith University
Member, Society for Medicinal Plant and Natural Product Research
Research scientist
Director, St John of God Subiaco Hospital Research network
Adjunct Professor School of Health Sciences, Curtin University
Adjunct Professor, Centre for Comparative Genomics, Murdoch University
Adjunct Associate Professor, School of Surgery and School of Pathology and
Laboratory Medicine, University of Western Australia
Adjunct Associate Professor, Faculty of Medicine, University of Notre Dame,
Western Australia
Founding Director, Australian Clinical Trials Alliance
Member, Research Committee, NHMRC
Member, Australian Health Ethics Committee, NHMRC:
Triennium 20102012
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1 These criteria should not be treated as universal rules or principles that are applicable to all clinical contexts. The criteria were developed in
response to a specific activityNHMRCs overview of the effectiveness of homeopathy for treating clinical conditions in humans.
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When there was a body of evidence addressing the intervention versus placebo, and another body of
evidence addressing the intervention versus another comparator, two separate evidence statements
were generally prepared (with all other comparators included in the one evidence statement).
Separate evidence statements were not developed where there was more than one specific type of
homeopathic intervention. For example, where one study examined X homeopathic treatment and
another examined Y homeopathic treatment, the evidence statement refers broadly to homeopathy
rather than the specific treatment. This approach is consistent with other studies that assess the
efficacy of an entire class of therapies: for example under the headings antibiotics or physiotherapy
for some conditions.
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statements. If the reviews still could not be split, the lower quality score was used in the
evidence statement to avoid any overestimation of the studys quality.
If the quality of studies was variable, the quality range was stated, for example poor
medium; poorgood.
If the authors did not assess quality then it was stated as unreported.
4. The number of participants (total number of participants across all studies and the range).
Number of participants was listed as the total number of participants ever randomised for each
question, and a range for the smallest to largest study.
Where there were only two included studies, the number of participants for each study was
stated, rather than the total number of participants or the range.
Where there was only one study, the description of the body of evidence included the size
ofthestudy described in words, as follows2:
< 50 : very small
50 to 149: small
150 to 499: medium
500 to 999: large
1000: very large
5. A description of the intervention.
Where all studies examined one specific homeopathic treatment (eg homeopathic Arnica),
thiswas explicitly stated. Otherwise, the intervention was simply described as homeopathy.
6. A description of the comparator.
As noted above, placebo and other comparators were addressed separately, in two distinct
evidence statements.
Where multiple other comparators were examined, these were referred to as other therapies,
with details provided in brackets.
Where only one or two other comparators were examined, the comparator was explicitly
described, rather than using the term other therapy.
7. A statement about the findings of the included studies / reviews.
A description of the findings of the included studies / reviews was only included in the evidence
statement where there were good quality studies of sufficient size, for example: The one
medium sized, good quality trial ([number] participants) did not detect a difference between
homeopathy and placebo in the treatment of people with [condition].
For the purposes of the homeopathy overview, studies were considered to be of sufficient size
where N>150 (i.e. those studies categorised as medium sized or larger), as the outcomes were
generally continuous outcomes.
If different systematic reviews reported different numbers of participants for the same study,
it was generally assumed that the study was of the smallest size reported to avoid any
overestimation of the sample size.
If the study quality was unreported, it was generally assumed to be poor quality to avoid any
overestimation of the studys quality.
2 Thresholds for descriptions of study sizes were determined as a general guide for intervention studies of this nature, based on the (generally)
continuous outcomes measured in the studies. The following study was considered in the development of these thresholds: Influence of trial
sample size on treatment effect estimates: meta-epidemiological study. BMJ2013;346:f2304.
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If different systematic reviews reported different quality scores for the same study, it
was generally assumed that the study was of the lowest quality reported to avoid any
overestimation of the studys quality.
In theory, the results of meta-analyses may have also been discussed in this part of the evidence
statement. However, it was considered that all of the meta-analyses for specific conditions
(i.e.those that had the potential to be included in evidence statements) had included studies
that were of poor methodological quality/had a high risk of bias. A decision was made to state
the findings of studies that were of good methodological quality and sufficient size in favour
ofmeta-analyses that included poor quality studies.
If there was more than one study that suggested that homeopathy is more effective than placebo
or as effective as other therapies but due to the number, size and/or quality of those studies the
findings are not reliable, a general statement to that effect was made, for example: These studies
are of insufficient [quality] / [size] / [quality and size] / [quality and/or size] / [quality or size] to
warrant further consideration of their findings.
In all other circumstances, no statement of findings was included in the evidence statement.
Where a systematic review did not identify any studies, this was stated and the date of the
systematic review was included, for example: One systematic review ([year]) did not identify any
prospectively designed and controlled studies that assessed the effectiveness of homeopathy in
people with [condition].
GRADE description
High
Moderate
Low
Very low
3 For further information on the GRADE methodology see: Grading Quality of Evidence and Strength of Recommendations. Grade Working Group.
BMJ V328, 19 June 2004.
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The LOC was then upgraded or downgraded depending on the limitations or strengths of the studies
contained in the systematic reviews (see TableB.ii).
Table B.ii: Upgrading and downgrading
Decrease grade if:
For the homeopathy overview, the information available for downgrading evidence was
predominantly as follows:
Quality: -1 or -2 depending on seriousness of limitation to study quality.
If quality of the included studies was not reported in the systematic review then those studies
were assumed to be poor quality (-2).
NB: if quality is assessed using Jadad then any score <5 could indicate serious or very serious
bias. Therefore it was often appropriate to give a range for the LOC (i.e. subtracting both -1 and
-2) e.g. moderate-low.
Precision: related to the number of participants in individual studies and as a whole. Small is
relative but in general any study with less than 150 participants is small.
Very sparse data = 50 (-2).
Sparse data = 51 149 (-1).
A level of judgement was required. For example, three small / very small studies with a total
sample size of 110 might be considered sparse to very sparse, so would be downgraded by 12
and a range presented.
The remaining GRADE factors were difficult to apply to an overview; however, downgrading based
on the quality of the systematic review/s was also appropriate in some situations (as a poorer quality
systematic review is more likely to result in bias).
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There are two approaches for designing studies to evaluate medicines; null hypothesis and estimation
of effect. The standard approach used in Health Technology Assessments is the null hypothesis,
with the onus of proof on those who are proposing that the treatment be used (e.g. manufacturers,
practitioners or researchers). Any claims about the effectiveness of a medicine are not accepted
without evidence from clinical trials that compare the treatment with placebo in patients with the
clinical condition.
In this review of homeopathy, the null hypothesis for each clinical condition was that homeopathy
has no effect as a treatment for that condition unless there was sufficient reliable evidence to
demonstrate otherwise. The only exceptions to this principle were:
where there were no studies (or only one small and/or poor/unknown quality study) identified
fora particular clinical condition; or
where the evidence was so poorly reported so as to be uninterpretable.
In these cases, the HWC determined that no conclusion could be drawn about effectiveness,
ratherthan assuming the null hypothesis.
In general, separate conclusions were not developed where there was more than one specific type of
homeopathic intervention. That is, where one study examined X homeopathic treatment and another
examined Y homeopathic treatment, the conclusion refers broadly to homeopathy rather than the
specific treatment. The only exception to this principle was for the condition Children with diarrhoea,
where there was a difference in the evidence base for combined homeopathy and individualised
homeopathy. In this instance, the conclusion sentence separately reflected the evidence base for each
type of homeopathy.
In the final concluding statement, the intervention is described as homeopathy even if a more
detailed description is provided in Element 1 of the evidence statement.
For studies that compared homeopathy with placebo, the null hypothesis assumed by the HWC
wasthat homeopathy is no more effective than placebo.
For studies that compare homeopathy with another therapy, the null hypothesis assumed by the
HWC was that homeopathy is not as effective as the other therapy. It is noted however, that due to
the scope of the homeopathy overview, the appropriateness of the comparator was generally not
assessed. For the purpose of framing the null hypothesis, an implicit assumption has been made that
the comparator is more effective than placebo (i.e. the concluding statement is based around whether
homeopathy is as effective as another treatment, without a consideration of the appropriateness
ofthat treatment). The HWC acknowledged that this could mean that homeopathy is found to be
aseffective as an ineffective treatment.
Further detail on the development of evidence statements is provided at Appendix C of the
OverviewReport.[2]
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15. Bornhft, G. and P. Matthiessen, eds. Homeopathy in healthcareEffectiveness, appropriateness,
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16. Bornhoft, G., et al., Effectiveness, safety and cost-effectiveness of homeopathy in general practice
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17. Gurtner, F., The report Homeopathy in healthcare: effectiveness, appropriateness, safety, costs is
not a Swiss report. Swiss Medical Weekly, 2012. 142: p. w13595.
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Weekly, 2012. 142: p. w13594.
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19. Higgins, J.P.T. and S. Green, eds. Cochrane Handbook for Systematic Reviews of Interventions
Version 5.1.0 [updated March 2011]. 2011, The Cochrane Collaboration.
20. Dean, M.E., et al., Homeopathy for mental fatigue: lessons from a randomized, triple blind,
placebo-controlled cross-over clinical trial. BMC complementary and alternative medicine, 2012.
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placebo-controlled trials of homoeopathy and allopathy. Lancet, 2005. 366 (9487): p. 72632.
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