June 19, 2002
ADMINISTRATIVE
ORDER
No. 129–A
series 2002
NATIONAL POLICY ON DIAGNOSIS AND
CHEMOTHERAPY FOR MALARIA
I. RATIONALE
Drug resistance has become a major problem hampering
current efforts in the control of malaria in the Philippines. Results of recent
studies show that in vivo determinations of treatment failure rates for
Chloroquine (CQ) and Sulfa–Pyramethamine (SP) monotherapy in sampled
population from different regions in the country far exceed the 25% WHO
benchmark for clinical failures (MCS, 1996 – 1997, Preliminary Report ENHR,
2000, ADS – MCP, 1997 – 2000 and WHO/RBM, 2000 – 2001). These high treatment
failure rates provide a very strong evidence of the Department of Health to
immediately review and change existing anti–malarial drug policy in the country
(WHO Guidelines, 2000).
In such cases as monotherapy failure, combination
therapy becomes the more viable alternative in improving efficacy of available
drugs. Therapeutic efficacy studies done in Compostela Valley showed 100%
efficacy of artemether–lumefantine combination, which would make it the
better choice in terms of efficacy, safety and tolerance profile and
availability as a fixed dose formulation (WHO, 2001). However, this combination
has been restricted to be used as a second – line drug in view of these
reasons: limited findings of its safety for very young children, pregnant women
and breastfeeding mothers and their babies and the inadequate capability of the
current health infrastructure in many endemic areas to provide confirmatory
diagnosis. The DOH therefore has to be given time to explore and further study
the use of artermisin–based combination before it is adopted as a first–line
treatment.
On the other hand, CQ+SP combination showed lower
treatment failure rates of >15% in the sampled population studied in Agusan
and Compostela Valley (ADS – MCP 2001 and WHO/RBM, 2001). To ensure that there
is always safe, effective and affordable treatment which is accessible to the
population at risk, the CQ+SP combination offers a better and more practical
anti–malarial option in the short term.
This administrative order prescribes policies and
guidelines for diagnosis and combination chemotherapy for malaria, with the
objective of reducing further development of drug resistance and ultimately
towards reducing morbidity and transmission and preventing complications and
mortality due to malaria.
II. COVERAGE
This order shall apply to all government (national and
local) and private health facilities nationwide.
III. GENERAL
POLICIES
A. The
new anti–malarial drug policy as prescribed herein and its implementation shall
be subject to continuous review and evaluation by technical experts.
B. Implementation
of this diagnosis and chemotherapy in the control of malaria shall always be
within the context of primary health care approach. Provision of services shall
be integrated with other health services available at the different levels of
health care in endemic areas.
C. Implementation
shall be done in phases. This is to allow the National Malaria Control Programme
to manage the increase in cost of diagnosis and treatment and for the regions
to strengthen and expand its capacity for implementation. Areas shall be
prioritized as follows:
1. Priority
1 – pilot areas for implementation will consist of project sites where capacity
building for drug policy implementation has already been carried out or
underway, malaria microscopy centers at the Rural Health Units are already
established or upgraded and tools and system for monitoring is being developed,
i.e. Palawan, Agusan del Sur, Roll Back Malaria sites in Compostela Valley,
Davao del Sur and Kalinga;
2. Priority
2 – category A provinces and areas who had epidemics in last 2 years.
3. Priority
3 – category B provinces
4. Priority
4 – all other endemic provinces
D. Advocacy,
training of health workers have to be conducted, systems need to be in place
and funding requirements need to be secured prior to the full implementation of
this policy.
E. Support
from and collaboration among government, non–government and private organizations
shall be a necessary requisite for its successful implementation.
IV. PROGRAM
POLICIES
A. Combination
treatment for malaria
B. Diagnosis
1. Microscopy
shall remain as the “gold standard” for diagnosing malaria. All area with a
functional laboratory shall at all times employ this standard.
2. To
ensure quality, a quality assessment and assurance system shall be put in
place. Specifically, slide validation of all confirmed positive and proportion
of negative smears shall be done by designated provincial/regional validators
at least once a year.
3. Diagnosis
through Rapid Diagnostic Test (RDTs) shall initially be implemented in pilot
areas until operational experience in its use has already been gained.
Eventually, its deployment will be limited to the following areas:
a. Areas
with no microscopy centers
b. Areas
which require two (2) hours travel to the nearest microscopy centers.
C. Treatment
D. Treatment
during emergency situations or epidemics
V. SUPPORT
SYSTEMS
A. Health
Human Resource Development
B. Logistics
Management System
C. Reporting
and Surveillance System
VI. ROLES
AND RESPONSIBILITIES
A. The
Center for Infectious Diseases
B. Centers
for Health Development
C. Local
Government Units
1. Provincial
Health Office (PHO)
2. Rural
Health Unit (RHU)
3. BHWs/FAWs/other
Volunteers
D. Non–Government
Organizations
VII. REPEALING
CLAUSE
Administrative Order No. 19 series 1996, all other
orders and related issuances inconsistent with the provisions of this issuance
are hereby rescinded.
VIII. EFFECTIVITY
This order takes effect immediately.
MANUEL M.
DAYRIT, MD, MSc
Secretary of
Health
This order
was deliberately shortened to only highlight responsibilities inherent to a
medical technologist.
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