OVERVIEW OF RBM IN NIGERIA IN NIGERIA: CURRENT TREATMENT POLICY DR. T. O. SOFOLA NATIONAL COORDINATOR
PREAMBLE
Generally, malaria causes 300-500 million illnesses and 1-2 million deaths every year.
In Nigeria Malaria is responsible for 60% of Out Patients visits 30% of childhood mortality 25% of infant mortality 11% of maternal deaths
N132 billion is lost to Malaria annually in form of treatment costs, prevention, loss of man-hours, etc.
CONTROL OF MALARIA IN NIGERIA
Several initiatives and programmes
RBM now on ground since 1999
Historic Summit in Abuja, April 25, 2000 (Abuja Declaration and Targets)
ROLL BACK MALARIA
A partnership involving governments, private sector, research organizations, civil society, media.
Aim to reduce malaria by half in 2010
Abuja Targets (By 2005); 60% prompt access to appropriate treatment in 24hrs 60% of (children Under 5yrs and pregnant women) use insecticide treated nets (ITNs) 60% pregnant women to use Intermittent Preventive Treatment (IPT) with SulfadoxinePyrimethamine
• • •
RBM STRATEGIC PLAN
PRIORITY ISSUES:
Case management including Home Treatment
Promotion of ITN Use
Intermittent Preventive Treatment (IPT) for Malaria in Pregnancy
Partnership
RBM PROCESS IN NIGERIA
Inception Phase Consensus Building Meetings Deskwork analysis Situation Analysis Collection of baseline data for monitoring and evaluation Fostering of effective Partnership through formation of Partners forum and National Malaria Control Committee Development of National and States Plans of Action, Strategic Plan. Development of time-bound implementation plans with specific Interventions and products.
RBM PROCESS IN NIGERIA
Implementation Stage: Focusing on these 1.
2.
Disease Management – improve access to quality affordable anti-malaria drugs, encouraging home care and training of health care providers. Disease Prevention – Promote use of ITNs, environmental management, and intermittent preventive treatment of malaria in pregnancy.
RBM PROCESS IN NIGERIA CONTD. 1.
IEC/Social Mobilization – for community action
3.
Operational Research to discover new tools and better interventions
5.
Health systems development – Improve quality of care and make facilities able to handle / refer cases
ITNs COVERAGE ITN Coverage, 2001-2005 60 50 40 coverage (%) 30 20 10 0 2001
2002
2003
2004
year
2005
Abuja
ACCESS TO TREATMENT Access to Treatment, 2001-2005 60 50 40 Cov (%) 30 20 10 0 2001
2002
2003
2004
year
2005
Abuja
INTERMITTENT PREVENTIVE TREATMENT – (IPT ) Coverage IPT, 2001-2005 60 50 40 Cov (%) 30 20 10 0 2001
2002
2003
2004
year
2005
Abuja
CASE MANAGEMENT
Improving Case Management involves: •
•
• •
•
Instituting evidence based treatment Policy through monitoring resistance trends. Capacity building to improve prescription practices among health professionals Encouraging Home Management of Malaria Making effective and affordable quality agespecific anti-malaria drugs at community and home levels Building capacity of community based health support personnel e.g. PMVs
ACCESS TO TREATMENT
ACHIEVEMENTS TO DATE
Policy on PPD accepted by Govt. PPDs produced by private sector (Public / Private Partnership ensured) PPDs in the market Capacity building of health professionals through cascade training Work on orientation of health workers and community agents has started Monitoring of drug efficacy through studies at sentinel sites were instituted DTET carried out in 2002, previous one was done in 1987 Social marketing of PPD has been piloted in three States. Guidelines on use of PPD produced Rapid assessment on the use of anti-malarial drugs conducted Consensus Meeting on Drug Policy Review
National Treatment Policy
First line drug – Chloroquine Second line drug – Sulphadoxine Pyrimethamine Criteria for second line drug: Ineffectiveness of the first line drugs Adverse Reaction to first line Resistance problems
National Treatment Policy Contd
MALARIA MGT WITH PRE-PACKAGED DRUG (PPD) REASONS FOR PPD
All patients grouped in 4 age-groups Chloroquine
•Reduce adulteration/fake drug Colour •Improve patients´compliance Yellow *Simplify dosage regimen no breaking of tablets etc.)
Agegroup
•Although drugs are best given according to bodyweight, in practice majority of the population do not have weighing-scales. Age is therefore used for PPD
Day 1
Day2
Day3
Below 1yr 75mg(1tab) 75mg(1tab)
75mg(1tab)
Blue
1 – 6yrs
150mg(1tab)
White
>6–12yrs
150mg x2tabs 150mg x2tabs 150mg x2tabs
Pink
>12 years
300mg x 2tabs 300mg x2 tab 300mg x1tab
150mg(1tab) 150mg(1tab)
Patients in 4 age-groups Sulphadoxine-pyrimethamine Colour Agegroup Single dose Paracetamol*
•It is colour coded, age specific to aid recognition by less educated
Yellow 2–24months 250+12.5mg x1tab 125mg x1tab Blue
2-6yrs
500+25mg x1tab
•It is labelled for manufacturers to protect and maintain quality & standards of their product
White
>6-12yrs
500+25mg x2tabs 500mg x1tab
500mg x1tab
Pink >12yrs 500+25mg x3tabs 500mg x2tab * Paracetamol is co-packed with SP and may be given thrice daily for 3 days 7
LESSONS LEARNED
Local production of PPDs feasible
PPDs available in the market
PPDs acceptable
CHALLENGES
There is need to: Work out a framework to update policy in line with results of the DTET Sustain and indeed improve on the public private collaboration through the process Use available evidence and lessons from other countries to go through the process efficiently Move through this process fast in collaboration with all relevant stakeholders
When we join hands, pictures like this will be a thing of the past THANK YOU!!!
THANK YOU