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PREFACE
APOC AT MID-POINT : SO FAR SO GOOD
PREFACE
APOC AT MID-POINT:
SOFAR
SOGOOD
The
African
Programme for Onchocerciasis Control (APOC) was launched in December 1995on the tidal wave of the
resounding successof the 2l-year old
Onchocerciasis Control Programmein West Africa (OCP). Six
yearslater and now at the mid-point of its
pre- determined existenceit
is time to take stock and plan for the second half.This
special Supplement contains a setof
articles that focus on somekey
areasof
theactivities of APOC in the first phase.
Eacharticle
makesa critical
appraisalof
the major achievements and shortcomingsof
the Programmefrom
the startof
operationsin
1996 andidentifies
the main challengesfor
Phase2. A
succinct accountof the
stateof affairs
at thebirth
of APOC would help to put the achievements and the challenges in better perspective.The ultimate goal of APOC is "to eliminate
onchocerciasis asa
diseaseof
publichealth
importance andan important
constraintto
socio-economic development throughoutAfrica".
The prescribed strategy by which this goal is to be attained is "the establishment of a self-sustainableivermectin
treatment programme"in
thehigh-risk
zonesof all
the endemic countries outside the OCParea.
Where feasible,control would
be effectedby local
vector eradication.The
five
mainpillars
aroundwhich
the successof APOC
was predicatedare:
1. The empowerrnent of the endemic communitieswithin
the contextof
Primary Health Care (PHC).2.
A
unique global partnership between the private andpublic
sectorsincluding
the affected communities themselves,forming
a formidable alliancein
pursuitof
a common objective. 3.The
development and opportunearrival on
the scene, through research,of
innovative tools and strategies that make the proposedcontrol
operationsboth
feasible and cost-effective. 4.The unprecedented commitment
of
a Pharmaceutical Company- Merck &
Co. Inc., to donateI
through the Mectizan@ Donation Programme
(MDP)
the ivermectin (Mectizan@,for
as longas
neededto treat
onchocerciasis,and 5. The vast
experienceof OCP and the
synergy derivable from the physicalproximity
and temporal overlapof
the two programmes.There were major concerns
also.
Notable among these was theprobability of
'donor-fatigue', which
haslargely
recededin
the faceof
the impressive Economic Rateof
Return (ERR) and general satisfactionwith APOC's
progress over the years. There were also some doubts about securing appropriatereceptivity
and commitmentof
the participating countries to the APOCinitiative
given the increasing andconflicting
demandsof
emerging diseases onnational budgets. A third and
daunting concernwas
relatedto the scientifically
derivedestimation that ivermectin would have to be
consumedby at least 65
o/oof the
target populationsof all
the hyper- and meso-endemic areas at least once every year for upwardsof
20 years
if
the objectiveof eliminating
onchocerciasisfrom
the continentis to
be achieved.The progress made towards overcoming these concerns are contained
in
the accompanying papers.There have been many changes since
APOC
commenced operations. The pre-APOC estimateof
numberof
people arisk
and to be treated has more than doubled as a resultof
the applicationof REMO/GIS.
The numberof
people treated every yearwith
ivermectin, usingAPOC's
Community-directed treatment(ComDT)
approach has risen sharplyfrom
8million
in
1996,to over 20 million in 2000.
Substantial capacitybuilding
has taken placeon all fronts, including diverse training
programmesthat range in content from
administrative competenceto skills
neededfor field operations. Devolution of
operational research to endemic country scientists and thepromotion
and empowermentof local
non-governmentalorganizations (NGDOs) by the International NGDOs are crucial
investments towardssustainability of the
programmethat augur well for other future health and
developmentprogrammes. The
prospectsof effectively
integratingCommunity
directed treatmentwith
2
Ivermectin (CDTI) into the health
system,and its potential as an entry point for
other programmes are very bright.The potential impact of APOC on the
disease spectrum andthe
health servicesof participating
countries areenorrnous. With the empowernent of the
endemic communitieswithin
the contextof
PHC the health care stakes and bar of performance have been raised to alevel that must be sustained in Phase 2 of APOC.
There are many challenges
to
be facedin APOC
Phase2.
Someof
these have beenidentified and discussed in the seven articles of this supplement. Most of
theseunderstandably have to do
with sustainability.
Sufficeit
to state thatif
these challenges are to be successfully met then the partnership that has broughtAPOC to this
commendable stagewould
haveto
remaincommitted.
The Managementof APOC
andits
support systems,like
the Technical Consultative Committee (TCC), need to be adequately strengthened so as to be able to copewith
the ever expanding scopeof activities.
This is more so now that OCP which has provided a substantial amountof
administrative and infrastructural back up to APOC has only a few more months beforewinding
up.As has been
observedin all previously
successfulpublic health
disease control programmes, notably the global smallpox eradication programme and OCP, contemporaneousscientific
researchis a sine qua non for ultimate success. APOC's main
investment in operational research is channeled throughWHO/TDR
where the searchfor
a macrofilaricide that is suitablefor
mass treatment and a newtool for
rapidmonitoring
of treatment continues.In this regard
it
is nice to end on a cheerfulnote.
As we were about to go to press, report of aTDR-APOC
supported multi-centre study has indicated that a rapid epidemiological methodfor identiffing
areas and levels of Loaloa
endemicity has been developed that would provide an importanttool for
dealingwith
one of the major challenges that is beingcaried
over fromAPOC phase I to
phase2, namely the
issueof
severe adverse events(SAE) following
treatmentwith
ivermectin in some areas where onchocerciasis and loiasis coexist.3
According to the Report of the External Mid-Term Evaluation, "APOC
has madesignificant
and satisfactory progress towards meeting itsobjectives". This
Supplement tells partof
the story onhow it
has done so,how
farit
has gone and how much fartherit
must go before the curtain is drawn on its operations.Dr. Azodoga
SEKETELI
Director,
African
Programme for Onchocerciasis Control (APOC)4
PARTNERSHIP AND PROMISE:
EVOTUTION OF THE AFRICAN RIVERBTINDNESS
CAMPAIGNS
1
Partnership and Promise: Evolution of the African Riverblindness Campaigns
AUTHORS:
B. BENroN,' J. BuMp,'''' B. Lrcse,3Atto
A.
SEKETELI,aADDRESSES OF AUTHORS:
Onchocerciasis Coordination Unit, The World Bank, 1818 H. Street
NW,
Washington, DC 20433, U.S.A.Institute of the History of Medicine, The Johns Hopkins University, 1900 E. Monument Street, Baltimore, Maryland 21205, U.S.A.
Human Development Network, Africa Region, The World Bank, 1818 H. Street NW, Washington, DC 20433, U.S.A.
African Programme for Onchocerciasis Control, 01 B.P. 549, Ouagadougou, Burkina Faso
Address
for
CorrespondenceDr
J. BumpInstitute
of theHistory
of Medicine, The JohnsHopkins University,
1900 E.Monument
Street,Baltimore, Maryland
21205, U.S.A E-mail: jbump@worldbank.org
Short running
title:
Partnership and Promise of APOC)
3.
4.
ABSTRACT
The article describes the evolution of the partnership between various health and developmental agencies that has sustained
the
campaign against riverblindnessin Africa. The
international community was oblivious to the devastating public health and socio-economic consequencesof
onchocerciasis
until
towards the end of the 1960s and the beginning of the 1970s when a UNDP- supported Missionto
WestAfrica
and avisit to
the sub-regionby
the Presidentof
the World Bank culminated,in
1974, in the inauguration of the Onchocerciasis Control Programme in WestAfrica (OCP).
OCP wasa
landmark eventfor
the Bank asit
representedits first
ever direct investment in a public healthinitiative.
The resounding success of the OCP is a testimony to thepower of the
partnershipwhich, with the
adventof the Mectizan Donation
Program, was emboldenedto
extend the scopeof
its activitiesto
encompass the remaining endemic areasof Africa
outsideOCP.
The paper discusses the progress that has been madein
consolidating the partnership and the prospectsof
adapting the various strategiesof
theAfrican
Programmefor
Onchocerciasis Control (APOC), such as the community-directed treatment(CDTI)
concept soas to entrench an integrated
approachthat couples strong regional coordination with
empowerment of local communities to address many other health
problems.INTRODUCTION
The control of West Africa's
riverblindnessis a glowing, but unlikely,
successstory
in international publichealth.
Despite its crippling effects, this once-widespread disease remainedvirtually
undetected during the colonialperiod.
Lost among the numerous and varied tropical diseases, onchocerciasis ranged unchecked throughoutmuch of the 20h century as
well,attracting international interest only in the last 50 years. Running since 1974,
the OnchocerciasisControl
Programmein West Africa (OCP) has eliminated
riverblindness (onchocerciasis) as a public health problem in thel0
countries whereit
operates. Inaugurated in 1995,the African
Programmefor
OnchocerciasisControl (APOC)
extended operations toinclude the remaining 19 infested
countrieson the African continent. Given the
low internationalprofile of
the disease and the technicaldifficulty of its
control,it is
particularly impressive that OCP and APOC have been successful. This article outlines how onchocerciasis becamevisible to two
previously independentcommunities-international
health experts and international development professionals-and follows the ongoing resultsof
their collaboration, the OCP and APOC programmes.Onchocerciasis
is a debilitating welter of skin
disease, blindness,and itching to
its sufferers(Buck, 1974).
These symptoms are the body's immunologic responseto millions of tiny
worms(microfilaria),
spewed forth by adult worms (macrofilaria), whichlive
coiledin
the human hostfor
10-14 years.If
removed and unwound, these adult worms routinely measure 60 or more centimeters long (Malatt andTaylor,
1992). Conveyedin
ajuvenile
phase via unluckybites of the aptly
namedblackfly
Simulium damnosum, onchocerciasis was,until
recently, endemic to WestAfrica
and even now remains a serious public health problem in the majorityof
countries on the
continent.
Commonly called riverblindness after its geographic locus and mostvisible symptom, those infected are cursed with interminable itching, thickening
and depigmentationof the skin,
andin
an averagel}Yo of
cases, permanentblindness. In
someheavily
infectedvillages of
pre-OCPWest Africa, this figure was
severaltimes higher-
blindness among adults
often ran
above30% (Waddy, 1969). When highly
prevalent, the disease eventually forces communities awayfrom
thefertile river
valleys asvillage
blindness rates reach devastatingproportions. With too few
able-bodied peopleleft to
tend fields, food shortages and economic collapse evict residents. Moving to hardscrabble highlands offers some)
respite
from
further infection,but is
not without its ownproblems-poor
soils andlittle
water cripple farmingefforts.
Since 1974, OCP has sought to end this scourge.Despite riverblindness' wide-ranging consequences,
it was an unlikely
targetof
the internationalhealth community. Except to the
affected communities, onchocerciasis wasinvisible until recently. [t went
unnoticedby colonial
administrations even asthey
fought schistosomiasis, sleeping sickness, syphilis, malaria, and a rangeof
other labor-related diseases.Its
transmissioncycle was not
describeduntil
1926(Blacklock, I926a, 1926b). It
was notdefinitively linked to
blindnessuntil
almost 1950(Waddy, 1949).
Riverblindnessis
also an exclusively rural disease, affecting only the poorest and most remotecommunities-populations with the fewest
resourcesand the
least accessto health services. Further, the
disease is technicallydifficult to
control becauseof
theworm's
long lifespan, the prevalenceof
infected populations,the vector's very long flight
range, andthe
absenceof
suitable pharmaceutical optionsbefore
1987. These factors combineto
suggest that onchocerciasiscould
have easily gone unchecked, ravaging locally, unnoticedinternationally. All
the more curious then, that the internationalhealth community
shouldfind one of its
greatest successesin
onchocerciasis control.Rising awareness among
international
health professionalsAfricans were
all
toofamiliar with
onchocerciasis, butfull
knowledgeof
its characteristics and symptoms eluded western medicsuntil
afterWorld
WarII.
During the colonial period,"craw- craw,"
asit
was then known, was identified as a skin disease. Reaffirming European notionsof
disease and place, craw-craw went unnoticed as one among countless
tropical afflictions. A
more precise understanding began to emerge
in
1875, when SurgeonJohn O'Neill
of the H.M.S.Decoy identified craw-craw as a
filarial
disease, that is, one caused by a parasiticworm.
Mooredoff
Cape Coast Castle, Ghana,O'Neill
borrowed six patients from Addah Fort Hospital, noting"[craw-craw's]
intractability, contagiousness, and irritating nature so aroused my attention thatI
was induced
to
bestow much time on its microscopic examination, and succeeded at length in discoveringa filaria..." (O'Neill,
1875,p.265). The filaria itself was later
described by Leuckartin
1893, who namedit
"Onchocercavolvulus."
The next breakthrough waited more than 30
years. In
a pairof
1926 publications, D. B.Blacklock of the Sir
Alfred
Lewis Jones Research Laboratory in Freetown, Sierra Leone cleverly unraveled the parasite's transmission and developmentcycle (Blacklock,1926a,
D). Blacklock4
traced the parasite through the blackfly
vector-Sizulium
damnosum-discovering that, aswith
malaria, the onchocerciasis parasite undergoes an intermediate maturation in the insect.These discoveries
of
riverblindness' cause and transmission cycle werefollowed by
adeepening understanding
of
the disease'seffects.
Though WestAfrican
blindness rates werelong known as
amongthe world's
highest,onchocerciasis-historically viewed as a
skindisease-has only
recently receivedit's
shareof the blame. In its
stead,the role of
other perennialculprits was magnified-Vitamin A deficiency and
trachoma,to
nametwo. A
tentative
link
between blindness and onchocerciasis had been made as early as 1916by
Robles(Luna,
1918),working in
Guatemala, wherethe
disease had been inadvertently imported byslave
traders(Nelson,
1991),and by Rodhain in
1920,working in the Belgian
Congo.Community observations
by
Hissettein
1931 were thefirst
indicationof
a major public healthproblem-studies in the
Sankururiver
areaof
Congo revealed amongthe
population 20o/oblindness and
50% "ocular complications." Finally, a definitive
studyby Waddy in
L949 conclusively linked onchocerciasis andAfrica's
rampant blindness. Present-day understandingsof
onchocerciasis consequently emphasizeblindness, in addition to the
long-identified dermatologic symptoms.As the
full
effects of the scourge became known, onchocerciasis attracted more and moreattention from European and American specialists; particularly well
represented were researchersfrom
ORSTOMT (assignedto
OCCGE2),reflecting
longstanding French colonial involvementin
theregion.
Manyof
ORSTOM's studies later proved crucial to OCP (Le Berre, 1966; Duke, 1990)Armed
with
knowledgeof
the disease andits
effects,public
health workers struggledwith
a limited arsenal. Chemotherapeutic options suramin, a macrofilaricide, (VanHoof,
1947)and
diethylcarbamazine(DEC), a microfilaricide, (Hewitt,
1947)both proved
unworkable outside the hospital because of severe side effects.A
surgical option, mass nodulectomy, proved ineffectivein trials (WHO 1987).
Vector control remained apossibility, but
struck many asunworkable in light of the environmental problems of
DDT
and the unsuccessful Global Malaria Eradication Programme of the 1950s and 1960s.Large-scale international attention
first
came to the disease inAfrica in
a 1968 technical conferencein
Tunisia(WHO
1969),initiated
largelyby
M6dicin-G6n6ral Pierre Richet, Dr.' Office de la Recherche Scientifique et Technique d'Outre-Mer (ORSTOM), now named " Institut de Recherche pour le Developpement (IRD)".
2 Organisation de Coordination et de Coop6ration pour la Lutte contre les Grandes Endemies.
5
Ansari, WHO's Chief of Parasitic Diseases (Duke, 1990), and an important paper later published
by B. B.
Waddy(1969).
Arrangedby USAID,
OCCGE, andWHO,
delegates convened to discuss the technicalfeasibility of
controlling onchocerciasisin
WestAfrica,
whereits
effects were most severe. Conference attendees concluded that given sufficient resources, control mightbe
possible,but would take two
decadesor more. Four years later, a
UNDP-supported Preparatory Assistance to Governments (PAG) mission leftfor
WestAfrica
to plan a long-term control strategy.The development assistance community becomes involved
Over the
courseof the
20'hcentury,
onchocerciasis worsenedin West Africa.
Growing populations, forced migration,climatic
changes, andcolonial
ambivalenceall
exacerbated an upswingin the
centuries-oldtide of infection (Hunter, 1966). On the
one hand,the
rising diseasetoll multiplied
the humanitarian and economic impactof
onchocerciasis. On the other hand, an unusually harsh seriesof
droughts intensified the needfor
agriculturaldevelopment-
particularly in the oncho-infested river valleys, with their better soils and ready water sources.The confluence of these two pressures exacted its cost in health and productivity, but also forged the alliance that would eventually succeed against the widening scourge.
By
1972, the international health community was alreadymobilizing to fight the disease.
Becauseof
the drought and famine, the international development community was also focused on the fateof
West
Africa.
Accordingly, and at the sametime
as thePAG
mission,World
Bank President Robert McNamara wentto
WestAfrica,
where he saw the broken villages andfallow
fieldsof
the endemic zones duringa flight to
Ouagadougou, UpperVolta
(now Burkina Faso), a then- common feafureof
the West-African savanna. From the air he saw curious clustersof
circularforms-the
surviving skeletons of once-occupied homes.Upon
landingin
Ouagadougou, McNamara, struckby the
devastationof the
disease, quickly arranged a specialtrip
to Bobo Dioulasso, Burkina Faso's second largest city, where hewould meet PAG mission
leaderB. B. Waddy and
French scientists, ReneLe Berre,
an entomologist, and Jean-JacquesPicq, a
microbiologistin the
Frenchmilitary (World
Bank, 1972). Deeply concerned, McNamara made his own investigation, discussing onchocerciasis at lengthwith
the scientistsin Africa.
Uponhis
returnto
Washington he continued his inquiry, making use of his extensive connections, including researchers at the Wilmer Eye Institute at the JohnsHopkins University.
McNamara became convincedthat control of the
disease was technically possible,given
enoughtime
andmoney-projected at 20
years and $120million
6
1972 dollars
(WHO,
1,973). Armedwith
personal conviction, McNamara threw his own weight and that of the institution he led behind the budding onchocerciasis control efforts.However,
in
managerial terms,the World Bank
wasnot
equippedto direct a
publichealth campaign.
In
fact, at that time, the World Bank had never even made a loanfor
a healthprogramme.
FinancingOCP would be the Bank's first initiative in the
sector,a
strikingdeparture
from the early '70s norm of large dams and
massiveinfrastructure
projects.Meanwhile, WHO already had scientists at work, and UNDP and FAO were developing
follow-
up agricultural plans. McNamara saw his comparative advantage-the World Bank could use its reputation and leveragewith
donorsto
fund the control programme and manage the finances.He insisted on unrestricted contributions made as grants only, and prepared donors
for
a lengthy campaign.The Onchocerciasis
Control
Programmein
WestAfrica
Through a combination of persistence, dedication, and happenstance, the Onchocerciasis Control Programme evolved
from
an ambitious planto a
sterling exampleof
diseasecontrol. At
the nexusof
health and development, riverblindness served as a rallying pointfor
many previouslydistant
groups.The
launchingof OCP in
1974 formalizedan
unprecedented collaboration between seven host countries,four
international organizations, andnine donors.
Sponsoring agencies included theWorld
Health Organization as the executor, theWorld
Bank as the fiscalagent, and the United Nations
Development Programmeand the Food and
Agriculture Organization sharingvarious
development planning responsibilities.This
partnership joinedintemational health
professionalswith their
counterpartsfrom the international
assistancecommunity. The
confluenceof
thesetwo
groups reflectedgrowing
appreciationfor
the importance of health to development.When Programme operations began
in
1974, the blackflies that transmit riverblindnesswere so
numerousthat
protection against themin
mostrural
areaswas impossible.
These swarnsof
flies were kept infective by a large parasite reservoir in the humanpopulation.
In the mid-1970s, entomologists recordedfly
biting rates in the thousands per person,per
dayin
someheavily infected areas (Walsh, 1977). In these and other so-called
"oncho
zones,"riverblindness reached devastating proportions, often infecting 90%o
or
moreof
the population(Crisp, 1956; Brown, 1962). Without a drug
treatment,the only effective
approach to onchocerciasiscontrol was to intemrpt
parasite transmissionby
substantially reducing the densityof
infectedflies.
The flies could be targeted at the larval stage because their breeding7
sites were confined to areas
of
fast-flowing water, such as rapids and damspillways.
Larvicide spraying could therefore be concentrated on these locations,killing
the disease-transmitting flies beforematurity.
Strict environmental monitoring and follow-up protective measures ensured the long-term healthof
non-targetfish, flora,
andfauna. Until
thelate
1980s,by
necessity, OCP was based exclusively on this strategy of vector control.Options expanded in the 1980s when Merck's Mectizan@ (ivermectin,
MSD)
was shown to be effective against the microfilariae that manifest riverblindness(Aziz
etal.,
1982a,1982b;Sutherland and Campbell 1990), without the harmful side effects
of
DEC (Greene etal.,
1985;Larviere et
al.,
1985; Awadzi etal.,
1986). Because ivermectin does notkill
adult worrns, which continueto
produce damaging microfilariae, keeping the symptomsat bay
therefore requires regular dosesfor
the remainderof
the adult worm'slife, up to
14years. The
advantagesof
ivermectin aretwofold.
First,it
relieves the symptoms and prevents further damage. Second, becauseit kills
thejuvenile
worrns, blackflies are lesslikely to
ingest (and later transmit) the parasites evenif
they do bite avictim
while he or shestill
harbors productive adultworms.
This second benefit, slowing transmission, is particularly helpful when beginning control efforts in new areas becauseit initially
reduces themicrofilarial
load in the population faster than larvicide spraying. In the original OCP area, control through larviciding had been mostly achieved by the time ivermectin became available, but the drug proved a key advantagein
heavily infected areas and added a therapeutic dimension to the programme, providingrelief for
victims and arrestingits progress. Additionally, World Bank staff, in
particularwere
intriguedby the
expansion possibilities held by the new drug.Following French regulatory approval
in
1987 (Brown andNeu,
1990), OCP conducted extensive field trials to assess ivermectin's public heath potential (Remme etal,
1990; Dadzie etal. 1991). It
was already known as a potent drugfor
individuals, but couldit
intemrpt regional transmission? What coverage would be necessary to protect communities? Underwriting these investigations wasMerck's
pledge to donate ivermectinin
whatever quantity needed andfor
aslong as necessary. Community trials were
supplementedwith
extensivemodeling
usingONCHOSIM, a
transmissionsimulator
developedwith OCP data by
researchersat
the Universityof
Rotterdam (Plaisier, 1990). These intensive epidemiological studies indicated thatwith long-term ivermectin
coveragealone-no larvicide spraying-it might be
possible to control riverblindness.The
African
Programmefor
OnchocerciasisControl
8
I
Emboldened
by their
successin West Africa and
empoweredby Merck's
donation, the riverblindness partnership embarked on a broadermission-defeating
the disease throughout the continent. Building on the knowledge and experience gained in OCP, the sponsoring agencies in 1995 launched a second programmeto
combat the restof Africa's
riverblindness, the African Programme for Onchocerciasis Control (APOC).APOC emphasizes the ivermectin strategy studied
initially
underOCP-using
long-term distributionof
the drugto
eliminate sickness and slow transmissionby
reducing the parasite reservoirin humans. Larviciding is
usedonly
peripherally becauseAPOC's
vast area makes spraying too costly, andthick
forests covering the area's principal rivers render aerial deliveryineffective,
aswell. APOC is
made possibleby Merck's
continued donationof
unlimitedsupplies of
Mectizan.
This generosity and the drug's effectiveness have facilitated the expansion of riverblindness control to the remaining infested areas of Africa.Riverblindness control based
on
ivermectin presents some advantages over larviciding alone, such as immediaterelief
for victims, but also raises new challenges, the largest of which involves sustaining a drug coverage threshold long enough to intemrpt transmission.With
rural diseases such as riverblindness, people who most need the drugs are often the hardestto
serve,living
beyond the reach of national health services. And riverblindness victims need doses every six to twelve months as long as they harbor even one adultworm.
Further, communities must take the drugfor two
decades or more to have anydefinitive
impact on transmission. For this reason, APOC's Community-Directed Treatmentinitiative
(Com-DT) has developed extensive networksof
CommunityDrug
Distributors(CDDs),
appointedby their
peersto work with
APOC's NGDO (non-governmental development organizations) partners to distribute Mectizan on a sustainable basis and to share knowledge of the disease. APOC's reliance on the regular and continued administrationof
the drug makes this distribution crucial to success.WHO's
expert epidemiologists estimate that communities at riskwill
need to take ivermectin for approximately20
continuous yearsto
eliminate the disease as apublic
healthproblem. During this
period, these scientists calculate, APOC must ensure at least 650/o treatment coverage throughout the affectedcommunities. In 2000,
membersof the
Community-Directed Treatment network achieved an average ivermectin coverageof
74%oin
the targeted communities(WHO
2001).These distribution efforts were augmented by a strong commitment to capacity-building: in the same year APOC trained
or
re-trained more than 77,000people.
The 22million
people now reached annuallyby
APOC represent less thanhalf of
thosewho will
be targeted as APOC expands over the next few years.9
OCP's
27
yearsof
operationsform the
knowledge baseon which APOC is
founded, thoughon the
surfaceit would
appear that thetwo
control strategies areunrelated. In
fact,APOC's
approach representsa natural evolution from OCP,
incorporatingnew
treatment strategiesbut relying
heavilyon
OCP's technology and fine-tuned databaseof
riverblindness epidemiology,which has been painstakingly
constructedover nearly three
decades. The involvementof
communitiesis
also a natural extensionof
the devolution integralto
OCP allalong. While the first staff
membersin
Ouagadougouwere primarily
Westerners, the Programme setout quickly to
hire and trainAfricans.
Since 1980,for
instance,all
Directors have beenAfricans.
Overall, OCP has funded several hundred graduate degrees,all
awarded to Africans who were working against riverblindness (Samba,1994). By
1984, ten years into the prograrnme, 96ohof the staff
wereAfrican. Now Africans
comprisemore
than 99o/oof
the personnel.In addition to devolution, OCP made groundbreaking contributions in other areas as well.
From the earliest days, OCP has embodied a culture
of
operations research, which has rescued the Programme more thanonce. Around
1980,for
instance, the blackflies began developing resistanceto
the main larvicide(Kurtak, 1990).
Thanksto
several yearsof
ongoing research, OCP scientists were able to develop and test alternatives. Using someof
these new options in arotation
overcamethe
resistancein the fly
population, restoringthe
effectivenessof
vectorcontrol.
Another majordifficulty
cameto light
when OCP entomologists discovered that thefly's
effectiveflight
range was 400 kilometers or more(WHO, 1987)-nearly
10 times original estimates(WHO, 1973).
The problem appeared as infectedflies
were discovered re-invading previously controlled areas (Garms etal., 1979).
Ongoing epidemiological and entomological research revealed the problemwhile
superb management and redoubled donor support allowed OCPto
expandinto
the nearby zones where newflies
had been discovered (Philippon et al.,1990). Similarly, APOC's
operationswere
underwrittenby
extensive preparatory research including epidemiological mapping (De Sole eral.,
1990), studying distribution methods (TDR,1996), examining the sustainability
of
the Com-DT approach(WHO,
2000), and investigating community compliance and the effects of ivermectin on skin disease (Brieger etal.,
1998).Future
ProspectsAPOC is
fundamentally about riverblindness,but the
ivermectindistribution
networkit
hascreated stands ready
to
serve as an essentialvehicle for
addressing other widespread health problems.As Merck
has donewith
Mectizan, several drug companies are preparedto
donate medicines that can be delivered via APOC at minimal cost to the poorest communities. Among10
the simplest and most effective would be vitamin
A
capsules, given freeby
Hoffman-LaRoche, whichwould
help prevent blindnessin
children and improve general healthin
the restof
thepopulation. Aside from the
health benefits,providing
additional drugswould
strengthen the position and effectivenessof
community Mectizan distributors. Great care must be taken not to overwhelm this nascent distribution network, butin
the caseof
vitaminA, little
training would be needed, and everyone can takeit.
Furtherbuilding
local capacityby
distributing vitaminA
would pave the wayfor
making available several other donated drugsin
the communities that have been the hardest to reach.The
full
value of APOC's distribution network lies in itspotential.
Init,
the international community has a ready pathway to deliver medicines to those who needit most.
Drugs already availableat no cost
includethe following, all of which
havethe
same dosing schedule asMectizan:
Vitamin A to prevent malnutrition, blindness, death
Azythromycin to cure trachoma, now the leading cause of blindness in
Africa
Ivermectin and albendazole to stop transmission of lymphatic filariasis (elephantiasis), one of Africa's leading causes of long-term disability
Despite recent, sharp reductions in price,
AIDS
medications arestill
quite expensive, but are amongthe many health
interventionsthat could
conceivablybe
delivered through this networkin
thefuture.
Oncefully
developed, there would bevirnrally
nolimit to
the materials that could be distributed, including health information, condoms, multivitamins, and vaccines.There is the very real possibility of knocking out not
just
one health problem, but several majordiseases-enough to dramatically improve public health overall, instead of just
making opportunities for diseases now of secondary importance.The Community Directed Treatment (Com-DT)
initiative
stands as afitting
codato
the legacy established byOCP.
What began as a top-down, vertical disease programme has evolvedinto a bottom-up,
integrated approachthat
couplesstrong regional
coordinationwith
the empowermentof local
communitiesto
addressnot only
onchocerciasis but, potentially, manyother health
problemsas well. For much of its history, OCP has been
conductedwith
helicopters, spraying againsta
formidable,but
solitaryfoe.
APOC has extendedthis
successwith the help of
Mectizanto
includelocal
communitiesnot
as passive beneficiaries,but
aspowerful agents impacting some
of
their own health outcomes. This grassroots involvement,if
fully
strengthened, would complete OCP's transformation from an external programme to afully
African-owned and managed region-wide health system.
1l
The success
of
OCP testifiesto
the powerof
this partnership,in which
sponsors have concentrated on their respective strengths and the donor community has lent unwavering supportfor
nearly threedecades-far
longer thanfor
any other operational development programme.Given the technical hurdles, this commitment has been essential to success and remains one
of
OCP'sfinest hallmarks. No
combinationof
shorter programmescould
have achieved these resultsnor
evolvedhorizontally, affording potentially much wider protection of the
publichealth.
The longstanding collaboration andgoodwill
developed onall
sidesof
this partnership have generated synergies greater than those imagined, andall
at remarkablylow cost.
Coverage has cost,at
everypoint in both
programrnes,far
lessthan
onedollar per
year,per
personprotected (Benton and Skinner, 1990; Benton, 1998).
OCP's
efforts
haveled to
widespread acclaim amongpublic
health practitioners, but perhaps more importantly, haveled to
broad-based supportfrom the
communities protected.This gtassroots
credibility is
the single most important factorin APOC's
success at Mectizan distribution, and portends a transformationin
theability
to deliver a wide rangeof
medicationsin
thefuture.
Development assistance prograrnmes havelong
sought comprehensive waysof
addressing widespread public health problems
while
ensuring sustainability, local involvement, and community empowerment. OCP and APOC have achieved these goalsby
virfueof
nearly30 years'
dynamic partnershipwith
increasinglyactive host
countriesand their
constituent populations, proficient intemational agencies, and unswervingly dedicated donors.ACKNOWLEDGEMENTS
We appreciate the valuable help given by Prof. O. O. Kale in the preparation of this paper. The assistance of Marline Alexis, Joyce Musya-Mpangu and Olympia Gjino of the Onchocerciasis Coordination unit of the World Bank is gratefully acknowledged.
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17
THE ACHIEVEMENTS AND CHALLENGES OF THE
AFRICAN PROGRA MME FOR ONCHOCERCIASTS
coNrRoL (apoc)
THB ACHIEVEMENTS AND CHALLENGES
OFTHE
AFRICAN PROGRAMME
FORONCHOCERCIASIS CONTROL (APOC)
AUTHORS
A. sprBrell,t
G. ADEoyE,2 A. EYAMBA,3 E. I.NORU*,4 p. DRAMEH,' u.v.
AMAZIGo,' M. NoMA,' F. AGBoroN,ly. AHoLou,'o.
o. xaLp6ANDK. y.DADZTE'ADDRESSES OF AUTHORS
l.
African Programme for Onchocerciasis Control (APOC), Ouagadougou, Burkina Faso2.
University of Lagos, Akoka, Yaba, Lagos, Nigeria3.
The Carter Center, Global 2000 River Blindness Program, Yaounde, Cameroon4.
Departmentof
Dermatology, Collegeof
Medicine, Universityof
Nigeria, Enugu Campus, Enugu, Nigeria5.
World Health Organization, Geneva, Switzerland6.
Departmentof
Preventiveand Social Medicine, University College Hospital,
Ibadan, Nigeria7.
01905 Osu - Accra, GhanaAddress
for
CoruespondenceDr.
Azodoga S6k6t6tiDirector, African
Programmefor
Onchocerciasis
Control
(APOC), 01 B. P. 549 Ouagadougou 01Burkina
FasoTel:
(226) 34.22.77 Faxz (226) 34.48.00E-mail:
seketelia@oncho.oms.bfShort running
title:
Achievements of APOCABSTRACT
The Community Directed Treatment
with
Ivermectin(CDTI)
strategyof
APOC has enabled the Programmeto
reach, empowerand bring relief to
remoteand
underserved onchocerciasis endemic communities.With CDTI,
geographical and therapeutic coverage rates have increased substantially,in
most areas,to
levels requiredto
eliminate onchocerciasis asa public
healthproblem.
Over 20million
people received treatmentin 2000.
APOC has also used REMO-GISeffectively to provide information on the geographical distribution and prevalence of
onchocerciasis, as a means
of
identifyingCDTl-priority
areas, and obtaining better estimatesof
the numbers
of
people to be treated.A
unique public/private sector partnership has been at theheart of APOC's relative success. Through efficient
capacitybuilding, the
Programme's operations havepositively
influencedand
strengthenedthe health
servicesof
participatingcountries.
These laudable achievements notwithstanding, APOC faces many challenges during the second phaseof
its operations when thefull
impactof
the Programme is expected to be felt.Notable among these
is
the sustainabilityof CDTI,
its effective integration into the health care system andexploiting its
potential as an entrypoint for
other health programmes such as thelymphatic filariasis elimination
programme,which would
featureon the
agendaof
many participating countriesduring APOC's
Phase2.
Executing these other programmes without compromisingthe
onchocerciasiscontrol
programmeitself is a major
challengeto
APOC.Success
in
meeting these challengeswill
depend on the continued wholehearted commitmentof
all partners especially governments of participating countries.
2
INTRODUCTION
The vast
majority of
thosewho
sufferfrom
and are exposedto
onchocerciasislive in Africa (WHO,
1995a). The most severe consequences of the disease is blindness, which may affect one third of the adult population of the most highly affected communities and the prevention of which has been the main clinical raison d'€trefor
initiating the Onchocerciasis Control Programme in WestAfrica
(OCP)in
1974(Tsalikis,
1993; Benton etal., 2001).
Howeverin
the last decade important pioneering studies, sponsored by the UNDPAVoTId Bank/WHO Special Programmefor
Research and Trainingin
Tropical Diseases(TDR),
have shown that onchocercal skin disease (OSD)is
associatedwith
a greater degreeof morbidity
than was hitherto appreciated. These studies demonstrated that severe OSD and intolerable itching cause alot of
suffering to millions of people particularlyin
the forest zone where the blinding formof
the disease is less prevalent.(Amazigo and Obikeze, 1991, Amazigo, 1993,
WHO,
1995b,).It
notonly
causes psychosocial problems, ostracism and stigma (Okello etal.,
1995;Owga
etal.,
1995,WHO,
l995b,Brieger etal.,
1998b)but OSD also
hasa
demonstrably negative socio-economicimpact on
farmers' productivity, breastfeeding and school attendance. (Amazigo 1994;Kim
eta|.,1997
; Oladepo elal.,
1997; Benton, 1998 ; Vlassoff et a1.,2000). The relative contributions of both major clinical patterns,ocular
and dermal,to the
burdenof
onchocercal diseaseand their
socio-economic consequences are considerable. (Kale, 1998).The principal strategy of OCP from its inception was vector
control.
However the advent of ivermectin (Mectizan@) and its donation by Merck&
Co.in
1987, free of charge for as long asneeded, provided a second string to OCP's operational
bow.
Thefirst
extensivefield
studies on the suitabilityof
the drug for use on a mass scale were conductedby
theOCP.
The favourable resultsof
these studies ledto
OCP adopting mass distributionof
Mectizan@ as an adjunct to vectorcontrol. It
even used the drug alonein
some areas(Awadzi
etal.,
1985; Dadzie et al., 1987, Remmeet al.,
1989; Dadzieet al.,
1990; Remmeet al.,
1990; Dadzieet al., l99l;
3
Whitworth et
al., l99l;1992
Guillet et.al.,
1995). The application of the two strategies by OCP has led to the virrual eliminationof
onchocerciasis as a public health problem and an obstacle to socio-economic developmentin the 1l
countriesof
OCP leadingto
the recognitionof
OCP asone
of the most
successful prograflrmesin the history of
development assistance(Kim
and Benton, 1995).The initial efforts
at mass distributionof
ivermectin outside OCP were madeby
non- govemmental development organizations (NGDOs) a few yearsprior
to the establishment of theAfrican
Programmefor
OnchocerciasisControl (APOC). The first of the
NGDO-facilitated distribution progralnmesin Africa
that cameto
be referredto
asthe
Ivermectin Distribution Programme(IDP) (Duke
andDadzie
1993),was
establishedNigeria in
1989.Many of
the pioneering NGDOs were alreadywell
known through their activitiesin
preventionof
blindness and were alreadywith the WHO
Preventionof
Blindness Programme(PBL). At
that time, outsideof
the OCP area, authoritiesin
most countries where the disease was endemicdid
not considerthe
disease asa public
health problem and there were thereforeno
programmes or structuresin
placefor its control.
The NGDOs soon recognised the needto
coordinate their separate and independent effortsif
they were to achieve their commongoal.
Thereforein
199?they
came togetherto form
theNGDO
Coordination Groupfor
IvermectinDistribution. By
1995,it
had become clear that membersof
the Coordination Group needed considerably more resources than they could generated on their ownif
there was to be any significant expansion inthe
scopeof their activities.
Furthermore the variousNGDOs
and programmes used mobile teams and the clinic-based and Community-Based Treatmentwith
Ivermectin(CBTI)
methods in the distributionof ivermectin.
These methods were clearly not appropriate or cost-effectivefor
large-scale sustainabledistribution of the drug. In
1995the
Task Forceon
Onchocerciasis Operational Research (OOR) of the TDR, in collaborationwith
the OCP, addressed the problem in a multi-country researchstudy.
The result was the developmentof
the methodof
distribution4
that has become known as the
Community-DirectedTreatment with Ivermectin
(CDTI) (WHO,l996a).Prior to this,
andin
responseto the
needof
the disparatecontrol
programmesof
the variousNGDOs for a rapid, reliable and
cost-effective methodof identifying
communitiesendemic for
onchocerciasisto be
targetedfor
treatment,the OOR
developedthe
Rapid Epidemiological Mapping of Onchocerciasis (REMO), (Ngoumou and Walsh, 1993; Ngoumou etal.,
1994l'WHO, 1995c).
The underlying concepts and designof REMO
drew heavily on the experiencein OCP.
TheWorld
Bank provided financial supportin
the developmentof
REMO, which has since become a key tool in the control armamentarium of APOC.This then was the scenario on the onchocerciasis front in Africa when APOC, inaugurated
in
December 1995, commenced operationsin
1996with
a mandate"to build
on the successof
OCP and establish sustainable control (of onchocerciasis) in the remaining 19 countries in
Africa
where the disease wasstill
a public health problem".(WHO,l996b).
The entire Programme wasmanifestly
predicatedon the window of opportunity provided by the Mectizan
Donation Programme(MDP).
Thusthe control
strategy prescribedfor APOC
was "community-based treatment prografirmeswith
the drug ivermectin, supplementedwith
vector eradicationin
a few isolatedfoci".
This paper is an overview
of
the achievementsof
APOCin
thefirst
(1996-2001)of
two planned phasesof its
operations, anda
considerationof the
challengesfor the
second phase(2002-2007). Six
companion articlesin this
supplementreview in
greaterdetail
some key aspects of the activities of APOC.The
Structure
ofAPOC
Governance: APOC has built a strong and effective partnership that unites the member countries
their
beneficiary communities, NGDOs, multilateral agencies, bilateral donors and the private5
sector,
Merck & Co. Inc. and the scientific community. The
organisationalframework
is designed to reflect this partnership.(WHO,l996b).
All
partners are represented on theJoint Action Forum (JAF),
the main governing bodyof
APOCwhich
has been meeting, annually as scheduled, to review and approve the proposed plans of action and budgets, assess global financing requirements and take decisionswith
regard to overall progralnme policies.The members of the Committee of Sponsoring Agencies (CSA) are the same as for OCP
viz. FAO, UNDP, WHO
andthe World Bank. The CSA
organizes medium andlong
term planningof
APOC and OCP activities, approves National Plans and Project Proposals and takes interim decisions on behalf of JAF.Programme
Management:
The headquartersof
APOC isin
Ouagadougou where a small core staff looks after the day-to-day affairs ofAPOC.
This core staff, in conjunctionwith
the NGDO liaisonoffice in
Geneva, has,in
spiteof
a heavy burdenof
work, maintained a high standardof operations.
APOC Management hasfaithfully
implemented programmepolicy,
facilitated and coordinated the activitiesof
the National Onchocerciasis Task Forces and their partner NGDOs and provided oversight on financial management.It
has also assistedin
the training of National and NGDO staff and facilitated the monitoring of projects.APOC is
supportedby a Technical Consultative Committee (TCC),
madeup of
10members. The TCC has successfully reviewed and recommended for approval 63 applications
for APOC funding of CDTI
projects, includingtheir
national support systemsin
additionto
four vector elimination projects.In the first
phaseof its
operationAPOC
has facilitatedthe formation of a National
Onchocerciasis Task Force (NOTF) in every participatingcountry.
Made upof
officials of the Ministries of Health(MoH)
and Programme Managers aswell
as all partner NGDOs operating in the country, NOTFs have made considerable improvement in their performance over the years.6