Got ACTs? Availability, price, market share and provider knowledge of anti-malarial medicines in public and private sector outlets in six malaria-endemic countries
- Kathryn A O'Connell1Email author,
- Hellen Gatakaa1,
- Stephen Poyer1,
- Julius Njogu1,
- Illah Evance1,
- Erik Munroe1,
- Tsione Solomon1,
- Catherine Goodman2,
- Kara Hanson2,
- Cyprien Zinsou3,
- Louis Akulayi4,
- Jacky Raharinjatovo5,
- Ekundayo Arogundade6,
- Peter Buyungo7,
- Felton Mpasela8,
- Chérifatou Bello Adjibabi9,
- Jean Angbalu Agbango10,
- Benjamin Fanomezana Ramarosandratana11,
- Babajide Coker12,
- Denis Rubahika13,
- Busiku Hamainza14,
- Steven Chapman15,
- Tanya Shewchuk1 and
- Desmond Chavasse1
© O'Connell et al; licensee BioMed Central Ltd. 2011
Received: 29 July 2011
Accepted: 31 October 2011
Published: 31 October 2011
Artemisinin-based combination therapy (ACT) is the first-line malaria treatment throughout most of the malaria-endemic world. Data on ACT availability, price and market share are needed to provide a firm evidence base from which to assess the current situation concerning quality-assured ACT supply. This paper presents supply side data from ACTwatch outlet surveys in Benin, the Democratic Republic of Congo (DRC), Madagascar, Nigeria, Uganda and Zambia.
Between March 2009 and June 2010, nationally representative surveys of outlets providing anti-malarials to consumers were conducted. A census of all outlets with the potential to provide anti-malarials was conducted in clusters sampled randomly.
28,263 outlets were censused, 51,158 anti-malarials were audited, and 9,118 providers interviewed. The proportion of public health facilities with at least one first-line quality-assured ACT in stock ranged between 43% and 85%. Among private sector outlets stocking at least one anti-malarial, non-artemisinin therapies, such as chloroquine and sulphadoxine-pyrimethamine, were widely available (> 95% of outlets) as compared to first-line quality-assured ACT (< 25%). In the public/not-for-profit sector, first-line quality-assured ACT was available for free in all countries except Benin and the DRC (US$1.29 [Inter Quartile Range (IQR): $1.29-$1.29] and $0.52[IQR: $0.00-$1.29] per adult equivalent dose respectively). In the private sector, first-line quality-assured ACT was 5-24 times more expensive than non-artemisinin therapies. The exception was Madagascar where, due to national social marketing of subsidized ACT, the price of first-line quality-assured ACT ($0.14 [IQR: $0.10, $0.57]) was significantly lower than the most popular treatment (chloroquine, $0.36 [IQR: $0.36, $0.36]). Quality-assured ACT accounted for less than 25% of total anti-malarial volumes; private-sector quality-assured ACT volumes represented less than 6% of the total market share. Most anti-malarials were distributed through the private sector, but often comprised non-artemisinin therapies, and in the DRC and Nigeria, oral artemisinin monotherapies. Provider knowledge of the first-line treatment was significantly lower in the private sector than in the public/not-for-profit sector.
These standardized, nationally representative results demonstrate the typically low availability, low market share and high prices of ACT, in the private sector where most anti-malarials are accessed, with some exceptions. The results confirm that there is substantial room to improve availability and affordability of ACT treatment in the surveyed countries. The data will also be useful for monitoring the impact of interventions such as the Affordable Medicines Facility for malaria.
In 2000, African Heads of State agreed in Abuja that by 2010 60% of people with malaria would be able to access "affordable and appropriate treatment within 24 hours of the onset of symptoms" . This target was increased to 80% in 2005 . Artemisinin-based Combination Therapy (ACT) is the first-line malaria treatment throughout most of the malaria-endemic world. Although public sector procurement of ACT has increased sharply in recent years, it was estimated that in 2009 less than 15% of children under five years of age received ACT when they had fever in 11 of 13 African countries, and only 32% received anti-malarials of any kind . Furthermore, the availability and use of oral artemisinin monotherapy [4, 5] is worrying given the risk of development of artemisinin resistance  and WHO's recommendation to countries to ban the importation and manufacturing of these drugs.
A variety of country-specific studies have raised important concerns about ACT supply that may explain these low levels of ACT use. Studies have generally found low availability of ACT and higher availability of monotherapies in both the public and private sector [7–9]. While ACT is typically free-of-charge or subsidized in the public and not-for-profit sector, in the private sector ACT is between ten and twenty times more expensive than non-artemisnin therapies, such as chloroquine and sulphadoxine-pyrimethamine (SP) [8, 10–12]. Provider knowledge that ACT is the first-line treatment for malaria is also low, particularly in the private sector [13–16].
Research addressing questions on the anti-malarial market is typically limited in geographical scope and utilizes a variety of different methods to ascertain price and availability. Data are typically collected in a few purposively selected geographical areas within one country, and at times include only certain outlet types or sectors. Studies are not typically designed with sufficient power to detect differences between sectors. With a few exceptions [14, 17–20], there is little evidence on the market share of anti-malarial medicines sold through the private retail sector, where most malaria treatment is sought.
The available data, therefore, fail to provide a firm evidence base from which to assess the current situation concerning ACT supply across countries, or to help evaluate the impact of important initiatives to improve this, such as the Affordable Medicines Facility for Malaria (AMFm), which provides heavily subsidized, quality assured, ACT to pilot countries . Standardized information on availability, price and market share of ACT and other anti-malarials in the public/not-for-profit and private sectors will inform such interventions and help gauge their relative success, guiding policy makers and programmers at the national and international levels.
To help address some of these gaps, Population Services International (PSI) in partnership with the London School of Hygiene and Tropical Medicine (LSHTM) launched a five-year multi-country research project in 2008 called ACTwatch to monitor anti-malarial supply and demand in seven malaria endemic countries in Africa and Asia. This involves multiple surveys of households and anti-malarial outlets, and a systematic analysis of the anti-malarial supply chain in Benin, Cambodia, the Democratic Republic of Congo (DRC), Madagascar, Nigeria, Uganda and Zambia .
This paper presents the results from ACTwatch outlet surveys carried out between March 2009 and June 2010 in the six sub-Saharan countries. An ACT was the first-line anti-malarial in all these countries at the time of the study, with artemether-lumefantrine and/or artesunate-amodiaquine the recommended combination. All countries recommended quinine for treatment of severe malaria, and SP for intermittent preventive treatment in pregnancy.
Design & sampling
A nationally representative sample of outlets providing anti-malarials to consumers was selected. Each country was first stratified using information on country size, malaria endemicity, geopolitical areas, or urbanization. Benin was designated as a single stratum; Madagascar, Uganda, and Zambia were divided into two strata; the DRC into four and Nigeria into six . Stratification was agreed in consultation with national authorities including the national malaria control programme and the national drug regulatory authority.
Following stratification, a one-stage probability-proportional-to-size (PPS) cluster design was used to select clusters within each stratum, with cluster population serving as the measure of size. The primary sampling unit, or cluster, selected was an administrative unit with 10,000 to 15,000 inhabitants. The proportion of outlets with any ACT in stock was used as a key indicator for sample size calculation, conservatively estimated at 40% for each country. A minimum of 290 outlets with anti-malarials in stock was needed to detect a 20% increase in this indicator, at 80% power, setting the level of significance at 5% and adjusting for an estimated design effect of 3. It was estimated that the selection of 19 clusters per stratum would provide at least this number of outlets stocking anti-malarials.
Within each selected cluster all outlet types with the potential to provide anti-malarials to consumers were sampled, with the identification of these outlet types based on available literature and local knowledge. The main types of outlets sampled included public and not-for profit health facilities, private health facilities, pharmacies, drug stores and grocery stores/kiosks. In addition, a range of other outlet types were considered relevant in specific countries, for example, market stalls in Benin, gargotes in Madagascar, itinerant vendors in Nigeria and Benin, and community health workers in Nigeria, Uganda and Madagascar.
As public health facilities and pharmacies are important providers of anti-malarials but are relatively uncommon, over-sampling was conducted for these outlet types. This booster sample was obtained by including public health facilities and pharmacies in the larger administrative area from which a given cluster was selected. For example, if the cluster was defined as the sub-district, the booster sample covered all public health facilities and pharmacies in the whole district within which the sub-district was located.
Training and fieldwork
The outlet surveys were conducted during the months of peak malaria transmission in each country. The survey data were collected by teams of between 21 and 76 enumerators with at least 12 years of education who were fluent in the local language. Interviewer training was provided over six days, focusing on outlet identification, informed consent procedures, and the procedures for completing the questionnaire.
Field workers were provided with a list of selected clusters and maps that illustrated their administrative boundaries, in addition to lists of public health facilities and pharmacies obtained from relevant authorities. Snowball sampling was also used by field workers to identify facilities that were not on official lists. In each selected cluster, fieldworkers conducted a census of all outlets that had the potential to provide anti-malarials. For each outlet that was identified during the census, the outlet type and location were noted, along with its longitude and latitude coordinates (obtained via hand-held global positioning units). A fieldworker then approached the outlet's main seller or provider and invited him or her to participate in the study. Providers who agreed to participate were asked two screening questions to determine whether (a) the outlet had stocked anti-malarials within the previous three months, and (b) anti-malarials were available on the day of the survey. All providers answering "yes" to at least one of these questions were deemed eligible for inclusion in the survey and the questionnaire was administered to these outlets. An interview with the staff member who was most likely to sell or prescribe medications was conducted.
The interview was carried out in the appropriate local language. Questionnaires were pre-tested and validated in each country before data collection.
The questionnaire consisted of two parts. A drug audit collected information on all anti-malarials found at the time of the interview, including information on brand and generic names, dose, manufacturer, amount sold in the last seven days, and retail price. The provider questionnaire collected information on provider demographics, anti-malarial treatment knowledge, anti-malarial storage conditions, stock-outs, and licensing.
Data collection lasted from one to five months in each country and took place between March 2009 and June 2010 (Benin, April 28th - May 13th 2009; the DRC, August 10th - October 27th 2009; Madagascar, April 27th - June 21st 2010; Nigeria August 4th - September 16th 2009; Uganda, March 16th - April 7th 2009; Zambia, April 14th - July 3rd 2009).
During data collection, approximately 80% of all questionnaires were reviewed by the team supervisor and 15-20% of all outlets were revisited by a supervisor or/and quality controller for quality control checks.
Double data entry was conducted using Microsoft Access (Microsoft Corporation, Redmond, Washington, USA) with built-in range and consistency checks. Entered data were triangulated with questionnaires, field supervision notes and daily activity logs filled by each interviewer in the field. Data were analysed using Stata 11.0 (StataCorp College Station, TX).
Stata survey settings were used to account for the stratified and clustered sampling strategy. Results were adjusted by sampling weights. Sampling weights were based on the inverse of the probability of selection to allow for the differences in strata and cluster sizes and the oversampling of public health facilities and pharmacies. Distribution of the outlets was assumed to be proportional to population size. Data analysis included descriptive summaries; between-group proportions were compared using chi-square analysis and median prices compared using the Wilcoxon rank sum test.
Description of Quality-Assured ACT classifications
First-line quality-assured ACTs:
Non first-line quality-assured ACTs:
Government recommended first-line treatments (regardless of strength) for uncomplicated malaria that appear on the WHO list of approved ACTs or the UNICEF procurement records.
Brands on these lists and audited in each country were:
ACTs that are not the government's recommended first-line treatment for uncomplicated malaria, but which appear on the WHO list of approved ACTs or the UNICEF procurement records.
Brands on these lists and audited in each country were:
Artefan 20/120; Coartem; Lumartem 20/120; Lumet 20/120
Arsuamoon; Artesunate & Amodiaquine from Ipca; Artesunate & Amodiaquine from Cipla; Falcimon Kit; Serenadose; Coarsucam; Winthrop
Artefan 20/120; Coartem 20/120; Lumartem 20/120
Arsuamoon; Artesunate & Amodiaquine from Ipca; Actipal 50/153; Winthrop; Coarsucam; Falcimon kit; Larimal
Artefan 20/120; Coartem 20/120;
Coartem D 20/120;
Coartem 20/120; Coartem D 20/120; Lumerax 20/120 *Arsuamoon; *Coarsucam; *Larimal
Coartem; Artefan 20/120; Lumartem 20/120
Larimal, Falcimon kit
Artefan 20/120; Coartem 20/120; Lumartem 20/120; Lumerax; Lumet 20/120
Availability was calculated using two methods. For each country, availability of anti-malarials was measured as the proportion of outlets with at least one anti-malarial in stock, among all censused outlets. Within each country, the availability of specific anti-malarial categories, restricted to those outlets that had anti-malarials in stock, was also calculated. Thus, for example, the availability of ACT was measured as the proportion of outlets stocking ACT, among all outlets with at least one anti-malarial in stock.
In a supplementary analysis, the availability in public health facilities was also measured as the proportion of facilities with different categories of anti-malarials in stock, among all censused public health facilities. This operationalized the expectation that public health facilities should stock anti-malarials.
Volumes and price
The volume sold/distributed and retail price of the anti-malarials recorded in the drug audit were standardized using the adult equivalent treatment dose (AETD) to allow meaningful comparisons between anti-malarials with different treatment courses. For the five countries that conducted surveys in 2009, prices were converted to US dollars using their average annual exchange rate . For Madagascar (where data were collected in 2010), local currency prices were adjusted to 2009 prices using the Madagascar consumer price index , and then converted to US dollars using the 2009 average exchange rate.
Prices per AETD are presented for the three anti-malarial categories believed to be most pertinent to policy level decisions; first-line quality-assured ACT, the most popular anti-malarial based on volume (defined by generic name), and oral artemisinin monotherapy.
Price measures include tablet anti-malarials only as this is the most common formulation. The price of non-tablet formulations, such as powders for reconstitution, suspensions, suppositories and syrups, was excluded. The price distributions for these non-tablet formulations tend to be different from those for tablets, with much higher medians, implying that it could be misleading to use one measure of central tendency for all formulations. However, measures of volume include all dosage forms to provide a complete assessment of anti-malarial market shares.
The study was approved by the local ethical review boards: Benin Ministry of Health, Authorization for Data Collection Number 3989/MS/DC/SGM/DRS/SCI/SA, 14th July 2008; Cambodia, Ministry of Health, National Ethics Review Committee, Reference Number 109 NECNR, 7th November 2008; Democratic Republic of Congo, Ministerie de L'Enarignement Superior at Universitaire, School of Public Health, Reference Number ESP/CF/020/2008, 11th June 2008; Madagascar, Ministry of Health du Planning Familial et de la Protection Sociale, Reference Number 206SANPFPS, 16th June 2008; Nigeria; Federal Department of Ministry of Health, Department of Public Health, Reference Number MH/1158/5/137, 20th October 2008; Uganda, Makerere University, Faculty of Medicine, Reference Number 2008-057, 1st September 2008; and Zambia, University of Zambia, Biomedical Ethical Research Committee, Reference Number 014-08-08, 2nd October 2008.
A total of 28,263 outlets across six countries were approached to participate in the surveys. In total, 348 outlets were closed down permanently, 665 outlets were not open, 299 eligible providers were not available for interview, 395 providers refused to participate and 301 outlets were excluded for other reasons. As a result, 26,255 outlets were screened for stocking anti-malarials. Of these, 9,118 outlets met the screening criteria and were administered the questionnaire (8,383 outlets were found to have at least one anti-malarial in stock and 735 outlets had no anti-malarials in stock at the time but reported having stocked anti-malarials in the past three months).
Among outlets stocking anti-malarials on the day of survey, 51,158 individual anti-malarial products were audited (66% tablets). The proportion of tablet formations in the audit varied by country (Benin, 73%, n=5, 232; the DRC, 58%, n=11, 939; Madagascar, 87%, n=5,579; Nigeria, n=61%; n=20,841; Uganda, 63%, n=5,784; and Zambia, 82%, n=1,783).
Proportion (N) of outlets censused with at least one anti-malarial in stock on the day of interview, by sector, outlet type and country¹
Community Health Worker
Private not-for-profit Health Facility
Private Health Facility
Other Outlet Types
In the private sector, stocking of anti-malarials was lower and varied by outlet type and country, ranging from 6% in Zambia to 36% in Benin. Private health facilities, pharmacies and drug stores were more likely to stock anti-malarials than grocery stores and other outlets, where stocking rates were generally less than 5%. Exceptions were grocery stores in Benin and Madagascar and market stalls in Benin, with around one in three of these outlets stocking anti-malarials.
Outlets with specific anti-malarial categories as a percentage of outlets with at least one anti-malarial in stock, by sector¹
First-line quality-assured ACT
Any non-artemisinin therapy
Oral artemisinin monotherapy
< 0.1 a
Availability of different categories of anti-malarials in public health facilities was also calculated among all censused public health facilities (see Additional File 1 Table 1). Among all public health facilities (excluding community health workers), stockage rates of first-line quality-assured ACT at the time of survey were as follows: Benin, 81%; the DRC, 82%; Madagascar, 80%; Nigeria 43%; Uganda, 72% and Zambia, 85%. The stocking rate of SP among all outlets in the public sector, used in intermittent preventive treatment of pregnant women (IPTp), also varied (Benin, 50%; the DRC, 70%; Madagascar, 46%; Nigeria 63%; Uganda, 62% and Zambia, 59%). Quinine injection, the government-recommended treatment for severe malaria for persons who cannot take oral medication, ranged in public sector availability as well: Benin, 61%; the DRC, 66%; Madagascar, 43%; Nigeria 16%; Uganda, 73% and Zambia, 53%.
First-line quality-assured ACT was free at public sector outlets in four of the six countries. In Benin and the DRC, where public-sector patients pay for anti-malarials, the median prices were $1.29 (Inter Quartile Range [IQR]: $1.29, $1.29) and $0.52 (IQR: $0.00, $1.29) respectively for an adult equivalent treatment dose (see Additional File 2 Table 2).
Median price in US dollar (inter-quartile range) for an adult-equivalent treatment dose in the private sector (tablet formulation only), by anti-malarial type
Median $ (IQR)
Oral Artemisinin Monotherapy
0.65 a (0.43, 1.08) N = 462
3.24 b (1.94, 5.77) N = 216
8.10 (8.07, 10.45) N = 56
0.39 a (0.26, 0.52) N = 1, 258
1.86 b (1.03, 3.61) N = 252
3.23 (2.45, 4.13) N = 956
0.36 a (0.36, 0.36) N = 1, 847
0.14 b (0.10, 0.57) N = 302
(0 and 7.33) N = 2
0.54 a (0.40, 0.81) N = 4, 061
6.40 b (5.05, 6.74) N = 372
3.24 (2.70, 3.77) N = 1, 438
0.50 a (0.30, 0.75) N = 653
4.48 b (2.49, 5.97) N = 81
9.55 (7.96, 11.94) N = 229
0.40 a (0.30, 0.61) N = 261
9.63 b (3.01, 11.04) N = 83
6.74 (5.72, 6.74) N = 16
The median private sector AETD price of the most popular anti-malarial in tablet form, either SP or chloroquine in each country, ranged from $0.36 (IQR: $0.36, $0.36) to $0.65 (IQR: $0.43, $1.08). This was significantly lower (p < 0.01) than the median price of the first-line quality-assured ACT in each country, with Madagascar as an exception, where the first-line quality-assured ACT was significantly less expensive than the most popular anti-malarial, chloroquine.
Overall, the median price of chloroquine tablets ranged from $0.24 (IQR: $0.24, $0.48) to $0.48 (IQR: $0.48, $0.48) and SP from $0.38 (IQR: $0.29, $ 0.48) to $0.65 (IQR: $0.43, $1.08) in the private sector (see Additional File 3 Table 3).
Median prices of oral artemisinin monotherapies in the private sector ranged from $3.23 in the DRC (IQR: $2.45, $4.13) to $9.55 in Uganda (IQR: $7.96, $11.94).
For most countries, non-artemisinin therapies dominated the overall market, followed by ACT and then oral artemisinin monotherapies. Exceptions to this finding were noted in Nigeria and the DRC where more oral artemisinin monotherapies were sold than ACT in the private sector. Across all countries quality-assured ACT accounted for less than 25% of total anti-malarial volumes; private-sector quality-assured ACT volumes represented less than 6% of the total market share. In the public/not-for-profit sector, SP made up the largest market share of non-artemisinin therapies (Benin, 11.6%; the DRC, 16.2%; Madagascar, 9.5%; Nigeria 1.4%; Uganda, 21.6%; Zambia, 34.1%).
Provider knowledge of first-line treatment and dosing regimens, by sector¹
Correctly state the recommended first-line treatment for uncomplicated malaria
Correctly state the dosing regimen of the first-line treatment for an adult
Correctly state the dosing regimen of the first-line treatment for a two year old
Each outlet was assessed for the availability of rapid diagnostic tests (RDTs) (see Additional File 4 Table 4). In the public/not-for-profit sector, availability varied considerably by country (Benin, 72%; the DRC, 36%; Madagascar, 43%; Nigeria, 7%; Uganda, 22% and Zambia, 86%). In the private sector, availability was less than 20% and significantly lower across all countries than in the public/not-for-profit sector.
This paper presents standardized, nationally representative data on the anti-malarial market in six sub-Saharan African countries between 2009 and 2010. The data confirm the low market share of ACT, reflecting a combination of low ACT availability in both the public/not-for-profit and private sectors, high ACT prices in the private sector and low provider ACT knowledge, particularly in the private sector. Other studies have highlighted similar challenges [8, 10, 11, 17, 28]. The following sub-sections describe the limitations of the ACTwatch outlet surveys, summarize the main findings according to availability, price, market share and provider knowledge, and address the policy implications of these results.
Strengths and limitations
The ACTwatch survey methodology allows for the measurement of anti-malarial availability and prices in a standardized way, on a nationally representative sample of outlets, with multiple steps to ensure data quality. When combined with the ACTwatch household survey , and the supply chain study on the structure and operation of the anti-malarial distribution chain, ACTwatch data provide a full picture of the anti-malarial market, with multiple uses for policy making.
Despite the study's strengths, the outlet survey data presented here have several limitations. 1) Providers may have had incentives to mis-report certain information, such as whether they stocked any anti-malarials, or specific anti-malarial categories, especially if this was not permitted by government regulations. Although interviewers stressed that they were not connected with any regulatory body, anti-malarial availability and stocks may have been under-reported. 2) Volumes were based purely on provider recall. Given the lack of sales records in most private outlets, this was felt to be the most logistically feasible method for estimating volumes, but it is likely that some recall bias was present. 3) Adult equivalent treatment dose calculations were used when calculating prices and volumes. This has the advantage of allowing direct comparability between drugs. However, it should be noted that in practice many customers will be obtaining drugs for children and/or purchasing incomplete doses . As a result, the price actually paid per customer may be considerably lower than the median price per AETD. Similarly, the actual number of customers to whom each drug was sold will be considerably higher than the volume of AETDs dispensed. It should also be noted that AETD prices presented in this paper do not include additional fees that may have been incurred for customers, such as consultation fees or service charges. 4) While price indicators were standardized according to the 2009 US dollar, it is acknowledged that there are different costs of living within countries and varying average or minimum wages, which make like-with-like comparisons across countries challenging. 5) Data were only collected at one point in the year, generally around the peak malaria transmission season. Seasonal variation may be expected, meaning in particular that anti-malarial availability and sales volumes may have been higher during the surveys than their annual averages, especially in countries with marked seasonal transmission, such as Madagascar and Zambia. 6) While a methodological strength of the survey is the full census of outlets in selected clusters, there are a number of practical implementation challenges with this method. Conducting a full census requires interviewers in the clusters to screen every outlet. It is acknowledged that some outlets with the potential to sell anti-malarials may have been missed, thus distorting the true figure of anti-malarial availability across countries.
Overall availability of ACT was low, particularly in the private sector. In the private sector, non-artemisinin therapies, typically chloroquine or SP, were by far the most abundant anti-malarial available while first-line quality-assured ACT was available in less than one-quarter of the anti-malarial stocking outlets. Oral artemisinin monotherapies were available in more than 40% of private sector anti-malarial-stocking outlets in the DRC and Nigeria. Within the public/not-for-profit sector, quality-assured ACT stockage rates ranged between 49%-92%.
When observing stocking rates for all public health facilities, availability of ACT hovered around 80%, but in Nigeria less than half of facilities had a quality assured ACT in stock. This suggests that maintaining a consistent supply to public health facilities may be difficult, a finding supported by other facility based research, which also highlights stock-outs as a common problem in public health facilities .
With one notable exception in Madagascar, first-line quality-assured ACT treatment in the private sector was significantly more expensive, between 5-23 times so, than the most popular anti-malarial (chloroquine or SP). Given the importance of the private sector in distributing anti-malarials, the higher cost of first-line quality-assured ACT is a concern. Although ACT is free or at a low price in the public sector, this is not where the majority of people seek treatment .
In Madagascar, the price of quality-assured ACT in the private sector is exceptionally low at $0.14. This is due to the presence of a socially-marketed ACT, which is sold nationally at a highly subsidized price through pharmacies and drug stores. This mirrors findings from a pilot subsidy programme in Tanzania which demonstrated that after the introduction of an ACT subsidy, ACT prices were as low as $0.58 in the private sector and did not differ significantly from the price paid for SP, the most common alternative .
Market share data highlight the dominant role of the private sector across all countries except Zambia, where 60% of all anti-malarials pass through the public/not-for-profit sector. Of the other countries, the private sector was the most important in Nigeria accounting for 98% of anti-malarial sales volumes, and elsewhere ranged from 58%-82%. Unfortunately, most of the anti-malarials sold through the private sector are non- artemisinin therapies, as well as concerning amounts of oral artemisinin monotherapies in the DRC and Nigeria (7%-8% of the total market). ACT comprised less than 25% of the total volume of anti-malarials distributed across all sectors. Quality-assured ACT fared even worse in the private sector, where it generally accounted for less than 6% of the total market share.
Of note, in Nigeria and the DRC, the market share of ACT was particularly low and more oral artemisinin monotherapies were sold than ACT in the private sector. In Nigeria, oral artemisinin monotherapy is less expensive than first-line quality-assured ACT treatment, perhaps explaining why higher volumes of oral artemisinin monotherapies are found.
Provider knowledge was generally lower in the private sector than in the public/not- for-profit sector. Other studies have shown that medicine seller knowledge of drugs and doses, particularly in the private sector, is often poor [13, 15, 16]. This is likely to be exacerbated by the relatively recent introduction of ACT in sub-Saharan Africa because these have new dosage requirements and more than one product may be available with different dosages .
Poor ACT availability in both public/not-for-profit and private sectors, as well as the high price observed in the private sector, and poor provider knowledge, serve as barriers to obtaining effective treatment. Of grave concern, quality-assured ACT availability in the public sector ranges between 43-85%. This suggests that there are issues within the public-sector supply chain that require urgent attention, especially in Nigeria and Uganda where stocking rates were lowest.
In the private sector, non-artemisinin therapies are more widely available and more commonly sold than other classes of anti-malarials; these medicines are also usually sold at a much lower price than ACT. Given the relative affordability and accessibility of non-artemisinin therapies, consumers have strong incentives to choose the 'wrong', ineffective, anti-malarial when seeking treatment.
Oral artemisinin monotherapy, discouraged for its potential to speed the spread of artemisinin resistance, was commonly available and sold at private outlets in the DRC and Nigeria. These disappointing findings should act as a rallying call given the Millennium Development Goal targets and that together these two nations account for nearly half of the total global burden of malaria disease . While all the ACTwatch countries have taken regulatory measures to withdraw the marketing authorization of oral artemisinin monotherapies, the manufacturing and marketing of these products is still ongoing (and many of these companies are located in Nigeria, though renewal licenses will not be granted to existing companies currently marketing oral artemisinin monotherapies ). This calls into question the effectiveness of current regulatory practices in countries where this drug is banned. Interventions such as tighter regulation and building awareness of issues with oral artemisinin monotherapies should be considered so that this national policy of public health significance is indeed followed. For other countries, availability of oral artemisinin monotherapy was low, suggesting a positive outcome from the 2006 WHO regulatory ban on oral artemisinin monotherapy, and heightened government response to the threat of artemisinin resistence.
As the majority of anti-malarials are delivered through the private sector, there is a clear need to consider how to handle the role of the private sector when developing anti-malarial drug policies. Some argue that emphasis should remain on the public sector, to attract more people to outlets where care is regulated and provided by qualified staff . Others argue that, given the current state of developing country health systems, while the public sector cannot be ignored, high private sector use is inevitable in many countries, and therefore strategies should be adopted to improve its quality . The extent to which the emphasis should be placed on the private sector continues to be debated  and data presented here provide evidence to help facilitate further discussion.
Prominent among private sector initiatives is the Affordable Medicines Facility for Malaria (AMFm), which began operations in pilot countries during 2010, and provides a mechanism for heavily subsidized, quality-assured ACT to be sold at a target retail price of $0.50 . However, there continues to be controversy about such initiatives, with some arguing that the subsidy will be captured by middle-men in the distribution chain; that market power in the private sector will lead to continued problems of affordability and inaccessibility by the poor; and that widespread availability of ACT without improving access to diagnosis will result in mis-use of ACT and fuel the development of resistance [35, 38].
Of the countries covered in this paper, Madagascar provides an interesting example of a setting where an ACT subsidy has been in operation since 2008. The subsidized ACT was open to all wholesalers registered or unregistered in the country and it was sold nationally through community health workers, pharmacies and rural drug stores. The ACT did not have over-the-counter status and had a recommended retail price of $0.05. In contrast to the other countries, the price of quality-assured ACT was lower than non-artemisinin therapies. However, accessibility remained low, as ACTwatch data show that less than 10% of private sector outlets stocking this type of ACT. Provider knowledge of the first-line treatment was also low (12%). As such, substantial gains in market share of ACT were not apparent, and rates of ACT use in febrile children remained less than 5% . Despite this, smaller scale pilots of ACT subsidies have shown impressive results [27, 32, 39]. Promising findings have also been demonstrated in Cambodia, where an ACT social marketing programme has been in place for the past 10 years .
The data suggest a need for interventions to address a full range of supply side issues that go above and beyond a price subsidy (i.e. targeting provider knowledge, increasing supply and product promotion). Interventions should also focus on demand creation through activities that include behaviour change communication, to encourage the stocking and uptake of ACT, particularly in the private sector. It remains to be seen how far the "supporting interventions, " (e.g. provider trainings and behaviour change communication, all to promote ACT utilization), being implemented as part of the AMFm and other initiatives will go in addressing these concerns.
ACTwatch provides standardized, nationally representative data on anti-malarial supply from multiple countries collected within 16 months. Data presented in this paper report on key, policy relevant indicators across countries. The results typically demonstrate the low availability, low market share and high price of ACT, at least in the private sector where most anti-malarials are being accessed, with some exceptions. Data from ACTwatch outlet surveys confirm that there is substantial room to improve availability and affordability of ACT treatment in six countries across sub-Saharan Africa, and in both the public/not-for-profit and private sectors. The data will also be useful for monitoring the impact of interventions such as the Affordable Medicines Facility for malaria. More detailed, country specific findings (for example, outlet anti-malarial availability by country strata) can be found in country reports on the ACTwatch website .
The authors are grateful to country teams who undertook the surveys. The authors are also grateful to Amin Abdinasir, Kelly Safreed-Harmon, Susan Duvall, Meg Kays, and Angus Spiers for comments on an earlier draft of the manuscript. We are indebted to the study participants and the enumerators for data collection.
This study received financial support from the Bill and Melinda Gates Foundation (#058992) and from the Global Fund to Fight AIDS, Tuberculosis and Malaria (PO 20013306).
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