But researchers warn that routine surveillance is crucial as poor quality medicines exist, leaving malaria patients at risk of dying and increasing the risk of drug resistance.
Previous reports had suggested that up to one third of antimalarials could be fake. Researchers from the Artemisinin-based Combination Therapy (ACT) Consortium at the London School of Hygiene & Tropical Medicine analysed 2,028 antimalarials from Tanzania and Cambodia. Samples were selected in a rigorous and representative way making this one of the most recent comprehensive data sets on antimalarial quality.[1]
Drugs were analysed in three independent laboratories in the UK and USA and classed as acceptable quality, falsified (fake drugs which do not contain the stated active pharmaceutical ingredient or API) or substandard (genuine medicines produced by authorised manufacturers which do not have the correct amount of API).[2]
No falsified drugs were found in either country. However, substandard drugs were found in 31% of samples in Cambodia and in 12% of samples in Tanzania.
In Tanzania, the study team used an "overt sampling" system, telling vendors that they were going to analyse the quality of their medicines. In Cambodia, researchers used overt sampling as well as a "mystery client" approach, where actors pretended to be patients with malaria, or their relatives, and bought the medicines offered to them. Both studies used a randomised approach to sampling of drug outlets, which differs from previous studies that mostly used non-representative methods for selecting drugs for analysis.
Dr Harparkash Kaur from the London School of Hygiene & Tropical Medicine, lead investigator of the drug quality programme of the ACT Consortium, said: "Although there have been alarming reports about the prevalence of fake antimalarials, our study provides ample data showing that the quality of drugs is not so bad based on comprehensive sampling and analysis presented here. This type of study is very cost intensive, both for the purchase and analysis of drugs. The lack of falsified medicines in Cambodia and Tanzania are reassuring, but the presence of substandard medicines is definitely a concern."
Dr Shunmay Yeung from the London School of Hygiene & Tropical Medicine, lead author of the study in Cambodia - one of the epicentres of resistance to artemisinin - said: "Falsified medicines have received much attention globally, but substandard drugs are far more prevalent and of great concern. Not only do they leave patients with malaria undertreated, which could be fatal, but they may also contribute to the development of resistance to ACTs, the most effective drugs for malaria. Generally, the fact that no falsified antimalarials were identified reflects the positive impact of the country's effort to control drug quality."
Dr Catherine Goodman from the London School of Hygiene & Tropical Medicine, who led the study in Tanzania, said: "There is an urgent need to strengthen the capacity of national medicine regulation authorities to develop robust estimates of drug quality that are affordable, representative and timely. Our study saved costs by collecting samples within a nationally representative survey that was already in place." In Tanzania, one fourth of the 1,737 medicines analysed were prequalified by the World Health Organization, and these were less likely to be of poor quality than those not prequalified. [3]
The lead investigators highlighted that results based on low cost convenience sampling approaches are still useful in drawing attention to the problem. However, alarming messages could be counter-productive by undermining the confidence in drugs and health care providers and systems.
These are the first published results from the ACT Consortium's large drug quality programme, which analysed over 10,000 samples from malaria endemic countries over five years. Results from Nigeria, Equatorial Guinea, Ghana and Rwanda will be published in the next few months.
The ACT Consortium studies in Tanzania and Cambodia are funded by a grant from the Bill & Melinda Gates Foundation to London School of Hygiene & Tropical Medicine. The Cambodia study also received support from the UK Department for International Development.
INFORMATION:
For more information or to request interviews contact Katie Steels, Media Manager at the London School of Hygiene & Tropical Medicine: Katie.Steels@lshtm.ac.uk and +44 (0)20 7927 2802.
Notes to Editors:
[1] The previous reports were based on studies that have predominantly used non-representative methods for selecting drugs for analysis, with study teams often selecting antimalarial sellers because they were easily accessible, or because they believed sellers were more likely to sell poor quality medicines based on their appearance or anecdotal reports. This "convenience approach" for sampling is not representative of the places where patients buy their medicines. Medicines in both studies were collected from private drug outlets only; in many countries these are one of the most common sources of treatment and their medicines tend to be less supervised than those delivered through the public sector.
[2] Falsified drugs carry false representations of their source or identity, and often contain none of the stated active ingredient. Counterfeit medicines are medicines that do not comply with intellectual property rights or that infringe trademark law. Substandard drugs can result from either inadequate quality control in the manufacturing process (meaning that they contain a lower or greater amount of the API than intended), or well manufactured medicines may become degraded if they are kept in inappropriate storage conditions, for example in high heat or humidity. Researchers used the analytical technique of high performance liquid chromatography for the quantitative analysis and mass spectrometry for the qualitative analysis. Based on USP and WHO pharmacopeia rules, drugs defined as being poor quality contain less than 90% or more than 110% of the stated API. In order for the ACT Consortium drug quality programme to apply such rules, they would have had to analyse 30 tablets per sample. However, some packets only had 6 tablets, which were shared between three laboratories. Therefore the ACT Consortium adopted the 85% to 115% API range. Results are sensitive to these limits.
[3] In order for a finished pharmaceutical product to be prequalified by the WHO, a comprehensive, scientific evaluation of the product is carried out based on information submitted by the manufacturer and on an inspection of the corresponding manufacturing facilities and clinical sites. More information is available at http://apps.who.int/prequal/
Collaborating institutions: Division of Parasitic Diseases and Malaria, US Centers for Disease Control and Prevention, Atlanta, Georgia; School of Chemistry and Biochemistry, Georgia Institute of Tehnology, Atlanta, Georgia; Ifakara Health Institute, Dar es Salaam, Tanzania; Cambodia National Malaria Centre.
About the ACT Consortium
The ACT Consortium is an international research collaboration working on 25 projects in 10 countries to answer key questions on malaria drug delivery. Since initiating activities in 2008, the Consortium has been working to optimise the use of Artemisinin-based Combination Therapy (ACT), the first-line treatment for the most dangerous form of malaria recommended by the World Health Organization. The projects investigate ways to improve the access and targeting of ACTs, as well as assessing their safety and quality. The ACT Consortium is based at the London School of Hygiene & Tropical Medicine and a member of the School's Malaria Centre. Learn more about the drug quality programme at http://www.actconsortium.org/drugquality and watch a video at https://vimeo.com/125049233. The ACT Consortium will host a drug quality event on 28 May 2015 in Geneva, Switzerland. Find out more information on the above website.
About the London School of Hygiene & Tropical Medicine
The London School of Hygiene & Tropical Medicine is a world-leading centre for research and postgraduate education in public and global health, with 3,900 students and more than 1,000 staff working in over 100 countries. The School is one of the highest-rated research institutions in the UK, and was recently cited as the world's leading research-focused graduate school. Our mission is to improve health and health equity in the UK and worldwide; working in partnership to achieve excellence in public and global health research, education and translation of knowledge into policy and practice. http://www.lshtm.ac.uk
