Battling the malaria iceberg with chloroquine in India
© Sharma; licensee BioMed Central Ltd. 2007
Received: 16 November 2006
Accepted: 07 August 2007
Published: 07 August 2007
The National Vector Borne Disease Control Programme (NVBDCP) of the Ministry of Health, Government of India is reporting about 2 million parasite positive cases each year, although case incidence is 30-fold or more under-estimated. Forty five to fifty percent of Plasmodium infections are caused by Plasmodium falciparum, the killer parasite. Anti-malaria drug policy (2007) of the NVBDC recommends chloroquine (CQ) as the first line of drug for the treatment of all malarias. In a Primary Health Centre (PHC) reporting 10% or more cases of CQ resistance in P. falciparum, ACT blister pack is recommended and, so far, the policy has been adopted in 261 PHCs of 71 districts. The NVBDCP still depends on CQ to combat malaria and, as a result, P. falciparum has taken deep roots in malaria-endemic regions, causing unacceptable levels of morbidity and mortality. This policy was a subject of criticism in recent Nature and Lancet articles questioning the World Bank's decision to supply CQ to the NVBDCP. Continuation of an outdated drug in the treatment of P. falciparum is counterproductive in fighting drug resistant malaria and in the containment of P. falciparum. Switchover to Artemisinin-based Combination Therapy (ACT) in the treatment of all P. falciparum cases, ban on artemisinin monotherapy and effective vector control (treated nets/efficient insecticide spraying) would be a rational approach to malaria control in India.
The National Vector Borne Disease Control Programme (NVBDCP) is reporting about 2 million parasite positive cases a year, 50% of these Plasmodium falciparum. The WHO estimates 100 million cases in the South East Asian Region, 70% of these occur in India [1, 2]. Independent studies by the Indian Council of Medical Research have unequivocally established that malaria incidence is hugely under-estimated [3–6]. Health is the state's responsibility, therefore, malaria control is carried out by the states, under the overall guidance of the NVBDCP. To monitor the impact of interventions surveillance is organized to detect malaria cases by examining fever cases in the entire country. In rural areas, blood smears are collected at fortnightly intervals by multi-purpose workers i.e. through Active Case Detection (ACD) and also collected at the Primary Health Centres (PHCs) i.e. Passive Case Detection (PCD). In urban areas, PCD is carried out at the malaria clinics. The blood smears are examined in the laboratory for parasite identification and results are used for follow-up action. Cases found positive are given radical treatment, as per the policy of the NVBDCP. This data is used in calculating epidemiological indices at the various levels of health services. PHCs reporting cases of drug failure are referred to the drug monitoring teams for further investigation on drug sensitivity in P. falciparum. If 25% (now reduced to 10%) of the cases tested show resistance to CQ, the drug policy is changed for the second line of drug. Thirteen NVBDCP teams routinely monitor P. falciparum drug sensitivity in the country. These teams are located in various regions so as to cover the entire country. P. falciparum monitoring for drug sensitivity is done using the World Health Organization (WHO) methodology of in vivo (28-day) test procedure for determining the status of resistance to CQ and other antimalarial drugs in P. falciparum. Malaria Drug Policy (2007) of the NVBDCP provides inter alia the following treatment guidelines countrywide .
1. All fever cases should preferably be investigated for malaria by microscopy or Rapid Detection Test (RDT).
2. The first line of treatment is chloroquine and the second line is ACT (artesunate+sulphadoxine/pyrimethamine) combination in case resistant to these formulations and to treat severe and complicated malaria, quinine will be the drug of choice.
3. Microscopically positive P. falciparum cases should be treated with chloroquine in therapeutic dose of 25 mg/kg body weight over three days and a single dose of primaquine 0,75 mg/kg body weight on the first day. The practice is to be followed at all levels including Voluntary Health Workers (VHWs) like Drug Distribution Centres (DDCs)/Fever Treatment Depots(FTDs)/Accredited Social Health Activist (ASHA) as well.
The antimalarial drug policy states that all Plasmodium vivax cases, undiagnosed fever cases, and clinical malaria cases should be treated with chloroquine in full therapeutic doses. ACT (artesunate+sulphadoxine/pyrimethamine) is the first line of antimalarial drug for treatment of P. falciparum in chloroquine resistant areas. Chloroquine, therefore, remains the main drug for the treatment of all malarias in India except in PHCs with 10% or more cases found resistant to it. The objective of this paper is to highlight the realistic and evidence-based malaria situation in the country, and how the changes in drug policy and efficient vector control can wipe out malaria, thus bringing out the importance of the WHO recommendation of a switch over to artemisinin-based fixed-dose combination therapy (ACT) to treat all P. falciparum cases (sensitive or resistant to CQ/SP).
Studies on re-emergence of malaria revealed countrywide presence and spread of P. falciparum e.g. P. falciparum is found in all states and union territories except Lakshadweep Island (Malaria situation 2002–2006, NVBDCP). It may be noted that P. falciparum occurrence is highly uneven in time and space [8, 9]. Furthermore, the NVBDCP is reporting malaria epidemics in five or six states each year, and frequent focal outbreaks . In some parts of the country, malaria epidemics cover two or more districts, dominated by P. falciparum [11–14]. Currently an epidemic of malaria is raging in Assam, a region more frequently visited by annual exacerbations [15, 16]. The country-wide presence of P. falciparum is facilitated by inter- and intra-state population movement, particularly for civil works, agriculture, rail road construction, rural urban migration; thus providing opportunities for the mutant strains to disseminate across district and state boundaries [17–19].
Malaria epidemiology and its control are complicated by poverty as it is a dominant disease in poverty stricken societies. For example, Indian states with population exceeding the national average of 26.1% population below poverty line (BPL) contributed 88% P. falciparum in 2000 . Addressing the plenary session of United Nations Conference on Human Environment at Stockholm,14 June 1972, the former Prime Minister of India Smt. Indira Gandhi said "Are not poverty and need the greatest polluters?  Poverty alleviation is on the national and United Nations agenda. How to fight poverty which is at the roots of all ills? Certainly malaria control is an important tool to alleviate human suffering caused by poverty and ill health. Therefore, priorities in malaria control should remain high, national and international bodies should work in tandem to eradicate this age old "King of all Diseases".
Plasmodium falciparum monitoring for drug sensitivity is conducted by thirteen NVBDCP teams. Monitoring is done on the line of WHO methodology of in vivo (28-day) standard techniques for determination of resistance in P falciparum to CQ and other antimalarials. India is a vast country, so it is difficult to generalize. However, between 1978 and June 2001, a total of 15,069 P. falciparum cases in 178 districts of 28 states and union territories have been completed. Of these 3,965 (26.3%) were sensitive to CQ; 7,661 (50.8) were S/RI; 2,142 RI resistant; 752 RII resistant (5%) and 549 (3.6%) RIII resistant to CQ . In 2004, the P. falciparum monitoring teams collected 45,966 blood smears, of which 4,756 were positive for malaria and 3,850 for P. falciparum (80.95%). Results based on CQ sensitivity of 209 samples, showed Adequate Clinical and Parasitological Response (ACPR) 98 (47.9%), Early Treatment Failure (ETF) 27 (12.9%) and Late Treatment Failure (LTF) 84 (40.2%). Drug resistance to CQ is presenting countrywide, although proportion of resistant strains varies greatly [28–33]. Already the Pfcrt K76T mutation, an important determinant of CQ resistance, is present in >95% of P. falciparum isolates . In addition to these clear indicators of resistance in the parasite populations, there are important changes in disease outcomes. For example, in patients with P. falciparum infections, acute renal and multi-organ failures have almost doubled in the last 5–7 years. Although it is not possible to attribute this directly to the decreasing efficacy of CQ, but it may be an important factor, as it has been in malaria-related deaths in African children . The deteriorating trends in P. falciparum demands urgent radical changes in antimalarial drug policy. ACT is currently used in 261 PHCs (71 districts) as against approximately 14,000 malaria endemic PHCs. The process of adoption to ACT is painfully slow and may take a long time, until then CQ remains the first line drug in India. In 2006 a series of articles in The Lancet [36–38] and Nature  concerned funding of antimalaria drugs by the World Bank. The Lancet paper criticized the World Bank for funding the purchase of CQ by the Indian government. There is substantial evidence that CQ is no longer effective against P. falciparum in many areas of India, and under those circumstances the purchase of CQ supports a dangerous public health practice. One response to the criticism was that CQ is used in India only to combat P. vivax, a species against which it is mostly still effective. This statement contradicts the drug policy of the NVBDCP which recommends the use of CQ to treat all malaria cases, including P. falciparum, the more lethal pathogen.
Malaria in Betul District, Madhya Pradesh, India
DDT (50% WP) sprayed
in mt against 200 mt required
Synthetic Pyrethroid sprayed in mt
CQ Tablets (150 mg base)
Total malaria cases
P. falciparum cases
The WHO recommends fixed dose artemisinin combination therapy for P. falciparum . In light of the clear evidence for CQ-resistance in P. falciparum, and the recommendation for using CQ as the treatment for all malaria, not just P. vivax, the NVBDCP should respond to the recommendation of the Lancet Viewpoint and abandon CQ, in favour of ACT. Indian states with high prevalence of P. falciparum have the problem of CQ resistance, although the proportion remains undetermined. CQ and sulphadoxine/pyrimethanine (SP) resistance is more pronounced in the north-eastern states and Orissa. Multidrug-resistant strains abound on the international borders with the Indian NE states [44–46]. Artesunate with SP combination (blister pack) is now recommended in drug resistant areas. In seven states in the northeastern region of the country, ACT is being introduced in one district in each state in the pilot phase. Further expansion would depend on the experience gained in the districts in north-eastern region. This switch over to ACT would take place in 71 districts in the country (261 PHCs, but there are approximately 14,000 high risk PHCs requiring ACT to treat P. falciparum), with provision to expand this coverage to adjacent PHCs reporting >10% CQ resistant P. falciparum. States have been advised to monitor the status of drug resistance in the adjacent PHCs for the expansion of ACT. PHCs lacking microscopic facility would be supplied with rapid diagnostic test kits to detect P. falciparum. Furthermore, artemisinin drugs are frequently used as monotherapy in the private sector, the racket of substandard and fake drugs , private sector working in isolation, government support to herbal drugs failing in scientific scrutiny  and indiscretion in the use of artemisinin are dangerous signals, and failure to address these problems may endanger life of patients and accelerate resistance. Thus the inertia may open the possibility of an epicenter of drug resistant malaria in South East Asia. Finally, withholding correct malaria treatment for unfounded reasons, lacking sound scientific basis and wise clinical judgment, is both unethical and discriminatory. Malaria is predominantly the disease of the poor lacking health equity. This inequity should be leveled by following correct drugs and drug schedule to the needy and unprotected for a relentless war against malaria. Setting the house in order is a formidable challenge. Therefore, inter alia policy issues must be addressed by the NVBDCP first and the foremost.
We are grateful to Dr Neeru Singh, Sr Dy Director, Regional Medical Research Centre for Tribals, Jabalpur, M.P. for providing useful inputs in the preparation of this manuscript.
- WHO: First meeting of the Regional Technical Advisory Group on Malaria, Manesar, Haryana, India 15–17. 2004, World Health Organization, Regional Office for South-East Asia, New Delhi SEA-MAL-239, 1-38. DecemberGoogle Scholar
- WHO: Strategic Plan to Roll Back Malaria in the South-East Asia Region. World Health Organization, Regional Office for South-East Asia, New Delhi SEA-MAL- 237, 1-25.
- Snow RW, Guerra CA, Noor AM, Myint HY, Hay SI: The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature. 2005, 434: 214-217. 10.1038/nature03342.PubMed CentralView ArticlePubMedGoogle Scholar
- Choudhury DS, Malhotra MS, Shukla RP, Ghosh SK, Sharma VP: Resurgence of malaria in Gadarpur PHC district Nainital, Uttar Pradesh. Indian J Malariol. 1983, 20: 49-58.Google Scholar
- Yadav RS, Bhatt RM, Kohli VK, Sharma VP: The burden of malaria in Ahmedabad city, India – a retrospective analysis of reported cases and deaths. Ann Trop Med Parasit. 2003, 97: 793-802. 10.1179/000349803225002642.View ArticlePubMedGoogle Scholar
- Sharma VP, Choudhury DS, Ansari MA, Malhotra MS, Menon PKB, Razdan RK, Batra CP: Studies on the true incidence of malaria in Kharkhoda (Distt. Sonepat, Haryana) and Kichha (distt. Nainital, U.P.) Primary Health Centers. Indian J Malariol. 1983, 20: 21-34.Google Scholar
- NVBDCP: Malaria Drug Policy. 2007, [http://www.nvdcp.gov.in/Doc/Revised %20 drug%20 policy.pdf]Google Scholar
- Sharma VP, Mehrotra KN: Malaria resurgence in India : A critical study. Soc Sci Med. 1986, 22: 835-845. 10.1016/0277-9536(86)90238-8.View ArticlePubMedGoogle Scholar
- Sharma VP: Re-emergence of malaria in India. Indian J Med Res. 1996, 103: 26-45.PubMedGoogle Scholar
- Malaria epidemics/outbreaks. [http://www.searo.who.int/EN/Section10/Section21/Section1987.htm]
- Raghavendra K, Subbarao SK, Sharma VP: An investigation in to the recent malaria outbreak of malaria in district Gurgaon, Haryana state. Curr Sci. 1997, 73: 766-770.Google Scholar
- Neeru Singh, Shukla MM, Chand SK, Sharma VP: Outbreak of falciparum malaria in submerged villages of Narayanganj PHC district Mandla due to Narmada irrigation project, Central India, Madhya Pradesh. Curr Sci. 1997, 73: 686-691.Google Scholar
- Neeru Singh , Sharma VP, Shukla MM, Gyan Chand: Malaria outbreak in Kundam block, district Jabalpur, M.P. Indian J Malariol. 1988, 25: 41-49.Google Scholar
- Singh Neeru , Shukla MM, Sharma VP, Saxena BN: A focus of high degree chloroquine resistant P falciparum in Mandla District (M.P.). Indian J Malariol. 1989, 26: 45-51.Google Scholar
- Malaria epidemic kills 50 in Assam. [http://in.news.yahoo.com/060418/43/63m3w.html]
- Dev V, Sharma VP: Persistent transmission of malaria in Sonapur PHC Kamrup district Assam. J Parasitol Dis. 1995, 19: 65-68.Google Scholar
- Kumar A, Sharma VP, Thavaselvam D: Malaria related to constructions in Panaji, Goa. Indian J Malariol. 1991, 28: 219-226.PubMedGoogle Scholar
- Adak T, Batra CP, Mittal PK, Sharma VP: Malaria outbreak in a hotel construction site in South Delhi. Indian J Malariol. 1994, 31: 126-131.PubMedGoogle Scholar
- Sharma RC, Sharma VP: Epidemiological implications of population migration: Part II Evidence of chloroquine resistant Plasmodium falciparum malaria in Kheda district Gujarat. Indian J Malariol. 1988, 25: 17-118.PubMedGoogle Scholar
- Sharma VP: Current scenario of malaria in India. Parassitologia. 1999, 41: 349-353.PubMedGoogle Scholar
- Sehgal PN, Sharma MID, Gogai S: Resistance to chloroquine in falciparum malaria in Assam State, India. J Comm Dis. 1973, 5: 175-180.Google Scholar
- Ray AP, Narasimham MVVL, Kondrashin AV, Anna-Kari Bill: P. falciparum containment programme. Ten years of operation in India (1978–1988). 1998, PfCP/Directorate of NMEP/WHO/SIDA, DelhiGoogle Scholar
- Singh Neeru , Nagpal AC, Saxena Ajay, Singh MP: Changing scenario of malaria in central India, the replacement of Plasmodium vivax by Plasmodium falciparum(1986–2000). Trop Med Int Health. 2004, 9: 364-371. 10.1046/j.1365-3156.2003.01181.x.View ArticlePubMedGoogle Scholar
- India Malaria Profile . [http://www.searo.who.int/LinkFiles/Malaria_Profile_India.pdf]
- Sharma VP: Malaria and poverty in India. Curr Sci. 2003, 84: 513-515.Google Scholar
- Department of Environment, Government of India: Indira Gandhi on Environment. 1984, 1-123.
- Malaria Drug Policy. Unpublished document . NVBDCP, 22-Sham Nath Marg Delhi-110054
- Singh N, Tyagi AK, Sharma VP: Drug resistant Plasmodium falciparum in Mandla district, Madhya Pradesh. Indian J Malariol. 1995, 32: 174-177.PubMedGoogle Scholar
- Ghosh SK, Choudhury DS, Chandrahas RK, Singh Neeru , Ramanaiah TV, Sharma VP: Drug resistant P. falciparum in Madras (Tamil Nadu) and District Jabalpur (Madhya Pradesh). Indian J Malariol. 1989, 26: 87-90.PubMedGoogle Scholar
- Sinha S, Dua VK, Sharma VP: Chloroquine resistant imported P. falciparum in an industrial complex at Hardwar. Indian J Malariol. 1989, 26: 123-125.PubMedGoogle Scholar
- Dua VK, Kar PK, Gupta NC, Kar I, Sharma VP: In vivo and in vitro sensitivity of Plasmodium falciparum to chloroquine in Chennai (Tamil Nadu), India. Indian J Malariol. 1997, 34: 1-7.PubMedGoogle Scholar
- Ghosh SK, Yadav RS, Sharma VP: Sensitivity status of Plasmodium falciparum to chloroquine, amodiaquine, quinine, mefloquine and sulfadoxine/pyrimethamine in a tribal population of district Sundergarh, Orissa. Indian J Malariol. 1992, 29: 211-218.PubMedGoogle Scholar
- Sinha S, Choudhury DS, Ghosh SK, Usha Devi C, Sharma VP: In vitro Chloroquine resistant Plasmodium falciparum in Calcutta and its sensitivity in Qinghaosu (Artemisinin). Indian J Malariol. 1987, 24: 107-110.PubMedGoogle Scholar
- Vathsala PG, Pramanik A, Dhanasekaran S, UshaDevi C, Pillai CR, Subbarao SK, Ghosh SK, Tiwari SN, Sathyanarayan TS, Deshpande PR, Mishra GC, Ranjit MR, Dash AP, Rangarajan PN, Padmanaban G: Widespread occurrence of the Plasmodium falciparum chloroquine resistance transporter (Pfcrt) gene haplotype SVMNT in P falciparum malaria in India. Am J Trop Med Hyg. 2004, 70: 256-259.PubMedGoogle Scholar
- Snow RW, Trape JF, Marsh K: The past, present and future of childhood malaria mortality in Africa. Trends Parasitol. 2001, 17: 593-597. 10.1016/S1471-4922(01)02031-1.View ArticlePubMedGoogle Scholar
- Time for the World Bank to act on malaria. The Lancet. 2006, 367: 1372-
- Attaran A, Barnes K, Bate R, Binka F, d'Allessandro U, Fanello C, Garrett Cl, Mutabingwa L, Roberts TK, D Sibley CH, Talisuna A, van Geertruyden JP, Watkins WM: The World Bank: fake financial and statistical accounts and medical malpractice in malaria treatment. The Lancet. 2006, 368: 247-252. 10.1016/S0140-6736(06)68545-0.View ArticleGoogle Scholar
- Sarbib JL, Nankarni G, Patel P: The booster program for malaria control: putting knowledge and money to work. The Lancet. 2006, 368: 253-257. 10.1016/S0140-6736(06)68437-7.View ArticleGoogle Scholar
- World Bank defends efforts to curb malaria. Nature. 2006, 440: 1096-1097. 10.1038/4401096b.
- Sharma VP: DDT: The fallen angel. Curr Sci. 2003, 85: 1532-1537.Google Scholar
- Sharma VP: Artemisinin drugs in the treatment of P. falciparum malaria in India. Curr Sci. 90: 1323-1324.
- Sharma VP: Malaria in Betul submitted to the Government of Madhya Pradesh, (Unpublished work). Tour report. 2006Google Scholar
- World Health Organization: FACTS and ACTS (Artemisinin based combination therapies). FACTS ON ACTS (Artemisinin-based combination therapies), Geneva. January 2006 update, [http://www.google.co.in/search?hl=en&q=WHO+FACTS+and+ACTs&btnG=Google+Search&meta]
- Mohapatra PK, Prakash A, Bhattacharya DR, Goswami BK, Mahanata J: Concurrent multidrug resistant Plasmodium falciparum from northeast India. J Assoc Phys India. 1999, 47 (8): 823-824.Google Scholar
- Mohapatra PK, Prakash A, Taison K, Negmu K, Gohain AC, Namchoom NS, Wange D, Bhattacharya DR, Goswami BK, Borgohain BK, Mahanata J: Evaluation of chloroquine (CQ) and sulphadoxine pyrimethamine (SP) therapy in uncomplicated falciparum malaria in Indo-Myanmar border areas. Trop Med Int Health. 2005, 10: 478-483. 10.1111/j.1365-3156.2005.01401.x.View ArticlePubMedGoogle Scholar
- Mohapatra PK, Namchoom NS, Prakash A, Bhattacharya DR, Goswami BK, Mahanata J: Therapeutic efficacy of anti-malarials in Plasmodium falciparum malaria in an Indo-Myanmar border area of Arunachal Pradesh. Indian J Med Res. 2003, 118: 71-76.PubMedGoogle Scholar
- South-east Asia awash with fake drugs. [http://www.guardian.co.uk/international/story/0,,2018238,00.html]
- Valecha N, Usha Devi C, Joshi Hema , Sahi VK, Sharma VP, Lal Shiv : Comparative efficacy of Ayush-64 vs. chloroquine in vivax malaria. Curr Sci. 2000, 78: 1120-1122.Google Scholar
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