- Open Access
Therapeutic assessment of chloroquine–primaquine combined regimen in adult cohort of Plasmodium vivax malaria from a tertiary care hospital in southwestern India
Malaria Journalvolume 14, Article number: 310 (2015)
The Erratum to this article has been published in Malaria Journal 2016 15:59
Of late there have been accounts of therapeutic failure and chloroquine resistance in Plasmodium vivax malaria especially from Southeast Asian regions. The present study was conducted to assess the therapeutic efficacy of chloroquine–primaquine (CQ–PQ) combined regimen in a cohort of uncomplicated P. vivax mono-infection.
A tertiary care hospital-based prospective study was conducted among adult cohort with mono-infection P. vivax malaria as per the World Health Organization’s protocol of in vivo assessment of anti-malarial therapeutic efficacy. Participants were treated with CQ 25 mg/kg body weight divided over 3 days and PQ 0.25 mg/kg body weight daily for 2 weeks.
Of a total of 125 participants recruited, 122 (97.6%) completed day 28 follow up, three (2.4%) participants were lost to follow-up. Eight patients (6.4%) were ascertained to have mixed P. vivax and Plasmodium falciparum infection by nested polymerase chain reaction test. The majority of subjects (56.8%, 71/125) became aparasitaemic on day 2 followed by 35.2% (44/125) on day 3, and 8% (10/125) on day 7, and remained so thereafter. Overall only one therapeutic failure (0.8%, 1/125) occurred on day 3 due to persistence of fever and parasitaemia.
CQ–PQ combined regimen remains outstandingly effective for uncomplicated P. vivax malaria and should be retained as treatment of choice in the study region. One case of treatment failure indicates possible resistance which warrants constant vigilance and periodic surveillance.
Plasmodium vivax accounts for more than 50% of total malaria burden in India . Chloroquine (CQ) in a dose of 25 mg/kg body weight over 3 days remains the recommended first-line treatment for all uncomplicated P. vivax malaria in India . Additionally, for radical cure, a primaquine (PQ) dose of 0.25 mg/kg body weight for 14 days has been recommended in all non-gravid adult P. vivax cases with normal glucose-6-phosphate dehydrogenase (G6PD) activity . Therapeutic and prophylactic failures of CQ in P. vivax have been observed in 23 countries across the globe, including India . However, true resistance to CQ in P. vivax has been confirmed in only ten countries across the globe, excluding India .
Therapeutic assessment remains the mainstay of monitoring the efficacies of anti-malarial regimens and is recommended to be undertaken once every 2 years . Surveillance of CQ–PQ combined regimen in P. vivax remains valid and provides useful indices where regional health policy mandates such . This study was undertaken to determine the therapeutic efficacy of CQ–PQ combined regimen in adult P. vivax mono-infection cohort as per WHO’s protocol .
Study design and patients
A prospective cohort study was conducted among microscopically proven symptomatic mono-infection P. vivax patients aged ≥18 years attending Kasturba Hospital (KH), Manipal from September 2012 until October 2014. Patients were excluded if they had other febrile illnesses including mixed malaria or P. vivax malaria treated with artesunate combination therapy or prior anti-malarial medication outside KH before presentation or pregnancy or unwillingness to provide a written informed consent.
Ethical approval (IEC 193/2011) was obtained from the institutional ethics committee of Kasturba Medical College and Kasturba Hospital, Manipal University, Manipal. Participation in study was strictly voluntary and each participant had privilege to retract their participation any time throughout the study. Patients’ information and study data were anonymized.
Sample size calculation
Presuming the proportion of anti-malarial treatment failure (ATF) of CQ–PQ combined regimen to be 5%, for a desired precision of 5% and confidence interval of 95%, a cohort of 73 microscopically proven P. vivax mono-infection cases were required . Furthermore, to adjust for a 20% expected loss to follow-up and 20% expected withdrawal/protocol violation the final required sample size was determined as 122 subjects.
Blood sample collection and processing
The date of initiation of anti-malarial medication and study enrolment were the same and was considered as day 0. Peripheral blood smear was examined on days 0, 2, 3, 7, 14, 21, and 28. Before initiation of anti-malarial medications, 1 ml venous blood sample was obtained from each participant in an ethylenediaminetetraacetic acid (EDTA) anticoagulated vacutainer and used for making peripheral smears, total leukocyte count and DNA extraction. On subsequent follow-up days capillary blood sample was obtained by finger prick on cleaned glass slides to prepare both thin and thick smears. Leishman’s stained thin and thick peripheral blood smears were examined to ascertain the P. vivax mono-infection and to estimate the parasite index (PI), respectively. DNA was extracted from 200 µL of EDTA anticoagulated blood using QIAamp DNA Blood Mini Kit as per the manufacturer’s instructions and stored at −20°C until conduct of nested polymerase chain reaction (nPCR) test for confirmation of the mono-infection with P. vivax malaria.
Axillary temperature was recorded on each respective follow-up day as mentioned above. Participants’ total leukocyte count per µL was estimated in constituent laboratory of KH, Manipal by Beckman Coulter® LH 750 Haematology Analyzer and used for PI calculation. PI was determined as the absolute number of asexual and/or sexual parasites present in 1 µL of peripheral blood, as described elsewhere . Peripheral blood smears were examined under Olympus CH20i microscope and a mean PI by three consecutive calculates was derived for further analysis. Relevant demographic and clinical data of participants were recorded using a customized proforma.
ATF was considered as the primary outcome. Anti-malarial therapeutic responses were classified as per WHO’s recommendation for P. vivax . However, for in-hospital patients ‘deteriorating clinical condition requiring hospitalization with presence of parasitaemia’ was not considered as ATF, owing to the study setting being a tertiary care hospital and the patients being hospitalized as per the clinicians’ judgement before the diagnosis of malaria and initiation of anti-malarial treatments.
Confirmation of Plasmodium vivax mono-infection by nPCR test
Small sub-unit ribosomal RNA was amplified using genus and species-specific oligonucleotide primers separately for only P. vivax and P. falciparum, as described by Snounou et al. , with modifications in the amplification conditions of the second reaction. All reactions were carried out in a final volume of 20 µL containing 2 mM MgCl2, 50 mM KCl, 10 mM Tris–HCl pH 8.3, 125 µM of each dNTPs, 250 nM of each oligonucleotide primers, 0.5 units of Taq DNA polymerase (Sigma-Aldrich) and 1 µL of template DNA. Product of the first amplification reaction was further amplified in second reaction as step 1: 94°C for 5 min; step 2: 94°C for 30 s; step 3: 55°C for 30 s; step 4: 72°C for 1 min; steps 2–4 for 10 cycles, then step 6: 94°C for 10 s; step 7: 60°C for 10 s; step 8: 72°C for 1 min; steps 6–8 for 20 cycles and then final extension at 72°C for 5 min followed by termination temperature at 4°C. Reference samples of mono-infection P. vivax and P. falciparum were procured from the National Institute of Malaria Research (ICMR), Sector 8, Dwarka, Delhi-110077 (India). DNA extracted from the reference samples were used as positive controls in every batch of nPCR tests. While, DNA extracted from a normal healthy volunteer was used as negative control.
On presentation, patients were treated symptomatically as required. After confirmation of P. vivax malaria, specific anti-malarial medications were prescribed as per the clinicians’ judgements and the national guideline for treatment of malaria . Resochin (chloroquine phosphate 250 mg) manufactured by Bayer Pharmaceuticals Private Limited Bayer House Central Avenue, Hiranandani Estate, Thane—400607, Maharashtra, India and Malirid (primaquine phosphate 7.5 mg) manufactured by IPCA Laboratories Pvt. Ltd. 123-AB, Kandivli Industrial Estate, Kandivli (West)Mumbai 400 067, Maharashtra, India was administered to the study cohort. All patients were instructed to take primaquine after having food and not to take while empty stomach. PQ was administered only after estimation of G6PD activity, i.e., immediately after completion of CQ dosage. Activity of erythrocytes’ G6PD enzyme was quantified by manual spectrophotometric kinetic ‘gold standard’ method. The enzyme activity was determined by measurement of increase in reduced form of nicotinamide adenine dinucleotide phosphate (NADPH) concentration, that strongly absorbs UV light (340 nm). Mild to moderate G6PD deficient patients’ were treated with 0.75 mg/kg stat dose of PQ follow by weekly once same dose for subsequent 7 weeks. Patients’ adherence to anti-malarial regimens was ascertained by direct observation for all inpatients during their hospital stay and for outpatients by passive reminder (group messages over mobile phones) and by documenting the emptied stripes of medicines on each follow-up day.
Gaussian distribution of continuous variables was determined by Kolmogorov–Smirnov test. Data having normal distribution were summarized as mean with standard deviation and compared by independent t test. Skewed data were summarized as median with interquartile range and compared by Mann–Whitney U test. Categorical variables were summarized as frequency with proportion and compared by either χ2 test or Fischer’s exact test. All tests of significance were two-tailed with a p value <0.05 indicating statistical significance. Parasite index was summarized as geometric mean with 95% confidence interval of geometric mean. The probability of therapeutic failure was assessed by life table analysis. Data analysis was done using Statistical Package for the Social Sciences version 15.0 (SPSS, South Asia, Bangalore, India).
Patients’ clinical-demographic profile
A total of 125 participants sustaining the study selection criteria were enrolled. Pertinent clinical and demographic characteristics of the study cohort have been summarized in Table 1. Significantly (p < 0.05) higher axillary temperature at presentation and longer defervescence time was noted among hospitalized than ambulatory care participants. Mean duration of hospitalization of inpatients was 4.3 ± 1.5 days.
Chloroquine (25 mg/kg body weight over 3 days) and primaquine (0.25 mg/kg body weight daily for 2 weeks) standard anti-malarial regimen for P. vivax was given to all subjects except one participant whose G6PD was low (5.5 U/gm Hb), thus was given a 45 mg stat PQ dose followed by weekly dose of 45 mg PQ for next 7 weeks. Mean G6PD activity in study cohort was determined as 15.2 ± 4.1 U/gm Hb and ranged from 5.5 to 27.2 U/gm Hb. A complete adherence for the prescribed CQ–PQ regimens was noted among study cohort. Empiric antibiotic (ceftriaxone) was administered to one (1.2%) inpatient.
A total of 122 (97.6%) participants completed day 28 follow-up. Three participants (2.4%) were lost to follow up after day 3. One of them remained parasitaemic on day 3 but had become afebrile within 24 h of hospitalization. Another two participants had become aparasitaemic by day 3 and their defervescence time was less than 24 h. More than half of the subjects (56.8%, 71/125) became aparasitaemic on day 2 followed by 35.2% (44/125) on day 3; and 8% (10/125) on day 7 and remained so thereafter to day 28 (Fig. 1). Despite having history of fever within preceding 3 days, 24% (30/125) subjects were afebrile at presentation and remained so throughout study duration. Among febrile population, time to defervescence by day 2 was noted in 95.8% (91/95), by day 3 in 97.9% and by day 7 all participants had become afebrile and remained so throughout the study (Fig. 1). Overall only one ATF (0.8%, 1/125) occurred on day 3 (persistence of fever and parasitaemia, 2,200 parasite/µL on day 0 to 9,652 parasite/µL on day 2 to 7,012 parasite/µL on day 3). After this time point, attending physician changed the anti-malarial medication of that patient from CQ to artemether–lumefantrine (480–2,880 mg) combination and PQ standard regimen. Subsequently, on day 7 the patient was found to become aparasitaemic and afebrile. This one case of ATF was indeed an early treatment failure (ETF), whereas all other participants did have adequate clinical and parasitological response (ACPR) . Due to only one valid survival function, i.e., therapeutic failure outcome, Kaplan–Meier plot could not be generated. The cumulative incidence of therapeutic failure by day 28 was only 1% (Table 2). No mortality occurred till 28 day follow up in the study cohort.
Nested PCR results
Nested PCR test confirmed a total of 116 (93.6%) participants to have P. vivax mono-infection. However, the test revealed mixed (P. vivax and P. falciparum) infections among total of eight (6.4%) subjects. The DNA sample of one participant (0.8%) could not be amplified. Notably, the one subject with therapeutic failure had PCR proven P. vivax mono-infection.
Prime index of suspicion of emergence/existence of resistance to anti-malarial drugs surfaces during therapeutic drug trials or surveillances. Present study was undertaken to determine the therapeutic efficacy of CQ–PQ combined regimen in P. vivax malaria. The KH, Manipal caters for over 200 malaria patients annually from southwestern India comprising Goa, coastal Karnataka and Kerala. Notably, P. vivax infection constitutes more than 55% of total annual malaria incidence in KH, Manipal. Male preponderance observed in the current study is a common finding and has also been reported from the same hospital [7–9]. Significantly, (p < 0.05) high axillary temperature at presentation and longer time to defervescence among inpatients than outpatients is a reflection of more sick/febrile patients receiving in hospital care. Notably, about 99% therapeutic efficacy of CQ–PQ combined regimen as observed in the present study was reported previously from the same hospital during the years 2007–2009 . However, the previous study did lack the confirmation of P. vivax mono-infection by PCR test and also did not have rigorous 28 days follow-up, as in the current study. Furthermore, similar therapeutic efficacy until day 28 has also been reported from other parts of India viz. 100% (41/41) from Mangalore , 98.1% (105/107) from Chennai  and 96.9% (63/65) from Gujarat  for CQ only and 100% (103/103) from Kolkata  for CQ–PQ combined regimen during the years 2003–2012. Notably, CQ–PQ combined regimen is known to have superior efficacy than CQ alone for preventing P. vivax recurrences [14–16]. Nonetheless, of the published literature from India, only a case report dating back over two decades confirms CQ failure in P. vivax despite having adequate plasma concentration of CQ .
The hub of global CQ resistance in P. vivax is in Indonesia [15, 18, 19]. Probable CQ-resistant P. vivax in India has been documented from north, northeast and western parts, whereas CQ remains sensitive throughout southern India . Importantly, surging CQ resistance in P. vivax across eastern neighbouring countries of India, including Myanmar , Thailand  and Vietnam  is a matter of concern and this urges an immediate implementation of effective preventive measures to check the invasion of any resistant P. vivax strain from those countries along with travellers and/or migrants.
Strengths and limitations
The present study poses considerable strength over studies which did not have PCR-proven mono-infection P. vivax cases. Statistically, valid sample size, robust analysis and standard methodology render the study outcomes legitimately comparable with parallel series across the globe. Outstanding therapeutic efficacy of CQ–PQ combined regimen for P. vivax malaria observed in the current study is augmenting evidence to support the continuation of the existing national anti-malarial drug policy for P. vivax malaria in India. The probably resistant case of one therapeutic failure could not be ascertained as truly resistant P. vivax strain. Arguably, persistence of fever and increasing parasitaemia from 2,200 parasite/µL on day 0 to 9,652 parasite/µL on day 2 and residual 7,012 parasite/µL on day 3 despite completion of CQ dosage features a true resistant P. vivax strain. However, this argument could possibly have been true only if CQ and desethylchloroquine concentration in participant’s blood [16, 23] was estimated on the day of therapeutic failure and/or analysis of molecular markers for CQ resistance [14, 24, 25] was done.
The nPCR test proved an insubstantial proportion of participants to have mixed malaria infection. However those entities of mixed malaria seemed inconsequential clinically as nPCR proven mixed malaria did not affect either the nature of illness or treatment/outcome and conclusions of the study. Notably, this inference of clinical inconsequentiality of merely nPCR-proven mixed malaria must be methodically evaluated further as it is beyond the scope of the current study. Lost to follow-up ensued in only three patients but seemingly they all had ACPR until their day 3 follow-up. However, we cannot rule out the possibility of treatment failure beyond day 3. Remarkably, this study did not assess the efficacy of CQ alone as per the WHO protocol , rather a permitted deviation from it i.e., assessment of CQ–PQ combined regimen as it was suitable in the respective study setting. Therefore, the findings of this study can only be applicable to population exempting any contraindications for PQ administration. Similar studies in future should withhold PQ administration till day 28 as recommended primarily by the WHO .
Therapeutic efficacy of CQ–PQ combined regimen in uncomplicated P. vivax malaria remains intact in the study region and thus must be continued as the treatment of choice for uncomplicated P. vivax malaria. Periodic surveillances must be conducted to remain vigilant for taking immediate measures to prevent the emergence and spread of anti-malarial resistance in P. vivax.
WHO (2014) World Malaria Report 2014. World Health Organization, Geneva
Directorate of National Vector Borne Disease Control Programme (2013) National Drug Policy on Malaria. 22-Shamnath Marg, Delhi-110054: Directorate General of Health Services: Ministry of Health and Family Welfare
WHO (2013) World Malaria Report 2013. World Health Organization, Geneva
WHO (2009) Methods for surveillance of antimalarial drug efficacy. World Health Organization, Geneva
Rishikesh K, Madivala SK, Prabhu P, Kamath A, Ashok H, Vidyasagar S et al (2015) Surmised total leucocyte counts miscalculate the parasite index of Plasmodium vivax malaria patients of tertiary and primary care settings in South-Western India. Malar J 14:163
Snounou G, Viriyakosol S, Zhu XP, Jarra W, Pinheiro L, do Rosario VE et al (1993) High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction. Mol Biochem Parasitol 61:315–320
Saravu K, Rishikesh K, Kamath A (2014) Determinants of mortality, intensive care requirement and prolonged hospitalization in malaria—a tertiary care hospital based cohort study from South-Western India. Malar J 13:370
Saravu K, Rishikesh K, Kamath A, Shastry AB (2014) Severity in Plasmodium vivax malaria claiming global vigilance and exploration-a tertiary care centre-based cohort study. Malar J 13:304
Saravu K, Rishikesh K, Parikh CR (2014) Risk factors and outcomes stratified by severity of acute kidney injury in malaria. PLoS One 9:e90419
Saravu K, Acharya V, Kumar K, Kumar R (2012) Plasmodium vivax remains responsive to chloroquine with primaquine treatment regimen: a prospective cohort study from tertiary care teaching hospital in southern India. Trop Dr 42:163–164
Poravuth Y, Socheat D, Rueangweerayut R, Uthaisin C, Pyae Phyo A, Valecha N (2011) Pyronaridine-artesunate versus chloroquine in patients with acute Plasmodium vivax malaria: a randomized, double-blind, non-inferiority trial. PLoS One 6:e14501
Shalini S, Chaudhuri S, Sutton PL, Mishra N, Srivastava N, David JK et al (2014) Chloroquine efficacy studies confirm drug susceptibility of Plasmodium vivax in Chennai, India. Malar J 13:129
Srivastava HC, Yadav RS, Joshi H, Valecha N, Mallick PK, Prajapati SK et al (2008) Therapeutic responses of Plasmodium vivax and P. falciparum to chloroquine, in an area of western India where P. vivax predominates. Ann Trop Med Parasitol 102:471–480
Ganguly S, Saha P, Guha SK, Das S, Bera DK, Biswas A et al (2013) In vivo therapeutic efficacy of chloroquine alone or in combination with primaquine against vivax malaria in Kolkata, West Bengal, India, and polymorphism in pvmdr1 and pvcrt-o genes. Antimicrob Agents Chemother 57:1246–1251
Price RN, von Seidlein L, Valecha N, Nosten F, Baird JK, White NJ (2014) Global extent of chloroquine-resistant Plasmodium vivax: a systematic review and meta-analysis. Lancet Infect Dis 14:982–991
Baird JK (2009) Resistance to therapies for infection by Plasmodium vivax. Clin Microbiol Rev 22:508–534
Dua VK, Kar PK, Sharma VP (1996) Chloroquine resistant Plasmodium vivax malaria in India. Trop Med Int Health 1:816–819
Ratcliff A, Siswantoro H, Kenangalem E, Wuwung M, Brockman A, Edstein M et al (2007) Therapeutic response of multidrug-resistant Plasmodium falciparum and P. vivax to chloroquine and sulfadoxine–pyrimethamine in southern Papua, Indonesia. Trans R Soc Trop Med Hyg 101:351–359
Sumawinata IW, Leksana B, Sutamihardja A, Subianto B, Fryauff DJ, Baird JK (2003) Very high risk of therapeutic failure with chloroquine for uncomplicated Plasmodium falciparum and P. vivax malaria in Indonesian Papua. Am J Trop Med Hyg 68:416–420
Yuan L, Wang Y, Parker DM, Gupta B, Yang Z, Liu H et al (2015) Therapeutic responses of Plasmodium vivax malaria to chloroquine and primaquine treatment in northeastern Myanmar. Antimicrob Agents Chemother 59:1230–1235
Phyo AP, Lwin KM, Price RN, Ashley EA, Russell B, Sriprawat K et al (2011) Dihydroartemisinin-piperaquine versus chloroquine in the treatment of Plasmodium vivax malaria in Thailand: a randomized controlled trial. Clin Infect Dis 53:977–984
Phan GT, de Vries PJ, Tran BQ, Le HQ, Nguyen NV, Nguyen TV et al (2002) Artemisinin or chloroquine for blood stage Plasmodium vivax malaria in Vietnam. Trop Med Int Health 7:858–864
Asih PB, Syafruddin D, Leake J, Sorontou Y, Sadikin M, Sauerwein RW et al (2011) Phenotyping clinical resistance to chloroquine in Plasmodium vivax in northeastern Papua, Indonesia. Int J Parasitol Drugs Drug Resist 1:28–32
Suwanarusk R, Chavchich M, Russell B, Jaidee A, Chalfein F, Barends M et al (2008) Amplification of pvmdr1 associated with multidrug-resistant Plasmodium vivax. J Infect Dis 198:1558–1564
Lu F, Lim CS, Nam DH, Kim K, Lin K, Kim TS et al (2011) Genetic polymorphism in pvmdr1 and pvcrt-o genes in relation to in vitro drug susceptibility of Plasmodium vivax isolates from malaria-endemic countries. Acta Trop 117:69–75
KS, KR and AK: conception and design; KR: participants’ follow-up, microscopy, nPCR tests and acquisition of data; KR, AK and KS: analysis and interpretation of data; KR wrote the first draft of the manuscript; KS and KR did critical revision of the manuscript for important intellectual content; MHH, SV, RVA, VA, JB, ABS, and KS did clinical management of the study participants. All authors agree to be accountable for all aspects of the work. All authors read and approved the final manuscript.
This study was supported by an extramural research grant (AMR/46/2011-ECD-I) from the Indian Council of Medical Research, New Delhi, India. The funding council had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Authors are immensely grateful to all the participants’ of this study. The operational support of Mr Sathish Kitta Madivala and Mr Prashantha Prabhu, Laboratory Assistants of the aforementioned project grant are thankfully acknowledged.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.