Efficacy of sulphadoxine-pyrimethamine with or without artesunate for the treatment of uncomplicated Plasmodium falciparum malaria in southern Mozambique: a randomized controlled trial

被引:17
作者
Allen, Elizabeth N. [1 ]
Little, Francesca [2 ]
Camba, Tunisio
Cassam, Yasmin
Raman, Jaishree [3 ]
Boulle, Andrew [4 ]
Barnes, Karen I. [1 ]
机构
[1] Univ Cape Town, Dept Med, Div Clin Pharmacol, ZA-7700 Rondebosch, South Africa
[2] Univ Cape Town, Dept Stat Sci, ZA-7700 Rondebosch, South Africa
[3] MRC, Malaria Res Lead Programme, Durban, South Africa
[4] Univ Cape Town, Sch Publ Hlth & Family Med, ZA-7700 Rondebosch, South Africa
关键词
CHLOROQUINE TREATMENT FAILURE; DIHYDROFOLATE-REDUCTASE; MOLECULAR MARKERS; DRUG EFFICACY; FOLLOW-UP; IN-VIVO; RESISTANCE; CHILDREN; MUTATIONS; PREDICTORS;
D O I
10.1186/1475-2875-8-141
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: An artemisinin-based combination therapy, artesunate (AS) plus sulphadoxine-pyrimethamine (SP), was compared to SP monotherapy to provide evidence of further treatment options in southern Mozambique. Methods: Between 2003 and 2005, 411 patients over one year and 10 kg with uncomplicated Plasmodium falciparum malaria were randomly allocated SP (25/1.25 mg per kg day 0) or AS/SP (as above plus 4 mg/kg artesunate days 0, 1 and 2). Allocation was concealed, but treatment was open-label except to microscopists. The primary objective was the relative risk of treatment failure, which was assessed using World Health Organization response definitions modified to a 42-day follow-up. Results: Of the 411 subjects enrolled, 359 (87.3%) completed the follow up period (SP n = 175, AS/SP n = 184). A survival analysis including 408 subjects showed that the polymerase chain reaction-adjusted cure rates were 90.4% (95% confidence interval [CI] 84.9%-93.9%) and 98.0% (95% CI 94.8%-99.3%) for SP and AS/SP respectively. Multivariable analysis showed that treatment with AS/ SP decreased the relative hazard of treatment failure by 80% compared to SP ( hazard ratio [HR] 0.2; 95% CI 0.1-0.6) and age over seven years decreased the relative hazard of failure by 70% (HR 0.3; 95% CI 0.1-0.9), when compared to younger age. However, having a quintuple dhfr/dhps mutation increased the relative hazard of failure compared to fewer mutations (HR 3.2; 95% CI 1.3-7.5) and baseline axillary temperature increased the relative hazard of failure by 50% for each degrees C increase (HR 1.5; 95% CI 1.1-2.2). Conclusion: While both treatments were efficacious, AS plus SP significantly decreased the relative hazard of treatment failure compared to SP monotherapy Artesunate plus sulphadoxine-pyrimethamine, but not sulphadoxine-pyrimethamine monotherapy, met the current WHO criteria of >95% efficacy for policy implementation.
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相关论文
共 34 条
[11]   PREDICTORS OF TREATMENT FAILURE IN MULTIPLE DRUG-RESISTANT FALCIPARUM-MALARIA - RESULTS FROM A 42-DAY FOLLOW-UP OF 224 PATIENTS IN EASTERN THAILAND [J].
FONTANET, AL ;
WALKER, AM .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1993, 49 (04) :465-472
[12]   Sulfadoxine-pyrimethamine effectiveness against Plasmodium falciparum malaria in Mpumalanga Province, South Africa [J].
Govere, JM ;
la Grange, JJ ;
Durrheim, DN ;
Freese, JA ;
Sharp, BL ;
Mabuza, A ;
Mngomezulu, N ;
Bredenkamp, BLF .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1999, 93 (06) :644-644
[13]   Age, temperature, and parasitaemia predict chloroquine treatment failure and anaemia in children with uncomplicated Plasmodium falciparum malaria [J].
Hamer, DH ;
MacLeod, WB ;
Addo-Yobo, E ;
Duggan, CP ;
Estrella, B ;
Fawzi, WW ;
Konde-Lule, JK ;
Mwanakasale, V ;
Premji, ZG ;
Sempértegui, F ;
Ssengooba, FP ;
Yeboah-Antwi, K ;
Simon, JL .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2003, 97 (04) :422-428
[14]  
HAVIID L, 2005, ACTA TROP ACTA TROP, V95, P270
[15]   Molecular markers for failure of sulfadoxine-pyrimethamine and chlorproguanil-dapsone treatment of Plasmodium falciparum malaria [J].
Kublin, JG ;
Dzinjalamala, FK ;
Kamwendo, DD ;
Malkin, EM ;
Cortese, JF ;
Martino, LM ;
Mukadam, RAG ;
Rogerson, SJ ;
Lescano, AG ;
Molyneux, ME ;
Winstanley, PA ;
Chimpeni, P ;
Taylor, TE ;
Plowe, CV .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (03) :380-388
[16]   ORAL ARTESUNATE IN THE TREATMENT OF UNCOMPLICATED HYPERPARASITEMIC FALCIPARUM-MALARIA [J].
LUXEMBURGER, C ;
NOSTEN, F ;
SHOTAR ;
RAIMOND, D ;
CHONGSUPHAJAISIDDHI, T ;
WHITE, NJ .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1995, 53 (05) :522-525
[17]   Artemisinin-based combination treatment of falciparum malaria [J].
Nosten, Francois ;
White, Nicholas J. .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2007, 77 (06) :181-192
[18]   World antimalarial resistance network (WARN) III: Molecular markers for drug resistant malaria [J].
Plowe, Christopher V. ;
Roper, Cally ;
Barnwell, John W. ;
Happi, Christian T. ;
Joshi, Hema H. ;
Mbacham, Wilfred ;
Meshnick, Steven R. ;
Mugittu, Kefas ;
Naidoo, Inbarani ;
Price, Ric N. ;
Shafer, Robert W. ;
Sibley, Carol H. ;
Sutherland, Colin J. ;
Zimmerman, Peter A. ;
Rosenthal, Philip J. .
MALARIA JOURNAL, 2007, 6 (1)
[19]   Mutations in Plasmodium falciparum dihydrofolate reductase and dihydropteroate synthase and epidemiologic patterns of pyrimethamine-sulfadoxine use and resistance [J].
Plowe, CV ;
Cortese, JF ;
Djimde, A ;
Nwanyanwu, OC ;
Watkins, WM ;
Winstanley, PA ;
EstradaFranco, JG ;
Mollinedo, RE ;
Avila, JC ;
Cespedes, JL ;
Carter, D ;
Doumbo, OK .
JOURNAL OF INFECTIOUS DISEASES, 1997, 176 (06) :1590-1596
[20]   Effects of artemisinin derivatives on malaria transmissibility [J].
Price, RN ;
Nosten, F ;
Luxemburger, C ;
terKuile, FO ;
Paiphun, L ;
Chongsuphajaisiddhi, T ;
White, NJ .
LANCET, 1996, 347 (9016) :1654-1658