A randomized, placebo-controlled, double-blind trial on sulfadoxine-pyrimethamine alone or combined with artesunate or amodiaquine in uncomplicated malaria.

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A randomized, placebo-controlled, double-blind trial on sulfadoxine-pyrimethamine alone or combined with artesunate or amodiaquine in uncomplicated malaria. / Mockenhaupt, Frank P; Ehrhardt, Stephan; Dzisi, Stephen Y; Teun Bousema, J; Wassilew, Nasstasja; Schreiber, Jonas; Anemana, Sylvester D; Cramer, Jakob; Otchwemah, Rowland N; Sauerwein, Robert W; Eggelte, Teunis A; Bienzle, Ulrich.

In: TROP MED INT HEALTH, Vol. 10, No. 6, 6, 2005, p. 512-520.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Mockenhaupt, FP, Ehrhardt, S, Dzisi, SY, Teun Bousema, J, Wassilew, N, Schreiber, J, Anemana, SD, Cramer, J, Otchwemah, RN, Sauerwein, RW, Eggelte, TA & Bienzle, U 2005, 'A randomized, placebo-controlled, double-blind trial on sulfadoxine-pyrimethamine alone or combined with artesunate or amodiaquine in uncomplicated malaria.', TROP MED INT HEALTH, vol. 10, no. 6, 6, pp. 512-520. <http://www.ncbi.nlm.nih.gov/pubmed/15941413?dopt=Citation>

APA

Mockenhaupt, F. P., Ehrhardt, S., Dzisi, S. Y., Teun Bousema, J., Wassilew, N., Schreiber, J., Anemana, S. D., Cramer, J., Otchwemah, R. N., Sauerwein, R. W., Eggelte, T. A., & Bienzle, U. (2005). A randomized, placebo-controlled, double-blind trial on sulfadoxine-pyrimethamine alone or combined with artesunate or amodiaquine in uncomplicated malaria. TROP MED INT HEALTH, 10(6), 512-520. [6]. http://www.ncbi.nlm.nih.gov/pubmed/15941413?dopt=Citation

Vancouver

Bibtex

@article{333f52b5b790487bb63d000bdb14c86a,
title = "A randomized, placebo-controlled, double-blind trial on sulfadoxine-pyrimethamine alone or combined with artesunate or amodiaquine in uncomplicated malaria.",
abstract = "The therapeutic efficacy of sulfadoxine-pyrimethamine (SP) alone, SP plus amodiaquine (AQ), and SP plus artesunate (AS) was assessed in a randomized, placebo-controlled, and double-blind trial among 438 children with uncomplicated Plasmodium falciparum malaria in northern Ghana. Clinical and parasitological responses were monitored for 28 days following treatment; 86%, 98% and 97% of SP-, SP + AQ-, and SP + AS-treated patients achieved adequate clinical and parasitological response (ACPR) within 2 weeks, respectively. Parasite clearance was better with SP + AS than with SP or SP + AQ treatment but re-infections were more common. Polymerase chain reaction (PCR)-corrected rates of ACPR at day 28 were 72.2% for SP, 94.1% for SP + AQ (P <0.0001), and 94.5% for SP + AS (P <0.0001). Gametocyte prevalence and density 1 week after treatment were highest in children treated with SP, and lowest in patients receiving SP + AS. No severe adverse events attributable to study medication were observed. In northern Ghana, more than one of four children suffered SP treatment failure within 4 weeks. Both SP + AQ and SP + AS are efficacious alternative therapeutic options in this region. Although SP + AS and SP + AQ treatments have virtually identical cure rates, rapid parasite clearance and pronounced gametocidal effects are the advantages of the former, whereas cost and a lower rate of late re-infections are those of the latter.",
author = "Mockenhaupt, {Frank P} and Stephan Ehrhardt and Dzisi, {Stephen Y} and {Teun Bousema}, J and Nasstasja Wassilew and Jonas Schreiber and Anemana, {Sylvester D} and Jakob Cramer and Otchwemah, {Rowland N} and Sauerwein, {Robert W} and Eggelte, {Teunis A} and Ulrich Bienzle",
year = "2005",
language = "Deutsch",
volume = "10",
pages = "512--520",
journal = "TROP MED INT HEALTH",
issn = "1360-2276",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - A randomized, placebo-controlled, double-blind trial on sulfadoxine-pyrimethamine alone or combined with artesunate or amodiaquine in uncomplicated malaria.

AU - Mockenhaupt, Frank P

AU - Ehrhardt, Stephan

AU - Dzisi, Stephen Y

AU - Teun Bousema, J

AU - Wassilew, Nasstasja

AU - Schreiber, Jonas

AU - Anemana, Sylvester D

AU - Cramer, Jakob

AU - Otchwemah, Rowland N

AU - Sauerwein, Robert W

AU - Eggelte, Teunis A

AU - Bienzle, Ulrich

PY - 2005

Y1 - 2005

N2 - The therapeutic efficacy of sulfadoxine-pyrimethamine (SP) alone, SP plus amodiaquine (AQ), and SP plus artesunate (AS) was assessed in a randomized, placebo-controlled, and double-blind trial among 438 children with uncomplicated Plasmodium falciparum malaria in northern Ghana. Clinical and parasitological responses were monitored for 28 days following treatment; 86%, 98% and 97% of SP-, SP + AQ-, and SP + AS-treated patients achieved adequate clinical and parasitological response (ACPR) within 2 weeks, respectively. Parasite clearance was better with SP + AS than with SP or SP + AQ treatment but re-infections were more common. Polymerase chain reaction (PCR)-corrected rates of ACPR at day 28 were 72.2% for SP, 94.1% for SP + AQ (P <0.0001), and 94.5% for SP + AS (P <0.0001). Gametocyte prevalence and density 1 week after treatment were highest in children treated with SP, and lowest in patients receiving SP + AS. No severe adverse events attributable to study medication were observed. In northern Ghana, more than one of four children suffered SP treatment failure within 4 weeks. Both SP + AQ and SP + AS are efficacious alternative therapeutic options in this region. Although SP + AS and SP + AQ treatments have virtually identical cure rates, rapid parasite clearance and pronounced gametocidal effects are the advantages of the former, whereas cost and a lower rate of late re-infections are those of the latter.

AB - The therapeutic efficacy of sulfadoxine-pyrimethamine (SP) alone, SP plus amodiaquine (AQ), and SP plus artesunate (AS) was assessed in a randomized, placebo-controlled, and double-blind trial among 438 children with uncomplicated Plasmodium falciparum malaria in northern Ghana. Clinical and parasitological responses were monitored for 28 days following treatment; 86%, 98% and 97% of SP-, SP + AQ-, and SP + AS-treated patients achieved adequate clinical and parasitological response (ACPR) within 2 weeks, respectively. Parasite clearance was better with SP + AS than with SP or SP + AQ treatment but re-infections were more common. Polymerase chain reaction (PCR)-corrected rates of ACPR at day 28 were 72.2% for SP, 94.1% for SP + AQ (P <0.0001), and 94.5% for SP + AS (P <0.0001). Gametocyte prevalence and density 1 week after treatment were highest in children treated with SP, and lowest in patients receiving SP + AS. No severe adverse events attributable to study medication were observed. In northern Ghana, more than one of four children suffered SP treatment failure within 4 weeks. Both SP + AQ and SP + AS are efficacious alternative therapeutic options in this region. Although SP + AS and SP + AQ treatments have virtually identical cure rates, rapid parasite clearance and pronounced gametocidal effects are the advantages of the former, whereas cost and a lower rate of late re-infections are those of the latter.

M3 - SCORING: Zeitschriftenaufsatz

VL - 10

SP - 512

EP - 520

JO - TROP MED INT HEALTH

JF - TROP MED INT HEALTH

SN - 1360-2276

IS - 6

M1 - 6

ER -