Efficacy of praziquantel against Schistosoma mekongi and Opisthorchis viverrini: a randomized, single-blinded dose-comparison trial

Autor: Youthanavanh Vonghachack, Jennifer Keiser, Phonepasong Ayé Soukhathammavong, Léonore Lovis, Penelope Vounatsou, Christoph Hatz, Khampheng Phongluxa, Peter Odermatt, Kongsap Akkhavong, Jürg Utzinger, Marcel Tanner, Tippi K Mak
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Male
Epidemiology
Gastroenterology
Opisthorchiasis
Praziquantel
030308 mycology & parasitology
0302 clinical medicine
Opisthorchis
Schistosomiasis
Opisthorchis viverrini
Child
Anthelmintics
Food-Borne Trematodes
0303 health sciences
biology
lcsh:Public aspects of medicine
3. Good health
Treatment Outcome
Infectious Diseases
Laos
Schistosoma mekongi
Schistosoma
Medicine
Female
Public Health
medicine.drug
Research Article
Neglected Tropical Diseases
medicine.medical_specialty
lcsh:Arctic medicine. Tropical medicine
Adolescent
Infectious Disease Control
Clinical Research Design
lcsh:RC955-962
030231 tropical medicine
Infectious Disease Epidemiology
03 medical and health sciences
Internal medicine
parasitic diseases
medicine
Parasitic Diseases
Animals
Humans
Clinical Trials
Adverse effect
Biology
business.industry
Public Health
Environmental and Occupational Health

lcsh:RA1-1270
Drug Policy
medicine.disease
biology.organism_classification
Confidence interval
Surgery
Parasitology
Preventive Medicine
business
Zoology
Helminthology
Zdroj: PLoS Neglected Tropical Diseases, Vol 6, Iss 7, p e1726 (2012)
PLoS Neglected Tropical Diseases
PLoS neglected tropical diseases
ISSN: 1935-2735
1935-2727
Popis: Background Schistosomiasis and opisthorchiasis are of public health importance in Southeast Asia. Praziquantel (PZQ) is the drug of choice for morbidity control but few dose comparisons have been made. Methodology Ninety-three schoolchildren were enrolled in an area of Lao PDR where Schistosoma mekongi and Opisthorchis viverrini coexist for a PZQ dose-comparison trial. Prevalence and intensity of infections were determined by a rigorous diagnostic effort (3 stool specimens, each examined with triplicate Kato-Katz) before and 28–30 days after treatment. Ninety children with full baseline data were randomized to receive PZQ: the 40 mg/kg standard single dose (n = 45) or a 75 mg/kg total dose (50 mg/kg+25 mg/kg, 4 hours apart; n = 45). Adverse events were assessed at 3 and 24 hours posttreatment. Principal Findings Baseline infection prevalence of S. mekongi and O. viverrini were 87.8% and 98.9%, respectively. S. mekongi cure rates were 75.0% (95% confidence interval (CI): 56.6–88.5%) and 80.8% (95% CI: 60.6–93.4%) for 40 mg/kg and 75 mg/kg PZQ, respectively (P = 0.60). O. viverrini cure rates were significantly different at 71.4% (95% CI: 53.4–84.4%) and 96.6% (95% CI: not defined), respectively (P = 0.009). Egg reduction rates (ERRs) against O. viverrini were very high for both doses (>99%), but slightly lower for S. mekongi at 40 mg/kg (96.4% vs. 98.1%) and not influenced by increasing diagnostic effort. O. viverrini cure rates would have been overestimated and no statistical difference between doses found if efficacy was based on a minimum sampling effort (single Kato-Katz before and after treatment). Adverse events were common (96%), mainly mild with no significant differences between the two treatment groups. Conclusions/Significance Cure rate from the 75 mg/kg PZQ dose was more efficacious than 40 mg/kg against O. viverrini but not against S. mekongi infections, while ERRs were similar for both doses. Trial Registration Controlled-Trials.com ISRCTN57714676
Author Summary Parasitic worm infections are of public health importance in Southeast Asia. Particularly, the blood-dwelling Schistosoma mekongi worm, which is acquired by skin contact with the infectious cercariae in freshwater, can lead to liver enlargement. An infection with Opisthorchis viverrini is obtained by consumption of undercooked freshwater fish, and this infection increases the risk of developing cholangiocarcinoma. A single oral dose of 40 mg/kg praziquantel is recommended for mass treatment of schistosomiasis and opisthorchiasis, while at the individual level, a total dose of 75 mg/kg divided into three doses, is currently common practice to treat O. viverrini infection. Diagnosis is based on stool examination under a microscope for detection of worm eggs, but is limited by the low sensitivity of the widely used Kato-Katz technique. In this study, we showed that a 75 mg/kg total dose of praziquantel (50 mg/kg+25 mg/kg given 4 hours apart) cleared significantly more O. viverrini infections than a single 40 mg/kg dose, but no difference was observed for S. mekongi. Solicited adverse event profiles were mainly mild and similar in both groups. Repeated stool examination before and after treatment was essential for an accurate assessment of drug efficacy in terms of cure rate, but showed no effect on assessing egg reduction rates.
Databáze: OpenAIRE