Mass diethylcarbamazine chemotherapy for control of bancroftian filariasis: comparative efficacy of standard treatment and two semi-annual single-dose treatments
Identifieur interne : 001240 ( Istex/Corpus ); précédent : 001239; suivant : 001241Mass diethylcarbamazine chemotherapy for control of bancroftian filariasis: comparative efficacy of standard treatment and two semi-annual single-dose treatments
Auteurs : D. W. Meyrowitsch ; P. E. Simonsen ; W. H. MakundeSource :
- Transactions of the Royal Society of Tropical Medicine and Hygiene [ 0035-9203 ] ; 1996.
Abstract
The efficacy of 2 strategies for control of bancroftian filariasis using mass diethylcarbamazine (DEC) chemotherapy was evaluated and compared in 2 endemic communities in Tanzania with pre-treatment microfilarial (mf) prevalences of 28·5% and 17·7%, and mf geometric mean intensities (GMI) of 588 mf/mL and 251 mf/mL, respectively. All individuals in the first community were offered DEC treatment with 6 mg/kg body weight given daily for 12 d (standard treatment). The second community was offered DEC treatment with 2 single doses of 6 mg/kg body weight given with an interval of 6 months (semi-annual single-dose treatment). Among those who were microfilaraemic before treatment, the mf clearance rates were 51·2% and 36·0%, and the mf GMIs were reduced by 98·6% and 92·2% one year after the start of the standard and the semi-annual regimens, respectively. At community level, the standard strategy and the semi-annual strategy reduced the mf prevalences to 15·1% and 11·6% (reductions of 47·0% and 34·5%) and the mf GMIs to 112 mf/mL and 102 mf/mL (reductions of 81·0% and 59·4%, respectively) one year after start of treatment. Both regimens resulted in remarkable improvements in small hydroceles among males presenting this condition before treatment. The lower efficacy of the semi-annual single-dose treatment in relation to the standard treatment in reducing microfilaraemias might be compensated for by continuing semi-annual treatments for a slightly longer period of time. Considering that the semi-annual treatment is easy to administer and more acceptable to the treated individuals, it may in the long run be a more feasible strategy for mass DEC chemotherapy than the standard treatment.
Url:
DOI: 10.1016/S0035-9203(96)90484-8
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<front><div type="abstract" xml:lang="en">The efficacy of 2 strategies for control of bancroftian filariasis using mass diethylcarbamazine (DEC) chemotherapy was evaluated and compared in 2 endemic communities in Tanzania with pre-treatment microfilarial (mf) prevalences of 28·5% and 17·7%, and mf geometric mean intensities (GMI) of 588 mf/mL and 251 mf/mL, respectively. All individuals in the first community were offered DEC treatment with 6 mg/kg body weight given daily for 12 d (standard treatment). The second community was offered DEC treatment with 2 single doses of 6 mg/kg body weight given with an interval of 6 months (semi-annual single-dose treatment). Among those who were microfilaraemic before treatment, the mf clearance rates were 51·2% and 36·0%, and the mf GMIs were reduced by 98·6% and 92·2% one year after the start of the standard and the semi-annual regimens, respectively. At community level, the standard strategy and the semi-annual strategy reduced the mf prevalences to 15·1% and 11·6% (reductions of 47·0% and 34·5%) and the mf GMIs to 112 mf/mL and 102 mf/mL (reductions of 81·0% and 59·4%, respectively) one year after start of treatment. Both regimens resulted in remarkable improvements in small hydroceles among males presenting this condition before treatment. The lower efficacy of the semi-annual single-dose treatment in relation to the standard treatment in reducing microfilaraemias might be compensated for by continuing semi-annual treatments for a slightly longer period of time. Considering that the semi-annual treatment is easy to administer and more acceptable to the treated individuals, it may in the long run be a more feasible strategy for mass DEC chemotherapy than the standard treatment.</div>
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<ce:text>Address for correspondence: Dr Paul E. Simonsen, Danish Bilharziasis Laboratory, Jaegersborg Alle 1D, 2920 Charlottenlund, Denmark.</ce:text>
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<ce:abstract><ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec><ce:simple-para>The efficacy of 2 strategies for control of bancroftian filariasis using mass diethylcarbamazine (DEC) chemotherapy was evaluated and compared in 2 endemic communities in Tanzania with pre-treatment microfilarial (mf) prevalences of 28·5% and 17·7%, and mf geometric mean intensities (GMI) of 588 mf/mL and 251 mf/mL, respectively. All individuals in the first community were offered DEC treatment with 6 mg/kg body weight given daily for 12 d (standard treatment). The second community was offered DEC treatment with 2 single doses of 6 mg/kg body weight given with an interval of 6 months (semi-annual single-dose treatment). Among those who were microfilaraemic before treatment, the mf clearance rates were 51·2% and 36·0%, and the mf GMIs were reduced by 98·6% and 92·2% one year after the start of the standard and the semi-annual regimens, respectively. At community level, the standard strategy and the semi-annual strategy reduced the mf prevalences to 15·1% and 11·6% (reductions of 47·0% and 34·5%) and the mf GMIs to 112 mf/mL and 102 mf/mL (reductions of 81·0% and 59·4%, respectively) one year after start of treatment. Both regimens resulted in remarkable improvements in small hydroceles among males presenting this condition before treatment. The lower efficacy of the semi-annual single-dose treatment in relation to the standard treatment in reducing microfilaraemias might be compensated for by continuing semi-annual treatments for a slightly longer period of time. Considering that the semi-annual treatment is easy to administer and more acceptable to the treated individuals, it may in the long run be a more feasible strategy for mass DEC chemotherapy than the standard treatment.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:keywords><ce:section-title>Keywords</ce:section-title>
<ce:keyword><ce:text><ce:italic>Wuchereria bancrofti</ce:italic>
</ce:text>
</ce:keyword>
<ce:keyword><ce:text>filariasis</ce:text>
</ce:keyword>
<ce:keyword><ce:text>mass chemotherapy</ce:text>
</ce:keyword>
<ce:keyword><ce:text>diethylcarbamazine</ce:text>
</ce:keyword>
<ce:keyword><ce:text>comparison of regimens</ce:text>
</ce:keyword>
</ce:keywords>
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<mods version="3.6"><titleInfo><title>Mass diethylcarbamazine chemotherapy for control of bancroftian filariasis: comparative efficacy of standard treatment and two semi-annual single-dose treatments</title>
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<titleInfo type="alternative" contentType="CDATA"><title>Mass diethylcarbamazine chemotherapy for control of bancroftian filariasis: comparative efficacy of standard treatment and two semi-annual single-dose treatments</title>
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<name type="personal"><namePart type="given">D.W.</namePart>
<namePart type="family">Meyrowitsch</namePart>
<affiliation>Danish Bilharziasis Laboratory, Jaegersborg Alle 1D, 2920 Charlottenlund, Denmark</affiliation>
<role><roleTerm type="text">author</roleTerm>
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</name>
<name type="personal"><namePart type="given">P.E.</namePart>
<namePart type="family">Simonsen</namePart>
<affiliation>Address for correspondence: Dr Paul E. Simonsen, Danish Bilharziasis Laboratory, Jaegersborg Alle 1D, 2920 Charlottenlund, Denmark.</affiliation>
<affiliation>Danish Bilharziasis Laboratory, Jaegersborg Alle 1D, 2920 Charlottenlund, Denmark</affiliation>
<role><roleTerm type="text">author</roleTerm>
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<name type="personal"><namePart type="given">W.H.</namePart>
<namePart type="family">Makunde</namePart>
<affiliation>Amani Medical Research Centre, P. O. Box 4, Amani, Tanzania</affiliation>
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<dateIssued encoding="w3cdtf">1996</dateIssued>
<dateModified encoding="w3cdtf">1995-08-18</dateModified>
<copyrightDate encoding="w3cdtf">1996</copyrightDate>
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<abstract lang="en">The efficacy of 2 strategies for control of bancroftian filariasis using mass diethylcarbamazine (DEC) chemotherapy was evaluated and compared in 2 endemic communities in Tanzania with pre-treatment microfilarial (mf) prevalences of 28·5% and 17·7%, and mf geometric mean intensities (GMI) of 588 mf/mL and 251 mf/mL, respectively. All individuals in the first community were offered DEC treatment with 6 mg/kg body weight given daily for 12 d (standard treatment). The second community was offered DEC treatment with 2 single doses of 6 mg/kg body weight given with an interval of 6 months (semi-annual single-dose treatment). Among those who were microfilaraemic before treatment, the mf clearance rates were 51·2% and 36·0%, and the mf GMIs were reduced by 98·6% and 92·2% one year after the start of the standard and the semi-annual regimens, respectively. At community level, the standard strategy and the semi-annual strategy reduced the mf prevalences to 15·1% and 11·6% (reductions of 47·0% and 34·5%) and the mf GMIs to 112 mf/mL and 102 mf/mL (reductions of 81·0% and 59·4%, respectively) one year after start of treatment. Both regimens resulted in remarkable improvements in small hydroceles among males presenting this condition before treatment. The lower efficacy of the semi-annual single-dose treatment in relation to the standard treatment in reducing microfilaraemias might be compensated for by continuing semi-annual treatments for a slightly longer period of time. Considering that the semi-annual treatment is easy to administer and more acceptable to the treated individuals, it may in the long run be a more feasible strategy for mass DEC chemotherapy than the standard treatment.</abstract>
<subject><genre>article-category</genre>
<topic>Chemotherapy and chemoprophylaxis</topic>
</subject>
<subject><genre>Keywords</genre>
<topic>Wuchereria bancrofti</topic>
<topic>filariasis</topic>
<topic>mass chemotherapy</topic>
<topic>diethylcarbamazine</topic>
<topic>comparison of regimens</topic>
</subject>
<relatedItem type="host"><titleInfo><title>Transactions of the Royal Society of Tropical Medicine and Hygiene</title>
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<titleInfo type="abbreviated"><title>TRSTMH</title>
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<originInfo><dateIssued encoding="w3cdtf">199601</dateIssued>
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<identifier type="ISSN">0035-9203</identifier>
<identifier type="PII">S0035-9203(00)X0175-7</identifier>
<part><date>199601</date>
<detail type="volume"><number>90</number>
<caption>vol.</caption>
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<detail type="issue"><number>1</number>
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<extent unit="issue pages"><start>1</start>
<end>96</end>
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<extent unit="pages"><start>69</start>
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<identifier type="istex">27F22946F7A08DF7FB92E13B7898A43E1D1E91AD</identifier>
<identifier type="DOI">10.1016/S0035-9203(96)90484-8</identifier>
<identifier type="PII">S0035-9203(96)90484-8</identifier>
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