Community-wide reduction in prevalence and intensity of intestinal helminths as a collateral benefit of lymphatic filariasis elimination programs.
Identifieur interne : 003B67 ( PubMed/Checkpoint ); précédent : 003B66; suivant : 003B68Community-wide reduction in prevalence and intensity of intestinal helminths as a collateral benefit of lymphatic filariasis elimination programs.
Auteurs : Madsen Beau De Rochars [Haïti] ; Abdel N. Direny ; Jacquelin M. Roberts ; David G. Addiss ; Jeanne Radday ; Michael J. Beach ; Thomas G. Streit ; Desire Dardith ; Jack Guy Lafontant ; Patrick J. LammieSource :
- The American journal of tropical medicine and hygiene [ 0002-9637 ] ; 2004.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Adulte d'âge moyen, Albendazole (administration et posologie), Albendazole (usage thérapeutique), Animaux, Antihelminthiques (administration et posologie), Antihelminthiques (usage thérapeutique), Diéthylcarbamazine (administration et posologie), Diéthylcarbamazine (usage thérapeutique), Enfant, Enfant d'âge préscolaire, Femelle, Filariose lymphatique (), Filariose lymphatique (traitement médicamenteux), Filariose lymphatique (épidémiologie), Fèces (parasitologie), Humains, Mâle, Nematoda (), Nourrisson, Nouveau-né, Parasitoses intestinales (), Parasitoses intestinales (parasitologie), Parasitoses intestinales (traitement médicamenteux), Parasitoses intestinales (épidémiologie), Prévalence, Répartition par âge, Surveillance sentinelle.
- MESH :
- administration et posologie : Albendazole, Antihelminthiques, Diéthylcarbamazine.
- parasitologie : Fèces, Parasitoses intestinales.
- traitement médicamenteux : Filariose lymphatique, Parasitoses intestinales.
- usage thérapeutique : Albendazole, Antihelminthiques, Diéthylcarbamazine.
- épidémiologie : Filariose lymphatique, Parasitoses intestinales.
- Adolescent, Adulte, Adulte d'âge moyen, Animaux, Enfant, Enfant d'âge préscolaire, Femelle, Filariose lymphatique, Humains, Mâle, Nematoda, Nourrisson, Nouveau-né, Parasitoses intestinales, Prévalence, Répartition par âge, Surveillance sentinelle.
English descriptors
- KwdEn :
- Adolescent, Adult, Age Distribution, Albendazole (administration & dosage), Albendazole (therapeutic use), Animals, Anthelmintics (administration & dosage), Anthelmintics (therapeutic use), Child, Child, Preschool, Diethylcarbamazine (administration & dosage), Diethylcarbamazine (therapeutic use), Elephantiasis, Filarial (drug therapy), Elephantiasis, Filarial (epidemiology), Elephantiasis, Filarial (prevention & control), Feces (parasitology), Female, Humans, Infant, Infant, Newborn, Intestinal Diseases, Parasitic (drug therapy), Intestinal Diseases, Parasitic (epidemiology), Intestinal Diseases, Parasitic (parasitology), Intestinal Diseases, Parasitic (prevention & control), Male, Middle Aged, Nematoda (drug effects), Prevalence, Sentinel Surveillance.
- MESH :
- chemical , administration & dosage : Albendazole, Anthelmintics, Diethylcarbamazine.
- chemical , therapeutic use : Albendazole, Anthelmintics, Diethylcarbamazine.
- drug effects : Nematoda.
- drug therapy : Elephantiasis, Filarial, Intestinal Diseases, Parasitic.
- epidemiology : Elephantiasis, Filarial, Intestinal Diseases, Parasitic.
- parasitology : Feces, Intestinal Diseases, Parasitic.
- prevention & control : Elephantiasis, Filarial, Intestinal Diseases, Parasitic.
- Adolescent, Adult, Age Distribution, Animals, Child, Child, Preschool, Female, Humans, Infant, Infant, Newborn, Male, Middle Aged, Prevalence, Sentinel Surveillance.
Abstract
Annual mass treatment with antifilarial drugs is the cornerstone of the global program to eliminate lymphatic filariasis (LF). Although the primary goal of the program is to interrupt transmission of LF, additional public health benefits also are expected because of the known anthelminthic properties of these drugs. Since rapid re-infection with intestinal helminths occurs following treatment, annual de-worming may not be sufficient to produce a lasting reduction in the prevalence and intensity of these infections. We conducted stool examinations in four sentinel communities before and approximately nine months after each of two rounds of mass drug administration (MDA) with diethylcarbamazine and albendazole in the context of an LF elimination program in Leogane, Haiti. At baseline, overall Ascaris, Trichuris, and hookworm infection prevalences were 20.9%, 34.0%, and 11.2%, respectively (n = 2,716 stools). Nine months after the second MDA, Ascaris, Trichuris and hookworm prevalences had decreased significantly, to 14.1%, 14.6%, and 2.0%, respectively (n = 814 stools). Infection intensity decreased significantly for all three parasites as well. These results demonstrate that substantial reductions in intestinal helminth infections are associated with mass treatment of filariasis in Haiti and are consistent with the conclusion that high levels of coverage for the LF program can decrease transmission of geohelminths.
PubMed: 15516644
Affiliations:
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pubmed:15516644Le document en format XML
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<term>Albendazole (therapeutic use)</term>
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<term>Anthelmintics (therapeutic use)</term>
<term>Child</term>
<term>Child, Preschool</term>
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<term>Infant, Newborn</term>
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<term>Prevalence</term>
<term>Sentinel Surveillance</term>
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<term>Adulte d'âge moyen</term>
<term>Albendazole (administration et posologie)</term>
<term>Albendazole (usage thérapeutique)</term>
<term>Animaux</term>
<term>Antihelminthiques (administration et posologie)</term>
<term>Antihelminthiques (usage thérapeutique)</term>
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<term>Diéthylcarbamazine (usage thérapeutique)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Filariose lymphatique ()</term>
<term>Filariose lymphatique (traitement médicamenteux)</term>
<term>Filariose lymphatique (épidémiologie)</term>
<term>Fèces (parasitologie)</term>
<term>Humains</term>
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<term>Nourrisson</term>
<term>Nouveau-né</term>
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<term>Parasitoses intestinales (épidémiologie)</term>
<term>Prévalence</term>
<term>Répartition par âge</term>
<term>Surveillance sentinelle</term>
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<term>Intestinal Diseases, Parasitic</term>
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<term>Parasitoses intestinales</term>
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<term>Intestinal Diseases, Parasitic</term>
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<term>Intestinal Diseases, Parasitic</term>
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<term>Parasitoses intestinales</term>
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<term>Antihelminthiques</term>
<term>Diéthylcarbamazine</term>
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<term>Age Distribution</term>
<term>Animals</term>
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<front><div type="abstract" xml:lang="en">Annual mass treatment with antifilarial drugs is the cornerstone of the global program to eliminate lymphatic filariasis (LF). Although the primary goal of the program is to interrupt transmission of LF, additional public health benefits also are expected because of the known anthelminthic properties of these drugs. Since rapid re-infection with intestinal helminths occurs following treatment, annual de-worming may not be sufficient to produce a lasting reduction in the prevalence and intensity of these infections. We conducted stool examinations in four sentinel communities before and approximately nine months after each of two rounds of mass drug administration (MDA) with diethylcarbamazine and albendazole in the context of an LF elimination program in Leogane, Haiti. At baseline, overall Ascaris, Trichuris, and hookworm infection prevalences were 20.9%, 34.0%, and 11.2%, respectively (n = 2,716 stools). Nine months after the second MDA, Ascaris, Trichuris and hookworm prevalences had decreased significantly, to 14.1%, 14.6%, and 2.0%, respectively (n = 814 stools). Infection intensity decreased significantly for all three parasites as well. These results demonstrate that substantial reductions in intestinal helminth infections are associated with mass treatment of filariasis in Haiti and are consistent with the conclusion that high levels of coverage for the LF program can decrease transmission of geohelminths.</div>
</front>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15516644</PMID>
<DateCreated><Year>2004</Year>
<Month>11</Month>
<Day>01</Day>
</DateCreated>
<DateCompleted><Year>2004</Year>
<Month>12</Month>
<Day>09</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0002-9637</ISSN>
<JournalIssue CitedMedium="Print"><Volume>71</Volume>
<Issue>4</Issue>
<PubDate><Year>2004</Year>
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<Title>The American journal of tropical medicine and hygiene</Title>
<ISOAbbreviation>Am. J. Trop. Med. Hyg.</ISOAbbreviation>
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<ArticleTitle>Community-wide reduction in prevalence and intensity of intestinal helminths as a collateral benefit of lymphatic filariasis elimination programs.</ArticleTitle>
<Pagination><MedlinePgn>466-70</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Annual mass treatment with antifilarial drugs is the cornerstone of the global program to eliminate lymphatic filariasis (LF). Although the primary goal of the program is to interrupt transmission of LF, additional public health benefits also are expected because of the known anthelminthic properties of these drugs. Since rapid re-infection with intestinal helminths occurs following treatment, annual de-worming may not be sufficient to produce a lasting reduction in the prevalence and intensity of these infections. We conducted stool examinations in four sentinel communities before and approximately nine months after each of two rounds of mass drug administration (MDA) with diethylcarbamazine and albendazole in the context of an LF elimination program in Leogane, Haiti. At baseline, overall Ascaris, Trichuris, and hookworm infection prevalences were 20.9%, 34.0%, and 11.2%, respectively (n = 2,716 stools). Nine months after the second MDA, Ascaris, Trichuris and hookworm prevalences had decreased significantly, to 14.1%, 14.6%, and 2.0%, respectively (n = 814 stools). Infection intensity decreased significantly for all three parasites as well. These results demonstrate that substantial reductions in intestinal helminth infections are associated with mass treatment of filariasis in Haiti and are consistent with the conclusion that high levels of coverage for the LF program can decrease transmission of geohelminths.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>De Rochars</LastName>
<ForeName>Madsen Beau</ForeName>
<Initials>MB</Initials>
<AffiliationInfo><Affiliation>Hopital Ste. Croix, Leogane, Haiti. mbeauder@nd.edu</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Direny</LastName>
<ForeName>Abdel N</ForeName>
<Initials>AN</Initials>
</Author>
<Author ValidYN="Y"><LastName>Roberts</LastName>
<ForeName>Jacquelin M</ForeName>
<Initials>JM</Initials>
</Author>
<Author ValidYN="Y"><LastName>Addiss</LastName>
<ForeName>David G</ForeName>
<Initials>DG</Initials>
</Author>
<Author ValidYN="Y"><LastName>Radday</LastName>
<ForeName>Jeanne</ForeName>
<Initials>J</Initials>
</Author>
<Author ValidYN="Y"><LastName>Beach</LastName>
<ForeName>Michael J</ForeName>
<Initials>MJ</Initials>
</Author>
<Author ValidYN="Y"><LastName>Streit</LastName>
<ForeName>Thomas G</ForeName>
<Initials>TG</Initials>
</Author>
<Author ValidYN="Y"><LastName>Dardith</LastName>
<ForeName>Desire</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lafontant</LastName>
<ForeName>Jack Guy</ForeName>
<Initials>JG</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lammie</LastName>
<ForeName>Patrick J</ForeName>
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<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
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<MeshHeading><DescriptorName UI="D009348" MajorTopicYN="N">Nematoda</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015995" MajorTopicYN="N">Prevalence</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018571" MajorTopicYN="N">Sentinel Surveillance</DescriptorName>
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</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2004</Year>
<Month>11</Month>
<Day>2</Day>
<Hour>9</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2004</Year>
<Month>12</Month>
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<Hour>9</Hour>
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<PubMedPubDate PubStatus="entrez"><Year>2004</Year>
<Month>11</Month>
<Day>2</Day>
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</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">15516644</ArticleId>
<ArticleId IdType="pii">71/4/466</ArticleId>
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<affiliations><list><country><li>Haïti</li>
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</list>
<tree><noCountry><name sortKey="Addiss, David G" sort="Addiss, David G" uniqKey="Addiss D" first="David G" last="Addiss">David G. Addiss</name>
<name sortKey="Beach, Michael J" sort="Beach, Michael J" uniqKey="Beach M" first="Michael J" last="Beach">Michael J. Beach</name>
<name sortKey="Dardith, Desire" sort="Dardith, Desire" uniqKey="Dardith D" first="Desire" last="Dardith">Desire Dardith</name>
<name sortKey="Direny, Abdel N" sort="Direny, Abdel N" uniqKey="Direny A" first="Abdel N" last="Direny">Abdel N. Direny</name>
<name sortKey="Lafontant, Jack Guy" sort="Lafontant, Jack Guy" uniqKey="Lafontant J" first="Jack Guy" last="Lafontant">Jack Guy Lafontant</name>
<name sortKey="Lammie, Patrick J" sort="Lammie, Patrick J" uniqKey="Lammie P" first="Patrick J" last="Lammie">Patrick J. Lammie</name>
<name sortKey="Radday, Jeanne" sort="Radday, Jeanne" uniqKey="Radday J" first="Jeanne" last="Radday">Jeanne Radday</name>
<name sortKey="Roberts, Jacquelin M" sort="Roberts, Jacquelin M" uniqKey="Roberts J" first="Jacquelin M" last="Roberts">Jacquelin M. Roberts</name>
<name sortKey="Streit, Thomas G" sort="Streit, Thomas G" uniqKey="Streit T" first="Thomas G" last="Streit">Thomas G. Streit</name>
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<country name="Haïti"><noRegion><name sortKey="De Rochars, Madsen Beau" sort="De Rochars, Madsen Beau" uniqKey="De Rochars M" first="Madsen Beau" last="De Rochars">Madsen Beau De Rochars</name>
</noRegion>
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</tree>
</affiliations>
</record>
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