Filaria associated clinical manifestations in children in an endemic area and morbidity control by immunomonitoring and optimal DEC therapy: Sevagram experience.
Identifieur interne : 004A33 ( PubMed/Curation ); précédent : 004A32; suivant : 004A34Filaria associated clinical manifestations in children in an endemic area and morbidity control by immunomonitoring and optimal DEC therapy: Sevagram experience.
Auteurs : B C Harinath ; M V Reddy ; B. Bhunia ; Y P Bhandari ; V K Mehta ; P. Chaturvedi ; N C Prajapati ; R K GuptaSource :
- Indian journal of clinical biochemistry : IJCB [ 0970-1915 ] ; 2000.
Abstract
Lymphatic filariasis is a major public health problem in India with 412 million people living in bancroftian endemic areas and is a major cause of clinical morbidity. Twenty million people are reported to suffer from chronic disease manifestations such as lymphoedema, hydrocele or elephantiasis. At least twice the number have been shown to suffer from acute and occult filarial infections in an endemic area without diagnosis. Due to non-availability of suitable diagnostic test for confirming filaria aetiology other than parasitological examination, no significant study on filariasis in children has been reported earlier. Studies in our laboratory for more than a decade showed usefulness of microfilarial excretory-secretory antigen in confirming filarial aetiology in acute and occult infections in adults as well as in children. This study reports acute and atypical manifestations such as lymphadenopathy, asthmatic bronchitis, pulmonary eosinophilia, mono-arthritis, recurrent URI, pneumonia, nutritional anemia, pain in abdomen etc. in children living in filaria endemic area having no microfilaraemia but showing filaria aetiology by immunomonitoring for the presence of antibody or antigen and responding to optimal DEC therapy.
DOI: 10.1007/BF02867551
PubMed: 23105275
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B C Harinath<affiliation><nlm:affiliation>JB Tropical Disease Research Centre and Department of Biochemistry, Mahatma Gandhi Institute of Medical Sciences, 442102 Sevagram, (Wardha) India.</nlm:affiliation><wicri:noCountry code="subField">(Wardha) India</wicri:noCountry></affiliation>Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Filaria associated clinical manifestations in children in an endemic area and morbidity control by immunomonitoring and optimal DEC therapy: Sevagram experience.</title><author><name sortKey="Harinath, B C" sort="Harinath, B C" uniqKey="Harinath B" first="B C" last="Harinath">B C Harinath</name><affiliation><nlm:affiliation>JB Tropical Disease Research Centre and Department of Biochemistry, Mahatma Gandhi Institute of Medical Sciences, 442102 Sevagram, (Wardha) India.</nlm:affiliation><wicri:noCountry code="subField">(Wardha) India</wicri:noCountry></affiliation></author><author><name sortKey="Reddy, M V" sort="Reddy, M V" uniqKey="Reddy M" first="M V" last="Reddy">M V Reddy</name></author><author><name sortKey="Bhunia, B" sort="Bhunia, B" uniqKey="Bhunia B" first="B" last="Bhunia">B. Bhunia</name></author><author><name sortKey="Bhandari, Y P" sort="Bhandari, Y P" uniqKey="Bhandari Y" first="Y P" last="Bhandari">Y P Bhandari</name></author><author><name sortKey="Mehta, V K" sort="Mehta, V K" uniqKey="Mehta V" first="V K" last="Mehta">V K Mehta</name></author><author><name sortKey="Chaturvedi, P" sort="Chaturvedi, P" uniqKey="Chaturvedi P" first="P" last="Chaturvedi">P. 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Bhunia</name></author><author><name sortKey="Bhandari, Y P" sort="Bhandari, Y P" uniqKey="Bhandari Y" first="Y P" last="Bhandari">Y P Bhandari</name></author><author><name sortKey="Mehta, V K" sort="Mehta, V K" uniqKey="Mehta V" first="V K" last="Mehta">V K Mehta</name></author><author><name sortKey="Chaturvedi, P" sort="Chaturvedi, P" uniqKey="Chaturvedi P" first="P" last="Chaturvedi">P. Chaturvedi</name></author><author><name sortKey="Prajapati, N C" sort="Prajapati, N C" uniqKey="Prajapati N" first="N C" last="Prajapati">N C Prajapati</name></author><author><name sortKey="Gupta, R K" sort="Gupta, R K" uniqKey="Gupta R" first="R K" last="Gupta">R K Gupta</name></author></analytic><series><title level="j">Indian journal of clinical biochemistry : IJCB</title><idno type="ISSN">0970-1915</idno><imprint><date when="2000" type="published">2000</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Lymphatic filariasis is a major public health problem in India with 412 million people living in bancroftian endemic areas and is a major cause of clinical morbidity. Twenty million people are reported to suffer from chronic disease manifestations such as lymphoedema, hydrocele or elephantiasis. At least twice the number have been shown to suffer from acute and occult filarial infections in an endemic area without diagnosis. Due to non-availability of suitable diagnostic test for confirming filaria aetiology other than parasitological examination, no significant study on filariasis in children has been reported earlier. Studies in our laboratory for more than a decade showed usefulness of microfilarial excretory-secretory antigen in confirming filarial aetiology in acute and occult infections in adults as well as in children. This study reports acute and atypical manifestations such as lymphadenopathy, asthmatic bronchitis, pulmonary eosinophilia, mono-arthritis, recurrent URI, pneumonia, nutritional anemia, pain in abdomen etc. in children living in filaria endemic area having no microfilaraemia but showing filaria aetiology by immunomonitoring for the presence of antibody or antigen and responding to optimal DEC therapy.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">23105275</PMID><DateCreated><Year>2012</Year><Month>10</Month><Day>29</Day></DateCreated><DateCompleted><Year>2012</Year><Month>10</Month><Day>30</Day></DateCompleted><DateRevised><Year>2013</Year><Month>05</Month><Day>30</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0970-1915</ISSN><JournalIssue CitedMedium="Print"><Volume>15</Volume><Issue>Suppl 1</Issue><PubDate><Year>2000</Year><Month>Aug</Month></PubDate></JournalIssue><Title>Indian journal of clinical biochemistry : IJCB</Title><ISOAbbreviation>Indian J Clin Biochem</ISOAbbreviation></Journal><ArticleTitle>Filaria associated clinical manifestations in children in an endemic area and morbidity control by immunomonitoring and optimal DEC therapy: Sevagram experience.</ArticleTitle><Pagination><MedlinePgn>118-26</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/BF02867551</ELocationID><Abstract><AbstractText>Lymphatic filariasis is a major public health problem in India with 412 million people living in bancroftian endemic areas and is a major cause of clinical morbidity. Twenty million people are reported to suffer from chronic disease manifestations such as lymphoedema, hydrocele or elephantiasis. At least twice the number have been shown to suffer from acute and occult filarial infections in an endemic area without diagnosis. Due to non-availability of suitable diagnostic test for confirming filaria aetiology other than parasitological examination, no significant study on filariasis in children has been reported earlier. Studies in our laboratory for more than a decade showed usefulness of microfilarial excretory-secretory antigen in confirming filarial aetiology in acute and occult infections in adults as well as in children. This study reports acute and atypical manifestations such as lymphadenopathy, asthmatic bronchitis, pulmonary eosinophilia, mono-arthritis, recurrent URI, pneumonia, nutritional anemia, pain in abdomen etc. in children living in filaria endemic area having no microfilaraemia but showing filaria aetiology by immunomonitoring for the presence of antibody or antigen and responding to optimal DEC therapy.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Harinath</LastName><ForeName>B C</ForeName><Initials>BC</Initials><AffiliationInfo><Affiliation>JB Tropical Disease Research Centre and Department of Biochemistry, Mahatma Gandhi Institute of Medical Sciences, 442102 Sevagram, (Wardha) India.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Reddy</LastName><ForeName>M V</ForeName><Initials>MV</Initials></Author><Author ValidYN="Y"><LastName>Bhunia</LastName><ForeName>B</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Bhandari</LastName><ForeName>Y P</ForeName><Initials>YP</Initials></Author><Author ValidYN="Y"><LastName>Mehta</LastName><ForeName>V K</ForeName><Initials>VK</Initials></Author><Author ValidYN="Y"><LastName>Chaturvedi</LastName><ForeName>P</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Prajapati</LastName><ForeName>N C</ForeName><Initials>NC</Initials></Author><Author ValidYN="Y"><LastName>Gupta</LastName><ForeName>R K</ForeName><Initials>RK</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>India</Country><MedlineTA>Indian J Clin Biochem</MedlineTA><NlmUniqueID>8708303</NlmUniqueID><ISSNLinking>0970-1915</ISSNLinking></MedlineJournalInfo><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Indian J Pediatr. 1991 May-Jun;58(3):378-80</RefSource><PMID 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Sep;55(3):333-7</RefSource><PMID Version="1">8842125</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Trans R Soc Trop Med Hyg. 1997 Jan-Feb;91(1):78-81</RefSource><PMID Version="1">9093637</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Braz J Med Biol Res. 1996 Aug;29(8):1005-8</RefSource><PMID Version="1">9181082</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 1997 Oct;57(4):483-6</RefSource><PMID Version="1">9347968</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Trans R Soc Trop Med Hyg. 1997 Nov-Dec;91(6):677-9</RefSource><PMID Version="1">9509177</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Trop Med Hyg. 1998 Aug;59(2):217-21</RefSource><PMID Version="1">9715935</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Trans R Soc Trop Med Hyg. 1998 Sep-Oct;92(5):513-5</RefSource><PMID Version="1">9861365</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Trop Med Parasitol. 1990 Dec;41(4):403-6</RefSource><PMID Version="1">2075384</PMID></CommentsCorrections></CommentsCorrectionsList><OtherID Source="NLM">PMC3454079</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">DEC therapy</Keyword><Keyword MajorTopicYN="N">Filariasis</Keyword><Keyword MajorTopicYN="N">children</Keyword><Keyword MajorTopicYN="N">immunomonitoring</Keyword><Keyword MajorTopicYN="N">morbidity</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>10</Month><Day>30</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2000</Year><Month>8</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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