A polymerase chain reaction for the diagnosis of Haemophilus influenzae type b disease in children and its evaluation during a vaccine trial

BACKGROUND.Determination of the etiology of pneumonia in young children is difficult because blood culture, the usual method of diagnosis, is positive in only a small proportion of cases. For this reason vaccine trials that include bacterial pneumonia as an endpoint must be large. OBJECTIVES.To dete...

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Veröffentlicht in:The Pediatric infectious disease journal 1998-04, Vol.17 (4), p.309-312
Hauptverfasser: HASSAN-KING, MUSA, ADEGBOLA, RICHARD, BALDEH, IGNATIUS, MULHOLLAND, KIM, OMOSIGHO, CHARLES, OPARAUGO, ANSLEM, USEN, STANLEY, PALMER, AYO, SCHNEIDER, GISELA, SECKA, OUSMAN, WEBER, MARTIN, GREENWOOD, BRIAN
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container_end_page 312
container_issue 4
container_start_page 309
container_title The Pediatric infectious disease journal
container_volume 17
creator HASSAN-KING, MUSA
ADEGBOLA, RICHARD
BALDEH, IGNATIUS
MULHOLLAND, KIM
OMOSIGHO, CHARLES
OPARAUGO, ANSLEM
USEN, STANLEY
PALMER, AYO
SCHNEIDER, GISELA
SECKA, OUSMAN
WEBER, MARTIN
GREENWOOD, BRIAN
description BACKGROUND.Determination of the etiology of pneumonia in young children is difficult because blood culture, the usual method of diagnosis, is positive in only a small proportion of cases. For this reason vaccine trials that include bacterial pneumonia as an endpoint must be large. OBJECTIVES.To determine whether a diagnostic test based on a polymerase chain reaction could be used as an alternative to conventional blood culture for diagnosis of invasive Haemophilus influenzae type b (Hib) infections in young children investigated during the course of a large vaccine trial. METHODS.DNA was extracted from blood culture supernatants and probed for the presence of Hib DNA with a PCR assay with primers derived from the cap gene locus of Hib. Results of the PCR assay were compared with those obtained by conventional culture techniques. RESULTS.Blood cultures were obtained from 1544 children with suspected pneumonia, meningitis or septicemia and from 31 healthy control children who were contacts of cases. Blood culture supernatants were tested for Hib DNA in the PCR test. The sensitivity and specificity of a positive PCR test in blood culture supernatant as against culture of Hib from any normally sterile site were 100 and 99%, respectively. Eleven children had positive Hib PCR tests on blood culture supernatants but were negative by culture. In one of these cases Hib was isolated from a lung aspirate and in two other patients H. influenzae strains other than Hib were obtained from the cerebrospinal fluid. Eight of these 11 children were in the control group. When the results of the PCR assay were used to determine vaccine efficacy, a value of 86% was obtained compared with a figure of 95% obtained when conventional culture techniques were used. CONCLUSIONS.An Hib PCR assay on blood culture supernatants proved to be sensitive and specific for the diagnosis of Hib disease in children. The distribution of PCR-positive, culture-negative cases between Hib-vaccinated and control groups paralleled that of culture-positive cases, suggesting that most of these children had been infected with Hib. A trial of a highly efficacious vaccine provides a novel way for evaluating new diagnostic tests for which there is no standard diagnostic test of 100% reliability.
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For this reason vaccine trials that include bacterial pneumonia as an endpoint must be large. OBJECTIVES.To determine whether a diagnostic test based on a polymerase chain reaction could be used as an alternative to conventional blood culture for diagnosis of invasive Haemophilus influenzae type b (Hib) infections in young children investigated during the course of a large vaccine trial. METHODS.DNA was extracted from blood culture supernatants and probed for the presence of Hib DNA with a PCR assay with primers derived from the cap gene locus of Hib. Results of the PCR assay were compared with those obtained by conventional culture techniques. RESULTS.Blood cultures were obtained from 1544 children with suspected pneumonia, meningitis or septicemia and from 31 healthy control children who were contacts of cases. Blood culture supernatants were tested for Hib DNA in the PCR test. The sensitivity and specificity of a positive PCR test in blood culture supernatant as against culture of Hib from any normally sterile site were 100 and 99%, respectively. Eleven children had positive Hib PCR tests on blood culture supernatants but were negative by culture. In one of these cases Hib was isolated from a lung aspirate and in two other patients H. influenzae strains other than Hib were obtained from the cerebrospinal fluid. Eight of these 11 children were in the control group. When the results of the PCR assay were used to determine vaccine efficacy, a value of 86% was obtained compared with a figure of 95% obtained when conventional culture techniques were used. CONCLUSIONS.An Hib PCR assay on blood culture supernatants proved to be sensitive and specific for the diagnosis of Hib disease in children. The distribution of PCR-positive, culture-negative cases between Hib-vaccinated and control groups paralleled that of culture-positive cases, suggesting that most of these children had been infected with Hib. 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All Rights Reserved.</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4158-abce8db166eaefa32fc6acb5da21b80acb3e547a1a345b34a14f421c9dcb9ee93</citedby><cites>FETCH-LOGICAL-c4158-abce8db166eaefa32fc6acb5da21b80acb3e547a1a345b34a14f421c9dcb9ee93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2223244$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9576385$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HASSAN-KING, MUSA</creatorcontrib><creatorcontrib>ADEGBOLA, RICHARD</creatorcontrib><creatorcontrib>BALDEH, IGNATIUS</creatorcontrib><creatorcontrib>MULHOLLAND, KIM</creatorcontrib><creatorcontrib>OMOSIGHO, CHARLES</creatorcontrib><creatorcontrib>OPARAUGO, ANSLEM</creatorcontrib><creatorcontrib>USEN, STANLEY</creatorcontrib><creatorcontrib>PALMER, AYO</creatorcontrib><creatorcontrib>SCHNEIDER, GISELA</creatorcontrib><creatorcontrib>SECKA, OUSMAN</creatorcontrib><creatorcontrib>WEBER, MARTIN</creatorcontrib><creatorcontrib>GREENWOOD, BRIAN</creatorcontrib><title>A polymerase chain reaction for the diagnosis of Haemophilus influenzae type b disease in children and its evaluation during a vaccine trial</title><title>The Pediatric infectious disease journal</title><addtitle>Pediatr Infect Dis J</addtitle><description>BACKGROUND.Determination of the etiology of pneumonia in young children is difficult because blood culture, the usual method of diagnosis, is positive in only a small proportion of cases. For this reason vaccine trials that include bacterial pneumonia as an endpoint must be large. OBJECTIVES.To determine whether a diagnostic test based on a polymerase chain reaction could be used as an alternative to conventional blood culture for diagnosis of invasive Haemophilus influenzae type b (Hib) infections in young children investigated during the course of a large vaccine trial. METHODS.DNA was extracted from blood culture supernatants and probed for the presence of Hib DNA with a PCR assay with primers derived from the cap gene locus of Hib. Results of the PCR assay were compared with those obtained by conventional culture techniques. RESULTS.Blood cultures were obtained from 1544 children with suspected pneumonia, meningitis or septicemia and from 31 healthy control children who were contacts of cases. Blood culture supernatants were tested for Hib DNA in the PCR test. The sensitivity and specificity of a positive PCR test in blood culture supernatant as against culture of Hib from any normally sterile site were 100 and 99%, respectively. Eleven children had positive Hib PCR tests on blood culture supernatants but were negative by culture. In one of these cases Hib was isolated from a lung aspirate and in two other patients H. influenzae strains other than Hib were obtained from the cerebrospinal fluid. Eight of these 11 children were in the control group. When the results of the PCR assay were used to determine vaccine efficacy, a value of 86% was obtained compared with a figure of 95% obtained when conventional culture techniques were used. CONCLUSIONS.An Hib PCR assay on blood culture supernatants proved to be sensitive and specific for the diagnosis of Hib disease in children. The distribution of PCR-positive, culture-negative cases between Hib-vaccinated and control groups paralleled that of culture-positive cases, suggesting that most of these children had been infected with Hib. A trial of a highly efficacious vaccine provides a novel way for evaluating new diagnostic tests for which there is no standard diagnostic test of 100% reliability.</description><subject>Bacteremia - diagnosis</subject><subject>Bacteremia - prevention &amp; control</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the respiratory system</subject><subject>Biological and medical sciences</subject><subject>Child, Preschool</subject><subject>Culture Media</subject><subject>Diphtheria-Tetanus-Pertussis Vaccine - administration &amp; dosage</subject><subject>Female</subject><subject>Gambia</subject><subject>Haemophilus Infections - diagnosis</subject><subject>Haemophilus Infections - prevention &amp; control</subject><subject>Haemophilus influenzae</subject><subject>Haemophilus influenzae type b - genetics</subject><subject>Haemophilus influenzae type b - isolation &amp; purification</subject><subject>Haemophilus Vaccines - administration &amp; dosage</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Meningitis, Haemophilus - diagnosis</subject><subject>Meningitis, Haemophilus - prevention &amp; control</subject><subject>Pneumonia, Bacterial - diagnosis</subject><subject>Pneumonia, Bacterial - prevention &amp; control</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Sensitivity and Specificity</subject><subject>Tetanus Toxoid - administration &amp; dosage</subject><subject>Tropical medicine</subject><subject>Vaccines, Combined - administration &amp; dosage</subject><subject>Vaccines, Conjugate - administration &amp; dosage</subject><issn>0891-3668</issn><issn>1532-0987</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksGO1SAUhonRjNfRRzBhYdxVodAWlpOJOiaTuNE1OaWnU5RChXYm12fwoeXOvd6dkQ2cc77_J-GHEMrZO850956V1cpGVlxrxWSpqkNLPSE73oi6Ylp1T8mOKc0r0bbqOXmR8_dCCMnZBbnQTdcK1ezI7yu6RL-fMUFGaidwgSYEu7oY6BgTXSekg4O7ELPLNI70BnCOy-T8lqkLo98w_AKk635B2hc048Gp2NjCDAkDhTBQt2aK9-A3eHQetuTCHQV6D9a6UOTJgX9Jno3gM7467Zfk28cPX69vqtsvnz5fX91WVvJGVdBbVEPP2xYBRxD1aFuwfTNAzXvFylFgIzvgIGTTCwlcjrLmVg-214haXJK3R98lxZ8b5tXMLlv0HgLGLZtOKyGZrP8L8rYpD8lUAdURtCnmnHA0S3IzpL3hzBwSM38TM-fEHlsH6evTHVs_43AWniIq8zenOWQLfkwQrMtnrK5rUUtZMHnEHqJfMeUffnvAZCYEv07mX_9F_AGlxbDW</recordid><startdate>199804</startdate><enddate>199804</enddate><creator>HASSAN-KING, MUSA</creator><creator>ADEGBOLA, RICHARD</creator><creator>BALDEH, IGNATIUS</creator><creator>MULHOLLAND, KIM</creator><creator>OMOSIGHO, CHARLES</creator><creator>OPARAUGO, ANSLEM</creator><creator>USEN, STANLEY</creator><creator>PALMER, AYO</creator><creator>SCHNEIDER, GISELA</creator><creator>SECKA, OUSMAN</creator><creator>WEBER, MARTIN</creator><creator>GREENWOOD, BRIAN</creator><general>Williams &amp; 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For this reason vaccine trials that include bacterial pneumonia as an endpoint must be large. OBJECTIVES.To determine whether a diagnostic test based on a polymerase chain reaction could be used as an alternative to conventional blood culture for diagnosis of invasive Haemophilus influenzae type b (Hib) infections in young children investigated during the course of a large vaccine trial. METHODS.DNA was extracted from blood culture supernatants and probed for the presence of Hib DNA with a PCR assay with primers derived from the cap gene locus of Hib. Results of the PCR assay were compared with those obtained by conventional culture techniques. RESULTS.Blood cultures were obtained from 1544 children with suspected pneumonia, meningitis or septicemia and from 31 healthy control children who were contacts of cases. Blood culture supernatants were tested for Hib DNA in the PCR test. The sensitivity and specificity of a positive PCR test in blood culture supernatant as against culture of Hib from any normally sterile site were 100 and 99%, respectively. Eleven children had positive Hib PCR tests on blood culture supernatants but were negative by culture. In one of these cases Hib was isolated from a lung aspirate and in two other patients H. influenzae strains other than Hib were obtained from the cerebrospinal fluid. Eight of these 11 children were in the control group. When the results of the PCR assay were used to determine vaccine efficacy, a value of 86% was obtained compared with a figure of 95% obtained when conventional culture techniques were used. CONCLUSIONS.An Hib PCR assay on blood culture supernatants proved to be sensitive and specific for the diagnosis of Hib disease in children. The distribution of PCR-positive, culture-negative cases between Hib-vaccinated and control groups paralleled that of culture-positive cases, suggesting that most of these children had been infected with Hib. A trial of a highly efficacious vaccine provides a novel way for evaluating new diagnostic tests for which there is no standard diagnostic test of 100% reliability.</abstract><cop>Baltimore, MD</cop><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Williams &amp; Wilkins</pub><pmid>9576385</pmid><doi>10.1097/00006454-199804000-00008</doi><tpages>4</tpages></addata></record>
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subjects Bacteremia - diagnosis
Bacteremia - prevention & control
Bacterial diseases
Bacterial diseases of the respiratory system
Biological and medical sciences
Child, Preschool
Culture Media
Diphtheria-Tetanus-Pertussis Vaccine - administration & dosage
Female
Gambia
Haemophilus Infections - diagnosis
Haemophilus Infections - prevention & control
Haemophilus influenzae
Haemophilus influenzae type b - genetics
Haemophilus influenzae type b - isolation & purification
Haemophilus Vaccines - administration & dosage
Human bacterial diseases
Humans
Infant
Infectious diseases
Male
Medical sciences
Meningitis, Haemophilus - diagnosis
Meningitis, Haemophilus - prevention & control
Pneumonia, Bacterial - diagnosis
Pneumonia, Bacterial - prevention & control
Polymerase Chain Reaction - methods
Sensitivity and Specificity
Tetanus Toxoid - administration & dosage
Tropical medicine
Vaccines, Combined - administration & dosage
Vaccines, Conjugate - administration & dosage
title A polymerase chain reaction for the diagnosis of Haemophilus influenzae type b disease in children and its evaluation during a vaccine trial
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