Helicobacter Genotyping and Detection in Peroperative Lavage Fluid in Patients with Perforated Peptic Ulcer

Introduction and Objectives Certain Helicobacter pylori genotypes are associated with peptic ulcer disease; however, little is known about associations between the H. pylori genotype and perforated peptic ulcer (PPU). The primary aim of this study was to evaluate which genotypes are present in patie...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of gastrointestinal surgery 2008-03, Vol.12 (3), p.555-560
Hauptverfasser: Komen, N. A. P., Bertleff, M. J. O. E., van Doorn, L. J., Lange, J. F., de Graaf, P. W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 560
container_issue 3
container_start_page 555
container_title Journal of gastrointestinal surgery
container_volume 12
creator Komen, N. A. P.
Bertleff, M. J. O. E.
van Doorn, L. J.
Lange, J. F.
de Graaf, P. W.
description Introduction and Objectives Certain Helicobacter pylori genotypes are associated with peptic ulcer disease; however, little is known about associations between the H. pylori genotype and perforated peptic ulcer (PPU). The primary aim of this study was to evaluate which genotypes are present in patients with PPU and which genotype is dominant in this population. The secondary aim was to study the possibility of determining the H. pylori status in a way other than by biopsy. Materials and Methods Serum samples, gastric tissue biopsies, lavage fluid, and fluid from the nasogastric tube were collected from patients operated upon for PPU. By means of PCR, DEIA, and LIPA the presence of the “cytotoxin associated gene” ( cagA ) and the genotype of the “vacuolating cytotoxin gene” were determined. Results Fluid from the nasogastric tube was obtained from 25 patients, lavage fluid from 26 patients, serum samples from 20 patients and biopsies from 18 patients. Several genotypes were found, of which the vacA s1 cagA positive strains were predominant. Additionally, a correlation was found between the H. pylori presence in biopsy and its presence in lavage fluid ( p  = 0.015), rendering the latter as an alternative for biopsy. Sensitivity and specificity of lavage fluid analysis were 100% and 67%, respectively. Conclusion This study shows the vacA s1 cagA positive strain is predominant in a PPU population. The correlation found between the H. pylori presence in biopsy and its presence in lavage fluid suggests that analysis of the lavage fluid is sufficient to determine the H. pylori presence. Risks associated with biopsy taking may be avoided.
doi_str_mv 10.1007/s11605-007-0303-z
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2231408</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2789663211</sourcerecordid><originalsourceid>FETCH-LOGICAL-c468t-58285f39e9f856fd18f25be9663e22d759724ac9d2ce412d728aa381b08da9753</originalsourceid><addsrcrecordid>eNp1kV1rFDEUhgdR-mV_gDcyIHg3mpOZfN0IUm0rLNQLC96FbObMNnU2GZPMSvvrm3UXrUKv8nLOc96cw1tVr4C8A0LE-wTACWuKbEhL2ub-WXUEUrRNxyl_XjRR0FDGvh9WxyndEgKCgDyoDkEowhWRR9WPSxydDUtjM8b6An3Id5Pzq9r4vv6EGW12wdfO118xhgmjyW6D9cJszArr83F2_e9mKaPPqf7l8s0WHUIhsS9yys7W16PF-LJ6MZgx4en-Pamuzz9_O7tsFlcXX84-LhrbcZkbJqlkQ6tQDZLxoQc5ULZExXmLlPaCKUE7Y1VPLXZQClQa00pYEtkbJVh7Un3Y-U7zco29LYtFM-opurWJdzoYp__teHejV2GjKW2hI7IYvN0bxPBzxpT12iWL42g8hjlpQagAqdoCvvkPvA1z9OU4DQDFTnAQhYIdZWNIKeLwZxUgehuk3gWpt3IbpL4vM68f3_B3Yp9cAegOSKXlVxgfff2k6wPXCqqu</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1112237617</pqid></control><display><type>article</type><title>Helicobacter Genotyping and Detection in Peroperative Lavage Fluid in Patients with Perforated Peptic Ulcer</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Komen, N. A. P. ; Bertleff, M. J. O. E. ; van Doorn, L. J. ; Lange, J. F. ; de Graaf, P. W.</creator><creatorcontrib>Komen, N. A. P. ; Bertleff, M. J. O. E. ; van Doorn, L. J. ; Lange, J. F. ; de Graaf, P. W.</creatorcontrib><description>Introduction and Objectives Certain Helicobacter pylori genotypes are associated with peptic ulcer disease; however, little is known about associations between the H. pylori genotype and perforated peptic ulcer (PPU). The primary aim of this study was to evaluate which genotypes are present in patients with PPU and which genotype is dominant in this population. The secondary aim was to study the possibility of determining the H. pylori status in a way other than by biopsy. Materials and Methods Serum samples, gastric tissue biopsies, lavage fluid, and fluid from the nasogastric tube were collected from patients operated upon for PPU. By means of PCR, DEIA, and LIPA the presence of the “cytotoxin associated gene” ( cagA ) and the genotype of the “vacuolating cytotoxin gene” were determined. Results Fluid from the nasogastric tube was obtained from 25 patients, lavage fluid from 26 patients, serum samples from 20 patients and biopsies from 18 patients. Several genotypes were found, of which the vacA s1 cagA positive strains were predominant. Additionally, a correlation was found between the H. pylori presence in biopsy and its presence in lavage fluid ( p  = 0.015), rendering the latter as an alternative for biopsy. Sensitivity and specificity of lavage fluid analysis were 100% and 67%, respectively. Conclusion This study shows the vacA s1 cagA positive strain is predominant in a PPU population. The correlation found between the H. pylori presence in biopsy and its presence in lavage fluid suggests that analysis of the lavage fluid is sufficient to determine the H. pylori presence. Risks associated with biopsy taking may be avoided.</description><identifier>ISSN: 1091-255X</identifier><identifier>EISSN: 1873-4626</identifier><identifier>DOI: 10.1007/s11605-007-0303-z</identifier><identifier>PMID: 17906908</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antigens, Bacterial - isolation &amp; purification ; Bacterial Proteins - isolation &amp; purification ; Bronchoalveolar Lavage Fluid - microbiology ; Female ; Fluids ; Gastroenterology ; Genotype ; Genotype &amp; phenotype ; Helicobacter Infections - epidemiology ; Helicobacter pylori - genetics ; Humans ; Infections ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Peptic Ulcer Perforation - microbiology ; Surgery ; Ulcers</subject><ispartof>Journal of gastrointestinal surgery, 2008-03, Vol.12 (3), p.555-560</ispartof><rights>The Society for Surgery of the Alimentary Tract 2007</rights><rights>The Society for Surgery of the Alimentary Tract 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-58285f39e9f856fd18f25be9663e22d759724ac9d2ce412d728aa381b08da9753</citedby><cites>FETCH-LOGICAL-c468t-58285f39e9f856fd18f25be9663e22d759724ac9d2ce412d728aa381b08da9753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11605-007-0303-z$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11605-007-0303-z$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17906908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komen, N. A. P.</creatorcontrib><creatorcontrib>Bertleff, M. J. O. E.</creatorcontrib><creatorcontrib>van Doorn, L. J.</creatorcontrib><creatorcontrib>Lange, J. F.</creatorcontrib><creatorcontrib>de Graaf, P. W.</creatorcontrib><title>Helicobacter Genotyping and Detection in Peroperative Lavage Fluid in Patients with Perforated Peptic Ulcer</title><title>Journal of gastrointestinal surgery</title><addtitle>J Gastrointest Surg</addtitle><addtitle>J Gastrointest Surg</addtitle><description>Introduction and Objectives Certain Helicobacter pylori genotypes are associated with peptic ulcer disease; however, little is known about associations between the H. pylori genotype and perforated peptic ulcer (PPU). The primary aim of this study was to evaluate which genotypes are present in patients with PPU and which genotype is dominant in this population. The secondary aim was to study the possibility of determining the H. pylori status in a way other than by biopsy. Materials and Methods Serum samples, gastric tissue biopsies, lavage fluid, and fluid from the nasogastric tube were collected from patients operated upon for PPU. By means of PCR, DEIA, and LIPA the presence of the “cytotoxin associated gene” ( cagA ) and the genotype of the “vacuolating cytotoxin gene” were determined. Results Fluid from the nasogastric tube was obtained from 25 patients, lavage fluid from 26 patients, serum samples from 20 patients and biopsies from 18 patients. Several genotypes were found, of which the vacA s1 cagA positive strains were predominant. Additionally, a correlation was found between the H. pylori presence in biopsy and its presence in lavage fluid ( p  = 0.015), rendering the latter as an alternative for biopsy. Sensitivity and specificity of lavage fluid analysis were 100% and 67%, respectively. Conclusion This study shows the vacA s1 cagA positive strain is predominant in a PPU population. The correlation found between the H. pylori presence in biopsy and its presence in lavage fluid suggests that analysis of the lavage fluid is sufficient to determine the H. pylori presence. Risks associated with biopsy taking may be avoided.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens, Bacterial - isolation &amp; purification</subject><subject>Bacterial Proteins - isolation &amp; purification</subject><subject>Bronchoalveolar Lavage Fluid - microbiology</subject><subject>Female</subject><subject>Fluids</subject><subject>Gastroenterology</subject><subject>Genotype</subject><subject>Genotype &amp; phenotype</subject><subject>Helicobacter Infections - epidemiology</subject><subject>Helicobacter pylori - genetics</subject><subject>Humans</subject><subject>Infections</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Peptic Ulcer Perforation - microbiology</subject><subject>Surgery</subject><subject>Ulcers</subject><issn>1091-255X</issn><issn>1873-4626</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kV1rFDEUhgdR-mV_gDcyIHg3mpOZfN0IUm0rLNQLC96FbObMNnU2GZPMSvvrm3UXrUKv8nLOc96cw1tVr4C8A0LE-wTACWuKbEhL2ub-WXUEUrRNxyl_XjRR0FDGvh9WxyndEgKCgDyoDkEowhWRR9WPSxydDUtjM8b6An3Id5Pzq9r4vv6EGW12wdfO118xhgmjyW6D9cJszArr83F2_e9mKaPPqf7l8s0WHUIhsS9yys7W16PF-LJ6MZgx4en-Pamuzz9_O7tsFlcXX84-LhrbcZkbJqlkQ6tQDZLxoQc5ULZExXmLlPaCKUE7Y1VPLXZQClQa00pYEtkbJVh7Un3Y-U7zco29LYtFM-opurWJdzoYp__teHejV2GjKW2hI7IYvN0bxPBzxpT12iWL42g8hjlpQagAqdoCvvkPvA1z9OU4DQDFTnAQhYIdZWNIKeLwZxUgehuk3gWpt3IbpL4vM68f3_B3Yp9cAegOSKXlVxgfff2k6wPXCqqu</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Komen, N. A. P.</creator><creator>Bertleff, M. J. O. E.</creator><creator>van Doorn, L. J.</creator><creator>Lange, J. F.</creator><creator>de Graaf, P. W.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080301</creationdate><title>Helicobacter Genotyping and Detection in Peroperative Lavage Fluid in Patients with Perforated Peptic Ulcer</title><author>Komen, N. A. P. ; Bertleff, M. J. O. E. ; van Doorn, L. J. ; Lange, J. F. ; de Graaf, P. W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-58285f39e9f856fd18f25be9663e22d759724ac9d2ce412d728aa381b08da9753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens, Bacterial - isolation &amp; purification</topic><topic>Bacterial Proteins - isolation &amp; purification</topic><topic>Bronchoalveolar Lavage Fluid - microbiology</topic><topic>Female</topic><topic>Fluids</topic><topic>Gastroenterology</topic><topic>Genotype</topic><topic>Genotype &amp; phenotype</topic><topic>Helicobacter Infections - epidemiology</topic><topic>Helicobacter pylori - genetics</topic><topic>Humans</topic><topic>Infections</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Peptic Ulcer Perforation - microbiology</topic><topic>Surgery</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Komen, N. A. P.</creatorcontrib><creatorcontrib>Bertleff, M. J. O. E.</creatorcontrib><creatorcontrib>van Doorn, L. J.</creatorcontrib><creatorcontrib>Lange, J. F.</creatorcontrib><creatorcontrib>de Graaf, P. W.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of gastrointestinal surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komen, N. A. P.</au><au>Bertleff, M. J. O. E.</au><au>van Doorn, L. J.</au><au>Lange, J. F.</au><au>de Graaf, P. W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Helicobacter Genotyping and Detection in Peroperative Lavage Fluid in Patients with Perforated Peptic Ulcer</atitle><jtitle>Journal of gastrointestinal surgery</jtitle><stitle>J Gastrointest Surg</stitle><addtitle>J Gastrointest Surg</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>12</volume><issue>3</issue><spage>555</spage><epage>560</epage><pages>555-560</pages><issn>1091-255X</issn><eissn>1873-4626</eissn><abstract>Introduction and Objectives Certain Helicobacter pylori genotypes are associated with peptic ulcer disease; however, little is known about associations between the H. pylori genotype and perforated peptic ulcer (PPU). The primary aim of this study was to evaluate which genotypes are present in patients with PPU and which genotype is dominant in this population. The secondary aim was to study the possibility of determining the H. pylori status in a way other than by biopsy. Materials and Methods Serum samples, gastric tissue biopsies, lavage fluid, and fluid from the nasogastric tube were collected from patients operated upon for PPU. By means of PCR, DEIA, and LIPA the presence of the “cytotoxin associated gene” ( cagA ) and the genotype of the “vacuolating cytotoxin gene” were determined. Results Fluid from the nasogastric tube was obtained from 25 patients, lavage fluid from 26 patients, serum samples from 20 patients and biopsies from 18 patients. Several genotypes were found, of which the vacA s1 cagA positive strains were predominant. Additionally, a correlation was found between the H. pylori presence in biopsy and its presence in lavage fluid ( p  = 0.015), rendering the latter as an alternative for biopsy. Sensitivity and specificity of lavage fluid analysis were 100% and 67%, respectively. Conclusion This study shows the vacA s1 cagA positive strain is predominant in a PPU population. The correlation found between the H. pylori presence in biopsy and its presence in lavage fluid suggests that analysis of the lavage fluid is sufficient to determine the H. pylori presence. Risks associated with biopsy taking may be avoided.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><pmid>17906908</pmid><doi>10.1007/s11605-007-0303-z</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1091-255X
ispartof Journal of gastrointestinal surgery, 2008-03, Vol.12 (3), p.555-560
issn 1091-255X
1873-4626
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2231408
source MEDLINE; SpringerNature Journals
subjects Adult
Aged
Aged, 80 and over
Antigens, Bacterial - isolation & purification
Bacterial Proteins - isolation & purification
Bronchoalveolar Lavage Fluid - microbiology
Female
Fluids
Gastroenterology
Genotype
Genotype & phenotype
Helicobacter Infections - epidemiology
Helicobacter pylori - genetics
Humans
Infections
Male
Medicine
Medicine & Public Health
Middle Aged
Peptic Ulcer Perforation - microbiology
Surgery
Ulcers
title Helicobacter Genotyping and Detection in Peroperative Lavage Fluid in Patients with Perforated Peptic Ulcer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T11%3A08%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Helicobacter%20Genotyping%20and%20Detection%20in%20Peroperative%20Lavage%20Fluid%20in%20Patients%20with%20Perforated%20Peptic%20Ulcer&rft.jtitle=Journal%20of%20gastrointestinal%20surgery&rft.au=Komen,%20N.%20A.%20P.&rft.date=2008-03-01&rft.volume=12&rft.issue=3&rft.spage=555&rft.epage=560&rft.pages=555-560&rft.issn=1091-255X&rft.eissn=1873-4626&rft_id=info:doi/10.1007/s11605-007-0303-z&rft_dat=%3Cproquest_pubme%3E2789663211%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1112237617&rft_id=info:pmid/17906908&rfr_iscdi=true