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Intestinal obstruction after lung transplantation in children with cystic fibrosis
Background/Purpose: Distal intestinal obstruction syndrome (DIOS) occurs in 15% of patients with cystic fibrosis (CF). The authors reviewed their experience to determine the incidence, risk factors, and natural history of adhesive intestinal obstruction and DIOS after lung transplantation. Methods:...
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Published in: | Journal of pediatric surgery 1999-10, Vol.34 (10), p.1489-1493 |
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container_title | Journal of pediatric surgery |
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creator | Minkes, R.K. Langer, J.C. Skinner, M.A. Foglia, R.P. O'Hagan, A. Cohen, A.H. Mallory, G.B. Huddleston, C.B. Mendeloff, E.N. |
description | Background/Purpose:
Distal intestinal obstruction syndrome (DIOS) occurs in 15% of patients with cystic fibrosis (CF). The authors reviewed their experience to determine the incidence, risk factors, and natural history of adhesive intestinal obstruction and DIOS after lung transplantation.
Methods:
Eighty-three bilateral transplants were performed in 70 CF patients between January 1990 and September 1998. All were on pancreatic enzymes preoperatively, and none had preoperative bowel preparation. Fifty-six patients (80%) had prior gastrostomy (n = 54) or jejunostomy (n = 2). Eighteen patients (25.7%) had a previous laparotomy for meconium ileus (n = 8), fundoplication (n = 4), liver transplant (n = 1), jejunal atresia (n = 1), Janeway gastrostomy takedown (n = 1), pyloromyotomy (n = 1), free air (n = 1), or appendectomy (n = 1).
Results:
After lung transplantation, 7 patients (10%) required laparotomy for bowel obstruction (6 during the same hospitalization, and 1 during a subsequent hospitalization). The causes of obstruction were adhesions only (n = 1), DIOS only (n = 2), and a combination of DIOS and adhesions (n = 4). Adhesiolysis was performed in the 5 patients with adhesions, and a small bowel resection was also performed in 1 patient. DIOS was treated by milking secretions distally without an enterotomy (n = 3) with an enterotomy and primary closure (n = 1) or with an end ileostomy and mucus fistula (n = 2). Five had recurrent DIOS early postoperatively. One resolved with intestinal lavage, 2 were treated successfully with hypaque disimpaction, and 2 underwent reoperation; 1 required an ileostomy. The most important risk factor for posttransplant obstruction was a previous major abdominal operation. Obstruction occurred in 7 of 18 (39%) who had undergone a prior laparotomy versus 0 of 52 who had not (
P < .001,
χ
2).
Conclusions:
(1) The incidence of intestinal obstruction is high after lung transplantation in children with CF. (2) Previous laparotomy is a significant risk factor. (3) Recurrent obstruction after surgery for this condition is common. (4) Preventive measures such as pretransplant bowel preparation and early postoperative bowel lavage may be beneficial in these patients. |
doi_str_mv | 10.1016/S0022-3468(99)90110-0 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69237457</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022346899901100</els_id><sourcerecordid>69237457</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-fceaf107f3ff2ce9a7af3f84d14149d32e1b2f83971ce4822c2bb5b9123f28483</originalsourceid><addsrcrecordid>eNqFkElLxDAYhoMozrj8BKUHET1Us3XanETEZWBAcDmHNP3iRDrpmKTK_HszC-rNU0LyfG_ePAgdEXxBMBldPmNMac74qDoT4lxgQnCOt9CQFIzkBWblNhr-IAO0F8I7xukYk100ILjgoiz4ED2NXYQQrVNt1tUh-l5H27lMmQg-a3v3lkWvXJi3ykW1urIu01PbNh5c9mXjNNOLFKAzY2vfBRsO0I5RbYDDzbqPXu9uX24e8snj_fjmepJrJnDMjQZlCC4NM4ZqEKpUaVvxhnDCRcMokJqaiomSaOAVpZrWdVELQpmhFa_YPjpd585999GnT8iZDRra1BS6PsiRoKzkRZnAYg3q1C94MHLu7Uz5hSRYLmXKlUy5NCWFkCuZEqe5480DfT2D5s_U2l4CTjaAClq1JonSNvxyNMUWNGFXawySjU8LXgZtwWlorAcdZdPZf5p8Az2ikhM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69237457</pqid></control><display><type>article</type><title>Intestinal obstruction after lung transplantation in children with cystic fibrosis</title><source>ScienceDirect Journals</source><creator>Minkes, R.K. ; Langer, J.C. ; Skinner, M.A. ; Foglia, R.P. ; O'Hagan, A. ; Cohen, A.H. ; Mallory, G.B. ; Huddleston, C.B. ; Mendeloff, E.N.</creator><creatorcontrib>Minkes, R.K. ; Langer, J.C. ; Skinner, M.A. ; Foglia, R.P. ; O'Hagan, A. ; Cohen, A.H. ; Mallory, G.B. ; Huddleston, C.B. ; Mendeloff, E.N.</creatorcontrib><description>Background/Purpose:
Distal intestinal obstruction syndrome (DIOS) occurs in 15% of patients with cystic fibrosis (CF). The authors reviewed their experience to determine the incidence, risk factors, and natural history of adhesive intestinal obstruction and DIOS after lung transplantation.
Methods:
Eighty-three bilateral transplants were performed in 70 CF patients between January 1990 and September 1998. All were on pancreatic enzymes preoperatively, and none had preoperative bowel preparation. Fifty-six patients (80%) had prior gastrostomy (n = 54) or jejunostomy (n = 2). Eighteen patients (25.7%) had a previous laparotomy for meconium ileus (n = 8), fundoplication (n = 4), liver transplant (n = 1), jejunal atresia (n = 1), Janeway gastrostomy takedown (n = 1), pyloromyotomy (n = 1), free air (n = 1), or appendectomy (n = 1).
Results:
After lung transplantation, 7 patients (10%) required laparotomy for bowel obstruction (6 during the same hospitalization, and 1 during a subsequent hospitalization). The causes of obstruction were adhesions only (n = 1), DIOS only (n = 2), and a combination of DIOS and adhesions (n = 4). Adhesiolysis was performed in the 5 patients with adhesions, and a small bowel resection was also performed in 1 patient. DIOS was treated by milking secretions distally without an enterotomy (n = 3) with an enterotomy and primary closure (n = 1) or with an end ileostomy and mucus fistula (n = 2). Five had recurrent DIOS early postoperatively. One resolved with intestinal lavage, 2 were treated successfully with hypaque disimpaction, and 2 underwent reoperation; 1 required an ileostomy. The most important risk factor for posttransplant obstruction was a previous major abdominal operation. Obstruction occurred in 7 of 18 (39%) who had undergone a prior laparotomy versus 0 of 52 who had not (
P < .001,
χ
2).
Conclusions:
(1) The incidence of intestinal obstruction is high after lung transplantation in children with CF. (2) Previous laparotomy is a significant risk factor. (3) Recurrent obstruction after surgery for this condition is common. (4) Preventive measures such as pretransplant bowel preparation and early postoperative bowel lavage may be beneficial in these patients.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/S0022-3468(99)90110-0</identifier><identifier>PMID: 10549754</identifier><identifier>CODEN: JPDSA3</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Cystic Fibrosis - surgery ; Female ; Humans ; Intestinal Obstruction - etiology ; Lung Transplantation ; Male ; Medical sciences ; Postoperative Complications ; Reoperation ; Retrospective Studies ; Risk Factors ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the respiratory system</subject><ispartof>Journal of pediatric surgery, 1999-10, Vol.34 (10), p.1489-1493</ispartof><rights>1999</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-fceaf107f3ff2ce9a7af3f84d14149d32e1b2f83971ce4822c2bb5b9123f28483</citedby><cites>FETCH-LOGICAL-c390t-fceaf107f3ff2ce9a7af3f84d14149d32e1b2f83971ce4822c2bb5b9123f28483</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&idt=1200252$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10549754$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Minkes, R.K.</creatorcontrib><creatorcontrib>Langer, J.C.</creatorcontrib><creatorcontrib>Skinner, M.A.</creatorcontrib><creatorcontrib>Foglia, R.P.</creatorcontrib><creatorcontrib>O'Hagan, A.</creatorcontrib><creatorcontrib>Cohen, A.H.</creatorcontrib><creatorcontrib>Mallory, G.B.</creatorcontrib><creatorcontrib>Huddleston, C.B.</creatorcontrib><creatorcontrib>Mendeloff, E.N.</creatorcontrib><title>Intestinal obstruction after lung transplantation in children with cystic fibrosis</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Background/Purpose:
Distal intestinal obstruction syndrome (DIOS) occurs in 15% of patients with cystic fibrosis (CF). The authors reviewed their experience to determine the incidence, risk factors, and natural history of adhesive intestinal obstruction and DIOS after lung transplantation.
Methods:
Eighty-three bilateral transplants were performed in 70 CF patients between January 1990 and September 1998. All were on pancreatic enzymes preoperatively, and none had preoperative bowel preparation. Fifty-six patients (80%) had prior gastrostomy (n = 54) or jejunostomy (n = 2). Eighteen patients (25.7%) had a previous laparotomy for meconium ileus (n = 8), fundoplication (n = 4), liver transplant (n = 1), jejunal atresia (n = 1), Janeway gastrostomy takedown (n = 1), pyloromyotomy (n = 1), free air (n = 1), or appendectomy (n = 1).
Results:
After lung transplantation, 7 patients (10%) required laparotomy for bowel obstruction (6 during the same hospitalization, and 1 during a subsequent hospitalization). The causes of obstruction were adhesions only (n = 1), DIOS only (n = 2), and a combination of DIOS and adhesions (n = 4). Adhesiolysis was performed in the 5 patients with adhesions, and a small bowel resection was also performed in 1 patient. DIOS was treated by milking secretions distally without an enterotomy (n = 3) with an enterotomy and primary closure (n = 1) or with an end ileostomy and mucus fistula (n = 2). Five had recurrent DIOS early postoperatively. One resolved with intestinal lavage, 2 were treated successfully with hypaque disimpaction, and 2 underwent reoperation; 1 required an ileostomy. The most important risk factor for posttransplant obstruction was a previous major abdominal operation. Obstruction occurred in 7 of 18 (39%) who had undergone a prior laparotomy versus 0 of 52 who had not (
P < .001,
χ
2).
Conclusions:
(1) The incidence of intestinal obstruction is high after lung transplantation in children with CF. (2) Previous laparotomy is a significant risk factor. (3) Recurrent obstruction after surgery for this condition is common. (4) Preventive measures such as pretransplant bowel preparation and early postoperative bowel lavage may be beneficial in these patients.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Cystic Fibrosis - surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Intestinal Obstruction - etiology</subject><subject>Lung Transplantation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Postoperative Complications</subject><subject>Reoperation</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the respiratory system</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkElLxDAYhoMozrj8BKUHET1Us3XanETEZWBAcDmHNP3iRDrpmKTK_HszC-rNU0LyfG_ePAgdEXxBMBldPmNMac74qDoT4lxgQnCOt9CQFIzkBWblNhr-IAO0F8I7xukYk100ILjgoiz4ED2NXYQQrVNt1tUh-l5H27lMmQg-a3v3lkWvXJi3ykW1urIu01PbNh5c9mXjNNOLFKAzY2vfBRsO0I5RbYDDzbqPXu9uX24e8snj_fjmepJrJnDMjQZlCC4NM4ZqEKpUaVvxhnDCRcMokJqaiomSaOAVpZrWdVELQpmhFa_YPjpd585999GnT8iZDRra1BS6PsiRoKzkRZnAYg3q1C94MHLu7Uz5hSRYLmXKlUy5NCWFkCuZEqe5480DfT2D5s_U2l4CTjaAClq1JonSNvxyNMUWNGFXawySjU8LXgZtwWlorAcdZdPZf5p8Az2ikhM</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>Minkes, R.K.</creator><creator>Langer, J.C.</creator><creator>Skinner, M.A.</creator><creator>Foglia, R.P.</creator><creator>O'Hagan, A.</creator><creator>Cohen, A.H.</creator><creator>Mallory, G.B.</creator><creator>Huddleston, C.B.</creator><creator>Mendeloff, E.N.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Intestinal obstruction after lung transplantation in children with cystic fibrosis</title><author>Minkes, R.K. ; Langer, J.C. ; Skinner, M.A. ; Foglia, R.P. ; O'Hagan, A. ; Cohen, A.H. ; Mallory, G.B. ; Huddleston, C.B. ; Mendeloff, E.N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-fceaf107f3ff2ce9a7af3f84d14149d32e1b2f83971ce4822c2bb5b9123f28483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Cystic Fibrosis - surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Intestinal Obstruction - etiology</topic><topic>Lung Transplantation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Postoperative Complications</topic><topic>Reoperation</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Minkes, R.K.</creatorcontrib><creatorcontrib>Langer, J.C.</creatorcontrib><creatorcontrib>Skinner, M.A.</creatorcontrib><creatorcontrib>Foglia, R.P.</creatorcontrib><creatorcontrib>O'Hagan, A.</creatorcontrib><creatorcontrib>Cohen, A.H.</creatorcontrib><creatorcontrib>Mallory, G.B.</creatorcontrib><creatorcontrib>Huddleston, C.B.</creatorcontrib><creatorcontrib>Mendeloff, E.N.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Minkes, R.K.</au><au>Langer, J.C.</au><au>Skinner, M.A.</au><au>Foglia, R.P.</au><au>O'Hagan, A.</au><au>Cohen, A.H.</au><au>Mallory, G.B.</au><au>Huddleston, C.B.</au><au>Mendeloff, E.N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intestinal obstruction after lung transplantation in children with cystic fibrosis</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>34</volume><issue>10</issue><spage>1489</spage><epage>1493</epage><pages>1489-1493</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><coden>JPDSA3</coden><abstract>Background/Purpose:
Distal intestinal obstruction syndrome (DIOS) occurs in 15% of patients with cystic fibrosis (CF). The authors reviewed their experience to determine the incidence, risk factors, and natural history of adhesive intestinal obstruction and DIOS after lung transplantation.
Methods:
Eighty-three bilateral transplants were performed in 70 CF patients between January 1990 and September 1998. All were on pancreatic enzymes preoperatively, and none had preoperative bowel preparation. Fifty-six patients (80%) had prior gastrostomy (n = 54) or jejunostomy (n = 2). Eighteen patients (25.7%) had a previous laparotomy for meconium ileus (n = 8), fundoplication (n = 4), liver transplant (n = 1), jejunal atresia (n = 1), Janeway gastrostomy takedown (n = 1), pyloromyotomy (n = 1), free air (n = 1), or appendectomy (n = 1).
Results:
After lung transplantation, 7 patients (10%) required laparotomy for bowel obstruction (6 during the same hospitalization, and 1 during a subsequent hospitalization). The causes of obstruction were adhesions only (n = 1), DIOS only (n = 2), and a combination of DIOS and adhesions (n = 4). Adhesiolysis was performed in the 5 patients with adhesions, and a small bowel resection was also performed in 1 patient. DIOS was treated by milking secretions distally without an enterotomy (n = 3) with an enterotomy and primary closure (n = 1) or with an end ileostomy and mucus fistula (n = 2). Five had recurrent DIOS early postoperatively. One resolved with intestinal lavage, 2 were treated successfully with hypaque disimpaction, and 2 underwent reoperation; 1 required an ileostomy. The most important risk factor for posttransplant obstruction was a previous major abdominal operation. Obstruction occurred in 7 of 18 (39%) who had undergone a prior laparotomy versus 0 of 52 who had not (
P < .001,
χ
2).
Conclusions:
(1) The incidence of intestinal obstruction is high after lung transplantation in children with CF. (2) Previous laparotomy is a significant risk factor. (3) Recurrent obstruction after surgery for this condition is common. (4) Preventive measures such as pretransplant bowel preparation and early postoperative bowel lavage may be beneficial in these patients.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>10549754</pmid><doi>10.1016/S0022-3468(99)90110-0</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Child Cystic Fibrosis - surgery Female Humans Intestinal Obstruction - etiology Lung Transplantation Male Medical sciences Postoperative Complications Reoperation Retrospective Studies Risk Factors Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the respiratory system |
title | Intestinal obstruction after lung transplantation in children with cystic fibrosis |
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