Pancreatic Enzyme Supplementation in Cystic Fibrosis Patients Before and After Fibrosing Colonopathy
BACKGROUND:In 1994 we cared for nine cystic fibrosis patients with fibrosing colonopathy. To evaluate the relationship between fibrosing colonopathy and supplemental pancreatic enzymes we reviewed our dosing of enzymes prior to fibrosing colonopathy development and then evaluated the subsequent effe...
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Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 1998-01, Vol.26 (1), p.80-84 |
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description | BACKGROUND:In 1994 we cared for nine cystic fibrosis patients with fibrosing colonopathy. To evaluate the relationship between fibrosing colonopathy and supplemental pancreatic enzymes we reviewed our dosing of enzymes prior to fibrosing colonopathy development and then evaluated the subsequent effect of drastically reducing pancreatic enzyme dose.
METHODS:We retrospectively reviewed pancreatic enzyme dosing for 267 cystic fibrosis patients with pancreatic insufficiency. The supplemental enzyme history of nine patients with fibrosing colonopathy was contrasted with the history of 258 nonaffected patients. The pancreatic enzyme doses of 75 patients taking at least 6,000 U lipase/kg/meal were systematically reduced to approximately 2,000 lipase units/kg/meal. We evaluated the effect of this dose reduction on change in height and weight z scores one year after achievement of stable enzyme dose.
RESULTS:In the year prior to diagnosis patients with fibrosing colonopathy took a significantly larger pancreatic enzyme dose, whether assessed by highest dose or cumulative dose, than did nonaffected patients. Similar results were observed after controlling for sex and age. All 75 patients on at least 6,000 U lipase/kg/meal were able to tolerate a significant reduction in dose while achieving clinically acceptable nutrient absorption, with no change over one year in height and weight z scores.
CONCLUSIONS:Our data demonstrate a strong relationship between very high doses of pancreatic enzyme supplementation and formation of fibrosing colonopathy. These very high doses do not appear to be needed for adequate nutrient absorption and growth. |
doi_str_mv | 10.1097/00005176-199801000-00014 |
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METHODS:We retrospectively reviewed pancreatic enzyme dosing for 267 cystic fibrosis patients with pancreatic insufficiency. The supplemental enzyme history of nine patients with fibrosing colonopathy was contrasted with the history of 258 nonaffected patients. The pancreatic enzyme doses of 75 patients taking at least 6,000 U lipase/kg/meal were systematically reduced to approximately 2,000 lipase units/kg/meal. We evaluated the effect of this dose reduction on change in height and weight z scores one year after achievement of stable enzyme dose.
RESULTS:In the year prior to diagnosis patients with fibrosing colonopathy took a significantly larger pancreatic enzyme dose, whether assessed by highest dose or cumulative dose, than did nonaffected patients. Similar results were observed after controlling for sex and age. All 75 patients on at least 6,000 U lipase/kg/meal were able to tolerate a significant reduction in dose while achieving clinically acceptable nutrient absorption, with no change over one year in height and weight z scores.
CONCLUSIONS:Our data demonstrate a strong relationship between very high doses of pancreatic enzyme supplementation and formation of fibrosing colonopathy. These very high doses do not appear to be needed for adequate nutrient absorption and growth.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/00005176-199801000-00014</identifier><identifier>PMID: 9443125</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Adolescent ; Biological and medical sciences ; Child ; Child, Preschool ; Colon - pathology ; Colonic Diseases - drug therapy ; Colonic Diseases - etiology ; Cystic Fibrosis - complications ; Cystic Fibrosis - drug therapy ; Digestive system ; Exocrine Pancreatic Insufficiency - drug therapy ; Exocrine Pancreatic Insufficiency - etiology ; Female ; Fibrosis ; Humans ; Lipase - administration & dosage ; Lipase - therapeutic use ; Male ; Medical sciences ; Pancreas - enzymology ; Pharmacology. Drug treatments ; Retrospective Studies</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 1998-01, Vol.26 (1), p.80-84</ispartof><rights>Lippincott-Raven Publishers</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4344-27367cccb5d3ccceb14c71e7e8735b71142aacdb6b763c91a520eca8dbfa1c183</citedby><cites>FETCH-LOGICAL-c4344-27367cccb5d3ccceb14c71e7e8735b71142aacdb6b763c91a520eca8dbfa1c183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2101621$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9443125$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stevens, John C</creatorcontrib><creatorcontrib>Maguiness, Karen M</creatorcontrib><creatorcontrib>Hollingsworth, Judy</creatorcontrib><creatorcontrib>Heilman, Douglas K</creatorcontrib><creatorcontrib>Chong, Sonny K. F</creatorcontrib><title>Pancreatic Enzyme Supplementation in Cystic Fibrosis Patients Before and After Fibrosing Colonopathy</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>BACKGROUND:In 1994 we cared for nine cystic fibrosis patients with fibrosing colonopathy. To evaluate the relationship between fibrosing colonopathy and supplemental pancreatic enzymes we reviewed our dosing of enzymes prior to fibrosing colonopathy development and then evaluated the subsequent effect of drastically reducing pancreatic enzyme dose.
METHODS:We retrospectively reviewed pancreatic enzyme dosing for 267 cystic fibrosis patients with pancreatic insufficiency. The supplemental enzyme history of nine patients with fibrosing colonopathy was contrasted with the history of 258 nonaffected patients. The pancreatic enzyme doses of 75 patients taking at least 6,000 U lipase/kg/meal were systematically reduced to approximately 2,000 lipase units/kg/meal. We evaluated the effect of this dose reduction on change in height and weight z scores one year after achievement of stable enzyme dose.
RESULTS:In the year prior to diagnosis patients with fibrosing colonopathy took a significantly larger pancreatic enzyme dose, whether assessed by highest dose or cumulative dose, than did nonaffected patients. Similar results were observed after controlling for sex and age. All 75 patients on at least 6,000 U lipase/kg/meal were able to tolerate a significant reduction in dose while achieving clinically acceptable nutrient absorption, with no change over one year in height and weight z scores.
CONCLUSIONS:Our data demonstrate a strong relationship between very high doses of pancreatic enzyme supplementation and formation of fibrosing colonopathy. These very high doses do not appear to be needed for adequate nutrient absorption and growth.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Colon - pathology</subject><subject>Colonic Diseases - drug therapy</subject><subject>Colonic Diseases - etiology</subject><subject>Cystic Fibrosis - complications</subject><subject>Cystic Fibrosis - drug therapy</subject><subject>Digestive system</subject><subject>Exocrine Pancreatic Insufficiency - drug therapy</subject><subject>Exocrine Pancreatic Insufficiency - etiology</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Humans</subject><subject>Lipase - administration & dosage</subject><subject>Lipase - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pancreas - enzymology</subject><subject>Pharmacology. Drug treatments</subject><subject>Retrospective Studies</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kdFuFCEUhonR1LX6CCZcGO-mcoCBmcu6aa1JE5vYXhOGOeOOMjDCTJr16aXudu8kIYTzfwfIByEU2AWwVn9iZdSgVQVt2zAou6pMkC_IBmqhKlmKL8mGca0rDqBekzc5_yyIljU7I2etlAJ4vSH9nQ0uoV1GR6_Cn_2E9Ps6zx4nDEupxkDHQLf7_ARcj12Kecz0riQlz_QzDjEhtaGnl8OC6RkJP-g2-hjibJfd_i15NVif8d1xPScP11f325vq9tuXr9vL28pJIWXFtVDaOdfVvSgLdiCdBtTYaFF3GkBya13fqU4r4VqwNWfobNN3gwUHjTgnHw_nzin-XjEvZhqzQ-9twLhmo1ultGp4AZsD6Mpjc8LBzGmcbNobYOZJsHkWbE6CzT_BpfX98Y61m7A_NR6NlvzDMbfZWT-k4nfMJ4wDA8WhYPKAPUZfvOVffn3EZHZo_bIz__te8Rcvh5P4</recordid><startdate>199801</startdate><enddate>199801</enddate><creator>Stevens, John C</creator><creator>Maguiness, Karen M</creator><creator>Hollingsworth, Judy</creator><creator>Heilman, Douglas K</creator><creator>Chong, Sonny K. F</creator><general>Lippincott-Raven Publishers</general><general>Lippincott</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>199801</creationdate><title>Pancreatic Enzyme Supplementation in Cystic Fibrosis Patients Before and After Fibrosing Colonopathy</title><author>Stevens, John C ; Maguiness, Karen M ; Hollingsworth, Judy ; Heilman, Douglas K ; Chong, Sonny K. F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4344-27367cccb5d3ccceb14c71e7e8735b71142aacdb6b763c91a520eca8dbfa1c183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Colon - pathology</topic><topic>Colonic Diseases - drug therapy</topic><topic>Colonic Diseases - etiology</topic><topic>Cystic Fibrosis - complications</topic><topic>Cystic Fibrosis - drug therapy</topic><topic>Digestive system</topic><topic>Exocrine Pancreatic Insufficiency - drug therapy</topic><topic>Exocrine Pancreatic Insufficiency - etiology</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Humans</topic><topic>Lipase - administration & dosage</topic><topic>Lipase - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pancreas - enzymology</topic><topic>Pharmacology. Drug treatments</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stevens, John C</creatorcontrib><creatorcontrib>Maguiness, Karen M</creatorcontrib><creatorcontrib>Hollingsworth, Judy</creatorcontrib><creatorcontrib>Heilman, Douglas K</creatorcontrib><creatorcontrib>Chong, Sonny K. F</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 gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stevens, John C</au><au>Maguiness, Karen M</au><au>Hollingsworth, Judy</au><au>Heilman, Douglas K</au><au>Chong, Sonny K. F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pancreatic Enzyme Supplementation in Cystic Fibrosis Patients Before and After Fibrosing Colonopathy</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>1998-01</date><risdate>1998</risdate><volume>26</volume><issue>1</issue><spage>80</spage><epage>84</epage><pages>80-84</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>BACKGROUND:In 1994 we cared for nine cystic fibrosis patients with fibrosing colonopathy. To evaluate the relationship between fibrosing colonopathy and supplemental pancreatic enzymes we reviewed our dosing of enzymes prior to fibrosing colonopathy development and then evaluated the subsequent effect of drastically reducing pancreatic enzyme dose.
METHODS:We retrospectively reviewed pancreatic enzyme dosing for 267 cystic fibrosis patients with pancreatic insufficiency. The supplemental enzyme history of nine patients with fibrosing colonopathy was contrasted with the history of 258 nonaffected patients. The pancreatic enzyme doses of 75 patients taking at least 6,000 U lipase/kg/meal were systematically reduced to approximately 2,000 lipase units/kg/meal. We evaluated the effect of this dose reduction on change in height and weight z scores one year after achievement of stable enzyme dose.
RESULTS:In the year prior to diagnosis patients with fibrosing colonopathy took a significantly larger pancreatic enzyme dose, whether assessed by highest dose or cumulative dose, than did nonaffected patients. Similar results were observed after controlling for sex and age. All 75 patients on at least 6,000 U lipase/kg/meal were able to tolerate a significant reduction in dose while achieving clinically acceptable nutrient absorption, with no change over one year in height and weight z scores.
CONCLUSIONS:Our data demonstrate a strong relationship between very high doses of pancreatic enzyme supplementation and formation of fibrosing colonopathy. These very high doses do not appear to be needed for adequate nutrient absorption and growth.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>9443125</pmid><doi>10.1097/00005176-199801000-00014</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Biological and medical sciences Child Child, Preschool Colon - pathology Colonic Diseases - drug therapy Colonic Diseases - etiology Cystic Fibrosis - complications Cystic Fibrosis - drug therapy Digestive system Exocrine Pancreatic Insufficiency - drug therapy Exocrine Pancreatic Insufficiency - etiology Female Fibrosis Humans Lipase - administration & dosage Lipase - therapeutic use Male Medical sciences Pancreas - enzymology Pharmacology. Drug treatments Retrospective Studies |
title | Pancreatic Enzyme Supplementation in Cystic Fibrosis Patients Before and After Fibrosing Colonopathy |
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