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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of pediatric gastroenterology and nutrition 1998-01, Vol.26 (1), p.80-84
Hauptverfasser: Stevens, John C, Maguiness, Karen M, Hollingsworth, Judy, Heilman, Douglas K, Chong, Sonny K. F
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 84
container_issue 1
container_start_page 80
container_title Journal of pediatric gastroenterology and nutrition
container_volume 26
creator Stevens, John C
Maguiness, Karen M
Hollingsworth, Judy
Heilman, Douglas K
Chong, Sonny K. F
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79667682</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79667682</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4344-27367cccb5d3ccceb14c71e7e8735b71142aacdb6b763c91a520eca8dbfa1c183</originalsourceid><addsrcrecordid>eNp1kdFuFCEUhonR1LX6CCZcGO-mcoCBmcu6aa1JE5vYXhOGOeOOMjDCTJr16aXudu8kIYTzfwfIByEU2AWwVn9iZdSgVQVt2zAou6pMkC_IBmqhKlmKL8mGca0rDqBekzc5_yyIljU7I2etlAJ4vSH9nQ0uoV1GR6_Cn_2E9Ps6zx4nDEupxkDHQLf7_ARcj12Kecz0riQlz_QzDjEhtaGnl8OC6RkJP-g2-hjibJfd_i15NVif8d1xPScP11f325vq9tuXr9vL28pJIWXFtVDaOdfVvSgLdiCdBtTYaFF3GkBya13fqU4r4VqwNWfobNN3gwUHjTgnHw_nzin-XjEvZhqzQ-9twLhmo1ultGp4AZsD6Mpjc8LBzGmcbNobYOZJsHkWbE6CzT_BpfX98Y61m7A_NR6NlvzDMbfZWT-k4nfMJ4wDA8WhYPKAPUZfvOVffn3EZHZo_bIz__te8Rcvh5P4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79667682</pqid></control><display><type>article</type><title>Pancreatic Enzyme Supplementation in Cystic Fibrosis Patients Before and After Fibrosing Colonopathy</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>Wiley Online Library All Journals</source><creator>Stevens, John C ; Maguiness, Karen M ; Hollingsworth, Judy ; Heilman, Douglas K ; Chong, Sonny K. F</creator><creatorcontrib>Stevens, John C ; Maguiness, Karen M ; Hollingsworth, Judy ; Heilman, Douglas K ; Chong, Sonny K. F</creatorcontrib><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><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 &amp; 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&amp;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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0277-2116
ispartof Journal of pediatric gastroenterology and nutrition, 1998-01, Vol.26 (1), p.80-84
issn 0277-2116
1536-4801
language eng
recordid cdi_proquest_miscellaneous_79667682
source MEDLINE; Journals@Ovid Complete; Wiley Online Library All Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T19%3A30%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pancreatic%20Enzyme%20Supplementation%20in%20Cystic%20Fibrosis%20Patients%20Before%20and%20After%20Fibrosing%20Colonopathy&rft.jtitle=Journal%20of%20pediatric%20gastroenterology%20and%20nutrition&rft.au=Stevens,%20John%20C&rft.date=1998-01&rft.volume=26&rft.issue=1&rft.spage=80&rft.epage=84&rft.pages=80-84&rft.issn=0277-2116&rft.eissn=1536-4801&rft.coden=JPGND6&rft_id=info:doi/10.1097/00005176-199801000-00014&rft_dat=%3Cproquest_cross%3E79667682%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=79667682&rft_id=info:pmid/9443125&rfr_iscdi=true