| pubmed-article:1083350 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0023895 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0010674 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0205054 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0231220 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C1998511 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0021149 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0750729 | lld:lifeskim |
| pubmed-article:1083350 | lifeskim:mentions | umls-concept:C0205373 | lld:lifeskim |
| pubmed-article:1083350 | pubmed:issue | 5 PT.1 | lld:pubmed |
| pubmed-article:1083350 | pubmed:dateCreated | 1976-7-6 | lld:pubmed |
| pubmed-article:1083350 | pubmed:abstractText | Fifteen (2.2%) of 693 patients with cystic fibrosis seen over an 18-year period developed clinical hepatic disease. In 13 patients all symptoms were secondary to portal hypertension. Ten had hypersplenism and 6 had variceal bleeding, including 3 who developed both conditions. All 5 patients who survived the initial episode of gastrointestinal bleeding underwent portal systemic shunting. A shunting procedure also was performed on 1 patients with hypersplenism but no variceal bleeding. No subsequent deterioration of intellectual function occurred in either the shunted or unshunted patients. Only 1 of the shunted patients showed progression of hepatic disease after surgery. These results suggest that portal systemic shunting is useful in the treatment of bleeding esophageal varices in cystic fibrosis. A sweat test to rule out cystic fibrosis should be included in the evaluation of any teenage or young adult patient with unexplained portal hypertension. | lld:pubmed |
| pubmed-article:1083350 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1083350 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1083350 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:1083350 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1083350 | pubmed:month | May | lld:pubmed |
| pubmed-article:1083350 | pubmed:issn | 0016-5085 | lld:pubmed |
| pubmed-article:1083350 | pubmed:author | pubmed-author:SternR CRC | lld:pubmed |
| pubmed-article:1083350 | pubmed:author | pubmed-author:IzantR JRJJr | lld:pubmed |
| pubmed-article:1083350 | pubmed:author | pubmed-author:BoatT FTF | lld:pubmed |
| pubmed-article:1083350 | pubmed:author | pubmed-author:DoershukC FCF | lld:pubmed |
| pubmed-article:1083350 | pubmed:author | pubmed-author:MatthewsL WLW | lld:pubmed |
| pubmed-article:1083350 | pubmed:author | pubmed-author:StevensD PDP | lld:pubmed |
| pubmed-article:1083350 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1083350 | pubmed:volume | 70 | lld:pubmed |
| pubmed-article:1083350 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1083350 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1083350 | pubmed:pagination | 645-9 | lld:pubmed |
| pubmed-article:1083350 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:1083350 | pubmed:meshHeading | pubmed-meshheading:1083350-... | lld:pubmed |
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| pubmed-article:1083350 | pubmed:meshHeading | pubmed-meshheading:1083350-... | lld:pubmed |
| pubmed-article:1083350 | pubmed:year | 1976 | lld:pubmed |
| pubmed-article:1083350 | pubmed:articleTitle | Symptomatic hepatic disease in cystic fibrosis: incidence, course, and outcome of portal systemic hunting. | lld:pubmed |
| pubmed-article:1083350 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1083350 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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