scholarly journals Pancreatitis in A Patient with Cystic Fibrosis Taking Ivacaftor

Children ◽  
2020 ◽  
Vol 7 (1) ◽  
pp. 6 ◽  
Author(s):  
Argyri Petrocheilou ◽  
Athanasios G. Kaditis ◽  
Ioanna Loukou

Pancreatitis is rare in pancreatic insufficient cystic fibrosis patients. While pancreatic insufficiency has been considered irreversible until now, in the current era of new therapies with modulators of the Cystic Fibrosis Transmembrane Regulator CFTR channel, there are reports of improvement of pancreatic exocrine function. We describe the case of an adolescent with cystic fibrosis who developed pancreatitis after the partial recovery of pancreatic function while taking ivacaftor. This case adds to the limited body of evidence that CFTR modulators lead to the improvement of pancreatic exocrine function in cystic fibrosis.

Suizo ◽  
2017 ◽  
Vol 32 (4) ◽  
pp. 699-705
Author(s):  
Hiroshi ISHIGURO ◽  
Kotoyo FUJIKI ◽  
Shiho KONDO ◽  
Miyuki NAKAKUKI ◽  
Yuka KOZAWA ◽  
...  

2017 ◽  
Author(s):  
Sabina Sabharwal

Although cystic fibrosis (CF) has historically been considered a pulmonary disease, with the increasing life expectancy of these patients, gastrointestinal manifestations are becoming more important. Moreover, nutritional status is closely linked to pulmonary function and, thus, overall mortality. This review discusses gastrointestinal (including nutritional, pancreatic, and hepatobiliary) manifestations of CF and their management. It also discusses studies that have been critical to our understanding of these manifestations of CF. This review contains 1 figure, 1 table, and 36 references. Key words: body mass index, constipation, cystic fibrosis transmembrane regulator, distal intestinal obstruction syndrome, pancreatic insufficiency


2017 ◽  
Author(s):  
Sabina Sabharwal

Although cystic fibrosis (CF) has historically been considered a pulmonary disease, with the increasing life expectancy of these patients, gastrointestinal manifestations are becoming more important. Moreover, nutritional status is closely linked to pulmonary function and, thus, overall mortality. This review discusses gastrointestinal (including nutritional, pancreatic, and hepatobiliary) manifestations of CF and their management. It also discusses studies that have been critical to our understanding of these manifestations of CF. This review contains 1 figure, 1 table, and 36 references. Key words: body mass index, constipation, cystic fibrosis transmembrane regulator, distal intestinal obstruction syndrome, pancreatic insufficiency


2005 ◽  
Vol 7 (3) ◽  
pp. 227-233 ◽  
Author(s):  
Susan S. Baker ◽  
Drucy Borowitz ◽  
Robert D. Baker

1984 ◽  
Vol 18 (11) ◽  
pp. 1107-1111 ◽  
Author(s):  
Mitchell E Geffner ◽  
Barbara M Lippe ◽  
Solomon A Kaplan ◽  
Robert M Itami ◽  
Baiba K Gillard ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A214-A214
Author(s):  
M VENTRUCCI ◽  
V PAOLETTI ◽  
L CORVAGLIA ◽  
M CAPRETTI ◽  
M MIDDONNO ◽  
...  

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