Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis

doi:10.3748/wjg.v21.i1.318

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Jan 7, 2015 (publication date) through Apr 25, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Jan 7, 2015; 21(1): 318-325
Published online Jan 7, 2015. doi: 10.3748/wjg.v21.i1.318

Table 3 Forced expired volume in 1 s (% predicted) comparing study patients and controls in the 5-year period prior to the study

FEV1	Study group		Control group		P-value
FEV1	n	Mean % predicted ± SD	n	Mean % predicted ± SD	P-value
1^st yr	17	68.8 ± 19.5	22	70.0 ± 16.9	0.837
2^nd yr	21	66.6 ± 19.1	29	71.0 ± 16.3	0.386
3^rd yr	21	69.7 ± 21.0	25	69.9 ± 18.2	0.978
4^th yr	21	67.7 ± 20.4	29	68.5 ± 18.6	0.876
5^th yr	22	70.7 ± 20.1	17	68.5 ± 19.8	0.691

Study group: Cystic fibrosis patients diagnosed with distal intestinal obstruction syndrome; Control group: Cystic fibrosis patients; n: Number of patients; SD: Standard deviation; FEV1: Forced expired volume after 1 s of blowing out; SD: Standard deviation. A P < 0.05 is considered statistically significant.

Citation: Lavie M, Manovitz T, Vilozni D, Levy-Mendelovich S, Sarouk I, Weintraubv I, Shoseyov D, Cohen-Cymberknoh M, Rivlin J, Efrati O. Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis. World J Gastroenterol 2015; 21(1): 318-325
URL: https://www.wjgnet.com/1007-9327/full/v21/i1/318.htm
DOI: https://dx.doi.org/10.3748/wjg.v21.i1.318