Quality of life assessment after Nissen fundoplication

Citation
A. Lochegnies et al., Quality of life assessment after Nissen fundoplication, ACT CHIR B, 101(1), 2001, pp. 20-24
Citations number
21
Categorie Soggetti
Surgery
Journal title
ACTA CHIRURGICA BELGICA
ISSN journal
00015458 → ACNP
Volume
101
Issue
1
Year of publication
2001
Pages
20 - 24
Database
ISI
SICI code
0001-5458(200102)101:1<20:QOLAAN>2.0.ZU;2-L
Abstract
The aim of this study was to evaluate the quality of life of 31 patients pr esenting with gastroesophageal reflux (GORD) and operated on by Nissen fund oplication. The series consisted of 23 men and 8 women; the median age was 39 years (range 22-65) and the median follow-up 36 months (range 18-74). We used a new questionnaire: the Gastrointestinal Quality of Life Index (GIQL I) that includes 36 items and uses a five graded Likert scale (from 0 to 4) giving a maximum score of 144. This score includes five dimensions : sympt oms, emotions, vitality, social relations and medical treatment. The pre- a nd postoperative GIQLI scores observed in the Nissen group and the score of a control group of 110 healthy patients were compared with each other. The preoperative score (71 +/- 21) was greatly impaired compared to the score (123 +/- 13) of the control group (p < 0.0001). The postoperative score (10 9 +/- 21) increased significantly (p < 0.0001) but remained statistically i nferior to the score of the control group (p < 0.005). The analysis of the dimensions showed that the postoperative score of the symptoms was lower in the Nissen group: 56 +/- 9 versus 66 +/- 6 in the control group (p < 0.000 5) whereas no statistical difference was found for the four other dimension s. This lower symptoms score was not due to recurrence of GORD symptoms but to the occurrence of flatulence and to the persistence of gurgling noises and gas bloating. In conclusion, the quality of life of the patients requir ing surgery for gastroesophageal reflux was greatly impaired, it largely im proved after Nissen fundoplication but did not reach the level of healthy p atients because of unrelated GORD gastrointestinal symptoms.