Prospective validation of the short form liver disease quality of life instrument

被引:47
作者
Kanwal, F. [3 ,4 ,5 ]
Spiegel, B. M. R. [5 ,6 ]
Hays, R. D. [2 ,6 ]
Durazo, F. [6 ]
Han, S. B. [6 ,7 ]
Saab, S. [6 ]
Bolus, R. [5 ]
Kim, S. J. [5 ]
Gralnek, I. M. [1 ]
机构
[1] Technion Israel Inst Technol, Rappaport Fac Med, Dept Gastroenterol, Rambam Med Ctr, IL-31096 Haifa, Israel
[2] RAND Corp, Santa Monica, CA USA
[3] St Louis Univ, Div Gastroenterol, St Louis, MO 63103 USA
[4] John Cochran VA Med Ctr, St Louis, MO USA
[5] Univ Calif Los Angeles, Ctr Outcomes Res & Educ, Los Angeles, CA USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Dept Internal Med, Los Angeles, CA 90095 USA
[7] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA
关键词
D O I
10.1111/j.1365-2036.2008.03817.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Despite the realization that health-related quality of life (HRQOL) is an important outcome in patients with liver disease, there is scarcity of disease-targeted HRQOL measures that have undergone prospective evaluation. Aim To validate prospectively the short form of liver disease quality of life instrument (the SF-LDQOL) in patients with advanced liver disease. Methods The SF-LDQOL includes 36 disease-targeted items representing nine domains: symptoms of liver disease, effects of liver disease, memory/concentration, sleep, hopelessness, distress, loneliness, stigma of liver disease and sexual problems. We administered the SF-LDQOL to 156 advanced liver disease patients at baseline and at 6-month follow-up. We estimated internal consistency reliability for multi-item scales, item discrimination across scale and evaluated construct validity by estimating the associations of SF-LDQOL scores with SF-36 scores, symptom severity and disability days. To evaluate the SF-LDQOL's responsiveness, we compared HRQOL changes for patients who received with those who did not receive liver transplantation (LT). Results The internal consistency reliability coefficients were >= 0.70 for seven of nine scales in baseline and for all scales in follow-up administration. The SF-LDQOL correlated highly with SF-36 scores, symptom severity, disability days and global health. Patients undergoing LT reported improved HRQOL compared with patients without LT and the responsiveness indices were excellent. Conclusions This study provides support for the reliability and validity of the SF-LDQOL in patients with advanced chronic liver disease. This instrument may be useful in everyday clinical practice and in future clinical trials.
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页码:1088 / 1101
页数:14
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