Frailty predicts mortality in patients with upper gastrointestinal bleed: a prospective cohort study

被引:1
作者
Guliyara, Mohammed Affan [1 ,2 ]
Ermerak, Goktug [1 ]
Levy, Miriam [1 ,2 ]
Koo, Jenn Hian [1 ,2 ]
Bassan, Milan [1 ,2 ,3 ]
机构
[1] Liverpool Hosp, Dept Gastroenterol & Hepatol, Liverpool, NSW, Australia
[2] Univ New South Wales, South Western Sydney Clin Sch, Kensington, NSW, Australia
[3] Liverpool Hosp, Dept Gastroenterol & Hepatol, Corner Elizabeth & Goulburn St, Liverpool, NSW 2170, Australia
关键词
Charlson comorbidity index; Clinical frailty scale; Upper gastrointestinal bleeding; OUTCOMES; IMPACT;
D O I
10.1111/jgh.16188
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimEvidence on the impact of frailty in patients with upper gastrointestinal bleed (UGIB) is limited. This study aims to define the role of frailty as defined by Canadian Study of Health and Aging clinical frailty scale (CSHA-CFS) in predicting mortality in UGIB. MethodsA prospective single-center cohort study was conducted over 21 months on all consecutive patients with UGIB. Data on demographics, lab parameters, Glasgow Blatchford score, CSHA-CFS, Charlson Comorbidity Index, and AIMS65 score was recorded. The primary outcome was all-cause inpatient mortality. The secondary outcomes were all-cause 30-day mortality, 30-day rebleeding, 30-day readmission, hospital length of stay (LoS), intensive care unit (ICU) admission, need for repeat endoscopy, and need for blood transfusion. The data were evaluated using univariate and multivariate analysis. ResultsThere were 298 eligible patients, of which 63% were males, median age was 68 years, 44% were from non-English-speaking background, and 72% had major comorbidities. The all-cause inpatient and 30-day mortality were 9.4% and 10.7%, respectively. In the multivariate analysis, CHSA-CFS was the independent predictor of all-cause inpatient mortality (OR 1.66; 95% CI 1.13-2.143; P = 0.010) and all-cause 30-day mortality (OR 1.83; 95% CI 1.26-2.67; P = 0.002). CHSA-CFS was not a significant predictor of 30-day rebleed, 30-day readmission, ICU admission, hospital LoS, or need for blood transfusion. ConclusionFrailty is an important independent predictor of mortality in patients with UGIB. Frailty assessment can guide clinical decision making and allow targeting of health-care resource (Australia/New Zealand Clinical Trial Registry number: ACTRN12622000821796).
引用
收藏
页码:1292 / 1298
页数:7
相关论文
共 23 条
  • [1] Evaluating the impact of frailty on periprocedural adverse events and mortality among patients with GI bleeding
    Acosta, Camilo J.
    Goldberg, David
    Amin, Sunil
    [J]. GASTROINTESTINAL ENDOSCOPY, 2021, 94 (03) : 517 - +
  • [2] Adler DG, 2004, GASTROINTEST ENDOSC, V60, P497
  • [3] [Anonymous], 2013, AC UPP GASTR BLEED A
  • [4] Bennie Ray Upchurch, 2021, UPP GASTR BLEED UGIB
  • [5] Charlson Comorbidity Index: A Critical Review of Clinimetric Properties
    Charlson, Mary E.
    Carrozzino, Danilo
    Guidi, Jenny
    Patierno, Chiara
    [J]. PSYCHOTHERAPY AND PSYCHOSOMATICS, 2022, 91 (01) : 8 - 35
  • [6] Mortality in Acute Upper Gastrointestinal Bleeding Is Uncommonly due to Persistent Hemorrhage
    Chason, Rebecca
    Singal, Amit
    Rockey, Don
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2013, 108 : S490 - S491
  • [7] Frailty in elderly people
    Clegg, Andrew
    Young, John
    Iliffe, Steve
    Rikkert, Marcel Olde
    Rockwood, Kenneth
    [J]. LANCET, 2013, 381 (9868) : 752 - 762
  • [8] Systematic Review of the Predictors of Recurrent Hemorrhage After Endoscopic Hemostatic Therapy for Bleeding Peptic Ulcers
    Elmunzer, B. Joseph
    Young, Scott D.
    Inadomi, John M.
    Schoenfeld, Philip
    Laine, Loren
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (10) : 2625 - 2632
  • [9] Kita S., 2022, COMP VARIOUS RISK SC, DOI [10.1186/s12245-020-00293-x, DOI 10.1186/S12245-020-00293-X]
  • [10] Frailty is independently associated with mortality in 11 001 patients with inflammatory bowel diseases
    Kochar, Bharati
    Cai, Winston
    Cagan, Andrew
    Ananthakrishnan, Ashwin N.
    [J]. ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2020, 52 (02) : 311 - 318