Platelet-to-White Blood Cell Ratio Is Associated with Adverse Outcomes in Cirrhotic Patients with Acute Deterioration
- Author(s)
- Jung Hee Kim; Sung-Eun Kim; ,Do-Seon Song; Hee-Yeon Kim; Eileen L. Yoon; Tae-Hyung Kim; Young-Kul Jung; Ki Tae Suk; Baek-Gyu Jun; Hyung-Joon Yim; Jung-Hyun Kwon; Sung-Won Lee; Seong-Hee Kang; Moon-Young Kim; Soung-Won Jeong; Jae-Young Jang; Jeong-Ju Yoo; Sang-Gyune Kim; Young-Joo Jin; Gab-Jin Cheon; Byung-Seok Kim; Yeon Seok Seo; Hyung-Su Kim; Dong-Hyun Sinn; Woo-Jin Chung; Hwi Young Kim; Han Ah Lee; Seung-Woo Nam; In-Hee Kim; Jung-Il Suh; Ji-Hoon Kim; Hee-Bok Chae; Joo-Hyun Sohn; Ju-Yeon Cho; Yoon-Jun Kim; Jin-Mo Yang; Jung-Gil Park; Won Kim; Hyun-Chin Cho; Dong Joon Kim
- Keimyung Author(s)
- Chung, Woo Jin
- Department
- Dept. of Internal Medicine (내과학)
- Journal Title
- J Clin Med
- Issued Date
- 2022
- Volume
- 11
- Issue
- 9
- Keyword
- platelet-to-white blood cell ratio; acute-on-chronic liver failure; liver cirrhosis; acute decompensation; adverse outcomes
- Abstract
- Background:
The platelet-to-white blood cell ratio (PWR) is a hematologic marker of the systemic inflammatory response. Recently, the PWR was revealed to have a role as an independent prognostic factor for mortality in patients with hepatitis B virus (HBV)-related acute-on-chronic failure (ACLF) and HBV-related liver cirrhosis (LC) with acute decompensation (AD). However, the prognostic role of the PWR still needs to be investigated in LC patients with AD. In this study, we analyzed whether the PWR could stratify the risk of adverse outcomes (death or liver transplantation (LT)) in these patients.
Methods:
A prospective cohort of 1670 patients with AD of liver cirrhosis ((age: 55.2 ± 7.8, male = 1226 (73.4%)) was enrolled and evaluated for 28-day and overall adverse outcomes.
Results:
During a median follow-up of 8.0 months (range, 1.9–15.5 months), 424 (25.4%) patients had adverse outcomes (death = 377, LT = 47). The most common etiology of LC was alcohol use (69.7%). The adverse outcome rate was higher for patients with a PWR ≤ 12.1 than for those with a PWR > 12.1. A lower PWR level was a prognostic factor for 28-day adverse outcomes (PWR: hazard ratio 1.707, p = 0.034) when adjusted for the etiology of cirrhosis, infection, ACLF, and the MELD score. In the subgroup analysis, the PWR level stratified the risk of 28-day adverse outcomes regardless of the presence of ACLF or the main form of AD but not for those with bacterial infection.
Conclusions:
A lower PWR level was associated with 28-day adverse outcomes, indicating that the PWR level can be a useful and simple tool for stratifying the risk of 28-day adverse outcomes in LC patients with AD.
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