| Literature DB >> 34326624 |
Yu-Pei Zhuang1, Hao-Jie Zhong1.
Abstract
The coronavirus disease 2019 (COVID-19) pandemic has greatly impacted health systems. Many guidelines on chronic liver diseases have been released to optimize the use of medical resources and patient management. However, most of these guidelines have been established through expert consensus because the existing data do not provide strong evidence for developing effective recommendations. As Wilson disease (WD) is a rare chronic liver disease, the impact of COVID-19 on the clinical status of patients with WD is unclear. The present study showed a marked shortage of medical resources for clinically managing patients with WD during the pandemic. Although patients with WD who consistently took anticopper therapy showed no significant differences in hepatic and extrahepatic markers before and after the pandemic, their complication incidences, especially the infection incidence, were significantly increased during the study period. Therefore, patients with WD should be encouraged to adhere to anticopper therapy and be closely monitored to prevent infections and other complications. The present study provides a clinical basis for further managing WD during the pandemic. ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.Entities:
Keywords: Anticopper therapy; Clinical status; Complications; Coronavirus disease 2019; Infections; Wilson disease
Year: 2021 PMID: 34326624 PMCID: PMC8311527 DOI: 10.3748/wjg.v27.i26.4248
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742
Clinical features and complications in patients with Wilson disease before and after coronavirus disease 2019
| Before COVID-19 ( | After COVID-19 ( |
| |
| Demographic characteristics | |||
| Age (yr) | 28.00 (23.00–33.00) | - | |
| Male sex | 37 (54.41) | - | |
| Hepatic features | |||
| Elevated ALT (> 40 U/L) | 16 (23.53) | 12 (17.65) | 0.424 |
| Elevated AST (> 35 U/L) | 13 (19.12) | 17 (25.00) | 0.388 |
| Elevated bilirubin (> 17.1 µmol/L) | 15 (22.06) | 13 (19.12) | 0.754 |
| Hypoproteinemia (albumin < 35 g/L) | 10 (14.71) | 12 (17.65) | 0.774 |
| Elevated PT (> 15 s) | 11 (16.18) | 13 (19.12) | 0.791 |
| Elevated INR (> 1.5) | 1 (1.47) | 2 (2.94) | 1.000 |
| Child-Pugh | 1.000 | ||
| A | 64 (94.12) | 65 (95.59) | |
| B/C | 4 (5.88) | 3 (4.41) | |
| Cirrhosis | 57 (83.82) | 57 (83.82) | 1.000 |
| Extrahepatic features | |||
| Neurological manifestations | 50 (73.5) | 49 (72.1) | 1.000 |
| Psychiatric manifestations | 3 (4.4) | 4 (5.9) | 1.000 |
| Kayser-Fleischer ring | 32 (47.1) | 35 (51.5) | 0.375 |
| Splenomegaly/splenectomy | 45 (66.2) | 47 (69.1) | 0.688 |
| Complications | |||
| Any complication | 8 (11.76) | 16 (23.53) | 0.021 |
| Ascites | 2 (1.5) | 5 (7.4) | 0.375 |
| Infections | 1 (1.5) | 8 (11.8) | 0.016 |
| Respiratory infection | 0 (0) | 5 (7.4) | 0.063 |
| Urinary infection | 0 (0) | 1 (1.5) | 1.000 |
| Gastrointestinal infection | 1 (1.5) | 2 (2.9) | 1.000 |
| SBP | 0 (0) | 1 (1.5) | 1.000 |
| PVT | 0 (0) | 0 (0) | - |
| Gastroesophageal varices | 5 (7.4) | 7 (10.3) | 0.500 |
| Variceal bleeding | 0 (0) | 1 (1.5) | 1.000 |
| Hepatic encephalopathy | 0 (0) | 0 (0) | - |
| Renal impairment | 0 (0) | 0 (0) | - |
| Liver failure | 0 (0) | 0 (0) | - |
| HCC | 0 (0) | 0 (0) | - |
Data are presented as medians (interquartile ranges) or n (%). ALT: Alanine transaminase; AST: Aspartate transaminase; HCC: Hepatocellular carcinoma; INR: International normalized ratio; PT: Prothrombin time; PVT: Portal vein thrombosis; SBP: Spontaneous bacterial peritonitis; COVID-19: Coronavirus disease 2019.