In Ethiopia, cirrhosis of the liver is the cause of close to one-third of deaths in adult medical wards [8]. However, the predictors of in-hospital mortality among cirrhotic patients have not been well-studied. This study aimed to assess these factors in two referral teaching hospitals and one medical center with specialized gastroenterology and hepatology services. A total of 356 cirrhotic patients were admitted to the three health facilities during the study period, of which, 299 patients fulfilled the inclusion criteria and were included in the final analysis. The majority (79.6%) of patients were males. The median age of the study participants was 45 (IQR, 36–56) years and Hepatitis B virus (32.1%) was the most common etiology. More than half (52.9%) of the patients were in the Child-Pugh class C category. The prevalence of in-hospital mortality was 25.4%. In the binary logistic regression, history of previous admission within one one-year period, Grade III or IV hepatic encephalopathy, AKI, HCC, and MELD-Na Score were found to be significantly associated with in-hospital mortality.
The median age of the patients admitted to the hospitals was 45 (IQR, 36–56) years. This relatively young age is concerning, as cirrhosis can significantly impact patients' quality of life and life expectancy. This can have major socioeconomic consequences and can lead to disability, lost productivity, and the need for significant medical care and support. A similar age group was reported in Ethiopia [9] and other African studies [11–13]. However, this age is lower than those found in previous US [14] and European [15] research. This could be because of the high viral hepatitis burden and a limited access to quality healthcare and liver disease screening in many African settings which can lead to delayed diagnoses, allowing earlier stages of hepatitis to progress further before patients receive appropriate management.
The majority (79.6%) of the patients in this study were males. A higher prevalence of cirrhosis in males was reported in multiple other studies [16–18]. The higher prevalence of liver cirrhosis and its complications in men is likely due to a combination of behavioral factors such as alcohol consumption, and biological factors such as lower levels of estrogen, which have been shown to have anti-fibrotic and anti-inflammatory effects on the liver that collectively increase their susceptibility to the development and progression of various liver diseases leading to cirrhosis [19].
In our study, the most common etiology was hepatitis B virus (32.1%) followed by alcohol (30.1%) and hepatitis C virus (13.4%). HBV was also reported as the leading cause of cirrhosis in other studies conducted in Ethiopia [7, 9]. Similar results were observed in research done in Togo [20], Ghana [21], Nigeria [22], and other Sub-Saharan African countries [23]. HCV is the major cause of cirrhosis in the Eastern Mediterranean region[2, 24] and North Africa [25, 26]. Alcohol was the dominant etiology in reports from India [18, 27], Thailand [28], and Colombia[16]. Although lower than the global average, the peculiar finding in our study, when compared to other similar studies in Ethiopia, is the increasing prevalence of alcohol related liver disease and MASLD. This can be linked to the increasing trends in hazardous alcohol consumption[29] and metabolic risk factors for MASLD such as diabetes[30] in Ethiopia. This was also evident in our study, which revealed that 17.1% of the patients had diabetes and 26.1% of the patients had comorbidities. This represents a substantial change from an earlier Ethiopian study that reported the prevalence of diabetes and comorbidities in general to be 6.4% and 11% respectively [10]. This finding aligns with the global pattern that indicates the impending eclipse of the influence of viral hepatitis by emergent metabolic CLDs [2].
Ascites (69.2%), UGIB (50.5%), and hepatic encephalopathy (44.8%) were the most common presentations in this study. This finding significantly differs from those of former studies conducted in Ethiopia which reported UGIB to be present in 10.2% and 25.7% of the cases [9, 10]. The figure in our study is also higher than those reported by researchers from the United States (8.6%), Madagascar (33.3%), and Colombia (17.3%) [11, 14, 16]. The primary reason for this is that patients are usually referred to these centers for therapeutic endoscopic interventions due to the restricted availability of these services at other hospitals. The most frequent precipitant of hepatic encephalopathy in our patients was likewise discovered to be UGIB, which may account for why our study's prevalence of hepatic encephalopathy was higher than that of previous investigations.
In this study, the in-hospital mortality rate was 25.4%. This is comparable with the 25.9% and 23.5% in-hospital mortality rates that have been reported from studies previously conducted in Madagascar and Colombia, respectively [11, 16]. However, this percentage was less than that reported by studies carried out in Saudi Arabia (35%), Ghana (41.9%), and the Ivory Coast (42.2%) and much greater than that reported in Pakistan (15.7%), Morocco (8.7%), and the US (6.6%). These discrepancies may have resulted from variances in the study settings, as the study in Saudi Arabia included patients admitted to the ICU, and the baseline characteristics of the patients. These attributes include the stage of the disease, related comorbidities, specific complications of liver cirrhosis that resulted in hospitalization, and the clinical condition of the patients at admission. The higher mortality rate seen in the current study compared to that of the US, Pakistan, and Morocco can also be attributed to patients' delayed presentations and the lack of treatment options, such as shunt surgeries, which serve as a bridge to more definitive options such as liver transplantation nationwide.
Hepatic encephalopathy is one of the most common complications of liver cirrhosis and results in a spectrum of neuropsychiatric symptoms caused by circulating gut-derived toxins of nitrogenous compounds. West Haven Grade III or IV hepatic encephalopathy was found to be an independent predictor of in-hospital mortality. Multiple similar findings were reported from Ghana, Morocco, Madagascar, and the United States [11, 25, 31, 32]. This underlines the need for prompt identification of hepatic encephalopathy and its precipitant at an earlier stage, followed by proper management.
History of previous admission within one year was 33.1% and was also found to be a predictor of in-hospital mortality in the logistic regression. A similar finding was reported in Spain and Canada [33, 34]. One possible explanation for the greater death rate in our patients with a history of readmission could be the substantially greater prevalence of hepatic encephalopathy (59.6% vs. 37.5%) in this group of patients than in the patients without such a history. Hepatic encephalopathy was also found to increase readmission and mortality in a study conducted in Italy [35]. This may also be exacerbated by the unavailability of rifaximin in Ethiopia, which has been demonstrated to lower the risk of overt hepatic encephalopathy recurrence [36].
Patients with cirrhosis may have acute kidney damage (AKI) for a variety of reasons. Some of these include hepatorenal syndrome (HRS), which is characterized by renal vasoconstriction secondary to splanchnic pooling of blood that reduces the effective circulating blood volume; decreased renal perfusion due to gastrointestinal bleeding; use of diuretics; diarrhea caused by the use of lactulose or infections; and so on [37]. Regardless of the etiology, AKI was associated with increased in-hospital mortality in our study, which is similar to the findings of studies in the United States and Turkey [38, 39]. This was also demonstrated in another systematic review and meta-analysis [40].
The MELD Na score was also found to be an independent predictor of in-hospital mortality in our study. Similar studies performed in Brazil, and Poland also showed that the MELD Na score predicts in-hospital mortality in cirrhotic patients [41, 42].
HCC was the other predictor of hospital mortality in this study. Similar findings were reported in other Sub-Saharan African countries such as Ivory Coast and Ghana [13, 43]. However, the presence of HCC was not found to be a predictor of in-hospital mortality in research done in the US [14]. Because of poor screening and surveillance of HCC in cirrhotic patients, 95% of HCC cases in Sub-Saharan Africa are diagnosed late in the advanced or terminal stages, whereas 40% of cases in high-income countries are diagnosed at an early stage [44]. This, combined with the very limited availability of curative therapies, may have contributed to the results observed in our study.
UGIB was not shown to predict in-hospital mortality. The literature shows mixed results on the effect of UGIB on in-hospital mortality. A previous study done in Ethiopia [10] and another study conducted in Ghana [12] showed a significant association. In contrast, a study from France [45] showed a different result. Endoscopic therapy and antibiotic prophylaxis were shown to be independent predictors of survival in the French study. The reduced mortality found in our study could be due to the relatively better availability of interventional endoscopic services in the centers where our research was conducted, coupled with the current standard use of short-term antibiotic prophylaxis for SBP.
The major limitation of our study emanates from its retrospective design. The information collected from the electronic medical records included medical history, physical examination, and laboratory and imaging investigations ordered and documented by the treating physicians. This led us to remove some important parameters, such as nutritional status assessment with body mass index, from our study because these parameters were not available in almost all of the patient files. A significant number of patients were also excluded from the study because of multiple missing variables in their workups.