Epidemiological Study of Chronic Blood-Borne Viral Hepatitis in a Tertiary Care Facility in Al-Baha, Saudi Arabia: Associations with Liver Enzymes and Treatment Results - Scorecard - MDSpire
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Epidemiological Study of Chronic Blood-Borne Viral Hepatitis in a Tertiary Care Facility in Al-Baha, Saudi Arabia: Associations with Liver Enzymes and Treatment Results
Clinical Scorecard: Epidemiological Study of Chronic Blood-Borne Viral Hepatitis in a Tertiary Care Facility in Al-Baha, Saudi Arabia: Associations with Liver Enzymes and Treatment Results
At a Glance
Category
Detail
Condition
Chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections
Key Mechanisms
Persistent viral infection causing liver inflammation, biochemical and histological liver disease, risk of cirrhosis and hepatocellular carcinoma
Target Population
Patients with chronic HBV or HCV infections attending a tertiary care hospital in Al-Baha region, Saudi Arabia
Care Setting
Tertiary care hospital (King Fahd Hospital), regional referral center
Key Highlights
HBV remains a significant health problem in Saudi Arabia despite vaccination programs, with ongoing cases of cirrhosis, hepatocellular carcinoma, and liver-related deaths.
HCV affects approximately 0.7% of the Saudi population with many untreated cases leading to risk of advanced liver disease.
Regional epidemiological data from Al-Baha is limited; this study uses retrospective clinical data from 2019-2022 to assess prevalence, liver enzyme associations, and treatment outcomes.
Guideline-Based Recommendations
Diagnosis
Chronic HBV defined by persistent HBsAg for ≥6 months or ongoing HBV DNA beyond acute phase.
Chronic HCV defined by presence of anti-HCV antibodies and detectable HCV RNA with evidence of chronic hepatitis beyond 4–6 months.
Use of ELISA and confirmatory immune assays for serological diagnosis.
Quantitative PCR assays for HBV DNA and HCV RNA viral load measurement.
Management
HBV vaccination as preventive measure; no vaccine available for HCV.
Direct-acting antiviral (DAA) therapy recommended for HCV with >95% cure rates.
Treatment decisions based on viral load, liver enzyme levels, and clinical assessment.
Monitoring and managing complications such as cirrhosis and hepatocellular carcinoma.
Monitoring & Follow-up
Regular liver function tests including ALT, AST, bilirubin, ALP, and GGT.
Follow-up viral load testing to assess treatment response and sustained virological response (SVR).
Clinical and biochemical monitoring for disease progression.
Risks
Risk of progression to decompensated cirrhosis and hepatocellular carcinoma if untreated.
Limited access to diagnosis and treatment increases risk of advanced disease.
Incomplete treatment adherence and follow-up may affect outcomes.
Patient & Prescribing Data
Patients with confirmed chronic HBV or HCV infection attending King Fahd Hospital in Al-Baha region.
Data on antiviral regimens and baseline labs were complete for treated patients; however, treatment duration, adherence, and follow-up viral load data were incomplete due to retrospective study design.
Clinical Best Practices
Implement mass HBV vaccination programs to reduce incidence.
Ensure early diagnosis through serological and molecular testing to initiate timely treatment.
Utilize direct-acting antivirals for HCV to achieve high cure rates.
Maintain comprehensive patient records to monitor treatment adherence and outcomes.
Conduct regular liver enzyme and viral load monitoring to guide management.
Address regional disparities by improving access to diagnosis and treatment in under-investigated areas like Al-Baha.