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

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

  • By

  • Talal A. Sallam

  • Rabei M. El-Badry

  • Turki H. Alkully

  • Hasan H. Alfahemi

  • Muhammad A. Halwani

  • Khaled I. Alzahrani

  • Manal A. Alghamdi

  • January 12, 2026

  • 0 min

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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

CategoryDetail
ConditionChronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections
Key MechanismsPersistent viral infection causing liver inflammation, biochemical and histological liver disease, risk of cirrhosis and hepatocellular carcinoma
Target PopulationPatients with chronic HBV or HCV infections attending a tertiary care hospital in Al-Baha region, Saudi Arabia
Care SettingTertiary 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.

References

Original Source(s)

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