Background: Human immunodeficiency virus (HIV), hepatitis B and C viruses (HBV and HCV), and dual or triple infections are serious public health issues. While most medications have significantly improved the management of mono-infections,...
moreBackground: Human immunodeficiency virus (HIV), hepatitis B and C viruses (HBV and HCV), and dual or triple infections are serious public health issues. While most medications have significantly improved the management of mono-infections, triple co-infection may be a greater challenge in the future. The aim is to determine triple Co-infection of hepatitis B, C and HIV at the Tertiary care centre of Northern India. Material and Methods: The present study was conducted at the Department of Medical Gastroenterology, Post Graduate Institute of Medical Sciences, North India. A total of 30,000 serum samples of Hepatitis B (11, 500), Hepatitis C (12000) and HIV (6500) confirmed patients were tested for co-infection with other viruses. Results: Out of the total pool of 30,000 patients, triple co-infection was seen only in 46 patients (0.15%), and except for one, all were male, the majority in the younger age group, sexually active and were intravenous drug abusers. Of the total pool of 30,000 patients, only 46 (0.15%) had triple co-infection. Of these 46 patients, 45 were male (97.77%), and 1 was female (2.23%). The largest number of patients were young males in the 20-30 years age group, i.e., 35 (76.08%), followed by the 30-40 years age group, with 6 patients (13.04%). There was predominance of patients belonging to rural background, i.e., 33 patients (71.73%), and only 13 patients (28.27%) resided in urban areas. In the marital analysis, 32 patients (69.56%) were unmarried, and 14 patients (31.44%) were married. Out of the total 46 patients, 35 (72.5%) gave a history of intravenous drug abuse, alcohol intake and were smokers. In the total study group of 46 patients, 28 (60.86%) had a history of previous surgery and tattooing. In the total pool of 46 patients, only 6 (13.04%) were admitted for having multiple sexual partners. Of 46 patients, 44 (95.65%) were non-cirrhotic, 1 (2.17%) had significant fibrosis (fibroscan score>7 kPa), and 1 (2.17%) was cirrhotic. All 46 patients were on the HARRT with TLE regimen, containing tenofovir & lamivudine, which have antiviral activity against HBV. All of them were treated with oral directly acting antivirals (DAA's) for HCV. Of 46 patients, 43 (93.47%) achieved sustained virological response, similar to what is seen in mono-infected HCV patients. Conclusion: The HBV, HCV and HIV triple co-infection was extremely low, that too in the hotspot of HBV & HCV mono and dual infections and is a positive sign. It can be attributed to mandatory HBV vaccination of every HIV and HCV patient, along with a multi-pronged strategy of reducing high-risk behaviour. Moreover, early detection and treatment of mono-infections reduced the risk of developing dual or triple co-infections in the future.