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2.
Science ; 376(6596): 906-907, 2022 05 27.
Article in English | MEDLINE | ID: covidwho-1865138
3.
World J Gastroenterol ; 27(47): 8199-8200, 2021 Dec 21.
Article in English | MEDLINE | ID: covidwho-1580315

ABSTRACT

In 2016, the World Health Assembly adopted a Global Health Sector Strategy on viral hepatitis, with targets set for the years 2020 and 2030 to achieve hepatitis elimination. The main target of hepatitis elimination strategy is to reduce the incidence of hepatitis B virus (HBV) and hepatitis C virus (HCV) by 90% and mortality by 65% in 2030. In last 5 years, the number of people receiving HCV treatment has increased from 1 million to 9.4 million; however, this number is far from the 2030 target of 40 million people receiving HCV treatment. HBV and HCV incidence rates are down from 1.4 million to 1.1 million annual deaths but this is far from the 2030 target of < 0.5 million deaths. The coronavirus disease 2019 pandemic has severely affected the efforts in the fight against hepatitis. No major donor has committed to investing in the fight against hepatitis. Time is running out. There is a need to speed up efforts in the fight against hepatitis to achieve hepatitis elimination by 2030.


Subject(s)
COVID-19 , Hepatitis B , Hepatitis C , Hepatitis, Viral, Human , Antiviral Agents/therapeutic use , Global Health , Hepacivirus , Hepatitis B/diagnosis , Hepatitis B/drug therapy , Hepatitis B/epidemiology , Hepatitis C/diagnosis , Hepatitis C/drug therapy , Hepatitis C/epidemiology , Hepatitis, Viral, Human/drug therapy , Humans , SARS-CoV-2
4.
World J Gastroenterol ; 27(26): 4004-4017, 2021 Jul 14.
Article in English | MEDLINE | ID: covidwho-1319755

ABSTRACT

Chronic viral hepatitis is a significant health problem throughout the world, which already represents high annual mortality. By 2040, chronic viral hepatitis due to virus B and virus C and their complications cirrhosis and hepatocellular carcinoma will be more deadly than malaria, vitellogenesis-inhibiting hormone, and tuberculosis altogether. In this review, we analyze the global impact of chronic viral hepatitis with a focus on the most vulnerable groups, the goals set by the World Health Organization for the year 2030, and the key points to achieve them, such as timely access to antiviral treatment of direct-acting antiviral, which represents the key to achieving hepatitis C virus elimination. Likewise, we review the strategies to prevent transmission and achieve control of hepatitis B virus. Finally, we address the impact that the coronavirus disease 2019 pandemic has had on implementing elimination strategies and the advantages of implementing telemedicine programs.


Subject(s)
COVID-19 , Hepatitis B, Chronic , Hepatitis C, Chronic , Hepatitis, Viral, Human , Liver Neoplasms , Antiviral Agents/therapeutic use , Hepatitis B, Chronic/diagnosis , Hepatitis B, Chronic/drug therapy , Hepatitis B, Chronic/epidemiology , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/drug therapy , Hepatitis C, Chronic/epidemiology , Hepatitis, Viral, Human/diagnosis , Hepatitis, Viral, Human/drug therapy , Hepatitis, Viral, Human/epidemiology , Humans , Liver Neoplasms/drug therapy , Liver Neoplasms/epidemiology , Liver Neoplasms/prevention & control
5.
AIDS Res Hum Retroviruses ; 37(8): 585-588, 2021 08.
Article in English | MEDLINE | ID: covidwho-1272954

ABSTRACT

In 2016, the World Health Organization developed a plan for viral hepatitis elimination by 2030. Globally, control of hepatitis B virus (HBV) and hepatitis C virus (HCV) are the most challenging aspects of viral hepatitis elimination. In many developed countries elimination of HBV could be targeted to special populations mostly immigrants from low resource settings. Elimination of HCV, however, remains a challenge globally. Barriers to HCV elimination include high cost of medications and the ability to engage specific at-risk populations as well as individuals who are out of medical care. In the context of the coronavirus disease 2019 (COVID-19) pandemic, treatment access and screening have been further negatively impacted by social distancing rules and COVID-19-related anxieties. This threatens to throw most countries off course in their elimination efforts. Before the pandemic, some states in the United States had scaled up their elimination efforts with plans to ramp up testing and treatment using Netflix-like payment models for HCV direct acting antiviral drugs. Most of these efforts have stalled on account of the health system's focus on COVID-19 control. To prevent further delays in achieving elimination targets, programs would need to explore new models of care that address COVID-19-related access hurdles. Systems that leverage technologies such as telemedicine and self-testing could help maintain treatment levels. Mathematical models estimate that COVID-19-related delays in 2020 could lead to 44,800 hepatocellular cancers and 72,300 liver-related deaths for the next decade.


Subject(s)
COVID-19/epidemiology , Disease Eradication/statistics & numerical data , Hepatitis, Viral, Human/epidemiology , Antiviral Agents/therapeutic use , Goals , Hepatitis C/diagnosis , Hepatitis C/drug therapy , Hepatitis C/epidemiology , Hepatitis, Viral, Human/diagnosis , Hepatitis, Viral, Human/drug therapy , Humans , Pandemics , SARS-CoV-2 , Time Factors
6.
ChemMedChem ; 16(9): 1403-1419, 2021 05 06.
Article in English | MEDLINE | ID: covidwho-1064335

ABSTRACT

Nucleoside and nucleotide analogues are structurally similar antimetabolites and are promising small-molecule chemotherapeutic agents against various infectious DNA and RNA viruses. To date, these analogues have not been documented in-depth as anti-human immunodeficiency virus (HIV) and anti-hepatitis virus agents, these are at various stages of testing ranging from pre-clinical, to those withdrawn from trials, or those that are approved as drugs. Hence, in this review, the importance of these analogues in tackling HIV and hepatitis virus infections is discussed with a focus on the viral genome and the mechanism of action of these analogues, both in a mutually exclusive manner and their role in HIV/hepatitis coinfection. This review encompasses nucleoside and nucleotide analogues from 1987 onwards, starting with the first nucleoside analogue, zidovudine, and going on to those in current clinical trials and even the drugs that have been withdrawn. This review also sheds light on the prospects of these nucleoside analogues in clinical trials as a treatment option for the COVID-19 pandemic.


Subject(s)
Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , Hepatitis, Viral, Human/drug therapy , Nucleosides/therapeutic use , Nucleotides/therapeutic use , COVID-19/epidemiology , Clinical Trials as Topic , Drug Repositioning , HIV/drug effects , HIV/enzymology , HIV Reverse Transcriptase/antagonists & inhibitors , Hepatitis Viruses/drug effects , Hepatitis Viruses/enzymology , Humans , Pandemics , RNA-Dependent RNA Polymerase/antagonists & inhibitors , Reverse Transcriptase Inhibitors/therapeutic use , SARS-CoV-2/drug effects , COVID-19 Drug Treatment
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