• Tidak ada hasil yang ditemukan

Hepatitis C elimination by 2030 in Malaysia: an achievable goal? rosmawati Mohamed

N/A
N/A
Protected

Academic year: 2024

Membagikan "Hepatitis C elimination by 2030 in Malaysia: an achievable goal? rosmawati Mohamed"

Copied!
1
0
0

Teks penuh

(1)

Letter

Journal of Virus Eradication 2019; 5 : 253

253

© 2019 the Authors. Journal of Virus Eradication published by Mediscript Ltd

this is an open access article published under the terms of a Creative Commons License.

Hepatitis C elimination by 2030 in Malaysia: an achievable goal?

rosmawati Mohamed1, Fatiha H Shabaruddin2*, Amirah Azzeri3, Scott A McDonald4,5 and Maznah Dahlui3

1 Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

2 Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmacy, University of Malaya, Kuala Lumpur, Malaysia

3 Centre of Population Health, Department of Social and Preventative Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

4 Centre for Infectious Disease Control, National Institute for Public Health and the environment, Bilthoven, the Netherlands

5 School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, Scotland

*Corresponding author: Fatiha H Shabaruddin Department of Clinical Pharmacy and Pharmacy Practice, Faculty of

Pharmacy, University of Malaya, Kuala Lumpur, Malaysia email: [email protected] to the editor: the World Health Organization (WHO) aims to achieve global hepatitis C elimination by 2030, defined as diag- nosis of 90% of infected individuals and treatment initiation of 80% of eligible individuals. Most lower- and middle-income countries face multifaceted challenges within their respective healthcare systems to achieve these targets, ranging from under- equipped healthcare infrastructure to funding constraints [1].

In Malaysia, a middle-income country in the Southeast Asia region, it is estimated that 90% of 380,000 individuals with chronic hepatitis C virus (HCV) infection are undiagnosed and untreated.

Presently, generic direct-acting antiviral (DAA) regimens are available only in specific Ministry of Health facilities, where the 23,000 individuals diagnosed with HCV will be treated in stages with sofosbuvir and daclatasvir (SOF + DAC) for 12 weeks for individuals without cirrhosis and 24 weeks for cirrhotic individuals, with the addition of ribavirin for individuals with genotype 3 compensated cirrhosis and all individuals with decompensated cirrhosis [2]. this regimen was obtained by Malaysia through a government-use compulsory licence for sofosbuvir, which then resulted in the originator company Gilead extending its voluntary licence scheme to Malaysia, making widespread access to other generic regimens, including sofosbuvir and velpatasvir (SOF + VeL), possible upon approval [3].

With the availability of these two DAA regimens, a cost-efficient stratified treatment strategy is now possible, where SOF + DAC can be used to treat non-cirrhotic individuals with HCV for 12 weeks and SOF + VeL can be used to treat cirrhotic individuals with HCV for 12 weeks [4]. Presently, the acquisition cost for generic SOF + DAC is lower than the estimated cost of generic SOF + VeL in Malaysia. the projected cost savings from using a stratified strategy [5], mainly due to the omission of ribavirin for genotype 3 compensated cirrhosis and the shorter treat- ment duration with SOF + VeL for cirrhotic individuals, would reduce the financial impact of HCV treatment on the national healthcare budget.

It is projected that in order to meet the WHO elimination targets by 2030, Malaysia will need a steep scale-up in the annual number of treatments initiated [6]. It has been proposed that the annual

number of individuals initiated on DAA treatment would need to increase from 5000 individuals in 2018 to 15,000 individuals annually by 2022, then rapidly scaled up further to reach 30,000 treatments initiated annually by 2025 [6]. When most eligible individuals have been treated, treatment initiation can reduce to 25,000 per year by 2029 and 2030, thereby achieving the WHO targets, which will subsequently lead to reductions in downstream financial and clinical consequences of HCV infection nationally [6]. A scaled-up treatment strategy of this magnitude is only feasible alongside a large-scale national screening programme to prevent saturation of the individual pool, since many individuals living with HCV in Malaysia are undiagnosed.

Currently, it is very challenging for Malaysia to meet the WHO elimination targets by 2030 due to constraints within the health- care infrastructure, as well as the huge financial and resource investments required to implement the necessary scaled-up treat- ment and screening programmes [6,7]. these challenges potentially highlight the need for realistic expectations and strategies with regard to the country’s goal and timeline to achieving HCV elimi- nation, which may include adopting simplified service delivery using public health approaches and task shifting to decentralise HCV testing and treatment to primary care facilities and com- munity-based harm reduction sites. Community engagement and collaborative efforts with local advocacy groups, including Positive Malaysian treatment Access and Advocacy Group and Hepatitis Free Malaysia, remain crucial towards achieving national HCV elimination targets.

References

1. World Health Organization. Progress report on access to hepatitis C treatment:

focus on overcoming barriers in low-and middle-income countries (2018). Available at: www.who.int/iris/handle/10665/260445 (accessed July 2019).

2. Omar H. real life experience of sofosbuvir/daclatasvir in Malaysia. Presentation at the 4th National Hepatitis Conference, Kuala Lumpur, Malaysia (March) (2019).

3. Cooke GS, Andrieux-meyer I, Applegate tL et al. Accelerating the elimination of viral hepatitis: a Lancet Gastroenterology and Hepatology Commission. Lancet Gastroenterol Hepatol 2019; 4: 135–184.

4. World Health Organization. Guidelines for the care and treatment of persons diag- nosed with chronic hepatitis C virus infection (2018). Available at: apps.who.int/

iris/bitstream/handle/10665/273174/9789241550345-eng.pdf?ua=1 (accessed July 2019).

5. Mohamed r, Shabaruddin FH, Dahlui M et al. estimated 5-year acquisition cost of direct acting antiviral (DAA) for the treatment of hepatitis C in Malaysia in 2018 to 2022. Hepatol Int 2018; S544.

6. McDonald SA, Azzeri A, Shabaruddin FH et al. Projections of the healthcare costs and disease burden due to hepatitis C infection under different treatment policies in Malaysia, 2018–2040. Appl Health Econ Health Policy 2018; 16: 845–857.

7. Hieber L, Hecht r, Soe-Lin S et al. A step-wise approach to a national hepatitis C screening strategy in Malaysia to meet 2030 targets: proposed strategy, coverage, and costs. Value Health Reg Issues 2019; 18: 112–120.

Letter

Referensi

Dokumen terkait

1 Department of Nutrition, Faculty of Medicine, University of Sumatera Utara, Medan, Indonesia 2 Department of Public Health, Faculty of Medicine, University of Sumatera Utara,

3 Department of Global Health, Hanoi Medical University, Hanoi 11521, Vietnam; [email protected] 4 Faculty of Public Health, Thai Nguyen University of Medicine and Pharmacy,

DOI: 10.1016/j.matpr.2020.06.538 Department of Mechanical Engineering, Faculty of Engineering, International Islamic University Malaysia, Kuala Lumpur, 53100, Malaysia Abstract This

TUNKU SARA TUNKU AHMAD Tunku Sara binti Tunku Ahmad Yahaya, Professor of Orthopaedic Surgery and member of the unit of upper limb and microsurgery, University Malaya, Kuala Lumpur,

Sen Che Azlan bin Taib Mohd Faris bin Hassan MLIS Programme, Faculty of Computer Science & Information Technology, University of Malaya 50603 Kuala Lumpur, Malaysia ABSTRACT

Ravindaran Maraya3 1The author is a research student in the Department of Indian Studies, University of Malaya, Kuala Lumpur, Malaysia.. [email protected] 2The author is a

[email protected] 2The author is a Senior Lecturer in the Department of Indian Studies, University Malaya, Kuala Lumpur, Malaysia.. [email protected] 3The author is a research

Geetha Govindasamy is a Senior Lecturer at the Department of East Asian Studies, Faculty of Arts and Social Sciences, University Of Malaya, Kuala Lumpur, Malaysia.. Iga, Tsukasa is a