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      Looking back to move forward: a twenty-year audit of herpes zoster in Asia-Pacific

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          Abstract

          Background

          Herpes zoster (HZ) is a prevalent viral disease that inflicts substantial morbidity and associated healthcare and socioeconomic burdens. Current treatments are not fully effective, especially among the most vulnerable patients. Although widely recommended, vaccination against HZ is not routine; barriers in Asia-Pacific include long-standing neglect of adult immunisation and sparse local data. To address knowledge gaps, raise awareness, and disseminate best practice, we reviewed recent data and guidelines on HZ from the Asia-Pacific region.

          Methods

          We searched PubMed, Scopus, and World Health Organization databases for articles about HZ published from 1994 to 2014 by authors from Australia, China, Hong Kong, India, Indonesia, Japan, Korea, Malaysia, New Zealand, the Philippines, Singapore, Taiwan, Thailand, and Vietnam. We selected articles about epidemiology, burden, complications, comorbidities, management, prevention, and recommendations/guidelines. Internet searches retrieved additional HZ immunisation guidelines.

          Results

          From 4007 retrieved articles, we screened-out 1501 duplicates and excluded 1264 extraneous articles, leaving 1242 unique articles. We found guidelines on adult immunisation from Australia, India, Indonesia, Malaysia, New Zealand, the Philippines, South Korea, and Thailand.

          HZ epidemiology in Asia-Pacific is similar to elsewhere; incidence rises with age and peaks at around 70 years – lifetime risk is approximately one-third. Average incidence of 3–10/1000 person-years is rising at around 5% per year. The principal risk factors are immunosenescence and immunosuppression. HZ almost always causes pain, and post-herpetic neuralgia is its most common complication. Half or more of hospitalised HZ patients have post-herpetic neuralgia, secondary infections, or inflammatory sequelae that are occasionally fatal. These disease burdens severely diminish patients’ quality of life and incur heavy healthcare utilisation.

          Conclusions

          Several countries have abundant data on HZ, but others, especially in South-East Asia, very few. However, Asia-Pacific countries generally lack data on HZ vaccine safety, efficacy and cost-effectiveness. Physicians treating HZ and its complications in Asia-Pacific face familiar challenges but, with a vast aged population, Asia bears a unique and growing burden of disease. Given the strong rationale for prevention, most adult immunisation guidelines include HZ vaccine, yet it remains underused. We urge all stakeholders to give higher priority to adult immunisation in general and HZ in particular.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12879-017-2198-y) contains supplementary material, which is available to authorized users.

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          Most cited references726

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          Prevention of herpes zoster: recommendations of the Advisory Committee on Immunization Practices (ACIP).

          These recommendations represent the first statement by the Advisory Committee on Immunization Practices (ACIP) on the use of a live attenuated vaccine for the prevention of herpes zoster (zoster) (i.e., shingles) and its sequelae, which was licensed by the U.S. Food and Drug Administration (FDA) on May 25, 2006. This report summarizes the epidemiology of zoster and its sequelae, describes the zoster vaccine, and provides recommendations for its use among adults aged > or =60 years in the United States. Zoster is a localized, generally painful cutaneous eruption that occurs most frequently among older adults and immunocompromised persons. It is caused by reactivation of latent varicella zoster virus (VZV) decades after initial VZV infection is established. Approximately one in three persons will develop zoster during their lifetime, resulting in an estimated 1 million episodes in the United States annually. A common complication of zoster is postherpetic neuralgia (PHN), a chronic, often debilitating pain condition that can last months or even years. The risk for PHN in patients with zoster is 10%-18%. Another complication of zoster is eye involvement, which occurs in 10%-25% of zoster episodes and can result in prolonged or permanent pain, facial scarring, and loss of vision. Approximately 3% of patients with zoster are hospitalized; many of these episodes involved persons with one or more immunocompromising conditions. Deaths attributable to zoster are uncommon among persons who are not immunocompromised. Prompt treatment with the oral antiviral agents acyclovir, valacyclovir, and famciclovir decreases the severity and duration of acute pain from zoster. Additional pain control can be achieved in certain patients by supplementing antiviral agents with corticosteroids and with analgesics. Established PHN can be managed in certain patients with analgesics, tricyclic antidepressants, and other agents. Licensed zoster vaccine is a lyophilized preparation of a live, attenuated strain of VZV, the same strain used in the varicella vaccines. However, its minimum potency is at least 14-times the potency of single-antigen varicella vaccine. In a large clinical trial, zoster vaccine was partially efficacious at preventing zoster. It also was partially efficacious at reducing the severity and duration of pain and at preventing PHN among those developing zoster. Zoster vaccine is recommended for all persons aged > or =60 years who have no contraindications, including persons who report a previous episode of zoster or who have chronic medical conditions. The vaccine should be offered at the patient's first clinical encounter with his or her health-care provider. It is administered as a single 0.65 mL dose subcutaneously in the deltoid region of the arm. A booster dose is not licensed for the vaccine. Zoster vaccination is not indicated to treat acute zoster, to prevent persons with acute zoster from developing PHN, or to treat ongoing PHN. Before administration of zoster vaccine, patients do not need to be asked about their history of varicella (chickenpox) or to have serologic testing conducted to determine varicella immunity.
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            Efficacy and safety of abatacept in lupus nephritis: a twelve-month, randomized, double-blind study.

            To compare the efficacy and safety of intravenous (IV) abatacept, a selective T cell costimulation modulator, versus placebo for the treatment of active class III or IV lupus nephritis, when used on a background of mycophenolate mofetil and glucocorticoids.
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              Pregabalin reduces pain and improves sleep and mood disturbances in patients with post-herpetic neuralgia: results of a randomised, placebo-controlled clinical trial.

              This study was designed to assess the efficacy and safety of pregabalin-a novel alpha(2)-delta ligand with analgesic, anxiolytic, and anticonvulsant activity-for treating neuropathic pain in patients with post-herpetic neuralgia (PHN). Two hundred and thirty-eight patients were randomised into this multicentre, doubleblind, placebo-controlled trial to receive 150 (n=81), 300 mg/day (n=76) pregabalin, or placebo (n=81) for 8 weeks. Among the exclusion criteria was failure to respond to previous treatment for PHN with gabapentin at doses > or =1200 mg/day. Endpoint mean pain scores were significantly reduced in patients receiving 150 or 300 mg/day pregabalin compared with placebo. Efficacy was observed as early as week 1 and was maintained throughout the study. Significantly more patients in both pregabalin groups (150 mg, 26%; 300 mg, 28%) were responders (> or =50% decrease in mean pain score from baseline to endpoint) than in the placebo group (10%). Additionally, by week 1 and for the study's duration, 150 and 300 mg/day pregabalin significantly reduced weekly mean sleep interference scores. More pregabalin-treated patients than placebo-treated patients reported that they were 'much improved' or 'very much improved'. Health-related quality-of-life (HRQoL) measurements using the SF-36 Health Survey demonstrated improvement in the mental health domain for both pregabalin dosages, and bodily pain and vitality domains were improved in the 300 mg/day group. The most frequent adverse events were dizziness, somnolence, peripheral oedema, headache, and dry mouth. Pregabalin efficaciously treated the neuropathic pain of PHN. Additionally, pregabalin was associated with decreased sleep interference and significant improvements in HRQoL measures.
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                Author and article information

                Contributors
                +886-2-28757830 , lkchen2@vghtpe.gov.tw
                harai@ncgg.go.jp
                lychen8@vghtpe.gov.tw
                mychou@vghks.gov.tw
                samsuridjal@yahoo.com
                birongdong@163.com
                tkojima-tky@umin.ac.jp
                idktkwon@gmail.com
                hoenam@rophiclinic.com.sg
                emfleung@yahoo.com.hk
                ck.vghks@gmail.com
                xhliu@medmail.com.cn
                dean@apolloimsr.edu.in
                jypan@nsc.com.sg
                hfpeng@vghtpe.gov.tw
                edpob2011@gmail.com
                philippoi@gmail.com
                stewart_christine@mac.com
                terapong_tantawichien@hotmail.com
                chunwonvicky@yahoo.co.kr
                Journal
                BMC Infect Dis
                BMC Infect. Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                15 March 2017
                15 March 2017
                2017
                : 17
                : 213
                Affiliations
                [1 ]ISNI 0000 0004 0604 5314, GRID grid.278247.c, , Center for Geriatrics and Gerontology, Taipei Veterans General Hospital, ; No. 201, Sec. 2, Shih-Pai Rd., Taipei, 11217 Taiwan
                [2 ]ISNI 0000 0001 0425 5914, GRID grid.260770.4, , Aging and Health Research Center, National Yang Ming University, ; Taipei, Taiwan
                [3 ]ISNI 0000 0004 1791 9005, GRID grid.419257.c, , National Center for Geriatrics and Gerontology, ; 7-340 Morioka-cho, Obu, Aichi 474-8511 Japan
                [4 ]ISNI 0000 0004 0572 9992, GRID grid.415011.0, , Center for Geriatrics and Gerontology, Kaohsiung Veterans General Hospital, ; No. 386 Ta-Chun 1st Rd., Kaohsiung, 81362 Taiwan
                [5 ]ISNI 0000000120191471, GRID grid.9581.5, Department of Internal Medicine, Faculty of Medicine, , University of Indonesia, ; Salemba Raya No. 6, Jakarta, 10430 Indonesia
                [6 ]ISNI 0000 0001 0807 1581, GRID grid.13291.38, The Center of Gerontology and Geriatrics, West China Medical School/West China Hospital, , Sichuan University, ; No. 37 Guo Xue Xiang, Renmin Nan Lu, Chengdu, Sichuan 610041 China
                [7 ]ISNI 0000 0001 2151 536X, GRID grid.26999.3d, Department of Geriatric Medicine, Graduate School of Medicine, , The University of Tokyo, ; 7-3-1, Jongo, Bunkyo-ku, Tokyo, 113-8655 Japan
                [8 ]ISNI 0000 0004 0647 1890, GRID grid.413395.9, , Division of Infectious Diseases, Daegu Fatima Hospital, ; 99 Ayang-ro, Dong-gu, Daegu, 710-600 Korea
                [9 ]Rophi Clinic, 38 Irrawaddy Rd. #07-54/55, Mount Elizabeth Novena Specialist Centre, Singapore, 329563 Singapore
                [10 ]Geriatric Medicine Centre (Healthy Ageing), Hong Kong Sanatorium and Hospital, 2 Village Rd. Happy Valley, Hong Kong S.A.R., China
                [11 ]ISNI 0000 0004 0572 9992, GRID grid.415011.0, , Division of Neurology, Department of Internal Medicine, Kaohsiung Veterans General Hospital, ; Kaohsiung, Taiwan
                [12 ]ISNI 0000 0000 9889 6335, GRID grid.413106.1, Division of Geriatrics, Department of Internal Medicine, , Peking Union Medical College Hospital, ; Beijing, 100730 China
                [13 ]Apollo Institute of Medical Sciences and Research, Apollo Health City Campus, Jubilee Hills, Hyderabad, 500096 India
                [14 ]ISNI 0000 0004 0640 6896, GRID grid.410763.7, , National Skin Centre, ; 1 Mandalay Rd., Singapore, 308205 Singapore
                [15 ]ISNI 0000 0004 0571 4942, GRID grid.416846.9, , Geriatric Center, St. Luke’s Medical Center, ; 279 E. Rodriguez Sr. Ave., Quezon City, 1102 Philippines
                [16 ]ISNI 0000 0000 8963 3111, GRID grid.413018.f, Division of Geriatrics, Department of Medicine, , University Malaya Medical Centre, ; Lembah Pantai, 59100 Kuala Lumpur, Malaysia
                [17 ]Ropata Medical Centre, Lower Hutt, 5010 New Zealand
                [18 ]ISNI 0000 0001 0244 7875, GRID grid.7922.e, Division of Infectious Diseases, Department of Medicine, , Chulalongkorn University, ; Bangkok, 10330 Thailand
                [19 ]ISNI 0000 0001 2171 7818, GRID grid.289247.2, Department of Family Medicine, College of Medicine, , Kyung Hee University, ; 1 Hoigi-dong, Dongdaemun-gu, Seoul, 130-720 Korea
                Article
                2198
                10.1186/s12879-017-2198-y
                5353949
                28298208
                a7361101-62ce-4bb2-b1ac-5392a0ed93bf
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 5 March 2016
                : 9 January 2017
                Categories
                Review
                Custom metadata
                © The Author(s) 2017

                Infectious disease & Microbiology
                asia-pacific,complications,epidemiology,healthcare burden,herpes zoster,immunisation,management,post-herpetic neuralgia,prevention,vaccine

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