Challenges for achieving safe and effective radical cure of Plasmodium vivax: a round table discussion of the APMEN Vivax Working Group

被引:58
作者
Thriemer, Kamala [1 ,2 ]
Ley, Benedikt [1 ,2 ]
Bobogare, Albino [3 ]
Dysoley, Lek [4 ,5 ]
Alam, Mohammad Shafiul [6 ]
Pasaribu, Ayodhia P. [7 ]
Sattabongkot, Jetsumon [8 ]
Jambert, Elodie [9 ]
Domingo, Gonzalo J. [10 ]
Commons, Robert [8 ]
Auburn, Sarah [8 ]
Marfurt, Jutta [8 ]
Devine, Angela [11 ,12 ]
Aktaruzzaman, Mohammad M. [13 ]
Sohel, Nayeem [13 ]
Namgay, Rinzin [14 ]
Drukpa, Tobgyel [14 ]
Sharma, Surender Nath [15 ]
Sarawati, Elvieda [16 ]
Samad, Iriani [16 ]
Theodora, Minerva [16 ]
Nambanya, Simone [17 ]
Ounekham, Sonesay [18 ]
Mudin, Rose Nanti Binti [18 ]
Da Thakur, Garib [19 ]
Makita, Leo Sora [20 ]
Deray, Raffy [21 ]
Lee, Sang-Eun [22 ]
Boaz, Leonard
Danansuriya, Manjula N. [23 ]
Mudiyanselage, Santha D. [23 ]
Chinanonwait, Nipon [24 ]
Kitchakarn, Suravadee [24 ]
Nausien, Johnny [25 ]
Naket, Esau [25 ]
Thang Ngo Duc [26 ]
Ha Do Manh [26 ]
Hong, Young S. [27 ]
Cheng, Qin [28 ]
Richards, Jack S. [29 ]
Kusriastuti, Rita [30 ,31 ]
Satyagraha, Ari [32 ]
Noviyanti, Rintis [32 ]
Ding, Xavier C. [33 ]
Khan, Wasif Ali [6 ]
Phru, Ching Swe [6 ]
Zhu Guoding [34 ]
Qi, Gao [34 ]
Kaneko, Akira [35 ,36 ]
Miotto, Olivo [11 ,37 ,38 ]
机构
[1] Menzies Sch Hlth Res, Global & Trop Hlth Div, Darwin, NT, Australia
[2] Charles Darwin Univ, Darwin, NT, Australia
[3] Natl Vector Borne Dis Control Programme, Honiara, Solomon Islands
[4] Natl Ctr Parasitol Entomol & Malaria Control, Phnom Penh, Cambodia
[5] Natl Inst Publ Hlth, Sch Publ Hlth, Phnom Penh, Cambodia
[6] Int Ctr Diarrheal Dis & Res, Dhaka, Bangladesh
[7] Univ Sumatera Utara, Fac Med, Dept Pediat, Medan, Indonesia
[8] Mahidol Univ, Fac Trop Med, Mahidol Vivax Res Unit, Bangkok, Thailand
[9] MMV, Geneva, Switzerland
[10] PATH, Diagnost Program, Seattle, WA USA
[11] Mahidol Oxford Trop Med Res Unit MORU, Bangkok, Thailand
[12] Univ Oxford, Nuffield Dept Med, Ctr Trop Med & Global Hlth, Oxford, England
[13] Director Gen Hlth Serv, Minist Hlth & Family Welf Malaria & Parasit Dis C, Dhaka, Bangladesh
[14] Minist Hlth Bhutan, Dept Publ Hlth, VDCP, Thimphu, Bhutan
[15] Natl Vector Borne Dis Control Programme, Directorate Gen Hlth Serv Minist Hlth & Family We, New Delhi, India
[16] Natl Malaria Control Program, Jakarta, Indonesia
[17] Natl Ctr Entomol Parasitol & Malaria Control, Viangchan, Laos
[18] Minist Hlth Malaysia, Vectorborne Dis Control Programme, Kuala Lumpur, Malaysia
[19] Minist Hlth & Populat, Dept Hlth Serv, Malaria Control Programme Epidemiol & Dis Control, Kathmandu, Nepal
[20] Natl Malaria Control Programme, Goroka, Papua N Guinea
[21] Malaria Control Programme, Dept Hlth, Manila, Philippines
[22] Ctr Dis Control & Prevent, Div Malaria & Parasit Dis, Seoul, South Korea
[23] Minist Hlth, Antimalaria Campaign, Colombo, Sri Lanka
[24] Minist Publ Hlth, Bur VectorBorne Dis Dept Dis Control, Bangkok, Thailand
[25] Natl Malaria Control Programme, Port Vila, Vanuatu
[26] NIMPE, Tam Ky, Vietnam
[27] Access Bio Inc, Monmouth, PA USA
[28] Australian Army Malaria Inst, Enoggera, Qld, Australia
[29] Burnet Inst, Ctr Biomed Res, Melbourne, Vic, Australia
[30] Minist Hlth, Vector Borne Dis Control, Jakarta, Indonesia
[31] Indonesian Parasit Assoc, Jakarta, Indonesia
[32] Eijkman Inst Mol Biol, Jakarta, Indonesia
[33] FIND, Geneva, Switzerland
[34] Jiangsu Inst Parasit Dis, Wuxi, Peoples R China
[35] Karolinska Inst, Stockholm, Sweden
[36] Osaka City Univ, Osaka, Japan
[37] Univ Oxford, Ctr Genom & Global Hlth, Wellcome Trust Ctr Human Genet, Oxford, England
[38] Wellcome Trust Sanger Inst, Hinxton, England
[39] Mahidol Univ, Fac Trop Med, Dept Mol Trop Med, Salaya, Nakhon Pathom, Thailand
[40] Univ Oxford, Oxford Big Data Inst, Malaria Atlas Project, Nuffield Dept Med, Oxford, England
[41] Malaria Consortium, London, England
[42] ICMR, MRHRU, Agartala, Tripura State, India
[43] Yayasan Pengembangan Kesehatan Dan Masyarakat Pap, Timika, Indonesia
[44] Res Inst Trop Med, Manila, Philippines
[45] Walter Eliza Hall Inst Med Res, Melbourne, Vic, Australia
[46] Univ Melbourne, Dept Med Biol, Parkville, Vic, Australia
[47] United States Agcy Int Dev, Presidents Malaria Initiat, Bangkok, Thailand
[48] World Hlth Org Western Pacif Region, Manila, Philippines
[49] WWARN, Oxford, England
[50] Univ Washington, Seattle, WA 98195 USA
关键词
Vivax malaria; P; vivax; Radical cure; Primaquine; APMEN; Tafenoquine; DIRECTLY-OBSERVED THERAPY; RAPID DIAGNOSTIC-TESTS; GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY; TREATMENT ADHERENCE; MALARIA TREATMENT; ARTEMETHER-LUMEFANTRINE; UNCOMPLICATED MALARIA; PRIMAQUINE TREATMENT; G6PD; CHLOROQUINE;
D O I
10.1186/s12936-017-1784-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The delivery of safe and effective radical cure for Plasmodium vivax is one of the greatest challenges for achieving malaria elimination from the Asia-Pacific by 2030. During the annual meeting of the Asia Pacific Malaria Elimination Network Vivax Working Group in October 2016, a round table discussion was held to discuss the programmatic issues hindering the widespread use of primaquine (PQ) radical cure. Participants included 73 representatives from 16 partner countries and 33 institutional partners and other research institutes. In this meeting report, the key discussion points are presented and grouped into five themes: (i) current barriers for glucose-6-phosphate deficiency (G6PD) testing prior to PQ radical cure, (ii) necessary properties of G6PD tests for wide scale deployment, (iii) the promotion of G6PD testing, (iv) improving adherence to PQ regimens and (v) the challenges for future tafenoquine (TQ) roll out. Robust point of care (PoC) G6PD tests are needed, which are suitable and cost-effective for clinical settings with limited infrastructure. An affordable and competitive test price is needed, accompanied by sustainable funding for the product with appropriate training of healthcare staff, and robust quality control and assurance processes. In the absence of quantitative PoC G6PD tests, G6PD status can be gauged with qualitative diagnostics, however none of the available tests is currently sensitive enough to guide TQ treatment. TQ introduction will require overcoming additional challenges including the management of severely and intermediately G6PD deficient individuals. Robust strategies are needed to ensure that effective treatment practices can be deployed widely, and these should ensure that the caveats are outweighed by the benefits of radical cure for both the patients and the community. Widespread access to quality controlled G6PD testing will be critical.
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页数:9
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