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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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Science Citation Index Expanded",{"EN":935,"VI":936},"SCIE database","Cơ sở dữ liệu SCIE","scie",[939,813],"SCIE","https:\u002F\u002Fmjl.clarivate.com\u002Fsearch-results?issn=1525-4135",[942,943],"03744874-dcbd-436b-8d5c-f6fa955ce005","53866f02-5006-4f8f-a807-ec8cf950fc52","https:\u002F\u002Fjournals.lww.com\u002Fjaids\u002Fpages\u002Fdefault.aspx",{"impactFactor":32,"impactFactorByYear":946,"i10Index":357,"i10IndexLast5Year":32,"totalPublication":357,"totalPublicationByYear":948,"totalCitation":949,"totalCitationByYear":950,"totalCitationPerPublication":953,"totalCitationPerPublicationByYear":954,"hindexLast5Year":357,"hindex":357},{"2012":129,"2013":947,"2014":132,"2016":46,"2017":48,"2018":145},19.5,{"2004":40,"2005":40,"2007":40,"2011":40,"2012":40,"2015":40,"2016":123},794,{"2004":329,"2005":158,"2007":565,"2011":951,"2012":952,"2015":436,"2016":574},240,155,99.25,{"2004":329,"2005":158,"2007":565,"2011":951,"2012":952,"2015":436,"2016":280},{"meta":956,"data":958},{"total":957},"61",[959,1395,1974,2529,2834,3349,4402,4760,4969,5315],{"id":960,"createTime":961,"updateTime":962,"relativeEntities":963,"slug":964,"properties":965,"entityType":984,"verifyStatus":26,"verifyTime":961,"verifyNote":985,"languages":986,"translateLanguages":987,"viewCount":32,"primaryUrl":988,"fullTextUrl":28,"authors":989,"publicationType":1151,"publisherRelationship":1152,"citationCount":1207,"citationInfo":1208,"publishDate":1211,"publishYear":1209,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":1212,"openAccess":28,"references":1213,"isForceReanalyzing":1394},"f66e04c1-ba14-4c06-b232-83e6648a24e2","2024-09-23T11:40:30.932+00:00","2025-01-24T13:15:39.643+00:00",[],"Narrowing-the-Gap-in-Life-Expectancy-Between-HIV-Infected-and-HIV-Uninfected-Individuals-With-Access-to-Care",{"mag":966,"keywords":968,"pmc":970,"openalex":972,"abstract":974,"title":977,"pm":980,"doi":982},{"VOID":967},"2322243210",{"VI":969},"",{"VOID":971},"5427712",{"VOID":973},"W2322243210",{"VI":975,"EN":976},"\u003Cjats:sec>\n            \u003Cjats:title>Thông Tin Nền:\u003C\u002Fjats:title>\n            \u003Cjats:p>Chưa có thông tin về việc khoảng cách sống còn giữa những người bị nhiễm HIV và những người không bị nhiễm HIV có quyền truy cập dịch vụ chăm sóc có còn tồn tại hay không.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Phương Pháp:\u003C\u002Fjats:title>\n            \u003Cjats:p>Chúng tôi đã tiến hành một nghiên cứu đoàn hệ trong khuôn khổ Kaiser Permanente California trong giai đoạn 1996–2011, sử dụng bảng tuổi thọ tạm thời để ước lượng số năm sống còn mong đợi (“tuổi thọ”) ở tuổi 20.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Kết Quả:\u003C\u002Fjats:title>\n            \u003Cjats:p>Trong số 24,768 người bị nhiễm HIV và 257,600 người không bị nhiễm HIV, có 2229 và 4970 trường hợp tử vong, tương ứng với tỷ lệ tử vong là 1827 và 326 trên 100,000 năm người. Trong giai đoạn 1996–1997, tuổi thọ mong đợi ở tuổi 20 cho những người bị nhiễm HIV và không bị nhiễm HIV lần lượt là 19.1 và 63.4 năm, với khoảng cách là 44.3 năm (khoảng tin cậy 95%: 38.4 đến 50.2). Tuổi thọ mong đợi ở tuổi 20 cho những người bị nhiễm HIV đã tăng lên 47.1 năm vào năm 2008 và 53.1 năm vào năm 2011, thu hẹp khoảng cách xuống còn 11.8 năm (8.9–14.8 năm) vào năm 2011. Trong giai đoạn 2008–2011, tuổi thọ mong đợi ở tuổi 20 cho những người bị nhiễm HIV dao động từ mức thấp nhất là 45.8 năm đối với người da đen và 46.0 năm đối với những người có tiền sử sử dụng thuốc tiêm cho đến mức cao nhất là 52.2 năm đối với người Latinh. Những người bị nhiễm HIV bắt đầu điều trị kháng retrovirus với số CD4 ≥500 tế bào trên một microlit có tuổi thọ mong đợi ở tuổi 20 là 54.5 năm trong giai đoạn 2008–2011, thu hẹp khoảng cách so với những người không bị nhiễm HIV xuống còn 7.9 năm (5.1–10.6 năm). Đối với những người bị nhiễm HIV này, khoảng cách còn thu hẹp thêm ở các nhóm phụ không có tiền sử nhiễm virus viêm gan B hoặc C, hút thuốc, lạm dụng thuốc\u002Falcohol, hoặc bất kỳ yếu tố nguy cơ nào trong số này.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Kết Luận:\u003C\u002Fjats:title>\n            \u003Cjats:p>Ngay cả khi được điều trị sớm và có quyền truy cập vào dịch vụ chăm sóc, vẫn tồn tại một khoảng cách 8 năm về tuổi thọ giữa những người bị nhiễm HIV so với những người không bị nhiễm HIV.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>","\u003Cjats:sec>\n            \u003Cjats:title>Background:\u003C\u002Fjats:title>\n            \u003Cjats:p>It is unknown if a survival gap remains between HIV-infected and HIV-uninfected individuals with access to care.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Methods:\u003C\u002Fjats:title>\n            \u003Cjats:p>We conducted a cohort study within Kaiser Permanente California during 1996–2011, using abridged life tables to estimate the expected years of life remaining (“life expectancy”) at age 20.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Results:\u003C\u002Fjats:title>\n            \u003Cjats:p>Among 24,768 HIV-infected and 257,600 HIV-uninfected individuals, there were 2229 and 4970 deaths, with mortality rates of 1827 and 326 per 100,000 person-years, respectively. In 1996–1997, life expectancies at age 20 for HIV-infected and HIV-uninfected individuals were 19.1 and 63.4 years, respectively, corresponding with a gap of 44.3 years (95% confidence interval: 38.4 to 50.2). Life expectancy at age 20 for HIV-infected individuals increased to 47.1 years in 2008 and 53.1 years by 2011, narrowing the gap to 11.8 years (8.9–14.8 years) in 2011. In 2008–2011, life expectancies at age 20 for HIV-infected individuals ranged from a low of 45.8 years for blacks and 46.0 years for those with a history of injection drug use to a high of 52.2 years for Hispanics. HIV-infected individuals who initiated antiretroviral therapy with CD4 ≥500 cells per microliter had a life expectancy at age 20 of 54.5 years in 2008–2011, narrowing the gap relative to HIV-uninfected individuals to 7.9 years (5.1–10.6 years). For these HIV-infected individuals, the gap narrowed further in subgroups with no history of hepatitis B or C infection, smoking, drug\u002Falcohol abuse, or any of these risk factors.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Conclusions:\u003C\u002Fjats:title>\n            \u003Cjats:p>Even with early treatment and access to care, an 8-year gap in life expectancy remains for HIV-infected compared with HIV-uninfected individuals.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>",{"EN":978,"VI":979},"Narrowing the Gap in Life Expectancy Between HIV-Infected and HIV-Uninfected Individuals With Access to Care","Giảm Thiểu Khoảng Cách Về Tuổi Thọ Giữa Những Người Bị Nhiễm HIV và Những Người Không Bị Nhiễm HIV Có Quyền Truy Cập Dịch Vụ Chăm Sóc",{"VOID":981},"27028501",{"VOID":983},"10.1097\u002Fqai.0000000000001014","PUBLICATION","Auto Verify",[31],[30],"https:\u002F\u002Fjournals.lww.com\u002F00126334-201609010-00006",[990,1009,1028,1045,1060,1077,1096,1115,1134],{"id":991,"sortIndex":32,"researcher":28,"roles":992,"affiliations":993,"properties":1002,"displayName":1006,"givenName":28,"familyName":28},"6df652a1-0d9b-4a7e-a9d4-c961eb1f7aae",[],[994],{"id":995,"sortIndex":32,"affiliation":996,"properties":28},"747d926e-d9d4-41fa-824d-61c912d2ccf0",{"id":995,"createTime":28,"updateTime":28,"relativeEntities":997,"slug":28,"properties":998,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1001,"statistic":28},[],{"title":999},{"VI":1000},"Division of Research, Kaiser Permanente Northern California, Oakland, CA",[],{"orcid":1003,"title":1005,"openalex":1007},{"VOID":1004},"https:\u002F\u002Forcid.org\u002F0000-0002-8552-414X",{"EN":1006},"Julia L. 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2002, Antiretroviral treatment for adult HIV infection in 2002: updated recommendations of the International AIDS Society-USA Panel., JAMA, 288, 222, 10.1001\u002Fjama.288.2.222",{"doi":1805},"10.1001\u002Fjama.288.2.222",{"id":28,"text":1807,"url":28,"identifiers":1808},"Berger, 1999, Chemokine receptors as HIV-1 coreceptors: roles in viral entry, tropism, and disease., Annu Rev Immunol, 17, 657, 10.1146\u002Fannurev.immunol.17.1.657",{"doi":1809},"10.1146\u002Fannurev.immunol.17.1.657",{"id":28,"text":1811,"url":28,"identifiers":1812},"Kilby, 1998, Potent suppression of HIV-1 replication in humans by T-20, a peptide inhibitor of gp41-mediated virus entry., Nat Med, 4, 1302, 10.1038\u002F3293",{"doi":1813},"10.1038\u002F3293",{"id":28,"text":1815,"url":28,"identifiers":1816},"Lalezari, 2003, A controlled Phase II trial assessing three doses of enfuvirtide (T-20) in combination with abacavir, amprenavir, ritonavir and efavirenz in non-nucleoside reverse transcriptase inhibitor-naive HIV-infected adults., Antivir Ther, 8, 279, 10.1177\u002F135965350300800403",{"doi":1817},"10.1177\u002F135965350300800403",{"id":28,"text":1819,"url":28,"identifiers":1820},"Lalezari, 2003, Enfuvirtide, an HIV-1 fusion inhibitor, for drug-resistant HIV infection in North and South America., N Engl J Med, 348, 2175, 10.1056\u002FNEJMoa035026",{"doi":1821},"10.1056\u002FNEJMoa035026",{"id":28,"text":1823,"url":28,"identifiers":1824},"Hatse, 2002, Chemokine receptor inhibition by AMD3100 is strictly confined to CXCR4., FEBS Lett, 527, 255, 10.1016\u002FS0014-5793(02)03143-5",{"doi":1825},"10.1016\u002FS0014-5793(02)03143-5",{"id":28,"text":1827,"url":28,"identifiers":1828},"Gerlach, 2001, Molecular interactions of cyclam and bicyclam non-peptide antagonists with the CXCR4 chemokine receptor., J Biol Chem, 276, 14153, 10.1074\u002Fjbc.M010429200",{"doi":1829},"10.1074\u002Fjbc.M010429200",{"id":28,"text":1831,"url":28,"identifiers":1832},"Schols, 1997, Inhibition of T-tropic HIV strains 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10.1128\u002FJVI.72.7.6040-6047.1998",{"doi":1869},"10.1128\u002FJVI.72.7.6040-6047.1998",{"id":28,"text":1871,"url":28,"identifiers":1872},"Fenyo, 1988, Distinct replicative and cytopathic characteristics of human immunodeficiency virus isolates., J Virol, 62, 4414, 10.1128\u002FJVI.62.11.4414-4419.1988",{"doi":1873},"10.1128\u002FJVI.62.11.4414-4419.1988",{"id":28,"text":1875,"url":28,"identifiers":1876},"Donzella, 1998, AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor., Nat Med, 4, 72, 10.1038\u002Fnm0198-072",{"doi":1877},"10.1038\u002Fnm0198-072",{"id":28,"text":1879,"url":28,"identifiers":1880},"De Clercq, 1994, Highly potent and selective inhibition of human immunodeficiency virus by the bicyclam derivative JM3100., Antimicrob Agents Chemother, 38, 668, 10.1128\u002FAAC.38.4.668",{"doi":1881},"10.1128\u002FAAC.38.4.668",{"id":28,"text":1883,"url":28,"identifiers":1884},"Harouse, 2003, CD8+ T cell-mediated CXC chemokine receptor 4-simian\u002Fhuman immunodeficiency virus suppression in dually infected rhesus macaques., Proc Natl Acad Sci USA, 100, 10977, 10.1073\u002Fpnas.1933268100",{"doi":1885},"10.1073\u002Fpnas.1933268100",{"id":28,"text":1887,"url":28,"identifiers":1888},"Datema, 1996, Antiviral efficacy in vivo of the anti-human immunodeficiency virus bicyclam SDZ SID 791 (JM 3100), an inhibitor of infectious cell entry., Antimicrob Agents Chemother, 40, 750, 10.1128\u002FAAC.40.3.750",{"doi":1889},"10.1128\u002FAAC.40.3.750",{"id":28,"text":1891,"url":28,"identifiers":1892},"Hendrix, 2000, Pharmacokinetics and safety of AMD-3100, a novel antagonist of the CXCR-4 chemokine receptor, in human volunteers., Antimicrob Agents Chemother, 44, 1667, 10.1128\u002FAAC.44.6.1667-1673.2000",{"doi":1893},"10.1128\u002FAAC.44.6.1667-1673.2000",{"id":28,"text":1895,"url":28,"identifiers":1896},"Bjorndal, 1997, Coreceptor usage of primary human immunodeficiency virus type 1 isolates varies according to biological phenotype., J Virol, 71, 7478, 10.1128\u002FJVI.71.10.7478-7487.1997",{"doi":1897},"10.1128\u002FJVI.71.10.7478-7487.1997",{"id":28,"text":1899,"url":28,"identifiers":1900},"Liles, 2003, Mobilization of hematopoietic progenitor cells in healthy volunteers by AMD3100, a CXCR4 antagonist., Blood, 102, 2728, 10.1182\u002Fblood-2003-02-0663",{"doi":1901},"10.1182\u002Fblood-2003-02-0663",{"id":28,"text":1903,"url":28,"identifiers":1904},"Vandamme, 1996, Quantification of HIV-1 RNA in plasma: comparable results with the NASBA HIV-1 RNA QT and the AMPLICOR HIV monitor test., J Acquir Immune Defic Syndr Hum Retrovirol, 13, 127, 10.1097\u002F00042560-199610010-00003",{"doi":1905},"10.1097\u002F00042560-199610010-00003",{"id":28,"text":1907,"url":28,"identifiers":1908},"Petropoulos, 2000, A novel phenotypic drug susceptibility assay for human immunodeficiency virus type 1., Antimicrob Agents Chemother, 44, 920, 10.1128\u002FAAC.44.4.920-928.2000",{"doi":1909},"10.1128\u002FAAC.44.4.920-928.2000",{"id":28,"text":1911,"url":28,"identifiers":1912},"Veazey, 2003, Use of a small molecule CCR5 inhibitor in macaques to treat simian immunodeficiency virus infection or prevent simian-human immunodeficiency virus infection., J Exp Med, 198, 1551, 10.1084\u002Fjem.20031266",{"doi":1913},"10.1084\u002Fjem.20031266",{"id":28,"text":1915,"url":28,"identifiers":1916},"Hatse, 2001, Mutation of Asp(171) and Asp(262) of the chemokine receptor CXCR4 impairs its coreceptor function for human immunodeficiency virus-1 entry and abrogates the antagonistic activity of AMD3100., Mol Pharmacol, 60, 164, 10.1124\u002Fmol.60.1.164",{"doi":1917},"10.1124\u002Fmol.60.1.164",{"id":28,"text":1919,"url":28,"identifiers":1920},"Palani, 2001, Discovery of 4-[(Z)-(4-bromophenyl)-(ethoxyimino)methyl]-1-[(2,4-dimethyl-3- pyridinyl)carbonyl]-4-methyl-1,4-bipiperidine N-oxide (SCH 351125): an orally bioavailable human CCR5 antagonist for the treatment of HIV infection., J Med Chem, 44, 3339, 10.1021\u002Fjm015526o",{"doi":1921},"10.1021\u002Fjm015526o",{"id":28,"text":1923,"url":28,"identifiers":1924},"Strizki, 2001, SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo., Proc Natl Acad Sci USA, 98, 12718, 10.1073\u002Fpnas.221375398",{"doi":1925},"10.1073\u002Fpnas.221375398",{"id":28,"text":1927,"url":28,"identifiers":1928},"Tsamis, 2003, Analysis of the mechanism by which the small-molecule CCR5 antagonists SCH-351125 and SCH-350581 inhibit human immunodeficiency virus type 1 entry., J Virol, 77, 5201, 10.1128\u002FJVI.77.9.5201-5208.2003",{"doi":1929},"10.1128\u002FJVI.77.9.5201-5208.2003",{"id":28,"text":1931,"url":28,"identifiers":1932},"Labrosse, 1998, Determinants for sensitivity of human immunodeficiency virus coreceptor CXCR4 to the bicyclam AMD3100., J Virol, 72, 6381, 10.1128\u002FJVI.72.8.6381-6388.1998",{"doi":1933},"10.1128\u002FJVI.72.8.6381-6388.1998",{"id":28,"text":1935,"url":28,"identifiers":1936},"Hatse, 2003, Mutations at the CXCR4 interaction sites for AMD3100 influence anti-CXCR4 antibody binding and HIV-1 entry., FEBS Lett, 546, 300, 10.1016\u002FS0014-5793(03)00609-4",{"doi":1937},"10.1016\u002FS0014-5793(03)00609-4",{"id":28,"text":1939,"url":28,"identifiers":1940},"Brandt, 2002, Association of chemokine-mediated block to HIV entry with coreceptor internalization., J Biol Chem, 277, 17291, 10.1074\u002Fjbc.M108232200",{"doi":1941},"10.1074\u002Fjbc.M108232200",{"id":28,"text":1943,"url":28,"identifiers":1944},"Soriano, 2002, Plasma stromal cell-derived factor (SDF)-1 levels, SDF1-3A genotype, and expression of CXCR4 on T lymphocytes: their impact on resistance to human immunodeficiency virus type 1 infection and its progression., J Infect Dis, 186, 922, 10.1086\u002F343741",{"doi":1945},"10.1086\u002F343741",{"id":28,"text":1947,"url":28,"identifiers":1948},"Derdeyn, 1999, Correlation between circulating stromal cell-derived factor 1 levels and CD4+ cell count in human immunodeficiency virus type 1-infected individuals., AIDS Res Hum Retroviruses, 15, 1063, 10.1089\u002F088922299310359",{"doi":1949},"10.1089\u002F088922299310359",{"id":28,"text":1951,"url":28,"identifiers":1952},"Connor, 1997, Change in coreceptor use correlates with disease progression in HIV-1-infected individuals., J Exp Med, 185, 621, 10.1084\u002Fjem.185.4.621",{"doi":1953},"10.1084\u002Fjem.185.4.621",{"id":28,"text":1955,"url":28,"identifiers":1956},"Scarlatti, 1997, In vivo evolution of HIV-1 co-receptor usage and sensitivity to chemokine-mediated suppression., Nat Med, 3, 1259, 10.1038\u002Fnm1197-1259",{"doi":1957},"10.1038\u002Fnm1197-1259",{"id":28,"text":1959,"url":28,"identifiers":1960},"Schramm, 2000, Viral entry through CXCR4 is a pathogenic factor and therapeutic target in human immunodeficiency virus type 1 disease., J Virol, 74, 184, 10.1128\u002FJVI.74.1.184-192.2000",{"doi":1961},"10.1128\u002FJVI.74.1.184-192.2000",{"id":28,"text":1963,"url":28,"identifiers":1964},"Malkevitch, 2001, Coreceptor choice and T cell depletion by R5, X4, and R5X4 HIV-1 variants in CCR5-deficient (CCR5delta32) and normal human lymphoid tissue., Virology, 281, 239, 10.1006\u002Fviro.2000.0807",{"doi":1965},"10.1006\u002Fviro.2000.0807",{"id":28,"text":1967,"url":28,"identifiers":1968},"Tersmette, 1989, Evidence for a role of virulent human immunodeficiency virus (HIV) variants in the pathogenesis of acquired immunodeficiency syndrome: studies on sequential HIV isolates., J Virol, 63, 2118, 10.1128\u002FJVI.63.5.2118-2125.1989",{"doi":1969},"10.1128\u002FJVI.63.5.2118-2125.1989",{"id":28,"text":1971,"url":28,"identifiers":1972},"Doranz, 2001, Safe use of the CXCR4 inhibitor ALX40-4C in humans., AIDS Res Hum Retroviruses, 17, 475, 10.1089\u002F08892220151126508",{"doi":1973},"10.1089\u002F08892220151126508",{"id":1975,"createTime":1976,"updateTime":1977,"relativeEntities":1978,"slug":1979,"properties":1980,"entityType":984,"verifyStatus":26,"verifyTime":1998,"verifyNote":985,"languages":1999,"translateLanguages":2000,"viewCount":32,"primaryUrl":2001,"fullTextUrl":28,"authors":2002,"publicationType":1151,"publisherRelationship":2096,"citationCount":834,"citationInfo":2151,"publishDate":2153,"publishYear":1209,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":2154,"openAccess":28,"references":2155,"isForceReanalyzing":1394},"07f9d496-74a3-4960-a4c3-455eee7d291a","2024-09-24T00:50:35.930+00:00","2025-01-24T13:16:38.890+00:00",[],"Global-Epidemiology-of-HIV-Infection-and-Related-Syndemics-Affecting-Transgender-People",{"mag":1981,"keywords":1983,"pmc":1984,"openalex":1986,"abstract":1988,"title":1991,"pm":1994,"doi":1996},{"VOID":1982},"2461527608",{"VI":969},{"VOID":1985},"4969059",{"VOID":1987},"W2461527608",{"VI":1989,"EN":1990},"\u003Cjats:sec>\n            \u003Cjats:title>Giới thiệu:\u003C\u002Fjats:title>\n            \u003Cjats:p>Các quần thể người chuyển giới đã bị thiếu vắng trong các nghiên cứu dịch tễ học về HIV và do đó cũng thiếu thốn trong các chương trình phòng ngừa, chăm sóc và điều trị HIV. Từ năm 2012, đã có sự gia tăng đáng kể trong nghiên cứu tập trung vào người chuyển giới. Các nghiên cứu làm nổi bật gánh nặng của bệnh HIV và những yếu tố nguy cơ, bao gồm các định kiến giao thoa, như là động lực của các tình trạng đồng hiện trong các quần thể người chuyển giới. Bài tổng quan này tổng hợp dịch tễ học HIV toàn cầu gần đây và mô tả những khoảng trống hiện tại trong nghiên cứu và can thiệp để thông tin hóa việc ưu tiên nghiên cứu HIV cho các quần thể người chuyển giới.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Phương pháp:\u003C\u002Fjats:title>\n            \u003Cjats:p>Một cuộc tổng quan có hệ thống đã được thực hiện đối với tài liệu y khoa được công bố giữa ngày 1 tháng 1 năm 2012 và ngày 30 tháng 11 năm 2015. Dữ liệu tập trung vào tỷ lệ nhiễm HIV, các yếu tố nguy cơ và các tình trạng đồng hiện trong các quần thể người chuyển giới.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Kết quả:\u003C\u002Fjats:title>\n            \u003Cjats:p>Các ước tính thay đổi đáng kể theo vị trí địa lý và tiểu quần thể. Những cá nhân chuyển nữ có tỷ lệ nhiễm HIV tập trung cao nhất trên thế giới với tỷ lệ xác nhận trong phòng thí nghiệm lên tới 40%. Dữ liệu khá hiếm về các cá nhân chuyển nam; tuy nhiên, chúng cho thấy khả năng có nguy cơ cao hơn cho nam chuyển giới có quan hệ tình dục với nam (MSM). Không có dữ liệu về tỷ lệ nhiễm bệnh cho người chuyển giới ở khu vực châu Phi hạ Sahara hoặc đông Âu\u002Ftrung Á. Các dữ liệu mới nổi liên tục hỗ trợ mối liên hệ của các điều kiện đồng hiện với nguy cơ HIV trong các quần thể người chuyển giới.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Thảo luận:\u003C\u002Fjats:title>\n            \u003Cjats:p>Giải quyết các điều kiện đồng hiện và những thách thức đặc thù về giới tính là rất quan trọng để đảm bảo sự tham gia và duy trì trong phòng ngừa HIV bởi các quần thể người chuyển giới. Nghiên cứu trong tương lai nên ưu tiên: lấp đầy các khoảng trống kiến thức trong dịch tễ học HIV; làm rõ cách thức mà định kiến hình thành các yếu tố đồng hiện để tạo ra HIV và những tác động tiêu cực khác đến sức khỏe của người chuyển giới; và hiểu cách thức để thực hiện hiệu quả các can thiệp HIV cho người chuyển giới.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>","\u003Cjats:sec>\n            \u003Cjats:title>Introduction:\u003C\u002Fjats:title>\n            \u003Cjats:p>Transgender populations have been underrepresented in HIV epidemiologic studies and consequently in HIV prevention, care, and treatment programs. Since 2012, there has been a dramatic increase in research focused on transgender people. Studies highlight the burden of HIV and risk determinants, including intersecting stigmas, as drivers of syndemics among transgender populations. This review synthesizes the most recent global epidemiology of HIV infection and describes current gaps in research and interventions to inform prioritization of HIV research for transgender populations.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Methods:\u003C\u002Fjats:title>\n            \u003Cjats:p>A systematic review was conducted of the medical literature published between January 1, 2012 and November 30, 2015. The data focused on HIV prevalence, determinants of risk, and syndemics among transgender populations.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Results:\u003C\u002Fjats:title>\n            \u003Cjats:p>Estimates varied dramatically by location and subpopulation. Transfeminine individuals have some of the highest concentrated HIV epidemics in the world with laboratory-confirmed prevalence up to 40%. Data were sparse among trans masculine individuals; however, they suggest potential increased risk for trans masculine men who have sex with men (MSM). No prevalence data were available for transgender people across Sub-Saharan Africa or Eastern Europe\u002FCentral Asia. Emerging data consistently support the association of syndemic conditions with HIV risk in transgender populations.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>\n          \u003Cjats:sec>\n            \u003Cjats:title>Discussion:\u003C\u002Fjats:title>\n            \u003Cjats:p>Addressing syndemic conditions and gender-specific challenges is critical to ensure engagement and retention in HIV prevention by transgender populations. Future research should prioritize: filling knowledge gaps in HIV epidemiology; elucidating how stigma shapes syndemic factors to produce HIV and other deleterious effects on transgender health; and understanding how to effectively implement HIV interventions for transgender people.\u003C\u002Fjats:p>\n          \u003C\u002Fjats:sec>",{"EN":1992,"VI":1993},"Global Epidemiology of HIV Infection and Related Syndemics Affecting Transgender People","Đại dịch toàn cầu về nhiễm virus HIV và các điều kiện đồng hiện liên quan đến sự ảnh hưởng của người chuyển giới",{"VOID":1995},"27429185",{"VOID":1997},"10.1097\u002Fqai.0000000000001087","2024-09-24T00:50:35.929+00:00",[31],[30],"https:\u002F\u002Fjournals.lww.com\u002F00126334-201608151-00002",[2003,2022,2041,2060,2079],{"id":2004,"sortIndex":32,"researcher":28,"roles":2005,"affiliations":2006,"properties":2015,"displayName":2019,"givenName":28,"familyName":28},"b58144f0-782a-4f60-bf7c-e884647a0da5",[],[2007],{"id":2008,"sortIndex":32,"affiliation":2009,"properties":28},"1696cd30-7c26-4d84-9f57-e2a0a832efbd",{"id":2008,"createTime":28,"updateTime":28,"relativeEntities":2010,"slug":28,"properties":2011,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2014,"statistic":28},[],{"title":2012},{"VI":2013},"Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD",[],{"orcid":2016,"title":2018,"openalex":2020},{"VOID":2017},"https:\u002F\u002Forcid.org\u002F0000-0001-6541-3787",{"EN":2019},"Tonia Poteat",{"VOID":2021},"A5054463066",{"id":2023,"sortIndex":40,"researcher":28,"roles":2024,"affiliations":2025,"properties":2034,"displayName":2038,"givenName":28,"familyName":28},"e9a02bc4-52ea-42fb-b4e4-93e1c538e349",[],[2026],{"id":2027,"sortIndex":32,"affiliation":2028,"properties":28},"97781e37-8195-44c1-8c86-1146660ae1ac",{"id":2027,"createTime":28,"updateTime":28,"relativeEntities":2029,"slug":28,"properties":2030,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2033,"statistic":28},[],{"title":2031},{"VI":2032},"Department of Epidemiology and Biostatistics, Western University, London, Canada",[],{"orcid":2035,"title":2037,"openalex":2039},{"VOID":2036},"https:\u002F\u002Forcid.org\u002F0000-0001-8498-9829",{"EN":2038},"Ayden I. 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10.1080\u002F09540120412331305098",{"doi":3286},"10.1080\u002F09540120412331305098",{"id":28,"text":3288,"url":28,"identifiers":3289},"Anand, 2010, Neurocognitive Impairment and HIV risk factors: a reciprocal relationship AIDS Behav., , 14, 1213",{},{"id":28,"text":3291,"url":28,"identifiers":3292},"Korthius, 2011, Improved quality of life for opioid-dependent patients receiving buprenorphine treatment in HIV clinics., J Acquir Immune Defic Syndr, 56, S39, 10.1097\u002FQAI.0b013e318209754c",{"doi":3293},"10.1097\u002FQAI.0b013e318209754c",{"id":28,"text":3295,"url":28,"identifiers":3296},"Parienti, 2008, Not all missed doses are the same: sustained NNRTI treatment interruptions predict HIV rebound at low-to-moderate adherence levels., PLoS One, 3, e2783, 10.1371\u002Fjournal.pone.0002783",{"doi":3297},"10.1371\u002Fjournal.pone.0002783",{"id":28,"text":3299,"url":28,"identifiers":3300},"Gardner, 2009, Antiretroviral medication adherence and the development of class-specific antiretroviral resistance., AIDS, 23, 1035, 10.1097\u002FQAD.0b013e32832ba8ec",{"doi":3301},"10.1097\u002FQAD.0b013e32832ba8ec",{"id":28,"text":3303,"url":28,"identifiers":3304},"Lima, 2009, The combined effect of modern highly active antiretroviral therapy regimens and adherence on mortality over time., J Acquir Immune Defic Syndr, 50, 529, 10.1097\u002FQAI.0b013e31819675e9",{"doi":3305},"10.1097\u002FQAI.0b013e31819675e9",{"id":28,"text":3307,"url":28,"identifiers":3308},"Egger, 2002, Prognosis of HIV-1-infected patients starting highly active antiretroviral therapy: a collaborative analysis of prospective studies., Lancet, 360, 119, 10.1016\u002FS0140-6736(02)09411-4",{"doi":3309},"10.1016\u002FS0140-6736(02)09411-4",{"id":28,"text":3311,"url":28,"identifiers":3312},"Kohli, 2005, Mortality in an urban cohort of HIV-infected and at-risk drug users in the era of highly active antiretroviral therapy., Clin Infect Dis, 41, 864, 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