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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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VWD may be disproportionately symptomatic in women of child‐bearing age. It may also occur less frequently as an acquired disorder (acquired von Willebrand syndrome). VWD is caused by deficiency or dysfunction of von Willebrand factor (VWF), a plasma protein that mediates platelet haemostatic function and stabilizes blood coagulation factor VIII. The pathophysiology, classification, diagnosis and management of VWD are relatively complex, but understanding them is important for proper diagnosis and management of patients with VWD. These evidence‐based guidelines for diagnosis and management of VWD from the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel (USA) review relevant publications, summarize current understanding of VWD pathophysiology and classification, and present consensus diagnostic and management recommendations based on analysis of the literature and expert opinion. 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In:http:\u002F\u002Fwww.eMedicine.com\u002Fped\u002Ftopic654.htm;26 January 2003.",{},{"id":28,"text":3330,"url":28,"identifiers":3331},"10.1055\u002Fs-2007-999756",{"doi":3330},{"id":28,"text":3333,"url":28,"identifiers":3334},"10.1097\u002F00001721-200110000-00055",{"doi":3333},{"id":28,"text":3336,"url":28,"identifiers":3337},"10.1097\u002F00043426-199703000-00012",{"doi":3336},{"id":28,"text":3339,"url":28,"identifiers":3340},"Rochelson B, 1991, The use of prophylactic desmopressin (DDAVP) in labor to prevent hemorrhage in a patient with Ehlers‐Danlos syndrome, N Y State J Med, 91, 268",{},{"id":3342,"createTime":3343,"updateTime":3343,"relativeEntities":3344,"slug":3345,"properties":3346,"entityType":972,"verifyStatus":26,"verifyTime":3343,"verifyNote":974,"languages":3359,"translateLanguages":28,"viewCount":32,"primaryUrl":3360,"fullTextUrl":28,"authors":3361,"publicationType":1164,"publisherRelationship":3400,"citationCount":3453,"citationInfo":3454,"publishDate":3456,"publishYear":1221,"citationAnalyzeStatus":883,"lastCitationAnalyze":28,"indexDatabases":3457,"openAccess":28,"references":3458,"isForceReanalyzing":2492},"b324bf0e-f4d7-4a4c-b2b7-af8d7c344c1e","2024-09-01T09:42:49.682+00:00",[],"Inherited-antithrombin-deficiency-a-review",{"openalex":3347,"mag":3349,"abstract":3351,"title":3353,"pm":3355,"doi":3357},{"VOID":3348},"W2115509671",{"VOID":3350},"2115509671",{"EN":3352},"\u003Cjats:p>\u003Cjats:bold>Summary. \u003C\u002Fjats:bold> Antithrombin (AT) is a potent inactivator of thrombin and factor Xa and the major inhibitor of blood coagulation. Inherited AT deficiencies are uncommon, with prevalences in the general population between 1 in 500 and 1 in 5000. They are either quantitative (type I) or qualitative (type II). Type II is subdivided into the more common, but less thrombogenic, type IIb deficiency caused by a defect in the heparin‐binding region of AT and the less common, but more thrombophilic, type IIa variant caused by mutations in the thrombin‐binding site. A pleiotropic type IIc deficiency also exists. In the evaluation of a thrombophilic individual, a functional AT assay (AT activity) should be used and the diagnosis of AT deficiency only established after acquired causes have been ruled out and repeat AT testing on an additional sample has been performed. A subsequent antigenic AT assay result leads to differentiation between type I and type II deficiency. Further specialized tests help subclassify the type II deficiencies, but this is typically not carried out for clinical purposes, even though it might be helpful to assess thrombosis risk. AT deficiency is associated with an increased risk for venous thromboembolism (VTE) and pregnancy loss. The association with arterial thrombosis is only weak. VTE prophylaxis and treatment management will be discussed in this article and existing treatment guidelines presented. The lack of data surrounding the use of AT concentrates and the resulting ambiguity as to when to use such concentrates will be discussed.\u003C\u002Fjats:p>",{"EN":3354},"Inherited antithrombin deficiency: a review",{"VOID":3356},"19141163",{"VOID":3358},"10.1111\u002Fj.1365-2516.2008.01830.x",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1365-2516.2008.01830.x",[3362,3381],{"id":3363,"sortIndex":32,"researcher":28,"roles":3364,"affiliations":3365,"properties":3374,"displayName":3378,"givenName":28,"familyName":28},"e973e1a8-ca79-44c7-b91d-52c7017a732f",[],[3366],{"id":3367,"sortIndex":32,"affiliation":3368,"properties":28},"540cf52b-aaaf-4d9d-97db-32cc858367f8",{"id":3367,"createTime":28,"updateTime":28,"relativeEntities":3369,"slug":28,"properties":3370,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3373,"statistic":28},[],{"title":3371},{"EN":3372},"Department of Internal Medicine, University of Minnesota School of Medicine, Minneapolis, MN",[],{"orcid":3375,"title":3377,"openalex":3379},{"VOID":3376},"https:\u002F\u002Forcid.org\u002F0000-0001-6998-662X",{"EN":3378},"Mrinal M. 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In the last few years, the number of patients with recessively transmitted coagulation deficiencies has increased in European countries with a high rate of immigration of Islamic populations, because in these populations, consanguineous marriages are frequent. Owing to the relative rarity of these deficiencies, the type and severity of bleeding symptoms, the underlying molecular defects and the actual management of bleeding episodes are not as well established as for haemophilia A and B. This article reviews these disorders in terms of their clinical manifestations and characterization of the molecular defects involved. 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for guidance on plasma derived medicinal products.: Committee for Proprietary Medicinal Products (CPMP). Document number CPMP\u002FBWP\u002F269\u002F95 rev 3 2001.",{},{"id":28,"text":4966,"url":28,"identifiers":4967},"10.1046\u002Fj.1365-2141.2002.03293.x",{"doi":4966},{"id":28,"text":4969,"url":28,"identifiers":4970},"10.1016\u002FS0140-6736(94)91878-3",{"doi":4969},{"id":28,"text":4972,"url":28,"identifiers":4973},"10.1055\u002Fs-2006-946908",{"doi":4972},{"id":28,"text":4975,"url":28,"identifiers":4976},"2007, Fourth case of transfusion‐associated vCJD infection in the United Kingdom, Euro Surveill, 12, E070118",{},{"id":28,"text":4978,"url":28,"identifiers":4979},"10.1016\u002Fj.tracli.2006.11.006",{"doi":4978},{"id":28,"text":4981,"url":28,"identifiers":4982},"10.1016\u002F0140-6736(92)90874-3",{"doi":4981},{"id":28,"text":4984,"url":28,"identifiers":4985},"10.1046\u002Fj.1365-2516.1999.00300.x",{"doi":4984},{"id":28,"text":4987,"url":28,"identifiers":4988},"10.1055\u002Fs-0038-1655911",{"doi":4987},{"id":28,"text":4990,"url":28,"identifiers":4991},"10.1055\u002Fs-0038-1651565",{"doi":4990},{"id":28,"text":4993,"url":28,"identifiers":4994},"10.1182\u002Fblood-2005-04-1371",{"doi":4993},{"id":28,"text":4996,"url":28,"identifiers":4997},"10.1182\u002Fblood-2006-11-056317",{"doi":4996},{"id":28,"text":4999,"url":28,"identifiers":5000},"10.1111\u002Fj.1365-2516.2006.01373.x",{"doi":4999},{"id":28,"text":5002,"url":28,"identifiers":5003},"10.1002\u002F9780470757260.ch14",{"doi":5002},{"id":28,"text":5005,"url":28,"identifiers":5006},"De Biasi R, 1991, The impact of a very high purity factor VIII concentrate on the immune system of human immunodeficiency virus‐infected hemophiliacs: a randomized, prospective, two‐year comparison with an intermediate purity concentrate, Blood, 78, 1919, 10.1182\u002Fblood.V78.8.1919.1919",{"doi":5007},"10.1182\u002Fblood.V78.8.1919.1919",{"id":28,"text":5009,"url":28,"identifiers":5010},"10.1016\u002FS0140-6736(94)92345-0",{"doi":5009},{"id":28,"text":3236,"url":28,"identifiers":5012},{"doi":3236},{"id":28,"text":5014,"url":28,"identifiers":5015},"10.1046\u002Fj.1365-2141.1997.d01-2015.x",{"doi":5014},{"id":28,"text":2091,"url":28,"identifiers":5017},{"doi":2091},{"id":28,"text":2097,"url":28,"identifiers":5019},{"doi":2097},{"id":28,"text":5021,"url":28,"identifiers":5022},"10.1111\u002Fj.1538-7836.2004.00944.x",{"doi":5021},{"id":28,"text":1948,"url":28,"identifiers":5024},{"doi":1948},{"id":28,"text":2046,"url":28,"identifiers":5026},{"doi":2046},{"id":28,"text":5028,"url":28,"identifiers":5029},"10.1002\u002F14651858.CD001884.pub2",{"doi":5028},{"id":28,"text":2136,"url":28,"identifiers":5031},{"doi":2136},{"id":28,"text":2021,"url":28,"identifiers":5033},{"doi":2021},{"id":5035,"createTime":5036,"updateTime":5036,"relativeEntities":5037,"slug":5038,"properties":5039,"entityType":972,"verifyStatus":883,"verifyTime":5036,"verifyNote":5052,"languages":5053,"translateLanguages":28,"viewCount":32,"primaryUrl":5054,"fullTextUrl":28,"authors":5055,"publicationType":1164,"publisherRelationship":5084,"citationCount":5138,"citationInfo":5139,"publishDate":5142,"publishYear":5140,"citationAnalyzeStatus":883,"lastCitationAnalyze":28,"indexDatabases":5143,"openAccess":28,"references":5144,"isForceReanalyzing":2492},"5074bfba-f2fb-439f-9cbb-5a94766c05ec","2024-09-12T16:29:04.286+00:00",[],"Nanofiltration-of-plasma-derived-biopharmaceutical-products",{"openalex":5040,"mag":5042,"abstract":5044,"title":5046,"pm":5048,"doi":5050},{"VOID":5041},"W2051724757",{"VOID":5043},"2051724757",{"EN":5045},"\u003Cjats:p>\u003Cjats:bold>Summary.\u003C\u002Fjats:bold> This review presents the current status on the use and benefits of viral removal filtration systems – known as nanofiltration – in the manufacture of plasma‐derived coagulation factor concentrates and other biopharmaceutical products from human blood origin.\u003C\u002Fjats:p>\u003Cjats:p>Nanofiltration of plasma products has been implemented at a production scale in the early 1990s to improve margin of viral safety, as a complement to the viral reduction treatments, such as solvent–detergent and heat treatments, already applied for the inactivation of human immunodeficiency virus, hepatitis B and hepatitis C virus. The main reason for the introduction of nanofiltration was the need to improve product safety against non‐enveloped viruses and to provide a possible safeguard against new infectious agents potentially entering the human plasma pool.\u003C\u002Fjats:p>\u003Cjats:p>Nanofiltration has gained quick acceptance as it is a relatively simple manufacturing step that consists in filtering protein solution through membranes of a very small pore size (typically 15–40 nm) under conditions that retain viruses by a mechanism largely based on size exclusion. Recent large‐scale experience throughout the world has now established that nanofiltration is a robust and reliable viral reduction technique that can be applied to essentially all plasma products. Many of the licensed plasma products are currently nanofiltered.\u003C\u002Fjats:p>\u003Cjats:p>The technology has major advantages as it is flexible and it may combine efficient and largely predictable removal of more than 4 to 6 logs of a wide range of viruses, with an absence of denaturing effect on plasma proteins. Compared with other viral reduction means, nanofiltration may be the only method to date permitting efficient removal of enveloped and non‐enveloped viruses under conditions where 90–95% of protein activity is recovered. New data indicate that nanofiltration may also remove prions, opening new perspectives in the development and interest of this technique. Nanofiltration is increasingly becoming a routine step in the manufacture of biopharmaceutical products.\u003C\u002Fjats:p>",{"EN":5047},"Nanofiltration of plasma‐derived biopharmaceutical products",{"VOID":5049},"12558776",{"VOID":5051},"10.1046\u002Fj.1365-2516.2003.00701.x","Author affiliation is 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BA, 1996, Evaluation of anti‐viral filters, Dev Biol Stand, 88, 91",{},{"id":28,"text":5182,"url":28,"identifiers":5183},"Viresolve, 2002, Virus and Application Filtration Guide",{},{"id":28,"text":5185,"url":28,"identifiers":5186},"Element Data Sheet F1 1996 OMEGA VR TM virus reduction membrane",{},{"id":28,"text":5188,"url":28,"identifiers":5189},"10.5360\u002Fmembrane.14.77",{"doi":5188},{"id":28,"text":5167,"url":28,"identifiers":5191},{"doi":5167},{"id":28,"text":5193,"url":28,"identifiers":5194},"Manabe S., 1996, Removal of virus through novel membrane filtration method, Dev Biol Stand, 88, 81",{},{"id":28,"text":5196,"url":28,"identifiers":5197},"Ide S. 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Millipore12\u002F99.",{},{"id":28,"text":5211,"url":28,"identifiers":5212},"Graf EG, 1999, Virus removal by filtration, Dev Biol Stand, 99, 89",{},{"id":28,"text":5214,"url":28,"identifiers":5215},"Brandwein H, 2000, Membrane filtration for virus removal, Dev Biol Stand, 102:157",{},{"id":28,"text":5217,"url":28,"identifiers":5218},"10.1046\u002Fj.1423-0410.1998.7530181.x",{"doi":5217},{"id":28,"text":5220,"url":28,"identifiers":5221},"Validation Guide VG‐DV20 Pall ULTIPOR VF Grade DV20 AB style virus removal filter cartridges.Pall BioPharmaceuticals 2000.",{},{"id":28,"text":5223,"url":28,"identifiers":5224},"Aranha‐CreadoH OshimaK JafariS HowardG BrandweinH.Virus retention by Ultipor VF grade DV50 membrane filters. Pall STR1543.",{},{"id":28,"text":5226,"url":28,"identifiers":5227},"Aranha‐Creado H, 1997, Virus retention by a hydrophilic triple‐layer PVDF microporous membrane filter, PDA J Pharm Sc Technol, 51, 119",{},{"id":28,"text":5229,"url":28,"identifiers":5230},"Burnouf T., 1993, Chromatographic removal of viruses from plasma derivatives, Dev Biol Stand, 81, 199",{},{"id":28,"text":5232,"url":28,"identifiers":5233},"Guidelines on Viral Inactivation and Removal Procedures Intended to Assure the Viral Safety of Human Blood Plasma Products. In:HorowitzB MinorP MorgenthalerJJ BurnoufT McIntoshR PadillaA Thorpe R. (drafting group) Geneva: WHO. BS\u002F01\u002F1941 2002(in press).",{},{"id":28,"text":4987,"url":28,"identifiers":5235},{"doi":4987},{"id":28,"text":5237,"url":28,"identifiers":5238},"Rosendaal FR, 1993, A sudden increase in factor VIII inhibitor development in multitransfused hemophilia patients in The Netherlands, Blood, 81, 10.1182\u002Fblood.V81.8.2180.2180",{"doi":5239},"10.1182\u002Fblood.V81.8.2180.2180",{"id":28,"text":5241,"url":28,"identifiers":5242},"10.1111\u002Fj.1423-0410.1994.tb01647.x",{"doi":5241},{"id":28,"text":5244,"url":28,"identifiers":5245},"10.1111\u002Fj.1423-0410.1989.tb00832.x",{"doi":5244},{"id":28,"text":5247,"url":28,"identifiers":5248},"10.1055\u002Fs-0037-1615389",{"doi":5247},{"id":28,"text":5250,"url":28,"identifiers":5251},"Mannucci PM, 1995, Preliminary evaluation of a nanofiltered factor IX concentrate, Thromb Haemost, 73, 737, 10.1055\u002Fs-0038-1653859",{"doi":5252},"10.1055\u002Fs-0038-1653859",{"id":28,"text":5254,"url":28,"identifiers":5255},"Yunoki M, 2000, A Forum for Exchanging Information on the Latest Developments in Virus Removal Filtration",{},{"id":28,"text":5257,"url":28,"identifiers":5258},"Feldman P, 1998, To Meet and Exchange Information on the Latest Developments in Virus Removal Technology, 47",{},{"id":28,"text":5260,"url":28,"identifiers":5261},"10.1016\u002F0378-4347(95)00107-T",{"doi":5260},{"id":28,"text":5263,"url":28,"identifiers":5264},"10.1006\u002Fbiol.1999.0242",{"doi":5263},{"id":28,"text":5266,"url":28,"identifiers":5267},"10.1159\u002F000204024",{"doi":5266},{"id":28,"text":5269,"url":28,"identifiers":5270},"10.1046\u002Fj.1365-2516.1999.t01-1-00284.x",{"doi":5269},{"id":28,"text":5272,"url":28,"identifiers":5273},"10.1111\u002Fj.1423-0410.1987.tb02979.x",{"doi":5272},{"id":28,"text":5275,"url":28,"identifiers":5276},"Romisch J, 1996, Nanofiltration in production of Beriplex P\u002FN: increasing the capacity of virus elimination while maintaining product quality, Beitr Infusionsther Transfusionsmed, 33, 220",{},{"id":28,"text":5278,"url":28,"identifiers":5279},"Nowak T, 1998, To Meet and Exchange Information on the Latest Developments in Virus Removal Technology, 16",{},{"id":28,"text":5281,"url":28,"identifiers":5282},"10.1016\u002FS0049-3848(00)00339-X",{"doi":5281},{"id":28,"text":5284,"url":28,"identifiers":5285},"Over J, 1998, To Meet and Exchange Information on the Latest Developments in Virus Removal Technology, 5",{},{"id":28,"text":5287,"url":28,"identifiers":5288},"10.1016\u002F0378-4347(94)00532-A",{"doi":5287},{"id":28,"text":5290,"url":28,"identifiers":5291},"10.1016\u002FS0165-022X(01)00221-4",{"doi":5290},{"id":28,"text":5293,"url":28,"identifiers":5294},"Maeno H, 2000, A Forum for Exchanging Information on the Latest Developments in Virus Removal Filtration, 21",{},{"id":28,"text":5296,"url":28,"identifiers":5297},"10.1046\u002Fj.1423-0410.2001.00114.x",{"doi":5296},{"id":28,"text":5299,"url":28,"identifiers":5300},"Chtourou S, A Forum for Exchanging Information on the 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21",{},{"id":28,"text":5344,"url":28,"identifiers":5345},"Maeno H, 2000, A Forum for Exchanging Information on the Latest Developments in Virus Removal Filtration, 22",{},{"id":28,"text":5347,"url":28,"identifiers":5348},"Poulle M, 1994, Large‐scale preparation of highly purified human C1‐inhibitor for therapeutic use, Blood Coag Fibrinolysis, 5, 543",{},{"id":28,"text":5350,"url":28,"identifiers":5351},"BunchC KavanaghC HeldebrantC BhattacharyaP CraigWC.Alpha‐1 Proteinase Inhibitor (A1PI) Virus Reduction Studies.XVII Congress of the International Society on Thrombosis and Haemostasis Washington DC USA August 1421 1999 no. 912 (Abstracts).",{},{"id":28,"text":5353,"url":28,"identifiers":5354},"Bunch C, 1999, A Forum for Exchanging Information on the Latest Developments in Virus Removal Technology, 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a bleeding disorder, but it is not the only reproductive tract abnormality that women with bleeding disorders experience. Women with bleeding disorders appear to be at an increased risk of developing haemorrhagic ovarian cysts and possibly endometriosis. As they grow older, they may be more likely to manifest conditions, which present with bleeding such as fibroids, endometrial hyperplasia and polyps. Women with bleeding disorders are more likely to undergo a hysterectomy and are more likely to have the operation at a younger age. During pregnancy, they may be at greater risk of miscarriage and bleeding complications. At the time of childbirth, women with bleeding disorders appear to be more likely to experience postpartum haemorrhage, particularly delayed or secondary postpartum haemorrhage. Vaginal or vulvar haematomas, extremely rare in women without bleeding disorders, are not uncommon. While women with bleeding disorders are at risk for the same obstetrical and gynaecological problems that affect all women, they appear to be disproportionately affected by conditions that manifest with bleeding.\u003C\u002Fjats:p>",{"EN":5446},"More than menorrhagia: a review of the obstetric and gynaecological manifestations of bleeding 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Lack of detailed natural history and outcomes data for neonates and toddlers with haemophilia hampers the provision of optimal management of the disorder. We report an analysis of prospective data collected from 580 neonates and toddlers aged 0–2 years with haemophilia enrolled in the Universal Data Collection (UDC) surveillance project of the Centers for Disease Control and Prevention (CDC). This study focuses on a cohort of babies with haemophilia whose diagnosis was established before the age of two. The mode of delivery, type and severity of haemophilia, onset and timing of haemorrhages, site(s) of bleeding, provision of prophylaxis with coagulation factor replacement therapy, and the role played by the federally funded Haemophilia Treatment Centers (HTC) in the management of these infants with haemophilia were evaluated. Seventy‐five per cent of haemophilic infants were diagnosed early, in the first month of life, especially those with a family history or whose mothers were known carriers; infants of maternal carriers were more likely to be delivered by C‐section. Involvement of an HTC prior to delivery resulted in avoidance of the use of assisted deliveries with vacuum and forceps. Bleeding from the circumcision site was the most common haemorrhagic complication, followed by intra‐ and extra‐cranial haemorrhages and bleeding from heel stick blood sampling. Eight per cent of the infants were administered factor concentrate within 24 h of birth; more than half were treated to prevent bleeding. 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