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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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von lebensmittelbedingten Infektionen",{"VOID":953},"10.1007\u002Fs00508-005-0423-y","PUBLICATION","Author affiliation is blank","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00508-005-0423-y",[958],{"id":959,"sortIndex":32,"researcher":28,"roles":960,"affiliations":962,"properties":963},"9cb11327-39eb-42e3-a556-98ea9e1c51c6",[961],"AUTHOR",[],{"title":964},{"VI":965},"Franz Allerberger","ARTICLE",{"url":956,"publisher":968,"properties":1010},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":969,"slug":872,"properties":970,"entityType":25,"verifyStatus":880,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":974,"manageAffiliations":979,"indexDatabases":990,"url":933,"thumbnailPath":28,"statistic":1005,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":971,"title":972,"eissn":973},{"VOID":875},{"EN":877},{"VOID":879},[975],{"id":883,"createTime":28,"updateTime":28,"relativeEntities":976,"label":977,"description":978,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":886},{},[980,985],{"id":890,"createTime":28,"updateTime":28,"relativeEntities":981,"slug":28,"properties":982,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":984,"statistic":28},[],{"title":983},{"EN":894},[896],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":986,"slug":28,"properties":987,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":989,"statistic":28},[],{"title":988},{"EN":902},[896],[991,998],{"id":906,"indexDatabase":992,"url":918,"indexYears":28,"academicFieldIds":997,"indexDatabaseRanking":28},{"id":908,"createTime":28,"updateTime":28,"relativeEntities":993,"label":994,"description":995,"key":915,"publicationTags":996,"standard":28},[],{"EN":911,"VI":911},{"EN":913,"VI":914},[917,813],[920],{"id":922,"indexDatabase":999,"url":928,"indexYears":929,"academicFieldIds":1004,"indexDatabaseRanking":932},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":1000,"label":1001,"description":1002,"key":781,"publicationTags":1003,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[931],{"impactFactor":32,"impactFactorByYear":1006,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":40,"totalPublicationByYear":1007,"totalCitation":32,"totalCitationByYear":1008,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1009,"hindexLast5Year":32,"hindex":32},{},{"2007":40},{},{},{"pages":1011,"volume":1013},{"VOID":1012},"576-578",{"VOID":5},"2005-09-01",2005,[932,917],false,{"id":1019,"createTime":1020,"updateTime":1021,"relativeEntities":1022,"slug":1023,"properties":1024,"entityType":954,"verifyStatus":26,"verifyTime":1021,"verifyNote":1033,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1034,"fullTextUrl":28,"authors":1035,"publicationType":966,"publisherRelationship":1064,"citationCount":28,"citationInfo":28,"publishDate":1112,"publishYear":1113,"citationAnalyzeStatus":880,"lastCitationAnalyze":28,"indexDatabases":1114,"openAccess":28,"references":28,"isForceReanalyzing":1017},"0030b021-e179-49d2-a5be-907a32ed87f8","2024-01-02T15:24:01.380+00:00","2025-02-01T05:22:23.947+00:00",[],"Profile-of-SARS-CoV-2",{"abstract":1025,"title":1027,"references":1029,"doi":1031},{"EN":1026},"The recent emergence of a new coronavirus (severe acute respiratory syndrome coronavirus‑2, SARS-CoV-2) that is transmitted efficiently among humans and can result in serious disease and\u002For death has become a global threat to public health and economy. In this article, we describe some of the most important characteristics of this new virus (including gaps in our understanding) and provide a perspective of ongoing activities for developing virus-specific countermeasures, such as vaccines and antiviral drugs.",{"EN":1028},"Profile of SARS-CoV-2",{"VOID":1030},"Andersen KG, Rambaut A, Lipkin WI, Holmes EC, Garry RF. The proximal origin of SARS-CoV‑2. Nat Med. 2020;26(4):450–2.\nForni D, Cagliani R, Clerici M, Sironi M. Molecular evolution of human Coronavirus genomes. Trends Microbiol. 2017;25(1):35–48.\nCui J, Li F, Shi Z‑L. Origin and evolution of pathogenic coronaviruses. Nat Rev Microbiol. 2019;17(3):181–92.\nKhamassi Khbou M, Daaloul Jedidi M, Bouaicha Zaafouri F, Benzarti Mh. Coronaviruses in farm animals: Epidemiology and public health implications. Veterinary Medicine and Science. 2020. https:\u002F\u002Fdoi.org\u002F10.1002\u002Fvms3.359\nGraham RL, Donaldson EF, Baric RS. 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Cell. 2020;181(4):905–913.e7.\nRobbiani DF, Gaebler C, Muecksch F, Lorenzi JCC, Wang Z, Cho A, et al. Convergent antibody responses to SARS-CoV‑2 in convalescent individuals. Nature. 2020;584(7821):437–42.\nZost SJ, Gilchuk P, Case JB, Binshtein E, Chen RE, Nkolola JP, et al. Potently neutralizing and protective human antibodies against SARS-CoV‑2. Nature. 2020;584(7821):443–9.\nHansen J, Baum A, Pascal KE, Russo V, Giordano S, Wloga E, et al. Studies in humanized mice and convalescent humans yield a SARS-CoV‑2 antibody cocktail. Science. 2020;369(6506):1010.\nZhang H, Penninger JM, Li Y, Zhong N, Slutsky AS. Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV‑2 receptor: molecular mechanisms and potential therapeutic target. Intensive Care Med. 2020;46(4):586–90.\nNathanson N, Kew OM. From emergence to eradication: the epidemiology of poliomyelitis deconstructed. Am J Epidemiol. 2010;172(11):1213–29.\nFulton CDM, Beasley DWC, Bente DA, Dineley KT. Long-term, West Nile virus-induced neurological changes: A comparison of patients and rodent models. Brain Behav Immun Health. 2020;7:100105.\nGraham RL, Baric RS. SARS-CoV-2: combating coronavirus emergence. Immunity. 2020;52(5):734–6.\nXie X, Muruato A, Lokugamage KG, Narayanan K, Zhang X, Zou J, et al. An infectious cDNA clone of SARS-CoV‑2. Cell Host Microbe. 2020;27(5):841–848.e3.\nWrobel AG, Benton DJ, Xu P, Roustan C, Martin SR, Rosenthal PB, et al. SARS-CoV‑2 and bat RaTG13 spike glycoprotein structures inform on virus evolution and furin-cleavage effects. 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Jahrestagung der Österreichischen Gesellschaft für Endokrinologie und Stoffwechsel, St. Wolfgang, 21.–22. April 2005",{"VOID":1188},"10.1007\u002Fs00508-005-0345-8","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00508-005-0345-8",[],{"url":1189,"publisher":1192,"properties":1234},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1193,"slug":872,"properties":1194,"entityType":25,"verifyStatus":880,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1198,"manageAffiliations":1203,"indexDatabases":1214,"url":933,"thumbnailPath":28,"statistic":1229,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1195,"title":1196,"eissn":1197},{"VOID":875},{"EN":877},{"VOID":879},[1199],{"id":883,"createTime":28,"updateTime":28,"relativeEntities":1200,"label":1201,"description":1202,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":886},{},[1204,1209],{"id":890,"createTime":28,"updateTime":28,"relativeEntities":1205,"slug":28,"properties":1206,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1208,"statistic":28},[],{"title":1207},{"EN":894},[896],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1210,"slug":28,"properties":1211,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1213,"statistic":28},[],{"title":1212},{"EN":902},[896],[1215,1222],{"id":906,"indexDatabase":1216,"url":918,"indexYears":28,"academicFieldIds":1221,"indexDatabaseRanking":28},{"id":908,"createTime":28,"updateTime":28,"relativeEntities":1217,"label":1218,"description":1219,"key":915,"publicationTags":1220,"standard":28},[],{"EN":911,"VI":911},{"EN":913,"VI":914},[917,813],[920],{"id":922,"indexDatabase":1223,"url":928,"indexYears":929,"academicFieldIds":1228,"indexDatabaseRanking":932},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":1224,"label":1225,"description":1226,"key":781,"publicationTags":1227,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[931],{"impactFactor":32,"impactFactorByYear":1230,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":40,"totalPublicationByYear":1231,"totalCitation":32,"totalCitationByYear":1232,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1233,"hindexLast5Year":32,"hindex":32},{},{"2007":40},{},{},{"pages":1235,"volume":1237},{"VOID":1236},"A13-A22",{"VOID":5},"2005-04-01",[932,917],{"id":1241,"createTime":1242,"updateTime":1243,"relativeEntities":1244,"slug":1245,"properties":1246,"entityType":954,"verifyStatus":26,"verifyTime":1243,"verifyNote":1033,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1255,"fullTextUrl":28,"authors":1256,"publicationType":966,"publisherRelationship":1326,"citationCount":28,"citationInfo":28,"publishDate":1374,"publishYear":1375,"citationAnalyzeStatus":880,"lastCitationAnalyze":28,"indexDatabases":1376,"openAccess":28,"references":28,"isForceReanalyzing":1017},"00c834df-a699-4073-87ba-e5701ee3d963","2024-02-10T15:10:01.343+00:00","2024-12-12T23:58:25.096+00:00",[],"Severe-Traumatic-Brain-Injury-in-Austria-III-Prehospital-status-and-treatment",{"abstract":1247,"title":1249,"references":1251,"doi":1253},{"EN":1248},"OBJECTIVES: The goal of this paper is to describe prehospital status and treatment of patients with severe TBI in Austria. PATIENTS AND METHODS: Data sets from 396 patients with severe TBI (Glasgow Coma Scale score \u003C 9) included by 5 Austrian hospitals were available. The analysis focused on incidence and\u002For degree of severity of typical clinical signs, frequency of use of different management options, and association with outcomes for both. ICU mortality, 90-day mortality, final outcome (favorable = good recovery or moderate disability; unfavorable = severe disability, vegetative state, or death) after 6 or 12 months, and ratio of observed (90-day) to predicted mortality (O\u002FE ratio) are reported for the selected parameters. Chi2-test, t-test, Fisher's exact test, and logistic regression were used to identify significant (p \u003C 0.05) differences for association with survival and favorable outcome (both coded as 1). RESULTS: The majority of patients were male (72%), mean age was 49 ± 21 years, mean injury severity score (ISS) was 27 ± 17, mean first GCS score was 5.6 ± 2.9, and expected hospital survival was 63 ± 30%. ICU mortality was 32%, 90-day mortality was 37%, and final outcome was favorable in 35%, unfavorable in 53%, unknown in 12%. We found that age > 60 years, ISS > 50 points, GCS score \u003C 4, bilateral changes in pupil size and reactivity, respiratory rate \u003C 10\u002Fmin, systolic blood pressure (SBP) \u003C 90 mm Hg, and heart rate \u003C 60\u002Fmin were associated with significantly higher ICU and 90-day mortality rates, and lower rates of favorable outcome. With regard to prognostic value the GCS motor response score is identical to the full GCS score. Administration of > 1000 ml of fluid and helicopter transport were associated with better outcomes than expected, while endotracheal intubation in the field had neither a positive nor a negative effect on outcomes. Administration of no or \u003C 500 ml of fluids was associated with worse outcomes than expected. Outcomes were better than expected in the few patients (5%) who received hypertonic saline. CONCLUSIONS: Age, ISS, and initial neuro status are the factors most closely associated with outcome. Hypotension must be avoided. Fluids should be given to restore and\u002For maintain SBP > 110 mm Hg. Helicopter transport should be arranged for more seriously injured patients.",{"EN":1250},"Severe Traumatic Brain Injury in Austria III: Prehospital status and treatment",{"VOID":1252},"Rusnak M, Janciak I, Majdan M, Wilbacher I, Mauritz W; for the Austrian Severe TBI Study Investigators (2007) Severe traumatic brain injury in Austria I: introduction to the study. Wien Klin Wochenschr 119: 23–28\nMarshall LF, Becker DP, Bowers SA, et al (1983) The National Traumatic Coma Data Bank. Part 1: design, purpose, goals, and results. J Neurosurg 59: 276–284\nBoyd CR, Tolson MA, Copes WS (1987) Evaluating trauma care: the TRISS method. Trauma Score and the Injury Severity Score. J Trauma 27: 370–378\nDownloaded from www.xlstat.com\u002F\nTeasdale G, Jennett B (1976) Assessment and prognosis of coma after head injury. Acta Neurochir (Wien) 34: 45–55\nBalestreri M, Czosnyka M, Chatfield DA, Steiner LA, Schmidt EA, Smielewski P, Matta B, Pickard JD (2004) Predictive value of Glasgow Coma Scale after brain trauma: change in trend over the past ten years. J Neurol Neurosurg Psychiatry 75 (1): 161–162\nThe Brain Trauma Foundation. The American Association of Neurological Surgeons. The Joint Section on Neurotrauma and Critical Care (2000) Guidelines for the management of severe brain trauma. J Neurotrauma 17: 457–627\nChoi SC, Narayan RK, Anderson RL, Ward JD (1988) Enhanced specificity of prognosis in severe head injury. J Neurosurg 69: 381–385\nTien HC, Cunha JR, Wu SN, Chughtai T, Tremblay LN, Brenneman FD, Rizoli SB (2006) Do trauma patients with a glasgow coma scale score of 3 and bilateral fixed and dilated pupils have any chance of survival? J Trauma 60: 274–278\nZafonte RD, Hammond FM, Mann NR, Wood DL, Millis SR, Black KL (1996) Revised trauma score: an additive predictor of disability following traumatic brain injury? Am J Phys Med Rehabil 75: 456–461\nChesnut RM, Marshall SB, Piek J, Blunt BA, Klauber MR, Marshall LF (1993) Early and late systemic hypotension as a frequent and fundamental source of cerebral ischemia following severe brain injury in the Traumatic Coma Data Bank. Acta Neurochir [Suppl] (Wien) 59: 121–125\nWright KD, Knowles CH, Coats TJ, Sutcliffe JC (1996) Efficient timely evacuation of intracranial haematoma — the effect of transport direct to a specialist centre: Injury 27: 719–721\nAmerican Association for the Surgery of Trauma; Child Neurology Society; International Society for Pediatric Neurosurgery; International Trauma Anesthesia and Critical Care Society; Society of Critical Care Medicine; World Federation of Pediatric Intensive and Critical Care Societies; National Center for Medical Rehabilitation Research; National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Synthes USA; International Brain Injury Association (2003) Guidelines for the acute medical management of severe traumatic brain injury in infants, children, and adolescents. J Trauma 54 [6 Suppl]: S235–S310\nGabriel EJ, Ghajar J, Jagoda A, Pons PT, Scalea T, Walters BC; Brain Trauma Foundation (2002) Guidelines for prehospital management of traumatic brain injury. J Neurotrauma 19: 111–174\nChesnut RM, Marshall LF, Klauber MR, Blunt BA, Baldwin N, Eisenberg HM, Jane JA, Marmarou A, Foulkes MA (1993) The role of secondary brain injury in determining outcome from severe head injury. J Trauma 34: 216–222\nJeremitsky E, Omert L, Dunham CM, Protetch J, Rodriguez A (2003) Harbingers of poor outcome the day after severe brain injury: hypothermia, hypoxia, and hypoperfusion. J Trauma 54: 312–319\nWinchell RJ, Hoyt DB (1997) Endotracheal intubation in the field improves survival in patients with severe head injury. Trauma Research and Education Foundation of San Diego. Arch Surg 132: 592–597\nDavis DP, Hoyt DB, Ochs M, Fortlage D, Holbrook T, Marshall LK, Rosen P (2003) The effect of paramedic rapid sequence intubation on outcome in patients with severe traumatic brain injury. J Trauma 54: 444–453\nDavis DP, Peay J, Sise MJ, Vilke GM, Kennedy F, Eastman AB, Velky T, Hoyt DB (2005) The impact of prehospital endotracheal intubation on outcome in moderate to severe traumatic brain injury. J Trauma 58: 933–939\nWang HE, Peitzman AB, Cassidy LD, Adelson PD, Yealy DM (2004) Out-of-hospital endotracheal intubation and outcome after traumatic brain injury. Ann Emerg Med 44: 439–450\nHelm M, Hauke J, Lampl L (2002) A prospective study of the quality of pre-hospital emergency ventilation in patients with severe head injury. Br J Anaesth 88: 345–349\nLal D, Weiland S, Newton M, Flaten A, Schurr M (2003) Pre-hospital hyperventilation after brain injury: a prospective analysis of prehospital and early hospital hyperventilation of the brain-injured patient. Prehospital Disaster Med 18: 20–23\nDavis DP, Heister R, Poste JC, Hoyt DB, Ochs M, Dunford JV (2005) Ventilation patterns in patients with severe traumatic brain injury following paramedic rapid sequence intubation. Neurocrit Care 2: 165–171\nDavis DP, Stern J, Sise MJ, Hoyt DB (2005) A follow-up analysis of factors associated with head-injury mortality after paramedic rapid sequence intubation. J Trauma 59: 486–490\nStocchetti N, Maas AI, Chieregato A, van der Plas AA (2005) Hyperventilation in head injury: a review. Chest 127: 1812–1827\nWerner C, Reeker W, Engelhard K, Lu H, Kochs E (1997) Ketamine racemate and S-(+)-ketamine. Cerebrovascular effects and neuroprotection following focal ischemia. Anaesthesist 46 [Suppl 1]: S55–S60\nBickell WH, Wall MJ Jr, Pepe PE, Martin RR, Ginger VF, Allen MK, Mattox KL (1994) Immediate versus delayed fluid resuscitation for hypotensive patients with penetrating torso injuries. N Engl J Med 331: 1105–1109\nSoreide E, Deakin Ch (2005) Pre-hospital fluid therapy in the critically injured patient — a clinical update. Injury 36: 1001–1010\nCooper DJ, Myles PS, McDermott FT, Murray LJ, Laidlaw J, Cooper G, Tremayne AB, Bernard SS, Ponsford J; HTS Study Investigators (2004) Prehospital hypertonic saline resuscitation of patients with hypotension and severe traumatic brain injury: a randomized controlled trial. JAMA 291: 1350–1357\nFinfer S, Bellomo R, Boyce N, French J, Myburgh J, Norton R; SAFE Study Investigators (2004) A comparison of albumin and saline for fluid resuscitation in the intensive care unit. N Engl J Med 350: 2247–2256\nNeff TA, Doelberg M, Jungheinrich C, Sauerland A, Spahn DR, Stocker R (2003) Repetitive large-dose infusion of the novel hydroxyethyl starch 130\u002F0.4 in patients with severe head injury. Anesth Analg 96: 1453–1459\nHarutjunyan L, Holz C, Rieger A, Menzel M, Grond S, Soukup J (2005) Efficiency of 7.2% hypertonic saline hydroxyethyl starch 200\u002F0.5 versus mannitol 15% in the treatment of increased intracranial pressure in neurosurgical patients — a randomized clinical trial [ISRCTN62699180]. Crit Care 9: R530–R540\nMauritz W, Schimetta W, Oberreither S, Polz W (2002) Are hypertonic hyperoncotic solutions safe for prehospital small-volume resuscitation? Results of a prospective observational study. Eur J Emerg Med 9: 315–319\nWade CE, Grady JJ, Kramer GC, Younes RN, Gehlsen K, Holcroft JW (1997) Individual patient cohort analysis of the efficacy of hypertonic saline\u002Fdextran in patients with traumatic brain injury and hypotension. J Trauma 42 [5 Suppl]: S61–S65\nDavis DP, Peay J, Serrano JA, Buono C, Vilke GM, Sise MJ, Kennedy F, Eastman AB, Velky T, Hoyt DB (2005) The impact of aeromedical response to patients with moderate to severe traumatic brain injury. 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Die Frage, ob diese Patienten im Vergleich zu nicht transplantierten Patienten ein reduziertes Überleben haben, wird unterschiedlich beantwortet. Für Mortalitätsunterschiede zwischen den Gruppen scheinen aber eher das Alter, die Dialysedauer und die damit verbundene höhere Komorbidität verantwortlich zu sein. Eine Studie, die den klinischen Verlauf bei Patienten mit Transplantatversagen an der Hämodialyse (HD) und an der PD verglichen hat, fand keinen signifikanten Überlebensunterschied zwischen den beiden Gruppen. Mehrere Studien zeigen einen schnelleren Rückgang der Nierenrestfunktion bei PD-Patienten mit chronischer Transplantatinsuffizienz im Vergleich zu nicht transplantierten Patienten. Ob die PD aber im Vergleich zur HD bei chronischer Transplantatinsuffizienz den Verlauf der renalen Clearance günstig beeinflusst, ist bisher noch nicht untersucht worden. Die bei transplantierten im Vergleich zu nicht transplantierten PD-Patienten nachweisbaren höheren peritonealen Transportraten könnten das technische Überleben beeinflussen. Die Frage nach Art und Ausmaß der Immunsuppression bei chronischer Transplantatinsuffizienz und die möglichen Auswirkungen auf Abstoßung, längeren Erhalt der Nierenrestfunktion und Infektionsrate wird kontrovers diskutiert. Immunsupprimierte transplantierte Patienten haben ein erhöhtes Risiko für gramnegative Peritonitiden, ein kürzeres Zeitintervall vom Beginn der Dialyse bis zum Auftreten der ersten Peritonitis, aber auch ein erhöhtes Risiko für Staphylococcus-aureus-Katheterinfektionen im Vergleich zu nicht transplantierten und zu diabetischen PD-Patienten. 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frequently bring their children to the Emergency Department (ED) because of the fever without apparent source (FWAS). To avoid possible complications, it is important to recognize serious bacterial infection (SBI) as early as possible. Various tests, including different clinical scores and scales, are used in the laboratory evaluation of patients. However, it is still impossible to predict the presence of SBI with complete certainty. Galetto-Lacour et al. developed and validated a risk index score, named Lab-score. Lab-score is based on the three predictive variables independently associated with SBI: procalcitonin (PCT), C-reactive protein (CRP), and urinary dipstick. The objective of this study was to assess the performance of the Lab-score in predicting SBI in well-appearing infants ≤ 180 days of age with FWAS, who presented to ED and were hospitalized with suspicion of having SBI. Based on this study findings, white blood cells count (WBC), CRP, PCT, and lab-score ≥ 3 were confirmed as useful biomarkers for differentiation between SBI and non-SBI. Also, receiver operating characteristic curve (ROC) analysis confirmed that all of them were useful for differentiation between SBI and non-SBI patients with the highest area under curve (AUC) calculated for the Lab-score. The results of this research confirmed its value, with calculated sensitivity of 67.7 % and specificity of 98.6 % in prediction of SBI in infants aged ≤ 180 days. Its value was even better in infants aged ≤ 90 days with sensitivity of 75 % and specificity of 97.7 %. In conclusion, we demonstrated the high value of lab-score in detecting SBI in infants under 6 months of age with FWAS.",{"EN":1648},"Lab-score is a valuable predictor of serious bacterial infection in infants admitted to hospital",{"VOID":1650},"Baraff L, Bass J, Fleisher G, et al. Practice guideline for the management of infants and children 0 to 36 months of age with fever without source. Pediatrics. 1993;92(1):1–12.\nVorwerk C, Manias K, Davies F, Coats T. Prediction of severe bacterial infection in children with an emergency department diagnosis of infection. Emerg Med J. 2011;28(11):948–51.\nBachur R, Harper M. Predictive model for serious bacterial infections among infants younger than 3 months of age. Pediatrics. 2001;108(2):311–6.\nTrautner B, Caviness A, Gerlacher G, Demmler G, Macias C. Prospective evaluation of the risk of serious bacterial infection in children who present to the emergency department with hyperpyrexia (temperature of 106 degrees F or higher). Pediatrics. 2006;118(1):34–40.\nHoffmann J. Neutrophil CD64: a diagnostic marker for infection and sepsis. Clin Chem Lab Med. 2009;47(8):903–16.\nAshkenazi-Hoffnung L, Livni G, Amir J, Bilavsky E. Serious bacterial infections in hospitalized febrile infants aged 90 days or younger: The traditional combination of ampicillin and gentamicin is still appropriate. Scand J Infect Dis. 2011;43(6–7):489–94.\nHuppler AR, Eickhoff JC, Wald ER. Performance of low-risk criteria in the evaluation of young infants with fever: review of the literature. Pediatrics. 2010;125(2):228–33.\nBilavsky E, Yarden-Bilavsky H, Ashkenazi S, Amir J. C-reactive protein as a marker of serious bacterial infections in hospitalized febrile infants. Acta Paediatr. 2009;98(11):1776–80.\nOlaciregui I, Hernandez U, Munoz J, Emparanza J, Landa J. Markers that predict serious bacterial infection in infants under 3 months of age presenting with fever of unknown origin. Arch Dis Child. 2009;94(7):501–5.\nAndreola B, Bressan S, Callegaro S, Liverani A, Plebani M, Da Dalt L. Procalcitonin and C-reactive protein as diagnostic markers of severe bacterial infections in febrile infants and children in the emergency department. Pediatr Infect Dis J. 2007;26(8):672–7.\nDagan R, Sofer S, Phillip M, Shachak E. Ambulatory care of febrile infants younger than 2 months of age classified as being at low-risk for having serious bacterial-infections. J Pediatr. 1988;112(3):355–60.\nBaker M, Bell L, Avner J. Outpatient management without antibiotics of fever in selected infants. N Engl J Med. 1993;329(20):1437–41.\nMarkic J, Jeroncic A, Polancec D, et al. CD15s is a potential biomarker of serious bacterial infection in infants admitted to hospital. Eur J Pediatr. 2013;172(10):1363–9.\nCommittee ACoEPCP, Fever. ACoEPCPSoP. Clinical policy for children younger than three years presenting to the emergency department with fever. Ann Emerg Med. 2003;42(4):530–45.\nJaskiewicz J, McCarthy C, Richardson A, et al. Febrile infants at low-risk for serious bacterial-infection—An appraisal of the Rochester criteria and implications for management. Pediatrics. 1994;94(3):390–6.\nLacour A, Zamora S, Gervaix A. A score identifying serious bacterial infections in children with fever without source. Pediatr Infect Dis J. 2008;27(7):654–6.\nGaletto-Lacour A, Zamora SA, Andreola B, et al. Validation of a laboratory risk index score for the identification of severe bacterial infection in children with fever without source. Arch Dis Child. 2010;95(12):968–73.\nBressan S, Gomez B, Mintegi S, et al. Diagnostic performance of the lab-score in predicting severe and invasive bacterial infections in well-appearing young febrile infants. Pediatr Infect Dis J. 2012;31(12):1239–44.\nPearson G, editor. Why children die: a pilot study 2006; England (South West, North East and West Midlands), Wales and Northern Ireland. London: CEMACH; 2008.\nNg P, Lam H. Diagnostic markers for neonatal sepsis. Curr Opin Pediatr. 2006;18(2):125–31.\nHui C, Neto G, Tsertsvadze A, et al. Diagnosis and management of febrile infants (0–3 months). Evid Rep Technol Assess (Full Rep). 2012(205):1–297.\nLacour A, Gervaix A, Zamora S, et al. Procalcitonin, IL-6, IL-8, IL-1 receptor antagonist and C-reactive protein as identificators of serious bacterial infections in children with fever without localising signs. Eur J Pediatr. 2001;160(2):95–100.\nGaletto-Lacour A, Zamora S, Gervaix A. Bedside procalcitonin and C-reactive protein tests in children with fever without localizing signs of infection seen in a referral center. Pediatrics. 2003;112(5):1054–60.\nHsiao A, Chen L, Baker M. Incidence and predictors of serious bacterial infections among 57-to 180-day-old infants. Pediatrics. 2006;117(5):1695–701.\nSanders S, Barnett A, Correa-Velez I, Coulthard M, Doust J. Systematic review of the diagnostic accuracy of C-reactive protein to detect bacterial infection in nonhospitalized infants and children with fever. J Pediatr. 2008;153(4):570–4.\nYo CH, Hsieh PS, Lee SH, et al. Comparison of the test characteristics of procalcitonin to C-reactive protein and leukocytosis for the detection of serious bacterial infections in children presenting with fever without source: a systematic review and meta-analysis. Ann Emerg Med. 2012;60(5):591–600.\nRudensky B, Sirota G, Erlichman M, Yinnon A, Schlesinger Y. Neutrophil CD64 expression as a diagnostic marker of bacterial infection in febrile children presenting to a Hospital Emergency Department. Pediatr Emerg Care. 2008;24(11):745–8.\nHodge G, Hodge S, Han P, Haslam R. Multiple leucocyte activation markers to detect neonatal infection. 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