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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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Expanded",{"EN":932,"VI":933},"SCIE database","Cơ sở dữ liệu SCIE","scie",[936,813],"SCIE","https:\u002F\u002Fmjl.clarivate.com\u002Fsearch-results?issn=0172-0643",[939,940],"5f55e015-9add-4a50-bbdf-b4dbac2e40b3","22fd6c38-3ec0-41e0-8ae8-a4290171207e","https:\u002F\u002Flink.springer.com\u002Fjournal\u002F246",{"impactFactor":32,"impactFactorByYear":943,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":567,"totalPublicationByYear":944,"totalCitation":32,"totalCitationByYear":945,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":946,"hindexLast5Year":32,"hindex":32},{},{"1980":40,"1982":40,"1983":40,"1985":40,"1989":40,"1991":123,"1993":123,"2002":40,"2003":40,"2006":42,"2007":123,"2008":45,"2009":42,"2011":46,"2012":42,"2013":45,"2014":48,"2017":42,"2018":40,"2019":45,"2020":40,"2021":46,"2022":123,"2023":42,"2024":40},{},{},{"meta":948,"data":950},{"total":949},"4715",[951,1074,1234,1342,1494,1639,1750,1899,2035,2156],{"id":952,"createTime":953,"updateTime":954,"relativeEntities":955,"slug":956,"properties":957,"entityType":966,"verifyStatus":26,"verifyTime":954,"verifyNote":967,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":968,"fullTextUrl":28,"authors":969,"publicationType":1017,"publisherRelationship":1018,"citationCount":28,"citationInfo":28,"publishDate":1070,"publishYear":1071,"citationAnalyzeStatus":880,"lastCitationAnalyze":28,"indexDatabases":1072,"openAccess":28,"references":28,"isForceReanalyzing":1073},"000954c9-a09f-4e67-b519-0b4433809cbe","2024-01-24T16:27:16.133+00:00","2025-02-26T18:02:33.937+00:00",[],"Clinical-Application-of-the-QRS-T-Angle-for-the-Prediction-of-Ventricular-Arrhythmias-in-Patients-with-the-Fontan-Palliation",{"abstract":958,"title":960,"references":962,"doi":964},{"EN":959},"Fontan palliation patients are at risk for ventricular arrhythmias post-operatively. This study aimed to evaluate whether differences in the spatial QRS-T angle can reliably predict ventricular arrhythmias in patients who had undergone Fontan palliation. A total of 117 patients who had the Fontan palliation and post-Fontan catheterization were included. Ventricular arrhythmias were identified in nine patients. Measurements of ECG parameters including QRS vector magnitude, QRS duration, corrected QT interval, and spatial peaks QRS-T angles were performed, and compared between those with and without ventricular arrhythmias. The only ECG parameter to distinguish those with versus those without VA was the SPQRS-T angle (p \u003C 0.001), which at a cut-off value of 102.9° gave sensitivity, specificity, positive and negative predictive values of 100.0, 57.0, 17.6 and 100.0%, respectively. Only the spatial peaks QRS-T angle differentiated those with and without ventricular arrhythmia development with a univariate HR 1.237 (95% CI 1.021–1.500) and a multivariate HR of 1.032 (1.009–1.056) when catheter measured parameters were taken into account. In Fontan patients, the spatial peaks QRS-T angle is a significant independent predictor of ventricular arrhythmias. Clinical usefulness of this parameter remains to be seen and should be tested prospectively.",{"EN":961},"Clinical Application of the QRS-T Angle for the Prediction of Ventricular Arrhythmias in Patients with the Fontan Palliation",{"VOID":963},"Fontan F, Baudet E (1971) Surgical repair of tricuspid atresia. Thorax 26:240–248\nGale AW, Danielson GK, McGoon DC et al (1979) Modified Fontan operation for univentricular heart and complicated congenital lesions. J Thorac Cardiovasc Surg 78:8310838\nTweddell JS, Nersesian M, Mussatto KA et al (2009) Fontan palliation in the modern era: factors impacting mortality and morbidity. Ann Thorac Surg 88:1291–1299\nPeters NS, Sommerville J (1992) Arrhythmias after the Fontan procedure. Br Heart J 68:199–204\nDeal BJ (2012) Late arrhythmias following Fontan surgery. World J Pediatr Congenit Heart Surg 3:194–200\nMertens L, Hagler DJ, Somerville J (1998) Protein-losing enteropathy after the Fontan operation: an international multicenter study. PLE study group. J Thorac Cardiovasc Surg 115:1063–1073\nRydberg A, Karlsson M, Hörnsten R (2008) Can analysis of heart rate variability predict arrhythmia in children with Fontan circulation? Pediatr Cardiol 29:50–55\nDurongpisikul K, Porter CJ, Cetta F et al (1998) Predictors of early- and late-onset supraventricular tachyarrhythmias after Fontan operation. Am Heart Assoc 98:1099–1107\nGelatt M, Hamilton RM, McCrindle BW et al (1994) Risk factors for atrial tachyarrhythmias after the Fontan operation. J Am Coll Cardiol 24:1735–1741\nTuzcu V, Ozkan B, Sullivan N et al (2000) P wave signal-averaged electrocardiogram as a new marker for atrial tachyarrhythmias in postoperative Fontan patients. J Am Coll Cardiol 36:602–607\nYamada T, Fukunami M, Shimonagata T et al (2001) Identification of sinus node dysfunction by use of P-wave signal-averaged electrocardiograms in paroxysmal atrial fibrillation: a prospective study. Am Heart J 142:286–293\nVoulgari C, Pagoni S, Tesfaye S et al (2013) The spatial QRS-T angle: implications in clinical practice. Curr Cardiol Rev 9:197–210\nCortez D, Graw S, Mestroni L (2016) In hypertrophic cardiomyopathy, the spatial peaks QRS-T angle identifies those with sustained ventricular arrhythmias. Clin Cardiol 39:459–463\nRautaharju PM, Prineas RJ, Wood J et al (2007) Electrocardiographic predictors of new-onset heart failure in men and in women free of coronary heart disease (from the Atherosclerosis in Communities [ARIC] study). Am J Cardiol 100:1437–1441\nTamazaki T, Froelicher VG, Myers J et al (2005) Spatial QRS-T angle predicts cardiac death in a clinical population. Heart Rhythm 2:73–78\nPoplock Potter SL, Holvqvist F, Platonov PG et al (2010) Detection of hypertrophic cardiomyopathy is improved when using advanced rather than strictly conventional 12-lead electrocardiogram. J Electrocardiol 43:713–718\nCortez D, Sharma N, Cavanagh J et al (2015) The spatial QRS-T angle outperforms the Italian and seattle ECG-based criteria for detections of hypertrophic cardiomyopathy. J Electrocardiol 48:826–833\nCortez D, Sharma N, Cavanaugh J, et al (2016) Lower spatial QRS-T angle rules out sustained ventricular arrhythmias in children with hypertrophic cardiomyopathy. Cardiol Young\nCortez D, Ruckdeschel E, McCanta AC et al (2015) Vectorcardiographic predictors of ventricular arrhythmia inducibility in patients with tetralogy of Fallot. J Electrocardiol 48:141–144\nCortez D, Barham W, Ruckdeschel E, et al (2016) Non-invasive predictors of ventricular arrhythmias in patients with tetralogy of Fallot undergoing pulmonary valve replacements. JACC Electrophysiol\nKors JA, van Herpen G, Sittig AC et al (1990) Reconstruction of the Frank vectorcardiogram from standard electrocardiographic leads: diagnostic comparison of different methods. Eur Heart J 11:1083–1092\nCortez D, Sharma N, Devers C, Devers E, Schlegel TT (2014) Visual transform applications for estimating the spatial QRS-T angle from the conventional 12-lead ECG: Kors is still most Frank. J Electrocardiol 47:12–19\nVoulgari C, Tentolouris N, Moyssakis I et al (2006) The spatial QRS-T angle: association with diabetes and left ventricular performance. Eur J Clin Investig 36:608–613\nRautaharju PM, Ge S, Nelson JC et al (2006) Comparison of mortality risk for electrocardiographic abnormalities in men and women with and without coronary heart disease (from the cardiovascular health study). Am J Cardiol 97:309–315\nRautaharju PM, Kooperberg C, Larson JC et al (2006) Electrocardiographic predictors of incidence congestive heart failure and all-cause mortality is postmenopausal women: the women’s health initiative. Circulation 113:481–489\nRautaharju PM, Kooperbert C, Larson JC et al (2006) Electrocardiographic abnormalities that predict coronary heart disease events and mortality in postmenopausal women: the Women’s Health Initiaive. Circulation 113:473–480\nKardys I, Kors JA, Van der Meer I et al (2003) Spatial QRS-T angle predicts cardiac death in a general population. Eur Heart J 24:1357–1364\nDilaveris P, Gialafos E, Pantazis A et al (2001) The spatial QRS-T angle as a marker of ventricular repolarisation in hypertension. J Hum Hypertens 15:63–70\nGhelani SJ, Keenan EM, Mah D et al (2016) Prolonged QRS mechanical dyssynchrony and ventricular dilation are associated with ventricular arrhythmias late after the Fontan. J Am Coll Cardio 67:936\nPeters S, Trummel M (2003) Diagnosis of arrhythmogenic right ventricular dysplasia-cardiomyopathy: value of standard ECG revisited. Ann Noninvasive Electrocardiol 8:238–245",{"VOID":965},"10.1007\u002Fs00246-017-1618-5","PUBLICATION","Auto Verify","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00246-017-1618-5",[970,986],{"id":971,"sortIndex":32,"researcher":28,"roles":972,"affiliations":974,"properties":983,"displayName":985,"givenName":28,"familyName":28},"c0104908-c177-441f-8490-decf7ed4139f",[973],"AUTHOR",[975],{"id":976,"sortIndex":32,"affiliation":977,"properties":28},"c9605def-1d89-4c23-872d-7166110535d6",{"id":976,"createTime":28,"updateTime":28,"relativeEntities":978,"slug":28,"properties":979,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":982,"statistic":28},[],{"title":980},{"EN":981},"University of Colorado School of Medicine, Aurora, USA",[],{"title":984},{"VI":985},"Tuong-Vi Tran",{"id":987,"sortIndex":40,"researcher":28,"roles":988,"affiliations":989,"properties":1014,"displayName":1016,"givenName":28,"familyName":28},"026b4ceb-1e26-48f2-a749-db312cfc617d",[973],[990,996,1005],{"id":976,"sortIndex":32,"affiliation":991,"properties":28},{"id":976,"createTime":28,"updateTime":28,"relativeEntities":992,"slug":28,"properties":993,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":995,"statistic":28},[],{"title":994},{"EN":981},[],{"id":997,"sortIndex":40,"affiliation":998,"properties":1004},"96ace4c3-76e2-4c08-b548-4614c5b1dcc4",{"id":997,"createTime":28,"updateTime":28,"relativeEntities":999,"slug":28,"properties":1000,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1003,"statistic":28},[],{"title":1001},{"VI":1002},"Electrophysiology fellow, Penn State Milton S. Hershey Medical Center, Hershey, USA",[],{},{"id":1006,"sortIndex":123,"affiliation":1007,"properties":1013},"b8b2e397-5a27-4f63-adc4-dc9327d493bc",{"id":1006,"createTime":28,"updateTime":28,"relativeEntities":1008,"slug":28,"properties":1009,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1012,"statistic":28},[],{"title":1010},{"VI":1011}," Clinical Sciences, Lund University, Lund, Sweden",[],{},{"title":1015},{"VI":1016},"Daniel Cortez","ARTICLE",{"url":968,"publisher":1019,"properties":1065},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1020,"slug":872,"properties":1021,"entityType":25,"verifyStatus":880,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1025,"manageAffiliations":1034,"indexDatabases":1045,"url":941,"thumbnailPath":28,"statistic":1060,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1022,"title":1023,"eissn":1024},{"VOID":875},{"EN":877},{"VOID":879},[1026,1030],{"id":883,"createTime":28,"updateTime":28,"relativeEntities":1027,"label":1028,"description":1029,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":886},{},{"id":889,"createTime":28,"updateTime":28,"relativeEntities":1031,"label":1032,"description":1033,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":892},{},[1035,1040],{"id":896,"createTime":28,"updateTime":28,"relativeEntities":1036,"slug":28,"properties":1037,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1039,"statistic":28},[],{"title":1038},{"EN":900},[],{"id":903,"createTime":28,"updateTime":28,"relativeEntities":1041,"slug":28,"properties":1042,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1044,"statistic":28},[],{"title":1043},{"EN":907},[909],[1046,1053],{"id":912,"indexDatabase":1047,"url":918,"indexYears":919,"academicFieldIds":1052,"indexDatabaseRanking":923},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":1048,"label":1049,"description":1050,"key":781,"publicationTags":1051,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[921,922],{"id":925,"indexDatabase":1054,"url":937,"indexYears":28,"academicFieldIds":1059,"indexDatabaseRanking":28},{"id":927,"createTime":28,"updateTime":28,"relativeEntities":1055,"label":1056,"description":1057,"key":934,"publicationTags":1058,"standard":28},[],{"EN":930,"VI":930},{"EN":932,"VI":933},[936,813],[939,940],{"impactFactor":32,"impactFactorByYear":1061,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":567,"totalPublicationByYear":1062,"totalCitation":32,"totalCitationByYear":1063,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1064,"hindexLast5Year":32,"hindex":32},{},{"1980":40,"1982":40,"1983":40,"1985":40,"1989":40,"1991":123,"1993":123,"2002":40,"2003":40,"2006":42,"2007":123,"2008":45,"2009":42,"2011":46,"2012":42,"2013":45,"2014":48,"2017":42,"2018":40,"2019":45,"2020":40,"2021":46,"2022":123,"2023":42,"2024":40},{},{},{"pages":1066,"volume":1068},{"VOID":1067},"1049-1056",{"VOID":1069},"38","2017-04-29",2017,[923,936],false,{"id":1075,"createTime":1076,"updateTime":1077,"relativeEntities":1078,"slug":1079,"properties":1080,"entityType":966,"verifyStatus":26,"verifyTime":1077,"verifyNote":967,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1089,"fullTextUrl":28,"authors":1090,"publicationType":1017,"publisherRelationship":1179,"citationCount":28,"citationInfo":28,"publishDate":1231,"publishYear":1232,"citationAnalyzeStatus":880,"lastCitationAnalyze":28,"indexDatabases":1233,"openAccess":28,"references":28,"isForceReanalyzing":1073},"001021ce-d872-4c74-a3e9-ce9b030acb59","2024-01-19T06:22:52.140+00:00","2025-01-28T22:23:35.755+00:00",[],"Evaluation-by-N-terminal-Prohormone-of-Brain-Natriuretic-Peptide-Concentrations-and-Ross-Scoring-of-the-Efficacy-of-Digoxin-in-the-Treatment-of-Heart-Failure-Secondary-to-Congenital-Heart-Disease-With-Left-to-Right-Shunts",{"abstract":1081,"title":1083,"references":1085,"doi":1087},{"EN":1082},"This study aimed to evaluate the effectiveness of digoxin in children with heart failure secondary to left-to-right shunt lesions and normal left ventricular systolic function. The study registered 37 such patients (ages 10 days to 24 months, groups 1 and 2) and used 20 healthy children as a control group (group 3). Left ventricular systolic function, as assessed by conventional echocardiography, was normal in all the subjects. Congestive heart failure was diagnosed by clinical evaluation and modified Ross scoring. Plasma N-terminal prohormone of brain natriuretic peptide (NT-proBNP) concentrations and complete blood counts were assessed in all the children. Group 1 was treated with digoxin, enalapril, and furosemide and group 2 with enalapril and furosemide. Approximately 1 month after starting treatment, the patients were reevaluated by physical and echocardiographic examinations, modified Ross scoring, plasma NT-proBNP concentrations, and complete blood counts. The pre- and posttreatment Ross scores of group 1 (p = 0.377) and group 2 (p = 0.616) did not differ significantly. The NT-proBNP values in both groups decreased after treatment (p = 0.0001). The pre- and posttreatment NT-proBNP values did not differ significantly in group 1 (p = 0.094)) and group 2 (p = 0.372). The pretreatment NT-proBNP values in groups 1 and 2 (p = 0.0001) were significantly higher than in the control group (p = 0.003). A smaller difference was observed between posttreatment NT-proBNP values in group 1 and the control group (p = 0.045). We found no significant difference between the posttreatment NT-proBNP values of group 2 and those of the control group (p = 0.271). The study showed that both treatments currently used to treat heart failure secondary to congenital heart disease with left-to-right shunts and preserved left ventricular systolic function are effective and do not differ significantly. Thus, digoxin does not provide any extra benefit in the treatment of such patients.",{"EN":1084},"Evaluation by N-terminal Prohormone of Brain Natriuretic Peptide Concentrations and Ross Scoring of the Efficacy of Digoxin in the Treatment of Heart Failure Secondary to Congenital Heart Disease With Left-to-Right Shunts",{"VOID":1086},"Penny DJ, Vick GW III (2010) Novel therapies in childhood heart failure: today and tomorrow. Heart Fail Clin 6:591–621 x\nO’Connor MJ, Rosenthal DN, Shaddy RE (2010) Outpatient management of pediatric heart failure. Heart Fail Clin 6:515–529 ix\nBarnes S, Shields B, Bonney W, Hardin J, Abdulla R (2004) The pediatric cardiology pharmacopoeia: 2004 update. Pediatr Cardiol 25:623–646\nKantor PF, Mertens LL (2010) Clinical practice: heart failure in children. Part I: clinical evaluation, diagnostic testing, and initial medical management. Eur J Pediatr 169:269–279\nTimberlake K, Kantor PF (2011) Pharmacologic therapy of heart failure in children: part of a special series on paediatric pharmacology, guest edited by Gianvincenzo Zuccotti, Emilio Clementi, and Massimo Molteni. Pharmacol Res 64:427–430\nRoss RD (2012) The Ross classification for heart failure in children after 25 years: a review and an age-stratified revision. Pediatr Cardiol 33:1295–1300\nJohnstone DE, Abdulla A, Arnold JM, Bernstein V, Bourassa M, Brophy J, Davies R, Gardner M, Hoeschen R, Mickleborough L et al (1994) Diagnosis and management of heart failure. Canadian Cardiovascular Society. Can J Cardiol 10(613–631):635–654\nNir A, Lindinger A, Rauh M, Bar-Oz B, Laer S, Schwachtgen L, Koch A, Falkenberg J, Mir TS (2009) NT-pro-B-type natriuretic peptide in infants and children: reference values based on combined data from four studies. Pediatr Cardiol 30:3–8\nKoch A, Zink S, Singer H (2006) B-type natriuretic peptide in paediatric patients with congenital heart disease. Eur Heart J 27:861–866\nCantinotti M, Giovannini S, Murzi B, Clerico A (2011) Diagnostic, prognostic, and therapeutic relevance of B-type natriuretic hormone and related peptides in children with congenital heart diseases. Clin Chem Lab Med 49:567–580\nGessler P, Knirsch W, Schmitt B, Rousson V, von Eckardstein A (2006) Prognostic value of plasma N-terminal pro-brain natriuretic peptide in children with congenital heart defects and open-heart surgery. J Pediatr 148:372–376\nPrice JF, Thomas AK, Grenier M, Eidem BW, O’Brian Smith E, Denfield SW, Towbin JA, Dreyer WJ (2006) B-type natriuretic peptide predicts adverse cardiovascular events in pediatric outpatients with chronic left ventricular systolic dysfunction. Circulation 114:1063–1069\nTan LH, Jefferies JL, Liang JF, Denfield SW, Dreyer WJ, Mott AR, Grenier MA, Dickerson HA, Price JF, Towbin JA, Ou CN, Chang AC (2007) Concentrations of brain natriuretic peptide in the plasma predicts outcomes of treatment of children with decompensated heart failure admitted to the intensive care unit. Cardiol Young 17:397–406\nPuddy VF, Amirmansour C, Williams AF, Singer DR (2002) Plasma brain natriuretic peptide as a predictor of haemodynamically significant patent ductus arteriosus in preterm infants. Clin Sci Lond 103:75–77\nMir TS, Marohn S, Laer S, Eiselt M, Grollmus O, Weil J (2002) Plasma concentrations of N-terminal pro-brain natriuretic peptide in control children from the neonatal to adolescent period and in children with congestive heart failure. Pediatrics 110:e76\nKunii Y, Kamada M, Ohtsuki S, Araki T, Kataoka K, Kageyama M, Nakagawa N, Seino Y (2003) Plasma brain natriuretic peptide and the evaluation of volume overload in infants and children with congenital heart disease. Acta Med Okayama 57:191–197\nShaddy RE (2001) Optimizing treatment for chronic congestive heart failure in children. Crit Care Med 29:S237–S240\nBautista-Hernandez V, Sanchez-Andres A, Portela F, Fynn-Thompson F (2011) Current pharmacologic management of pediatric heart failure in congenital heart disease. Curr Vasc Pharmacol 9:619–628\nBerman W Jr, Yabek SM, Dillon T, Niland C, Corlew S, Christensen D (1983) Effects of digoxin in infants with congested circulatory state due to a ventricular septal defect. N Engl J Med 308:363–366\nKimball TR, Daniels SR, Meyer RA, Hannon DW, Tian J, Shukla R, Schwartz DC (1991) Effect of digoxin on contractility and symptoms in infants with a large ventricular septal defect. Am J Cardiol 68:1377–1382\nKothari SS (1997) Does digoxin still have a role in congestive heart failure? Indian J Pediatr 64:833–837\nRedington AN, Carvalho JS, Shinebourne EA (1989) Does digoxin have a place in the treatment of the child with congenital heart disease? Cardiovasc Drugs Ther 3:21–24\nNir A, Bar-Oz B, Perles Z, Brooks R, Korach A, Rein AJ (2004) N-terminal pro-B-type natriuretic peptide: reference plasma levels from birth to adolescence: elevated levels at birth and in infants and children with heart diseases. Acta Paediatr 93:603–607\nKoch A, Singer H (2003) Normal values of B type natriuretic peptide in infants, children, and adolescents. Heart 89:875–878\nRoss RD, Bollinger RO, Pinsky WW (1992) Grading the severity of congestive heart failure in infants. Pediatr Cardiol 13:72–75\nReithmann C, Reber D, Kozlik-Feldmann R, Netz H, Pilz G, Welz A, Werdan K (1997) A post-receptor defect of adenylyl cyclase in severely failing myocardium from children with congenital heart disease. Eur J Pharmacol 330:79–86\nSchiller NB, Shah PM, Crawford M, DeMaria A, Devereux R, Feigenbaum H, Gutgesell H, Reichek N, Sahn D, Schnittger I et al (1989) Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms. J Am Soc Echocardiogr 2:358–367\nJain S, Vaidyanathan B (2009) Digoxin in management of heart failure in children: should it be continued or relegated to the history books? Ann Pediatr Cardiol 2:149–152\nYoshibayashi M, Kamiya T, Saito Y, Nakao K, Nishioka K, Temma S, Itoh H, Shirakami G, Matsuo H (1995) Plasma brain natriuretic peptide concentrations in healthy children from birth to adolescence: marked and rapid increase after birth. Eur J Endocrinol 133:207–209\nMir TS, Flato M, Falkenberg J, Haddad M, Budden R, Weil J, Albers S, Laer S (2006) Plasma concentrations of N-terminal brain natriuretic peptide in healthy children, adolescents, and young adults: effect of age and gender. Pediatr Cardiol 27:73–77\nCardoso J, Brito MI, Ochiai ME, Novaes M, Berganin F, Thicon T, Ferreira EC, Regina K, Reis CM, Barretto AC (2010) Anemia in patients with advanced heart failure. Arq Bras Cardiol 95:524–528\nRalli S, Horwich TB, Fonarow GC (2005) Relationship between anemia, cardiac troponin I, and B-type natriuretic peptide levels and mortality in patients with advanced heart failure. Am Heart J 150:1220–1227\nWu YR, Chen SB, Huang MR, Zhang YQ, Sun K, Chen S (2005) Diagnostic value of plasma concentration of pro-brain natriuretic peptide in congestive heart failure in pediatric patients with ventricular septal defects. Zhonghua Er Ke Za Zhi 43:161–164\nZhang SR, Zhang YH, Xu Q, Qiu HX, Chen Q (2009) Values of brain natriuretic peptide and N-terminal pro-brain natriuretic peptide in evaluation of cardiac function in children with congenital heart disease. Zhongguo Dang Dai Er Ke Za Zhi 11:429–432",{"VOID":1088},"10.1007\u002Fs00246-013-0683-7","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00246-013-0683-7",[1091,1106,1121,1136,1149,1164],{"id":1092,"sortIndex":32,"researcher":28,"roles":1093,"affiliations":1094,"properties":1103,"displayName":1105,"givenName":28,"familyName":28},"69d28533-e45c-4ab3-9585-5f2e2ef4f716",[973],[1095],{"id":1096,"sortIndex":32,"affiliation":1097,"properties":28},"89e4c839-aa97-4289-860e-41d06f863d65",{"id":1096,"createTime":28,"updateTime":28,"relativeEntities":1098,"slug":28,"properties":1099,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1102,"statistic":28},[],{"title":1100},{"VI":1101},"Department of Pediatric Cardiology, Faculty of Medicine, Inonu University, Malatya, Turkey",[],{"title":1104},{"VI":1105},"Ozlem 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Images of the Aortopulmonary Window With an Interrupted Aortic Arch",{"VOID":1242},"Kutsche LM, Van Mierop LH (1987) Anatomy and pathogenesis of aorticopulmonary septal defect. Am J Cardiol 59:443–447\nValsangiacomo ER, Smallhorn JF (2002) Images in cardiovascular medicine: prenatal diagnosis of aortopulmonary window by fetal echocardiography. Circulation 105:E192\nBagtharia R, Trivedi KR, Burkhart HM, Williams WG, Freedom RM, Van Arsdell GS, McCrindle BW (2004) Outcomes for patients with an aortopulmonary window, and the impact of associated cardiovascular lesions. Cardiol Young 14:473–480\nKonstantinov IE, Karamlou T, Williams WG, Quaegebeur JM, del Nido PJ, Spray TL, Caldarone CA, Blackstone EH, McCrindle BW (2006) Surgical management of aortopulmonary window associated with interrupted aortic arch: a Congenital Heart Surgeons Society study. J Thorac Cardiovasc Surg 131(1136–1141):e1132\nHayashi G, Inamura N, Kayatani F, Kawazu Y, Hamamichi Y (2010) Prenatal diagnosis of aortopulmonary window with interrupted aortic arch by fetal echocardiography. Fetal Diagn Ther 27:97–100",{"VOID":1244},"10.1007\u002Fs00246-012-0613-0","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00246-012-0613-0",[1247,1262,1275],{"id":1248,"sortIndex":32,"researcher":28,"roles":1249,"affiliations":1250,"properties":1259,"displayName":1261,"givenName":28,"familyName":28},"b3ef7cef-815e-4072-b967-96b8f95ddf7b",[973],[1251],{"id":1252,"sortIndex":32,"affiliation":1253,"properties":28},"6a7a6493-678e-420f-8a11-026c9ac61d8a",{"id":1252,"createTime":28,"updateTime":28,"relativeEntities":1254,"slug":28,"properties":1255,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1258,"statistic":28},[],{"title":1256},{"VI":1257},"Department of Obstetrics and Gynecology, School of Medicine, Keio University, Shinjuku-ku, Japan",[],{"title":1260},{"VI":1261},"Ikuko 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this study, we aimed to assess levels of serum B cell lymphoma 2 (sBcl-2) in children, which has been implicated in the etiopathogenesis of pulmonary hypertension (PH), as well its association with tissue Doppler echocardiographic imaging (TDI) data and parameters used in the follow-up of PH. The sBcl-2 level was assessed in 35 children with PH (24 had eisenmenger syndrome, and 11 had idiopathic PH) and in 38 healthy children as controls. TDI was performed on 25 patients whose cardiac anatomy allowed the test. The respective sBcl-2 values in patients and controls were 35.69 ± 18.83 and 2.66 ± 7.95 ng\u002Fml (p \u003C 0.001). The sBcl-2 levels were significantly greater in the New York Heart Association (NYHA) functional class 3 patients than those in the NYHA class 2 patients (p = 0.033). The sBcl-2 value in patients who walked \u003C475 m in the 6-min walk distance (6MWD) test was significantly greater than in those who walked ≥475 m (p = 0.038). The sBcl-2 level showed a negative correlation with ejection time measured at the septal anulus (p = 0.026) and a positive correlation with interventricular septum-Tei (p = 0.018). The results of this study showed for the first time that there is an increase in the levels of sBcl-2 as an inflammatory marker and that the sBcl-2 levels are associated with prognostic parameters in children with PH. Because sBcl-2 levels were greater in patients who walked \u003C475 meters during the 6MWD test, we suggest 475 ms as the cut-off value for the 6MWD test to differentiate between a good and a bad prognosis.",{"EN":1352},"Serum Bcl-2 Values in Children with Pulmonary Hypertension",{"VOID":1354},"Chang SM, Lin CC, Hsiao SH, Lee CY, Yang SH, Lin SK et al (2007) Pulmonary hypertension and left heart function: insights from tissue Doppler imaging and myocardial performance index. Echocardiography 24(4):366–373\nColombel M, Symmans F, Gil S, O’Toole KM, Chopin D, Benson M et al (1993) Detection of the apoptosis-suppressing oncoprotein bc1-2 in hormone-refractory human prostate cancers. Am J Pathol 143(2):390–400\nCowan KN, Jones PL, Rabinovitch M (1999) Regression of hypertrophied rat pulmonary arteries in organ culture is associated with suppression of proteolytic activity, inhibition of tenascin-C, and smooth muscle cell apoptosis. Circ Res 84(10):1223–1233\nCowan KN, Heilbut A, Humpl T, Lam C, Ito S, Rabinovitch M (2000) Complete reversal of fatal pulmonary hypertension in rats by a serine elastase inhibitor. Nat Med 6(6):698–702\nde Jong D, Prins FA, Mason DY, Reed JC, van Ommen GB, Kluin PM (1994) Subcellular localization of the bcl-2 protein in malignant and normal lymphoid cells. Cancer Res 54(1):256–260\nEcarnot-Laubriet A, Assem M, Poirson-Bichat F, Moisant M, Bernard C, Lecour S et al (2002) Stage-dependent activation of cell cycle and apoptosis mechanisms in the right ventricle by pressure overload. Biochim Biophys Acta 1586(3):233–242\nFontanini G, Vignati S, Bigini D, Mussi A, Lucchi M, Angeletti CA et al (1995) Bcl-2 protein: a prognostic factor inversely correlated to p53 in non-small-cell lung cancer. Br J Cancer 71(5):1003–1007\nGalie N, Hoeper MM, Humbert M, Torbicki A, Vachiery JL, Barbera JA et al (2009) Guidelines for the diagnosis and treatment of pulmonary hypertension: the Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT). Eur Heart J 30(20):2493–2537\nGibbons GH, Dzau VJ (1994) The emerging concept of vascular remodeling. New Engl J Med 330(20):1431–1438\nGoldstein JC, Waterhouse NJ, Juin P, Evan GI, Green DR (2000) The coordinate release of cytochrome c during apoptosis is rapid, complete and kinetically invariant. Nat Cell Biol 2(3):156–162\nGurbanov E, Shiliang X (2006) The key role of apoptosis in the pathogenesis and treatment of pulmonary hypertension. Eur J Cardiothorac Surg 30(3):499–507\nHassoun PM, Mouthon L, Barbera JA, Eddahibi S, Flores SC, Grimminger F et al (2009) Inflammation, growth factors, and pulmonary vascular remodeling. J Am Coll Cardiol 54(1 Suppl):S10–S19\nHuang JB, Liu YL, Sun PW, Lv XD, Bo K, Fan XM (2010) Novel strategy for treatment of pulmonary arterial hypertension: enhancement of apoptosis. Lung 188(3):179–189\nLevy M, Maurey C, Celermajer DS, Vouhe PR, Danel C, Bonnet D et al (2007) Impaired apoptosis of pulmonary endothelial cells is associated with intimal proliferation and irreversibility of pulmonary hypertension in congenital heart disease. J Am Coll Cardiol 49(7):803–810\nMartin B, Paesmans M, Berghmans T, Branle F, Ghisdal L, Mascaux C et al (2003) Role of Bcl-2 as a prognostic factor for survival in lung cancer: a systematic review of the literature with meta-analysis. Br J Cancer 89(1):55–64\nMiyamoto S, Nagaya N, Satoh T, Kyotani S, Sakamaki F, Fujita M et al (2000) Clinical correlates and prognostic significance of six-minute walk test in patients with primary pulmonary hypertension. Comparison with cardiopulmonary exercise testing. Am J Respir Crit Care Med 161(2 Pt 1):487–492\nPaciocco G, Martinez FJ, Bossone E, Pielsticker E, Gillespie B, Rubenfire M (2001) Oxygen desaturation on the six-minute walk test and mortality in untreated primary pulmonary hypertension. Eur Respir J 17(4):647–652\nSilvestrini R, Veneroni S, Daidone MG, Benini E, Boracchi P, Mezzetti M et al (1994) The Bcl-2 protein: a prognostic indicator strongly related to p53 protein in lymph node-negative breast cancer patients. J Natl Cancer Inst 86(7):499–504\nSimonneau G, Gatzoulis MA, Adatia I, Celermajer D, Denton C, Ghofrani A et al (2013) Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 24(62(25 Suppl)):D34–D41\nSitbon O, Humbert M, Nunes H, Parent F, Garcia G, Herve P et al (2002) Long-term intravenous epoprostenol infusion in primary pulmonary hypertension: prognostic factors and survival. J Am Coll Cardiol 40(4):780–788\nStenmark KR, Fagan KA, Frid MG (2006) Hypoxia-induced pulmonary vascular remodeling: cellular and molecular mechanisms. Circ Res 99(7):675–691\nTanaka K, Iwamoto S, Gon G, Nohara T, Iwamoto M, Tanigawa N (2000) Expression of survivin and its relationship to loss of apoptosis in breast carcinomas. Clin Cancer Res 6(1):127–134\nYeo TC, Dujardin KS, Tei C, Mahoney DW, McGoon MD, Seward JB (1998) Value of a Doppler-derived index combining systolic and diastolic time intervals in predicting outcome in primary pulmonary hypertension. 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data exist regarding the efficacy and safety of the Amplatzer ductal occluder (ADO) type 1 device in the Asian region. This retrospective study, conducted between August 2001 and April 2011, attempted device placement for 231 patients (165 females and 66 males) with a median age of 7.4 years (range, 3 months to 64 years) and an average weight of 19.4 kg (range, 4.1–81.0 kg). Among the patients in this study, 66 (28.6%) had pulmonary hypertension, ten (4.3%) had trisomy 21, and eight (3.5%) had other congenital cardiac anomalies. The mean narrowest patent ductus arteriosus (PDA) diameter was 4.2 mm (range, 1.3–10 mm), and the ampulla size was 9.6 mm (range, 4–20 mm). Successful implantation was achieved for 229 patients (99.1%). Complete angiographic occlusion was achieved for 201 patients (87.8%) at the end the procedure. Follow-up data were available for 129 patients (66%). At the follow-up assessment, complete echocardiographic occlusion was seen in 128 patients (99.2%) after 1 month and in 100% of the patients after 6 months. The significant morbidities involved one device embolization and one dislodgment, for which surgical retrieval was performed. No mortalities occurred during the study period, and no late clinical adverse events occurred during the follow-up period. Occlusion of the PDA using ADO is safe, effective, and applicable for a wide range of PDA sizes including large PDAs in small symptomatic infants and in adults. 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citation_publication_date=2006; citation_pages=e7-e10; citation_id=CR8\ncitation_journal_title=J Am Coll Cardiol; citation_title=Catheter closure of moderate- to large-sized patent ductus arteriosus using the new Amplatzer duct occluder: immediate and short-term results; citation_author=J Masura, KP Walsh, B Thanopoulous, C Chan, J Bass, U Goussous, P Gavora, ZM Hijazi; citation_volume=31; citation_publication_date=1998; citation_pages=878-882; citation_doi=10.1016\u002FS0735-1097(98)00013-8; citation_id=CR9\ncitation_journal_title=Catheter Cardiovasc Interv; citation_title=Interventional treatment of patent ductus arteriosus in 2004; citation_author=JW Moore, DS Levi, SD Moore, DJ Schneider, F Berdjis; citation_volume=64; citation_publication_date=2005; citation_pages=91-101; citation_doi=10.1002\u002Fccd.20243; citation_id=CR10\ncitation_journal_title=J Am Coll Cardiol; citation_title=Multicenter USA Amplatzer patent ductus arteriosus occlusion device trial: initial and one-year results; citation_author=RH Pass, ZM Hijazi, DT Hsu, V Lewis, WE Hellenbrand; citation_volume=44; citation_publication_date=2004; citation_pages=513-519; citation_doi=10.1016\u002Fj.jacc.2004.03.074; citation_id=CR11\ncitation_journal_title=Radiol Clin North Am; citation_title=Catheter closure of patent ductus arteriosus: 62 cases treated without thoracotomy; citation_author=W Portsmann, L Wierny, H Warnke, G Gerstberger, PA Romaniuk; citation_volume=9; citation_publication_date=1971; citation_pages=203-218; citation_id=CR12\ncitation_journal_title=Pediatr Cardiol; citation_title=Transcatheter closure of patent arteriosus: successful use in a 3.5 kg infant; citation_author=WJ Rashkind, CC Cuaso; citation_volume=1; citation_publication_date=1979; citation_pages=3-7; citation_doi=10.1007\u002FBF02307335; citation_id=CR13\ncitation_journal_title=Circulation; citation_title=Nonsurgical closure of patent ductus arteriosus: clinical application of the Rashkind PDA occluder system; 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report describes an infant with heterotaxy syndrome and severe hypoplasia of the left heart who presented with profound cyanosis at birth despite a large patent ductus arteriosus. Pulmonary venous return was difficult to demonstrate by echocardiography. Angiography showed total anomalous pulmonary venous return via a plexus that drained through the paravertebral veins and bilateral superior vena cavae. Autopsy confirmed these findings, and histopathology demonstrated severe occlusive changes within the pulmonary veins.",{"EN":1649},"Hypoplastic Left Heart Syndrome and Pulmonary Veno-occlusive Disease in an Infant",{"VOID":1651},"Brann S, Brawn WJ, Faro R, Sreeram N (1995) Neonatal pulmonary vascular disease in hypoplastic left heart syndrome. Ann Thorac Surg 60:433–434\nCanter CE, Moorhead S, Huddleston CB, Spray TL (1993) Restrictive atrial septal communication as a determinant of outcome of cardiac transplantation for hypoplastic left heart syndrome. Circulation 88(Suppl 2):456–460\nFeinstein JA, Benson DW, Dubin AM et al (2012) Hypoplastic left heart syndrome: current considerations and expectations. J Am Coll Cardiol 59:1–42\nFrance NE, Brown RJK (1971) Congenital pulmonary lymphangiectasis: report of 11 examples with specific reference to cardiovascular findings. Arch Dis Child 46:528–532\nGlatz JA, Tabbutt S, Gaynor JW, Rome JJ, Montenegro L, Spray TL, Rychik J (2007) Hypoplastic left heart syndrome with atrial level restriction in the era of prenatal diagnosis. Ann Thorac Surg 84:1633–1638\nLuciani G, Pessotto R, Mombello A, Mazzucco A (1999) Hypoplastic left heart syndrome with restrictive atrial septal defect and congenital pulmonary lymphangiectasis. Cardiovasc Pathol 8:49–51\nRychik J, Rome JJ, Collins MH, DeCampli WM, Spray TL (1999) The hypoplastic left heart syndrome with intact atrial septum: atrial morphology, pulmonary vascular histopathology, and outcome. J Am Coll Cardiol 34:554–560\nStasik C, Goldberg C, Bove E, Devaney E, Ohye R (2006) Current outcomes and risk factors for the Norwood procedure. J Thorac Cariodvasc Surg 131:412–417",{"VOID":1653},"10.1007\u002Fs00246-012-0498-y","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00246-012-0498-y",[1656,1671,1684],{"id":1657,"sortIndex":32,"researcher":28,"roles":1658,"affiliations":1659,"properties":1668,"displayName":1670,"givenName":28,"familyName":28},"cbb8b4a9-9899-4935-9be6-99a827df44b7",[973],[1660],{"id":1661,"sortIndex":32,"affiliation":1662,"properties":28},"b18ad19f-1a6d-494c-9f9d-48ef19fb7332",{"id":1661,"createTime":28,"updateTime":28,"relativeEntities":1663,"slug":28,"properties":1664,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1667,"statistic":28},[],{"title":1665},{"VI":1666},"Pediatric Cardiology, University of Virginia, Charlottesville, USA",[],{"title":1669},{"VI":1670},"Marise D’Souza",{"id":1672,"sortIndex":40,"researcher":28,"roles":1673,"affiliations":1674,"properties":1681,"displayName":1683,"givenName":28,"familyName":28},"2db3fa2f-20fa-45ee-b60e-be80d11149c3",[973],[1675],{"id":1661,"sortIndex":32,"affiliation":1676,"properties":28},{"id":1661,"createTime":28,"updateTime":28,"relativeEntities":1677,"slug":28,"properties":1678,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1680,"statistic":28},[],{"title":1679},{"VI":1666},[],{"title":1682},{"VI":1683},"Jeffrey Vergales",{"id":1685,"sortIndex":123,"researcher":28,"roles":1686,"affiliations":1687,"properties":1694,"displayName":1696,"givenName":28,"familyName":28},"815b5726-7ea7-41ee-8d1c-c95619f0e5d4",[973],[1688],{"id":1661,"sortIndex":32,"affiliation":1689,"properties":28},{"id":1661,"createTime":28,"updateTime":28,"relativeEntities":1690,"slug":28,"properties":1691,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1693,"statistic":28},[],{"title":1692},{"VI":1666},[],{"title":1695},{"VI":1696},"K. 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Chúng tôi trình bày một trường hợp của một trẻ em mắc PAVC, người sau đó phát triển hẹp tĩnh mạch phổi tiến triển như một biểu hiện của bệnh lý của cô bé.","Patients with partial atrioventricular canal defect (PAVC) who present with congestive heart failure within the first year of life are usually found to have associated left-sided obstructive lesions. We present a case of a child with PAVC who subsequently developed progressive pulmonary venous stenosis as a manifestation of her disease.",{"EN":1761,"VI":1762},"Pulmonary Venous Stenosis as an Associated Manifestation of Left-Sided Obstructive Lesions in an Infant with Partial Atrioventricular Canal Defect","Hẹp Tĩnh Mạch Phổi Như Một Biểu Hiện Liên Quan Của Các Tổn Thương Tắc Nghẽn Bên Trái Ở Một Trẻ Sơ Sinh Có Khuyết Tật Kênh Nhĩ Thất Bán Phần",{"VI":1764},"khuyết tật kênh nhĩ thất bán phần, hẹp tĩnh mạch phổi, suy tim sung huyết, tắc nghẽn bên trái, bệnh lý tim mạch nhi khoa",{"VOID":1766},"RM King FJ Puga GK Danielson et al. (1986) ArticleTitlePrognostic factors and surgical treatment of partial atrioventricular canal Circulation 74 IssueID(suppl 1 42–46\nTC Koutlas ND Bridges JW Gaynor et al. (1997) ArticleTitlePediatric lung transplantation—are there surgical contraindications? Transplantation 63 269–274 Occurrence Handle9020329 Occurrence Handle1:STN:280:ByiC2s3isVE%3D\nGF Lacour J Zoghbi AE Serraf et al. (1999) ArticleTitleSurgical management of progressive pulmonary venous obstruction after repair of total anomalous pulmonary venous connection J Thorac Cardiovasc Surg 117 679–687\nPB Manning JE Mayer SP Sanders et al. (1994) ArticleTitleUnique features and prognosis of primum ASD presenting in the first year of life Circulation 90 II-30–II-35 Occurrence Handle1:STN:280:ByqD2czislY%3D\nCJ McMahon CE Mullins HG El Said (2003) ArticleTitleIntrastent sonotherapy in pulmonary vein restenosis: a new treatment for a recalcitrant problem Heart 89 IssueID2 E6 Occurrence Handle12527692 Occurrence Handle10.1136\u002Fheart.89.2.e6 Occurrence Handle1:STN:280:DC%2BD3s%2FitVOmuw%3D%3D\nHK Najm WG Williams S Chuaratanaphong et al. (1998) ArticleTitlePrimum atrial septal defect in children: early results, risk factors, and freedom from re-operation Ann Thorac Surg 66 829–835 Occurrence Handle9768938 Occurrence Handle10.1016\u002FS0003-4975(98)00607-9 Occurrence Handle1:STN:280:DyaK1cvjvFyktg%3D%3D\nMA Portman SD Beder JL Ankeney et al. (1985) ArticleTitleA 20-year review of ostium primum defect repair in children Am Heart J 110 1054–1058 Occurrence Handle3904374 Occurrence Handle10.1016\u002F0002-8703(85)90209-1 Occurrence Handle1:STN:280:BimD2cjkvFc%3D\nTL Spray ND Bridges (1992) ArticleTitleSurgical management of congenital and acquired pulmonary vein stenosis Pediatr Cardiac Surg Annu Semin Thorac Cardiovasc Surg 2 177–188\nS Stewart C Alexson J Manning (1987) ArticleTitlePartial atrioventricular canal defect: the early and late results of operation Ann Thorac Surg 45 527–529\nDF Wax AP Rocchini (1998) ArticleTitleTranscatheter management of venous stenosis Pediatr Cardiol 19 59–65 Occurrence Handle9396849 Occurrence Handle10.1007\u002Fs002469900247 Occurrence Handle1:STN:280:DyaK1c%2FmtV2htA%3D%3D",{"VOID":1768},"10.1007\u002Fs00246-005-8640-8","2025-01-23T09:34:16.306+00:00",[30],"https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00246-005-8640-8",[1773,1788,1803,1816,1831],{"id":1774,"sortIndex":32,"researcher":28,"roles":1775,"affiliations":1776,"properties":1785,"displayName":1787,"givenName":28,"familyName":28},"1da49c49-94bc-450d-9e9d-5209d8414d11",[973],[1777],{"id":1778,"sortIndex":32,"affiliation":1779,"properties":28},"0d1adc96-209c-4c90-a63e-5e9379a1e8e6",{"id":1778,"createTime":28,"updateTime":28,"relativeEntities":1780,"slug":28,"properties":1781,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1784,"statistic":28},[],{"title":1782},{"VI":1783},"Department of Pediatrics, Lillie Frank Abercrombie Section of Pediatric Cardiology, Baylor College of Medicine, Texas Children’s Hospital, Houston, USA",[],{"title":1786},{"VI":1787},"J. 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We found little difference between the magnitude of left-to-right shunt obtained with Doppler echocardiography and that with radioangioscintigraphy for a whole group of patients (N= 55, −11.42% to 12.04%) and for subgroups of ASD (n= 24, −12.49% to 12.19%) and VSD (n= 31, −10.69% to 12.23%). 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Evaluation is currently limited to imaging techniques that fail to provide an adequate overview of the intraluminal and luminal pathology perpetuating our limited understanding of this condition. Optical coherence tomography (OCT) is an imaging modality which provides intraluminal profiling with microstructural detail through optical reflective technology. We sought to evaluate whether its use was technically feasible in pediatric PVS and whether the imaging data provided potentially useful outputs for clinical utility. Eleven patients were prospectively selected from our cardiac catheterization for OCT evaluation of their pulmonary veins (PV) during elective catheterization for PVS. Measurements were taken both pre and post intervention using both manual and automated tools. Stent morphology was characterized. Eleven patients had evaluation of 34 pulmonary veins, with 7 patients having more than one assessment, for a total of 25 overall catheterizations. Most patients were female (75%). Median age at cardiac catheterization was 35 months (range 5–45 months). Median weight of subjects was 10.6 kg (3.7–14.2) with a median BSA documented at 0.505 m2 (0.21–0.57). Median number of pulmonary veins involved was 3, (range 1–5 veins) and median contrast volume of 2.9 mL\u002Fkg (0.7–3.7) given. Median radiation dose (DAP) was 6095 µGy·cm2 (1670–12,400). Median number of previous cardiac catheterizations was 7 (range 1–11). All of the vessels with a diameter \u003C 5 mm were adequately visualized. Of all the OCT images acquired, in 15 vessels (44%) contrast was used to clear the vessels from blood as an angiogram was required at the time, in the other 19 vessels (56%), saline was used with adequate imaging. There were no complications related to OCT. OCT is technically feasible to use in pediatric patients without any directly related complications. It provides intraluminal anatomy in children with both native and treated pulmonary venous stenosis when vessel size is less than 5 mm.",{"EN":2166},"Technical Feasibility on the Use of Optical Coherence Tomography in the Evaluation of Pediatric Pulmonary Venous Stenosis",{"VOID":2168},"Sadr IM, Tan PE, Kieran MW, Jenkins KJ (2000) Mechanism of pulmonary vein stenosis in infants with normally connected veins. Am J Cardiol 86(5):577\nLatson LA, Prieto LR (2007) Congenital and acquired pulmonary vein stenosis. Circulation 115(1):103–108\nVanderlaan RD, Rome J, Hirsch R, Ivy D, Caldarone CA (2020) Pulmonary vein stenosis: Treatment and challenges. J Thorac Cardiovasc Surg. 2020 Jun 27. https:\u002F\u002Fwww.jtcvs.org\u002Farticle\u002FS0022-5223(20)31796-7\u002Fabstract. Accessed 21 Dec 2020\nPatel JD, Briones M, Jones S, Suthar D, Gray R, Petit CJ (2020) Medical and invasive management of congenital and acquired pulmonary vein stenosis. Curr Treat Options Pediatr 6(3):170–181\ndel Cerro MJ, Moledina S, Haworth SG, Ivy D, Dabbagh MA, Banjar H et al (2016) Cardiac catheterization in children with pulmonary hypertensive vascular disease: consensus statement from the pulmonary vascular research institute, pediatric and congenital heart disease task forces. Pulm Circ 6(1):118–125\nKalfa D, Belli E, Bacha E, Lambert V, di Carlo D, Kostolny M et al (2018) Outcomes and prognostic factors for postsurgical pulmonary vein stenosis in the current era. J Thorac Cardiovasc Surg 156(1):278–286\nCory MJ, Ooi YK, Kelleman MS, Vincent RN, Kim DW, Petit CJ (2017) Reintervention is associated with improved survival in pediatric patients with pulmonary vein stenosis. JACC Cardiovasc Interv 10(17):1788–1798\nEsch JJ, Porras D, Bergersen L, Jenkins KJ, Marshall AC (2015) Systemic embolic complications of pulmonary vein angioplasty in children. Pediatr Cardiol 36(7):1357–1362\nCallahan R, Esch JJ, Wang G, Ireland CM, Gauvreau K, Jenkins KJ (2020) Systemic sirolimus to prevent in-stent stenosis in pediatric pulmonary vein stenosis. Pediatr Cardiol 41(2):282–289\nCallahan R, Kieran MW, Baird CW, Colan SD, Gauvreau K, Ireland CM et al (2018) Adjunct targeted biologic inhibition agents to treat aggressive multivessel intraluminal pediatric pulmonary vein stenosis. J Pediatr 198:29-35.e5\nPazos-López P (2016) Pulmonary vein stenosis: etiology, diagnosis and management. World J Cardiol 8(1):81\nKoestenberger M, Friedberg MK, Nestaas E, Michel-Behnke I, Hansmann G (2016) Transthoracic echocardiography in the evaluation of pediatric pulmonary hypertension and ventricular dysfunction. Pulm Circ 6(1):15–29\nVyas HV, Greenberg SB, Krishnamurthy R (2011) MR imaging and CT evaluation of congenital pulmonary vein abnormalities in neonates and infants. 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