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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. 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347, 1227, 10.1056\u002FNEJMoa020989\nJacobson, 1995, Ten-year results of a comparison of conservation with mastectomy in the treatment of stage I and II breast cancer, N Engl J Med, 332, 907, 10.1056\u002FNEJM199504063321402\nvan Dongen, 2000, Long-term results of a randomized trial comparing breast-conserving therapy with mastectomy: European Organization for Research and Treatment of Cancer 10801 trial, J Natl Cancer Inst, 92, 1143, 10.1093\u002Fjnci\u002F92.14.1143\nSarrazin, 1989, Ten-year results of a randomized trial comparing a conservative treatment to mastectomy in early breast cancer, Radiother Oncol, 14, 177, 10.1016\u002F0167-8140(89)90165-5\nBlichert-Toft, 1992, Danish randomized trial comparing breast conservation therapy with mastectomy: six years of life-table analysis, J Natl Cancer Inst Monogr, 19\nHuang, 2002, Classifying local disease recurrences after breast conservation therapy based on location and histology: new primary tumors have more favorable outcomes than 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radiotherapy and surgery for the treatment of ductal carcinoma in situ of the breast: a meta-analysis of 2 randomized trials, Radiother Oncol, 100, 195, 10.1016\u002Fj.radonc.2011.02.005\nMauri, 2005, Neoadjuvant versus adjuvant systemic treatment in breast cancer: a meta-analysis, J Natl Cancer Inst, 97, 188, 10.1093\u002Fjnci\u002Fdji021\nBuzdar, 2005, Significantly higher pathologic complete remission rate after neoadjuvant therapy with trastuzumab, paclitaxel, and epirubicin chemotherapy: results of a randomized trial in human epidermal growth factor receptor 2-positive operable breast cancer, J Clin Oncol, 23, 3676, 10.1200\u002FJCO.2005.07.032\nLiedtke, 2008, Response to neoadjuvant therapy and long-term survival in patients with triple-negative breast cancer, J Clin Oncol, 26, 1275, 10.1200\u002FJCO.2007.14.4147\nChen, 2004, Breast conservation after neoadjuvant chemotherapy: the MD Anderson cancer center experience, J Clin Oncol, 22, 2303, 10.1200\u002FJCO.2004.09.062\nAlpert, 2005, Ipsilateral breast tumor recurrence after breast conservation therapy: outcomes of salvage mastectomy vs. salvage breast-conserving surgery and prognostic factors for salvage breast preservation, Int J Radiat Oncol Biol Phys, 63, 845, 10.1016\u002Fj.ijrobp.2005.02.035\nSchnitt, 1985, Breast relapse following primary radiation therapy for early breast cancer. II. Detection, pathologic features and prognostic significance, Int J Radiat Oncol Biol Phys, 11, 1277, 10.1016\u002F0360-3016(85)90242-1\nKurtz, 1991, Is breast conservation after local recurrence feasible?, Eur J Cancer, 27, 240, 10.1016\u002F0277-5379(91)90505-8\nVoogd, 1999, Histological determinants for different types of local recurrence after breast-conserving therapy of invasive breast cancer, Eur J Cancer, 35, 1828, 10.1016\u002FS0959-8049(99)00220-8\nKomoike, 2003, Repeat lumpectomy for patients with ipsilateral breast tumor recurrence after breast-conserving surgery. 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Systemic therapy for treating locoregional recurrence in women with breast cancer. 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2017, Standardizing hysteroscopy teaching: development of a curriculum using the Delphi method, Surg Endosc, 31, 5389, 10.1007\u002Fs00464-017-5620-z\nLopes, 2017, An overview of the results of hysterosonography prior to in vitro fertilization, JBRA Assist Reprod, 21, 302\nBouzid, 2016, Feasibility and diagnostic value of hysterosonography performed in bleeding time in the exploration of abnormal uterine bleeding, J Gynecol Obstet Biol Reprod, 45, 1067, 10.1016\u002Fj.jgyn.2016.03.008\nde Kroon, 2003, Saline contrast hysterosonography in abnormal uterine bleeding: a systematic review and meta-analysis, Int J Obstet Gynaecol, 110, 938, 10.1111\u002Fj.1471-0528.2003.02472.x\nDudiak, 2001, Hysterosonography: a key to what is inside the uterus, Ultrasound Q, 17, 73, 10.1097\u002F00013644-200106000-00002\nDeffieux, 2013, Prevention of the complications related to hysteroscopy: guidelines for clinical practice, J Gynecol Obstet Biol Reprod, 42, 1032, 10.1016\u002Fj.jgyn.2013.09.008\nDreisler, 2019, Asherman's syndrome: current perspectives on diagnosis and management, Int J Womens Health, 11, 191, 10.2147\u002FIJWH.S165474\nSalle, 1999, Transvaginal sonohysterographic evaluation of intrauterine adhesions, J Clin Ultrasound, 27, 131, 10.1002\u002F(SICI)1097-0096(199903\u002F04)27:3\u003C131::AID-JCU5>3.0.CO;2-3\nSoares, 2000, Diagnostic accuracy of sonohysterography, transvaginal sonography, and hysterosalpingography in patients with uterine cavity diseases, Fertil Steril, 73, 406, 10.1016\u002FS0015-0282(99)00532-4\nBerridge, 2004, Saline infusion sonohysterography: technique, indications, and imaging findings, J Ultrasound Med, 23, 97, 10.7863\u002Fjum.2004.23.1.97\nSabry, 2018, Diagnostic value of three-dimensional saline infusion sonohysterography in the evaluation of the uterus and uterine cavity lesions, Pol J Radiol, 83, e482, 10.5114\u002Fpjr.2018.80132\nWamsteker, 1988, Diagnostic and therapeutic applications of hysteroscopy, Ned Tijdschr Geneeskd, 132, 2041\nCapella-Allouc, 1999, Hysteroscopic treatment of severe Asherman's syndrome and subsequent fertility, Hum Reprod, 14, 1230, 10.1093\u002Fhumrep\u002F14.5.1230\nFernandez, 2012, Total adhesions treated by hysteroscopy: must we stop at two procedures?, Fertil Steril, 98, 980, 10.1016\u002Fj.fertnstert.2012.06.032\nThubert, 2015, Influence of auto-cross-linked hyaluronic acid gel on pregnancy rate and hysteroscopic outcomes following surgical removal of intra-uterine adhesions, Eur J Obstet Gynecol Reprod Biol, 193, 65, 10.1016\u002Fj.ejogrb.2015.06.025\nWarembourg, 2015, Prevention and treatment of intra-uterine synechiae: review of the literature, J Gynecol Obstet Biol Reprod, 44, 366, 10.1016\u002Fj.jgyn.2014.10.014\nZhang, 2018, Therapeutic effect of human umbilical cord-derived mesenchymal stem cells on injured rat endometrium during its chronic phase, Stem Cell Res Ther, 9, 36, 10.1186\u002Fs13287-018-0777-5\nFernandez, 2012, Post-curettage and aspiration synechiae: is there value in an anti-adhesion agent?, J Gynecol Obstet Biol Reprod, 41, H8, 10.1016\u002FS0368-2315(12)70004-2\nGrimbizis, 2013, The ESHRE-ESGE consensus on the classification of female genital tract congenital anomalies, Gynecol Surg, 10, 199, 10.1007\u002Fs10397-013-0800-x\nRikken, 2018, The randomised uterine septum transsection trial (TRUST): design and protocol, BMC Womens Health, 18, 1, 10.1186\u002Fs12905-018-0637-6\nGarbin, 1997, Transcervical hysteroplasty: indications, techniques and results. 125 cases, Contracept Fertil Sex, 25, 843\nNagel, 1993, Hysteroscopic metroplasty in the diethylstilbestrol-exposed uterus and similar nonfusion anomalies: effects on subsequent reproductive performance; a preliminary report, Fertil Steril, 59, 502, 10.1016\u002FS0015-0282(16)55789-6\nFernandez, 2011, Surgical approach to and reproductive outcome after surgical correction of a T-shaped uterus, Hum Reprod, 26, 1730, 10.1093\u002Fhumrep\u002Fder056\nGarbin, 1998, Hysteroscopic metroplasty in diethylstilboestrol-exposed and hypoplastic uterus: a report on 24 cases, Hum Reprod, 13, 2751, 10.1093\u002Fhumrep\u002F13.10.2751\nMcIlwaine, 2015, A prospective study of the use of the Myosure resectoscope to manage endometrial polyps in an outpatient setting, Aust N Z J Obstet Gynaecol, 55, 482, 10.1111\u002Fajo.12382\nNoventa, 2015, Intrauterine morcellator devices: the icon of hysteroscopic future or merely a marketing image? A systematic review regarding safety, efficacy, advantages, and contraindications, Reprod Sci, 22, 1289, 10.1177\u002F1933719115578929\nScheiber, 2016, A prospective multicenter registry of patients undergoing hysteroscopic morcellation of uterine polyps and myomas, J Gynecol Surg, 32, 318, 10.1089\u002Fgyn.2016.0008\nRodriguez, 2019, Endometrial resection and ablation techniques for heavy menstrual bleeding, Cochrane Database Syst Rev\nKalampokas, 2018, Endometrial cancer after endometrial ablation or resection for menorrhagia, Int J Gynaecol Obstet, 142, 84, 10.1002\u002Fijgo.12503\nPhilip, 2018, Evaluation of NovaSure® global endometrial ablation in symptomatic adenomyosis: a longitudinal study with a 36 month-follow-up, Eur J Obstet Gynecol Reprod Biol, 227, 46, 10.1016\u002Fj.ejogrb.2018.04.001\nLou, 2019, The second generation endometrial ablation (NovaSure) improves efficacy of levonorgestrel-releasing intrauterine system in management of adenomyosis, Zhejiang Univ Med Sci, 48, 136\nThiel, 2014, Evaluation of the Novasure endometrial ablation procedure in women with uterine cavity length over 10cm, J Obstet Gynaecol Can, 36, 491, 10.1016\u002FS1701-2163(15)30562-4\nCooper, 2019, Laparoscopic supracervical hysterectomy versus endometrial ablation for women with heavy menstrual bleeding (HEALTH): a parallel-group, open-label, randomised controlled trial, Lancet, 394, 1425, 10.1016\u002FS0140-6736(19)31790-8\nFlorio, 2012, Hysteroscopic treatment of the cesarean-induced isthmocele in restoring infertility, Curr Opin Obstet Gynecol, 24, 180, 10.1097\u002FGCO.0b013e3283521202\nCalzolari, 2019, Prevalence of infertility among patients with isthmocele and fertility outcome after isthmocele surgical treatment: a retrospective study, Ochsner J, 19, 204, 10.31486\u002Ftoj.18.0048\nMunro, 2011, The flexible FIGO classification concept for underlying causes of abnormal uterine bleeding, Semin Reprod Med, 29, 391, 10.1055\u002Fs-0031-1287663\nBettocchi, 2009, A new hysteroscopic technique for the preparation of partially intramural myomas in office setting (OPPIuM technique): a pilot study, J Minim Invasive Gynecol, 16, 748, 10.1016\u002Fj.jmig.2009.07.016\nFernandez, 2011, Update on the management of menometrorrhagia: new surgical approaches, Gynecol Endocrinol, 27, 1131, 10.3109\u002F09513590.2011.634261\nDi SpiezioSardo, 2017, The role of hysteroscopy in the diagnosis and treatment of adenomyosis, BioMed Res Int, 2017, e2518396, 10.1155\u002F2017\u002F2518396\nGeorgiou, 2018, Hysteroscopic tissue removal system (MyoSure) for the resection of polyps, sub-mucosal leiomyomas and retained products of conception in an out-patient setting: a single UK institution experience, Eur J Obstet Gynecol Reprod Biol, 231, 147, 10.1016\u002Fj.ejogrb.2018.10.030\nFaivre, 2009, Hysteroscopic management of residual trophoblastic tissue and reproductive outcome: a pilot study, J Minim Invasive Gynecol, 16, 487, 10.1016\u002Fj.jmig.2009.04.011\nRein, 2011, Hysteroscopic management of residual trophoblastic tissue is superior to ultrasound-guided curettage, J Minim Invasive Gynecol, 18, 774, 10.1016\u002Fj.jmig.2011.08.003\nGulec, 2010, Osseous metaplasia of the endometrium, BMJ Case Rep, 2010, 10.1136\u002Fbcr.04.2010.2931\nGrigore, 2018, Ultrasound features of osseous metaplasia of the endometrium – Case series and review of the literature, Clin Imaging, 52, 260, 10.1016\u002Fj.clinimag.2018.08.006\nMadaan, 2015, Osseous metaplasia of the endometrium and successful hysteroscopic resection: a report of two cases and a review of the literature, Asian J Endosc Surg, 8, 63, 10.1111\u002Fases.12153\nCarin, 2015, Intra uterine devices removal during office hysteroscopy: about 36 cases, J Gynecol Obstet Biol Reprod, 44, 653, 10.1016\u002Fj.jgyn.2014.09.005",{"ES":842},"Histeroscopia quirúrgica",{"VOID":844},"10.1016\u002Fs1283-081x(22)46715-4","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS1283081X22467154",[847,862,874,886],{"id":848,"sortIndex":114,"researcher":26,"roles":849,"affiliations":850,"properties":859},"f42177e7-b479-4a2e-9318-73c4c4f0608d",[696],[851],{"id":26,"sortIndex":36,"affiliation":852,"properties":26},{"id":853,"createTime":854,"updateTime":854,"relativeEntities":855,"slug":26,"properties":856,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"447a96c6-b3eb-4b3c-b24e-d1019f48f79f","2024-02-12T14:44:19.701+00:00",[],{"title":857},{"VI":858},"Service de gynécologie obstétrique, Hôpital Bicêtre, GHU Sud, AP–HP, 78, rue du Général-Leclerc, 94270 Le Kremlin-Bicêtre, France",{"title":860},{"VI":861},"E. 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Rev., 21, 671, 10.1210\u002Fer.21.6.671\nApter, 1993, Gonadotropin-releasing hormone pulse generator activity during pubertal transition in girls: pulsatile and diurnal patterns of circulating gonadotropins, J. Clin. Endocrinol. Metab., 76, 940, 10.1210\u002Fjc.76.4.940\nIbanez, 1998, Possible genesis of polycystic ovary syndrom in the periadolescent girl, Curr. Opin. Endocrinol Diab, 5, 19, 10.1097\u002F00060793-199802000-00004\nvan Hooff, 2004, Predictive value of menstrual cycle pattern, body mass index, hormone levels and polycystic ovaries at age 15 years for oligo-amenorrhoea at age 18 years, Hum. Reprod., 19, 383, 10.1093\u002Fhumrep\u002Fdeh079\nLobo, 1991, Ovarian hyperandrogenism and androgen producing tumors, Endocrinol. Metab. Clin. North Am., 20, 773, 10.1016\u002FS0889-8529(18)30244-5\nYoung, 1985, Ovarian Sertoli-Leydig cell tumors: a clinicopathological analysis of 207 cases, Am. J. Surg. Pathol., 9, 543, 10.1097\u002F00000478-198508000-00001\nCaron, 1993, Androgenic granulosa cell tumor of the ovary: in vivo hormonal studies, J. Endocrinol. Invest., 16, 545, 10.1007\u002FBF03348903\nAbbott, 2002, Developmental origin of polycystic ovary syndrome-a hypothesis, J. Endocrinol., 174, 1, 10.1677\u002Fjoe.0.1740001\nStrauss, 1999, Molecular mysteries of polycystic ovary syndrome, Mol. Endocrinol., 13, 800, 10.1210\u002Fme.13.6.800\nDunaif, 1997, Insulin resistance and the polycystic ovarian syndrome: mechanism and implications for pathogenesis, Endocr. Rev., 18, 774, 10.1210\u002Fer.18.6.774\nWebber, 2003, Formation and early development of follicles in the polycystic ovary, Lancet, 362, 1017, 10.1016\u002FS0140-6736(03)14410-8\nDewailly, 1997, Definition, clinical manifestations, and prevalance of PCOS, 259\nZacur, 1997, Prolactin abnormalities in PCOS, 287\n2004, The Rotterdam ESHRE\u002FASRM sponsored PCOS consensus workshop group, Hum. Reprod., 19, 41\nBalen, 2003, Ultrasound assessment of the polycystic ovary: international consensus definitions, Hum. Reprod. Update, 9, 505, 10.1093\u002Fhumupd\u002Fdmg044\nForest, 1992, Formes non classiques dites « tardives » du déficit en 21-hydroxylase : diagnostic différentiel avec les hétérozygotes et conseil génétique, Rev. Fr. Endocrinol. Clin., 33, 47\nDewailly, 1997, Pathophysiology and clinical manifestations of nonclassic 21-hydroxylase deficiency, 173\nAzziz, 1997, Idiopathic Hirsutism: definition, prevalence and inheritance, 529\nCortet-Rudelli, 1997, Drug-induced androgen excess, 613\nNelson-DeGrave, 2004, Valproate potentiates androgen biosynthesis in human ovarien theca cells, Endocrinology, 145, 799, 10.1210\u002Fen.2003-0940\nDiamanti-Kandarakis, 1997, Cushing's disease and androgen excess, 569\nDeroubaix-Allard, 1997, Acromegaly and androgen excess, 585\nAzziz, 1997, Diagnosis, screening, and treatment of nonclassic 21-hydroxylase deficiency, 181\nSpritzer, 1990, Cyproterone acetate versus hydrocortisone treatment in late-onset adrenal hyperplasia, J. Clin. Endocrinol. Metab., 70, 642, 10.1210\u002Fjcem-70-3-642\nIbanez, 2004, Flutamide-metformin plus ethinylestradiol-drospirenone for lipolysis and antiatherogenesis in young women with ovarian hyperandrogenism: the key role of early, low-dose flutamide, J. Clin. Endocrinol. Metab., 89, 4716, 10.1210\u002Fjc.2004-0047\nKorytkowski, 1995, Metabolic effects of oral contraceptives in women with polycystic ovary syndrome, J. Clin. Endocrinol. 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Three cases of pulmonary edema, Minerva Ginecol, 56, 491\nKaraman, 2004, Pulmonary edema after ritodrine therapy during pregnancy and subsequent cesarean section with epidural anesthesia, Clin Exp Obstet Gynecol, 31, 67\nHamel, 2002, [Pulmonary edema and tocolysis with beta-agonists], Rev Mal Respir, 19, 241\nMilos, 1988, Maternal pulmonary edema complicating beta-adrenergic therapy of preterm labor, AJR Am J Roentgenol, 151, 917, 10.2214\u002Fajr.151.5.917\nEvron, 1983, [Pulmonary edema occurring after isoxsuprine treatment for preterm labor], Harefuah, 105, 287\nBenedetti, 1982, Maternal pulmonary edema during premature labor inhibition, Obstet Gynecol, 59\nStubblefield, 1978, Pulmonary edema occurring after therapy with dexamethasone and terbutaline for premature labor: a case report, Am J Obstet Gynecol, 132, 341, 10.1016\u002F0002-9378(78)90907-9\nNagey, 1982, Pulmonary complications of isoxsuprine therapy in the gravida, Obstet Gynecol, 59\nJacobs, 1980, Maternal pulmonary edema resulting from betamimetic and glucocorticoid therapy, Obstet Gynecol, 56, 56\nGuernsey, 1981, Pulmonary edema associated with the use of betamimetic agents in preterm labor, Am J Hosp Pharm, 38, 1942\nBrosset, 1982, Cardiac complications of ritodrine in mother and baby, Lancet, 1, 1468, 10.1016\u002FS0140-6736(82)92476-X\nCarson, 2002, Atrial fibrillation in pregnancy associated with oral terbutaline, Obstet Gynecol, 100, 1096\nAbramovici, 1980, Maternal pulmonary edema occurring after therapy with ritodrine for premature uterine contractions, Acta Obstet Gynecol Scand, 59, 555, 10.3109\u002F00016348009155450\nDordević, 2002, [Successful resuscitation of a patient with prolonged tocolytic therapy and an emergency cesarean section], Vojnosanit Pregl, 59, 325, 10.2298\u002FVSP0203325D\nMagnus, 1987, [Myocardial infarction during tocolysis with sympathomimetics], Tidsskr Nor Laegeforen, 107, 943\nKotoujansky, 1985, [Tocolysis using salbutamol in cases of cardiac rhythm disorders in the mother. Apropos of 4 cases], J Gynecol Obstet Biol Reprod, 14, 915\nZhang, 2014, Ritodrine-induced agranulocytosis in pregnancy, J Obstet Gynaecol, 34, 533, 10.3109\u002F01443615.2014.914481\nYasuda, 2012, Agranulocytosis associated with intravenous ritodrine hydrochloride therapy: two case reports by different mechanisms, J Obstet Gynaecol Res, 38, 574, 10.1111\u002Fj.1447-0756.2011.01756.x\nKikkawa, 2008, Granulocyte-colony stimulating factor for the treatment of ritodrine-induced neutropenia, J Obstet Gynaecol Res, 34, 286, 10.1111\u002Fj.1447-0756.2008.00773.x\nMuro, 1991, Ritodrine-induced agranulocytosis, Int J Gynaecol Obstet, 36, 329, 10.1016\u002F0020-7292(91)90488-Q\nVerriello, 2009, Rhabdomyolysis caused by tocolytic therapy with ritodrine hydrochloride, Neuromuscul Disord, 19, 718, 10.1016\u002Fj.nmd.2009.06.364\nNasu, 2006, Rhabdomyolysis caused by tocolysis with oral ritodrine hydrochloride in a pregnant patient with myotonic dystrophy, Gynecol Obstet Invest, 1, 53, 10.1159\u002F000088531\nRosene, 1982, Cerebral ischemia associated with parenteral terbutaline use in pregnant migraine patients, Am J Obstet Gynecol, 143, 405, 10.1016\u002F0002-9378(82)90081-3\nHudgens, 1993, Sudden death associated with terbutaline sulfate administration, Am J Obstet Gynecol, 169, 120, 10.1016\u002F0002-9378(93)90144-8\nMilliez, 1980, A case report of maternal death associated with betamimetics and betamethasone administration in premature labor, Eur J Obstet Gynecol Reprod Biol, 11, 95, 10.1016\u002F0028-2243(80)90014-3\nRäsänen, 1990, The effects of ritodrine infusion on fetal myocardial function and fetal hemodynamics, Acta Obstet Gynecol Scand, 69, 487, 10.3109\u002F00016349009013323\nGokay, 2001, Changes in fetal hemodynamics with ritodrine tocolysis, Ultrasound Obstet Gynecol, 18, 44, 10.1046\u002Fj.1469-0705.2001.00453.x\nBrar, 1988, Maternal and fetal blood flow velocity waveforms in patients with preterm labor: effect of tocolytics, Obstet Gynecol, 72, 209\nWitter, 2009, In utero beta 2 adrenergic agonist exposure and adverse neurophysiologic and behavioral outcomes, Am J Obstet Gynecol, 201, 553, 10.1016\u002Fj.ajog.2009.07.010\nConnors, 2005, Beta2-adrenergic receptor activation and genetic polymorphisms in autism: data from dizygotic twins, J Child Neurol, 20, 876, 10.1177\u002F08830738050200110401\nPitzer, 2001, Child development after maternal tocolysis with beta-sympathomimetic drugs, Child Psychiatry Hum Dev, 31, 165, 10.1023\u002FA:1026419720410\nHadders-Algra, 1986, Long-term follow-up of children prenatally exposed to ritodrine, Br J Obstet Gynaecol, 93, 156, 10.1111\u002Fj.1471-0528.1986.tb07880.x\nFreysz, 1977, A long term evaluation of infants who received a beta-mimetic drug while in utero, J Perinat Med, 5, 94, 10.1515\u002Fjpme.1977.5.2.94\nGidaya, 2016, In utero exposure to β-2-adrenergic receptor agonist drugs and risk for autism spectrum disorders, Pediatrics, 137, e20151316, 10.1542\u002Fpeds.2015-1316\nNICE. 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London: National Institute for Health and Care Excellence (UK); 2015.\nRomero, 2000, An oxytocin receptor antagonist (atosiban) in the treatment of preterm labor: a randomized, double-blind, placebo-controlled trial with tocolytic rescue, Am J Obstet Gynecol, 182, 1173, 10.1067\u002Fmob.2000.95834\nvan Vliet, 2016, Nifedipine versus atosiban for threatened preterm birth (APOSTEL III): a multicentre, randomised controlled trial, Lancet, 387, 2117, 10.1016\u002FS0140-6736(16)00548-1\nAl-Omari, 2006, Atosiban and nifedipine in acute tocolysis: a comparative study, Eur J Obstet Gynecol Reprod Biol, 128, 129, 10.1016\u002Fj.ejogrb.2005.12.010\nSalim, 2012, Nifedipine compared with atosiban for treating preterm labor: a randomized controlled trial, Obstet Gynecol, 120, 1323, 10.1097\u002FAOG.0b013e3182755dff\nSeinen, 2013, [Maternal pulmonary oedema due to the use of atosiban in cases of multiple gestation], Ned Tijdschr Geneeskd, 157, A5316\nFernández, 2011, Severe non-cardiogenic pulmonary oedema secondary to atosiban and steroids, Int J Obstet Anesth, 20, 189, 10.1016\u002Fj.ijoa.2010.09.003\nFerguson, 1990, A comparison of tocolysis with nifedipine or ritodrine: analysis of efficacy and maternal, fetal, and neonatal outcome, Am J Obstet Gynecol, 163, 105, 10.1016\u002FS0002-9378(11)90679-6\nSilberschmidt, 2008, Nifedipine concentration in maternal and umbilical cord blood after nifedipine gastrointestinal therapeutic system for tocolysis, BJOG, 115, 480, 10.1111\u002Fj.1471-0528.2007.01630.x\nClouqueur, 2015, [Adverse effects of calcium channels blockers used as tocolytic treatment], J Gynecol Obstet Biol Reprod, 44, 341, 10.1016\u002Fj.jgyn.2014.12.012\nFlenady, 2014, Calcium channel blockers for inhibiting preterm labour and birth, Cochrane Database Syst Rev, CD002255\nAra, 2008, A prospective randomised trial of nifedipine versus placebo in preterm labour, Bangladesh J Obstet Gynaecol, 23, 61, 10.3329\u002Fbjog.v23i2.4962\nZhang, 2002, [Clinical observations on the prevention and treatment of premature labor with nifedipine], Hua Xi Yi Ke Da Xue Xue Bao, 33, 288\nBejan-Angoulvant, 2015, [Calcium channel blockers pharmacology and their use as tocolytics], J Gynecol Obstet Biol Reprod, 44, 305, 10.1016\u002Fj.jgyn.2014.12.010\nParant, 2015, [Use of calcium channel blockers (CCB) for tocolysis in France and abroad], J Gynecol Obstet Biol Reprod, 44, 312, 10.1016\u002Fj.jgyn.2014.12.016\nLe Ray, 2010, [Nifedipine or nicardipine in management of threatened preterm delivery: an observational population-based study], J Gynecol Obstet Biol Reprod, 39, 490, 10.1016\u002Fj.jgyn.2010.04.004\nLaas, 2012, [Comparison of the rate of maternal complications of nifedipine and nicardipine in cases of preterm labor: historical study on two consecutive periods], J Gynecol Obstet Biol Reprod, 41, 631, 10.1016\u002Fj.jgyn.2012.04.020\nMcGuirl J, Arzuaga B, Lee BH. 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Pediatr Cardiol 2012;33:60–4.\nSmith, 2007, Randomized double-blind placebo-controlled trial of transdermal nitroglycerin for preterm labor, Am J Obstet Gynecol, 196, 10.1016\u002Fj.ajog.2006.10.868\nHaghighi, 2005, Isosorbide dinitrate for treatment of preterm labor, Int J Gynaecol Obstet, 89, 274, 10.1016\u002Fj.ijgo.2005.03.004\nDuckitt, 2014, Nitric oxide donors for treating preterm labour, Cochrane Database Syst Rev, CD002860\nAmorim, 2009, [Transdermal nitroglycerin versus oral nifedipine administration for tocolysis: a randomized clinical trial], Rev Bras Ginecol Obstet, 31, 552\nCrowther, 2014, Magnesium sulphate for preventing preterm birth in threatened preterm labour, Cochrane Database Syst Rev, CD001060\nReinebrant, 2015, Cyclo-oxygenase (COX) inhibitors for treating preterm labour, Cochrane Database Syst Rev, CD001992\nErny, 1986, The effects of oral administration of progesterone for premature labor, Am J Obstet Gynecol, 154, 525, 10.1016\u002F0002-9378(86)90595-8\nChawanpaiboon, 2011, Comparison of success rate of nifedipine, progesterone, and bed rest for inhibiting uterine contraction in threatened preterm labor, J Obstet Gynaecol Res, 37, 787, 10.1111\u002Fj.1447-0756.2010.01434.x\nSu, 2014, Progestational agents for treating threatened or established preterm labour, Cochrane Database Syst Rev, CD006770\nKCE. Prévention de l’accouchement prématuré chez les femmes à risque – Évaluation de quelques mesures courantes. https:\u002F\u002Fkce.fgov.be\u002Ffr\u002Fpr%C3%A9vention-de-l%E2%80%99accouchement-pr%C3%A9matur%C3%A9-chez-les-femmes-%C3%A0-risque-%E2%80%93-evaluation-de-quelques-mesures.\n[No authors listed]. Practice Bulletin No. 159: Management of Preterm Labor. Obstet Gynecol 2016;127:e29–38.\nOrganisation mondiale de la santé. Recommandations de l’OMS sur les interventions visant à améliorer l’issue des naissances prématurées. Août 2015. http:\u002F\u002Fapps.who.int\u002Firis\u002Fbitstream\u002F10665\u002F200219\u002F1\u002FWHO_RHR_15.16_fre.pdf?ua=1.\nVeille, 1985, Maternal cardiovascular adaptations to twin pregnancy, Am J Obstet Gynecol, 153, 261, 10.1016\u002FS0002-9378(85)80109-5\nDodd, 2012, Oral betamimetics for maintenance therapy after threatened preterm labour, Cochrane Database Syst Rev, 12, CD003927\nChawanpaiboon, 2014, Terbutaline pump maintenance therapy after threatened preterm labour for reducing adverse neonatal outcomes, Cochrane Database Syst Rev, CD010800\nHan, 2013, Magnesium maintenance therapy for preventing preterm birth after threatened preterm labour, Cochrane Database Syst Rev, CD000940\nNaik Gaunekar, 2013, Maintenance therapy with calcium channel blockers for preventing preterm birth after threatened preterm labour, Cochrane Database Syst Rev, CD004071\nRoos, 2013, Effect of maintenance tocolysis with nifedipine in threatened preterm labor on perinatal outcomes: a randomized controlled trial, JAMA, 309, 41, 10.1001\u002Fjama.2012.153817\nParry, 2014, The NIFTY study: a multicentre randomised double-blind placebo-controlled trial of nifedipine maintenance tocolysis in fetal fibronectin-positive women in threatened preterm labour, Aust N Z J Obstet Gynaecol, 54, 231, 10.1111\u002Fajo.12179\nPapatsonis, 2013, Maintenance therapy with oxytocin antagonists for inhibiting preterm birth after threatened preterm labour, Cochrane Database Syst Rev, CD005938\nVogel, 2014, Combination of tocolytic agents for inhibiting preterm labour, Cochrane Database Syst Rev, CD006169\nManuck, 2015, Tocolysis for women with early spontaneous preterm labor and advanced cervical dilation, Obstet Gynecol, 126, 954, 10.1097\u002FAOG.0000000000001095\nde Veciana, 1995, Tocolysis in advanced preterm labor: impact on neonatal outcome, Am J Perinatol, 12, 294, 10.1055\u002Fs-2007-994478\nAmon, 2000, Tocolysis with advanced cervical dilatation, Obstet Gynecol, 95, 358\nKlauser, 2016, Tocolysis in women with advanced preterm labor: a secondary analysis of a randomized clinical trial, J Matern Fetal Neonatal Med, 29, 696, 10.3109\u002F14767058.2015.1018171",{"ES":1321},"Fármacos tocolíticos",{"VOID":1323},"10.1016\u002Fs1283-081x(19)42003-1","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS1283081X19420031",[1326,1341,1356],{"id":1327,"sortIndex":36,"researcher":26,"roles":1328,"affiliations":1329,"properties":1338},"b43820b1-e054-4ee3-ac76-3d9ee61394fc",[696],[1330],{"id":26,"sortIndex":36,"affiliation":1331,"properties":26},{"id":1332,"createTime":1333,"updateTime":1333,"relativeEntities":1334,"slug":26,"properties":1335,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"28f2c27d-a0a5-47ac-889a-e2fbc3dcd77a","2023-11-30T06:21:53.446+00:00",[],{"title":1336},{"VI":1337},"Service de gynécologie obstétrique, Hôpital Femme-Mère-Enfant, Hospices civils de Lyon, 59, boulevard Pinel, 69677 Bron cedex, France",{"title":1339},{"VI":1340},"M. 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INVS; novembre 2014.\nBulletin des réseaux de surveillance des infections sexuellement transmissibles (IST) - Rénago, Rénachla et RésIST : données au 31 décembre 2012. Saint-Maurice : InVS, 2015, consultation en ligne : http:\u002F\u002Fwww.invs.sante.fr\u002FDossiers-thematiques\u002FMaladies-infectieuses\u002FVIH-sida-IST\u002FInfections-sexuellement-transmissibles-IST\u002FBulletins-des-reseaux-de-surveillance-des-IST.\nBowen, 2015, Increase in incidence of congenital syphilis—United States, 2012-2014, MMWR Morb Mortal Wkly Rep, 64, 1241, 10.15585\u002Fmmwr.mm6444a3\nBerwald, 2009, Self-administered vaginal swabs are a feasible alternative to physician-assisted cervical swabs for sexually transmitted infection screening in the emergency department, Acad Emerg Med, 16, 360, 10.1111\u002Fj.1553-2712.2009.00359.x\nMiettinen, 1993, Test performance of erythrocyte sedimentation rate and C-reactive protein in assessing the severity of acute pelvic inflammatory disease, Am J Obstet Gynecol, 169, 1143, 10.1016\u002F0002-9378(93)90271-J\nAlthaus, 2012, Towards more robust estimates of the transmissibility of Chlamydia trachomatis, Sex Transm Dis, 39, 402, 10.1097\u002FOLQ.0b013e318248a550\nDavies, 2013, Risk of pelvic inflammatory disease after Chlamydia infection in a prospective cohort of sex workers, Sex Transm Dis, 40, 230, 10.1097\u002FOLQ.0b013e31827b9d75\nDavies, 2014, Heterogeneity in risk of pelvic inflammatory diseases after Chlamydia infection: a population-based study in Manitoba, Canada, J Infect Dis, 210, S549, 10.1093\u002Finfdis\u002Fjiu483\nHammerschlag, 1989, Chlamydial infections, J Pediatr, 114, 727, 10.1016\u002FS0022-3476(89)80128-3\nLanjouw, 2016, 2015 European guideline on the management of Chlamydia trachomatis infections, Int J STD AIDS, 27, 333, 10.1177\u002F0956462415618837\nLand, 2006, Chlamydia antibody testing in subfertile women, Drugs Today, 42, 35\nRenault, 2011, Time to clearance of Chlamydia trachomatis ribosomal RNA in women treated for chlamydial infection, Sex Health, 8, 69, 10.1071\u002FSH10030\nChan, 2016, Extragenital infections caused by Chlamydia trachomatis and Neisseria gonorrhoeae: a review of the literature, Infect Dis Obstet Gynecol, 2016, 5758387, 10.1155\u002F2016\u002F5758387\nTrebach, 2015, Neisseria gonorrhoeae and Chlamydia trachomatis among women reporting extragenital exposures, Sex Transm Dis, 42, 233, 10.1097\u002FOLQ.0000000000000248\nTully, 1981, A newly discovered mycoplasma in the human urogenital tract, Lancet, 1, 1288, 10.1016\u002FS0140-6736(81)92461-2\nTaylor-Robinson, 2011, Mycoplasma genitalium: from chrysalis to multicolored butterfly, Clin Microbiol Rev, 24, 498, 10.1128\u002FCMR.00006-11\nHaggerty, 2011, Mycoplasma genitalium: an emerging cause of pelvic inflammatory disease, Infect Dis Obstet Gynecol, 2006\nOliphant, 2016, Pelvic inflammatory disease associated with Chlamydia trachomatis but not Mycoplasma genitalium in New Zealand, Sex Health, 13, 43, 10.1071\u002FSH14238\nLillis, 2011, Utility of urine, vaginal, cervical, and rectal specimens for detection of Mycoplasma genitalium in women, J Clin Microbiol, 49, 1990, 10.1128\u002FJCM.00129-11\nJernberg, 2008, Azithromycin and moxifloxacin for microbiological cure of Mycoplasma genitalium infection: an open study, Int J STD AIDS, 19, 676, 10.1258\u002Fijsa.2008.008038\nJensen, 2016, 2016 European guideline on Mycoplasma genitalium infections, J Eur Acad Dermatol Venereol, 30, 1650, 10.1111\u002Fjdv.13849\nKokkayil, 2015, Ureaplasma: current perspectives, Indian J Med Microbiol, 33, 205, 10.4103\u002F0255-0857.154850\nZdrodowska-Stefanow, 2006, Ureaplasma urealyticum and Mycoplasma hominis infection in women with urogenital diseases, Adv Med Sci, 51, 250\nKataoka, 2006, Association between preterm birth and vaginal colonization by mycoplasmas in early pregnancy, J Clin Microbiol, 44, 51, 10.1128\u002FJCM.44.1.51-55.2006\nSilver, 2014, Trichomonas vaginalis as a cause of perinatal morbidity: a systematic review and meta-analysis, Sex Transm Dis, 41, 369, 10.1097\u002FOLQ.0000000000000134\nWorld Health Organisation. 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Évaluation de l’intérêt de la recherche des papillomavirus humains (HPV) dans le dépistage des lésions précancéreuses et cancéreuses du col de l’utérus. Mai 2004.\nTamalet, 2016, Genotyping and follow-up of HR-HPV types detected by self-sampling in women from low socioeconomic groups not participating in regular cervical cancer screening in France, J Clin Virol, 78, 102, 10.1016\u002Fj.jcv.2016.02.027\nHaut Conseil de la Santé Publique : Avis sur les infections à HPV des jeunes filles : révision de l’âge de vaccination. Janvier 2013.\nChemlal, 2013\nJoura, 2015, A 9-valent HPV vaccine against infection and intraepithelial neoplasia in women, N Engl J Med, 372, 711, 10.1056\u002FNEJMoa1405044\nHaute Autorité de santé. 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