Telephone follow-up after early medical abortion using Australia's first low sensitivity urine pregnancy test

被引:1
|
作者
Melville, Catriona [1 ,2 ]
Goldstone, Philip [1 ]
Moosa, Nisreen [1 ]
机构
[1] MSI Australia, Melbourne, Vic, Australia
[2] MSI Australia, GPO Box 1635, Melbourne, Vic 3001, Australia
关键词
induced abortion; low-sensitivity urine pregnancy test; medical abortion; self-testing; telephone follow-up; HUMAN CHORIONIC-GONADOTROPIN; HCG; MIFEPRISTONE; TERMINATION; MISOPROSTOL;
D O I
10.1111/ajo.13731
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BackgroundFollow-up after early medical abortion (EMA) in Australia often entails tracking serum human chorionic gonadotropin levels or performing ultrasonography in-clinic. In other countries, methods of follow-up such as using a low-sensitivity urine pregnancy test (LSUPT), telephone evaluation and a questionnaire have been demonstrated to be safe and acceptable. AimsTo evaluate the safety and efficacy of telephone follow-up after EMA using an LSUPT and questionnaire. Materials and MethodsA prospective observational cohort study of patients undergoing telephone follow-up after EMA using an LSUPT and questionnaire was conducted from March 26 to July 31, 2020. Outcomes of patients who returned to clinic because of a positive LSUPT were evaluated and adverse event rates were calculated. Routinely collected adverse event information was used to compare complication rates during the evaluation period with that prior to introduction of the LSUPT. ResultsDuring the study period, 2223 patients underwent the new protocol. One hundred and ninety-seven patients had a positive LSUPT at their telephone follow-up. One hundred and thirty-two had an incomplete abortion, 11 had a continuing pregnancy, 53 had a complete abortion and one left the clinic before full assessment. ConclusionsIntroduction of telephone follow-up with an at-home LSUPT reduced the number of patients requiring unnecessary clinic appointments, with over 90% of patients completing their follow-up at home. Complication rates during the study period were found to be at least comparable with previously identified organisational adverse events.
引用
收藏
页码:797 / 802
页数:6
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