Nonpalpable implant removals at centre of experience in France: a cohort study.

IF 1.9 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Gautier Chene, Pia Akl, Ana Gjorgjievska-Delov, Emanuele Cerruto, Stephanie Moret, Erdogan Nohuz
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引用次数: 0

Abstract

Objective(s): Management and localisation strategies to remove nonpalpable contraceptive implants may be difficult. We aimed to evaluate our imaging modalities to identify deep implant and patient outcomes related to removal.

Study design: In this retrospective study, we reviewed all cases referred to our specialised centre for nonpalpable contraceptive implants from January 2018 to August 2022.

Results: Out of the cohort studied, 47 female subjects exhibited nonpalpable implants. The implant was nonpalpable for thirty-six patients (76,6%) immediately after the insertion whereas it was not palpable several months after the insertion for eleven patients (23.4%). Twelve patients (25.5%) had one or more failed removal attempts before referral.All 47 implants were successfully visualised via ultrasound in the upper arm: 40 implants (85.1%) were located in the subdermal tissue, 4 (8.5%) were intrafascial and 3 (6.4%) were intramuscular. Depth of the implant was 4.0 mm [1.7 - 12.0]. No clinical factors were statistically associated with differences in depth or location (subdermal vs subfascial). Removal procedures were mainly under local anaesthesia in 74.5% of cases in an outpatient setting. There were two Clavien-Dindo grade 1 complications (one case of cutaneous scar dehiscence and one transient postoperative neuropathic complaint in the upper arm resolved within 3 months under analgetics).

Conclusions: Identification of deep implants requires following the ultrasound modality protocol. Ultrasound detection makes easy and safe implant removal. Training programs for the insertion as well as for the removal of correct and incorrect inserted implants should be continued and developed all around the world.

法国经验中心的非可触及植入物取出:一项队列研究。
研究设计:在这项回顾性研究中,我们回顾了自2018年1月至2022年8月期间因不可触及的避孕植入物而转诊至本专业中心的所有病例:在所研究的群体中,有 47 名女性受试者表现出植入物无法触及的情况。有 36 名患者(76.6%)在植入后立即无法触及植入物,而有 11 名患者(23.4%)在植入数月后无法触及植入物。12 名患者(25.5%)在转诊前曾尝试过一次或多次移除植入物,但均以失败告终:所有 47 个植入体均可通过超声波在上臂成功观察到:40 个植入体(85.1%)位于皮下组织,4 个(8.5%)位于筋膜内,3 个(6.4%)位于肌肉内。植入深度为 4.0 毫米 [1.7 - 12.0]。在统计学上,没有临床因素与植入深度或位置(皮下与筋膜下)的差异相关。74.5%的病例在门诊环境下进行了局部麻醉。有两例克拉维恩-丁多 1 级并发症(一例皮肤疤痕开裂,一例术后上臂一过性神经痛,在镇痛药作用下 3 个月内缓解):结论:深部植入物的识别需要遵循超声模式规程。结论:深部植入物的识别需要遵循超声模式方案,通过超声检测可以轻松安全地取出植入物。应在全球范围内继续开展和发展关于正确插入和错误插入植入物的插入和移除培训计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
11.80%
发文量
63
审稿时长
>12 weeks
期刊介绍: The Official Journal of the European Society of Contraception and Reproductive Health, The European Journal of Contraception and Reproductive Health Care publishes original peer-reviewed research papers as well as review papers and other appropriate educational material.
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