de Jongh Frank W, Kooiman Laurens B R, Sanches Elijah E, Pouwels Sjaak, Ingels Koen J A O, Wehrens Kim M E, Tan Liang T
Department of Plastic- Reconstructive- and Hand surgery, Haaglanden Medical Center, Den Haag.
Department of Intensive Care Medicine, Elisabeth-Tweesteden Ziekenhuis, Tilburg.
Int J Surg Protoc. 2023 Nov 16;28(1):31-36. doi: 10.1097/SP9.0000000000000011. eCollection 2024 Mar.
The aim of this study is to prospectively evaluate the new minimal invasive (MINE) browlift technique with possibly superior results and minimal visible scarring.
A prospective observational study will be performed on all available data from patients who will undergo a browlift procedure in the HMC from 1 June 2021 till 31 May 2024. Our goal is to include at least 50 patients. Inclusion criteria are: patients with medical (i.e. brow ptosis and facial paralysis) or cosmetic indication, patients with sufficient understanding of the Dutch or English language and willingness to participate in extra study specific follow-up moments and filling in of questionnaires. Exclusion criteria are: less than 18 years of age and patients with previous brow or eyelid surgery. Patients will be photographed preoperatively and postoperatively using the VECTRA camera.
Scarring after procedure; functionality of eyebrow movement; amount of correction in brow ptosis, measured in VECTRA; longevity of procedure in months; aesthetic result as assessed by questionnaires and adverse effects of procedure will be measured.
The database management software 'Castor' will be used to store and collect the data from the questionnaire. The Medical Research Ethics Committee found this study not eligible to be submitted to the Dutch Medical Research Involving Human Subjects Acts (WMO). Written consent will be obtained from all patients.
本研究的目的是前瞻性地评估新的微创(MINE)提眉技术,该技术可能具有更好的效果和最小的可见疤痕。
将对2021年6月1日至2024年5月31日在HMC接受提眉手术的患者的所有可用数据进行前瞻性观察研究。我们的目标是纳入至少50名患者。纳入标准为:有医学(即眉下垂和面瘫)或美容适应症的患者,对荷兰语或英语有充分理解且愿意参与额外的特定研究随访阶段并填写问卷的患者。排除标准为:年龄小于18岁以及既往有眉部或眼睑手术史的患者。将使用VECTRA相机在术前和术后对患者进行拍照。
术后疤痕;眉部运动功能;用VECTRA测量的眉下垂矫正量;手术持续时间(以月为单位);通过问卷评估的美学效果以及手术的不良反应。
将使用数据库管理软件“Castor”来存储和收集问卷数据。医学研究伦理委员会认为本研究不符合提交至荷兰涉及人类受试者的医学研究法案(WMO)的条件。将获得所有患者的书面同意。