Shufaro Yoel, Cohen Mor, Wertheimer Avital, Altman Eran, Wolff Leor, Sapir Onit, Ben-Haroush Avi, Hochberg Alyssa
Infertility and in vitro fertilization (IVF) Unit, Beilinson Hospital, Rabin Medical Center, 39 Jabotinsky Street, Petah Tikva, 4941492, Israel.
The Faculty of Medicine, Tel Aviv University, Ramat Aviv, Tel Aviv, Israel.
J Med Internet Res. 2025 Aug 6;27:e72607. doi: 10.2196/72607.
Ovarian follicles and endometrial thickness are monitored repeatedly for assisted reproduction, burdening patients and clinics. Self-scans with a home ultrasound device can relieve this.
We aimed to evaluate the reliability of self-scans using the smartphone-based Pulsenmore follicle count vaginal self-scan device (FC) versus in-clinic (IC) sonographies, in ovarian stimulation for in-vitro fertilization or fertility preservation.
This study is a single-center, interventional, controlled, prospective study including 44 patients without pelvic pathologies undergoing stimulation for in-vitro fertilization (2022-2024). Following training, patients used a vaginal home ultrasound device to scan their uterus and ovaries with remote guidance by a sonographer in each cycle check-point. Clinical decisions were based on standard IC sonographies. FC and IC results were compared for image quality, endometrial thickness, and follicle count or size. Aspirated oocyte numbers were compared to the follicles recorded at the last visit by home and IC scans. Absolute differences in follicular count and endometrial thickness between IC and FC scans were compared using means, SDs, and 95% CIs. The Spearman correlation (r) analyzed the relations between IC and FC outcomes. All tests applied were 2-tailed, with a P value of ≤5% considered statistically significant. Patient and sonographer satisfaction were assessed via surveys.
Of 44 patients, 34 completed this study. The mean age was 34.7 (SD 4.0) years, and BMI was 25.8 (SD 5.0) kg/m². A total of 65% (22/34) pursued fertility preservation and 35% (12/34) aimed to conceive. The image quality scores of all home scans were at a minimum suitable level, with most of better quality. FC measurements closely matched IC findings for key clinical parameters: antral follicle count (mean FC 11.94, SD 6.62 vs mean IC 15.23, SD 10.2, ρ=0.86, P<.001); number of stimulated follicles ≥10 mm (FC 12.19, SD 6.27 vs IC 13.5, SD 8.87, ρ=0.84, P<.001); identification of the leading follicle >14 mm (achieved in 87% of FC scans); and follicular number or size pretriggering. The aspirated oocyte or last-visit stimulated follicles (>10 mm; FC 1.12, SD 0.6 vs IC 1.06, SD 0.56, ρ=0.82, P<.001), mature oocytes or follicles >13 mm ratios (FC 1.28, SD 1.11 vs IC 1.04, SD 0.77, ρ=0.88, P<.001), and endometrial thickness pretriggering (FC 9.87, SD 2.2 mm vs IC 9.63, SD 2.7 mm, ρ=0.54, P=.002) were well-correlated between the home and standard scans, with 87.1% concordance in identifying endometrial adequacy (≥7 mm). In the patient survey, 82% (28/34) expressed interest in future use of the FC device. In the sonographer survey, 91% (31/34) demonstrated patient improvement.
The home ultrasound device was feasible, comparable, and well-correlated with standard IC scans, laying the basis for remote home-based monitoring of follicular development during ovarian stimulation. We believe this also applies to monitoring milder stimulations and even natural cycles.
在辅助生殖过程中,需要反复监测卵巢卵泡和子宫内膜厚度,给患者和诊所带来负担。使用家用超声设备进行自我扫描可以缓解这一问题。
我们旨在评估使用基于智能手机的Pulsenmore卵泡计数阴道自我扫描设备(FC)进行自我扫描与临床超声检查(IC)相比,在体外受精或生育力保存的卵巢刺激中的可靠性。
本研究是一项单中心、干预性、对照、前瞻性研究,纳入了44例无盆腔病变且正在接受体外受精刺激的患者(2022 - 2024年)。经过培训后,患者在每个周期检查点使用家用阴道超声设备,在超声检查医师的远程指导下扫描子宫和卵巢。临床决策基于标准的IC超声检查。比较FC和IC的结果,包括图像质量、子宫内膜厚度以及卵泡计数或大小。将吸出的卵母细胞数量与在家中和IC扫描最后一次检查时记录的卵泡数量进行比较。使用均值、标准差和95%置信区间比较IC和FC扫描之间卵泡计数和子宫内膜厚度的绝对差异。Spearman相关性(r)分析IC和FC结果之间的关系。所有应用的检验均为双侧检验,P值≤5%被认为具有统计学意义。通过调查评估患者和超声检查医师的满意度。
44例患者中,34例完成了本研究。平均年龄为34.7(标准差4.0)岁,体重指数为25.8(标准差5.0)kg/m²。共有65%(22/34)的患者进行生育力保存,35%(12/34)的患者旨在怀孕。所有家用扫描的图像质量评分至少处于合适水平,大多数质量更好。FC测量结果与IC检查在关键临床参数上密切匹配:窦卵泡计数(FC均值11.94,标准差6.62,IC均值15.23,标准差10.2,ρ = 0.86,P <.001);直径≥10 mm的刺激卵泡数量(FC 12.19,标准差6.27,IC 13.5,标准差8.87,ρ = 0.84,P <.001);识别直径>14 mm的主导卵泡(在87%的FC扫描中实现);以及触发前的卵泡数量或大小。吸出的卵母细胞或最后一次检查时刺激卵泡(>10 mm;FC 1.12,标准差0.6,IC 1.06,标准差0.56,ρ = 0.82,P <.001)、成熟卵母细胞或直径>13 mm的卵泡比例(FC 1.28,标准差1.11,IC 1.04,标准差0.77,ρ = 0.88,P <.0