Subjects
This study was conducted after approval by the institutional review board at Medical Park Shonan and Medical Park Yokohama between November 2019 and March 2020. Our patients, who were aged between 20 and 45 years old with BMI values of ≤ 30 kg/m2, gave informed consent to participate in the study. We also measured the dominant follicle (follicle with a mean diameter ≥ 10 mm) in each ovary in patients undergoing controlled ovarian stimulation (COS). Data were obtained from follicle images suitable for evaluation that were either collected by the patient or by the doctor. Patients exhibiting development of ≥ 4 follicles in either ovary were excluded from the study as it would be difficult to identify the individual follicles.
COS techniques
The COS protocol is described as follows: (a) The CC-Gn method: the patient is administered clomiphene citrate at a dose of 50 mg/day from day 3 of the menstrual cycle and recombinant follicle-stimulating hormone (rec-FSH) or human menopausal gonadotrophin (HMG) at a dose of 225 IU on day 5 administered on alternate days; (b) The letrozole-FSH method: the patient is administered letrozole at a dose of 5 mg/day from day 3 to day 7 of the menstrual cycle and then receives rec-FSH injections at a dose of 150 IU on consecutive days from day 7 until the date of hCG administration; (c) The letrozole method: the patient is administered letrozole at a dose of 5 mg/day from day 3 of the menstrual cycle on consecutive days; (d) The short method: the patient is administered a GnRH agonist (buserelin acetate at a dose of 300 μg/day) from day 2 of the menstrual cycle and HMG at a dose of 300 IU/day on consecutive days from day 3, with hCG administered when the dominant follicle diameter reaches 18 mm. The selection of one of these stimulation methods is left to the discretion of the attending physician.
Follicle self-measurements by the patients using TAUS
The follicle diameter was measured on day 10 of the menstrual cycle or later. First, the patient ensured that their bladder was full, then they laid in the supine position and used a pocket-sized ultrasound device, known as the miruco (Japan Sigmax Co., Ltd., Osaka, Japan), that was fitted with an attached 3.5 MHz convex probe. The patient used the probe to perform a transabdominal scan to determine the transverse cross-section of the left and right ovaries. To do this, the patient scrolled down the left and right sides of the hypogastric region to capture both ovaries in their entirety, and then they stored the resulting videos (Fig. 1a). The entire procedure was performed under the guidance of a highly experienced gynecologist. Next, the acquired videos were stored on a tablet (ASUS) and sent to a computer (Lenovo Thinkpad X280, Lenovo, Tokyo, Japan). The individual ovarian follicle diameters were measured as follows. The maximum ovarian cross-sectional measurement was identified in the videos and saved as a still image. Next, the still images were uploaded to the image processing software ImageJ version 1.51n (National Institute of Health, Bethesda, MD, USA). These images were displayed at a resolution of 1920 × 1080 pixels on a 21.5-inch liquid crystal display sub-monitor (LCD-MF244ED, I-O DATA Co., Ltd., Kanazawa, Japan), and then the maximum follicle diameter and the diameter of the follicle on the line perpendicular to this diameter were calculated based on the scale used for US images. The mean value of these two values was taken as the abdominal transverse diameter (Fig. 1b).
Follicle measurements by the doctor using TVUS
After TAUS was completed, the doctor who provided guidance during TAUS performed TVUS. The patient was placed in the lithotomy position, and the measurements were taken using a SONOVISTA FX, premium edition (Konica Minolta, Inc., Tokyo, Japan). The dominant follicle in both ovaries was first identified, then the probe was aligned and rotated 90° to obtain the sagittal and coronal cross-sectional measurements. The maximum diameter of both follicles, and the length of the lines perpendicular to these diameters, were measured using the SONOVISTA FX premium edition display, and the mean values for each cross-sectional diameter were taken as the vaginal sagittal (VS) and vaginal coronal (VC) diameters.
Questionnaire
A questionnaire was conducted to enquire whether the patients who performed follicle self-measurement preferred TAUS to TVUS after the measurements were completed.
Statistical analysis
We evaluated the accuracy and precision of follicular size measurements from the pocket-sized US device to confirm whether the same follicular size was depicted in both the mobile US and TVUS images.
- Evaluation of accuracy
(1) Detection bias
Detection bias was defined as ≥ 1 mm.
(2) Sample size
There were ≥ 48 target follicles in each group.
(3) Analysis method
We tested AT vs. VS and AT vs. VC using the paired t-test to determine the presence of statistically significant differences.
- Evaluation of precision
The cross-sectional diameters measured using the two aforementioned measurement methods were different. For this reason, we were unable to exclude differences between the cross-sectional diameters measured during imaging when comparing the precision of the two measurement methods. The size of the individual ovarian follicles was also different. In consideration of the above, as shown in equations (I), (II) and (III) below, we calculated the amount of variance for the difference in follicle sizes obtained using TAUS and TVUS.
σAT-VS2・・・(I)
σAT-VC2・・・(II)
σVS-VC2・・・(III)
(III) clarifies the fact that with the TVUS cross-sectional diameter, it is the difference in the type of cross-section (sagittal or coronal) that is the dominant factor. Accordingly, during the comparison of image precision, we calculated the variance ratio to (III), i.e., (I)/(III) and (II)/(III), and performed a comparative evaluation.
Interclass correlation coefficient
The reliability of the measurements obtained using TVUS and TAUS were evaluated using the interclass correlation coefficient (ICC). The ICC ranged from 0 to 1, and the values were defined as follows: < 0.20 slight, 0.21 to 0.40 fair, 0.41 to 0.60 moderate, 0.61 to 0.80 substantial, and 0.81 to 1.00 almost perfect [14].
Statistical analysis was performed using Minitab version 19, and a p value < 0.05 was considered statistically significant.