Microsoft Word - GOI217BF

نویسندگان

  • T. Toshiyuki Hata
  • Daisaku Senoh
  • K. Ken Makihara
  • Osamu Takamiya
  • M. Manabu Kitao
چکیده

Transvaginal Doppler color flow mapping was performed on 8 Japanese women (normal, 1; menopause, 2; uterine myoma, 1; endometriosis, 2; pregnant, 2). In all 8, bilateral uterine arteries and branches could be clearly identified in shades of blue and/or red. The color flows were abundant in the pregnant women. Transvaginal Doppler color flow mapping is expected to be an important diagnostic tool for assessing uterine arterial blood flows in physiologic and pathologic conditions of the pelvis. Toshiyuki Hata, MD, Department of Obstetrics and Gynecology, Shimane Medical Universtiy, Izumo 693 (Japan) real-time two-dimensional Doppler mode, the flow directed toward the transducer was displayed in shades of red, the flow directed away from the transducer was in shades of blue and the maximal velocity of the flow that exceeded the Nyquist limits was presented as color aliasing. Pulse repetition frequencies of this apparatus were from 4 to 26 kHz. Blood flow velocities were displayed within a 30–80° sector at depths ranging from 4 to 22 cm. This apparatus Introduction With recent advances in Doppler ultrasound equipment, numerous reports on the assessment of uterine arterial blood flow velocity waveform have been done with pulsed (PW) or continuous wave (CW) Doppler ultrasound [1–3]. Transabdominal Doppler color flow mapping (DCFM) has also been done in nonpregnant or pregnant women and patients with gynecologic diseases [4–7]. However, to our knowledge, there has been no report of transvaginal DCFM in the female pelvis. We report here our preliminary findings of transvaginal DCFM, in various clinical conditions. Materials and Methods D ow nl oa de d by : 54 .7 0. 40 .1 1 11 /3 /2 01 7 6: 14 :0 9 P M Transvaginal DCFM was performed on 8 Japanese women (normal, 1; menopause, 2; uterine myoma, 1; endometriosis, 2; pregnant, 2) at Shimane Medical University Hospital. Permission for the study was obtained from each patient. Fig. 1. Special probe used in the study, a Whole view, b Leading edge of the probe. The apparatus used was an Aloka SSD-870 with a special probe for the use of transesophageal scanning (Aloka UST-5228S-5, 5 MHz transducer; fig. 1.). The probe was 70 cm in length and 9 mm in diameter and the tip was 12X9 mm. This probe is flexible and bends 120° anteriorly and 90° posteriorly about 5 cm from the tip by means of a manual controller. The imaging plane of the ultrasound was vertical and perpendicular to the axis of the probe. In the 218 Hata/Hata/Senoh/Makihara/Aoki/Takamiya/Kitao/Umaki allows for simultaneous real-time imaging and PW Doppler tracing. In the real-time twodimensional and PW Doppler modes, velocities can be measured up to 6.2 m/s. Wall filters (100 Hz) were used to eliminate low-frequency signals occurring from noise. After voiding, the patient was placed in the lithotomy position and the probe was inserted into the posterior fornix of the vagina. Transverse scanning by the real-time two-dimensional Doppler mode was performed and we searched for uterine arterial blood flows located at the lateral sides of the uterus. On the real-time two-dimensional Doppler ultrasonogram, the sampling point on the line of the PW Doppler beam was placed at the region of interest, where the color flow was clearly noted. Results and Discussion In normal nonpregnant women, bilateral uterine arteries were clearly noted (fig. 2). Moreover, DCFM revealed thin uterine arteries, even during the menopause. In the case of adenomyosis, DCFM showed increased vascularities of both uterine arteries (fig. 3). Abundant color flows were evident in the pregnant women (fig. 4). Consequently, bilateral uterine arteries and branches could be clearly identified in all 8 women. Transabdominal DCFM has been done in nonpregnant or pregnant women and patients with gynecologic diseases [4–7] and is especially useful for assessment of tumor vascularities in trophoblastic diseases [8, 9]. However, DCFM and/or blood flow velocity waveform cannot be detected by the transabdominal approach in some patients, for example, in those with uterine cervical cancer [6]. This may be because uterine cervical cancer most often occurs in older women and the uterus is relatively small. Therefore, there are limitations using transabdominal DCFM. Fleischer et al. [10] reported transvaginal CW Doppler examination without real-time imaging of the vessels and successful examinations could be performed by pattern recognition of each blood flow velocity waveform [3]. However, CW Doppler ultrasound has no range resolution, and blood flow patterns do change with the menstrual cycle and in the presence of pathology [6, 11]. We performed transvaginal DCFM for an exact identification of uterine arteries and branches and to place the sampling point of the PW Doppler mode at the region of interest. Consequently, bilateral uterine arteries and branches could be clearly noted in shades of blue and/or red in all 8 women. Transvaginal DCFM is expected to be an important part of the armamentarium of the gynecologist attempting to assess uterine arterial blood flow in the female pelvis, under physiologic and pathologic conditions. Acknowledgements We thank M. Ohara for comments and Aloka Co. Ltd. for use of the transesophageal probe. D ow nl oa de d by : 54.70.40.11-11/3/20176:14:09PM ReferencesCampbell S, Griffin DR, Pearce JM, et al: New Doppler technique for assessing uteroplacentalblood flow. Lancet 1983;i: 675–677.Trudinger BJ, Giles WB, Cook CM: Flow velocity waveforms in the maternal uteroplacental andfetal umbilical circulations. Am J Obstet Gynecol 1985;152:155–163.Schulman H, Fleischer A, Faumakides G, et al: Development of uterine artery compliance inpregnancy as detected by Doppler ultrasound. Am J Obstet Gynecol 1986;155:1031–1036.Shimamoto K, Sakuma S, Ishigaki T, et al: Intratumoral blood flow: Evaluation with colorDoppler echography. Radiology 1987;165:683–685.Hata K, Hata T, Aoki S, et al: Evaluation of female intrapelvic blood vessels and theirhemodynamics with real-time two-dimensional Doppler ultrasound. Acta Obstet Gynaecol Jap1988;40:67–73.Hata T, Hata K, Yamane Y, et al: Real-time two-dimensional and pulsed Doppler ultrasounddetection of intrapelvic neoplas-tic tumors and abnormal pathogenic changes: Preliminary report.J Cardiovasc Ultrasonog 1988;7:135–141.Hata K, Hata T, Aoki S, et al: Changes in myometrial arcuate arterial compliance during thereproductive cycle as assessed by real-time two-dimensional and color flow pulsed Dopplerultrasound. J Cardiovasc Ultrasonog 1988;7, in press.Hata T, Hata K, Senoh D, et al: Syncytial endometritits: Realtime two-dimensional Dopplersonographic and pelvic angio-graphic features (letter). Am J Roentgenol 1988; 151:831.Aoki S, Hata T, Hata K, et al: Doppler color flow mapping of an invasive mole. Gynecol ObstetInvest 1989;27:52–54. Fleischer A, Schulman H, Farmakides G, et al: Uterine artery Doppler velocimetry in pregnantwoman with hypertension. Am J Obstet Gynecol 1986;154:806–813.Taylor KJW, Burns PN, Wells PNT et al: Ultrasound Doppler flow studies of the ovarian anduterine arteries. Br J Obstet Gynaecol 1985;92:240–246. Downloadedby: 54.70.40.11-11/3/20176:14:09PM

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تاریخ انتشار 2009