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首页> 外文期刊>Journal of Perinatal Medicine >Evaluation of a device for objective determination of cervical consistency: a pilot study of device's validity on uterine specimens obtained by total abdominal hysterectomy for benign uterine disease.
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Evaluation of a device for objective determination of cervical consistency: a pilot study of device's validity on uterine specimens obtained by total abdominal hysterectomy for benign uterine disease.

机译:评估用于客观确定宫颈一致性的设备:该设备在通过全腹子宫切除术治疗良性子宫疾病的子宫标本上的有效性的初步研究。

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摘要

A new device in assessment of cervical consistency by means of resistance to electrical current was compared to observations made by traditional clinical assessment of the cervix. The cervix of 50 specimens obtained consecutively at a series of total abdominal hysterectomies done for benign disease was evaluated for cervical consistency first by palpation preoperatively and then by the new device, using 5 prototypes, after the specimen was removed. Obtained results showed that intra-observer error for all five prototypes averaged 1.28 +/- 2.5% (mean +/- standard deviation), whereas inter-observer error was 8.44 +/- 7.9%. Stratified by clinical cervical consistency as soft, moderate and firm, there was a statistically significant difference in the resistance to electrical current (f = 29.0, r2 = 0.19, p < 0.0001). Resistance to electrical current was highest for firm cervices, less for those of moderate consistency, and least for soft ones (21.8 +/- 2.73, 19.6 +/- 2.91 and 15.6 +/- 4.09 ohms, respectively). In conclusion, measurements of cervical resistance obtained objectively by a new device reliably correlated with traditional clinical assessment of cervical consistency.
机译:将一种通过电流抗性评估宫颈一致性的新装置与传统的宫颈临床评估结果进行了比较。在术前先行触诊,然后通过新装置,使用5个原型,在取下标本后,对一系列针对良性疾病进行的一系列腹部全子宫切除术连续获得的50个标本的宫颈进行宫颈一致性检查。获得的结果表明,所有五个原型的观察者内部误差平均为1.28 +/- 2.5%(平均+/-标准偏差),而观察者之间的误差为8.44 +/- 7.9%。根据临床颈椎的一致性将其分层为软,中度和牢固,对电流的电阻存在统计学上的显着差异(f = 29.0,r2 = 0.19,p <0.0001)。坚硬的子宫颈对电流的电阻最高,中等硬度的子宫颈的电流电阻较小,软的子宫颈的电阻最小(分别为21.8 +/- 2.73、19.6 +/- 2.91和15.6 +/- 4.09欧姆)。总之,通过新设备客观获得的宫颈抵抗力的测量结果与传统的宫颈一致性临床评估可靠地相关。

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