Sinha Manju, Hegde Aparna, Sinha Rakesh, Goel Sunita
Bombay Endoscopy Academy and Centre for Minimally Invasive Surgery, BEAMS Hospital for Women, Khar, Mumbai, India.
J Minim Invasive Gynecol. 2007 Mar-Apr;14(2):161-8. doi: 10.1016/j.jmig.2006.09.017.
To describe the clinical test parotid area sign, which is used to assess fluid absorption during resectoscopic surgery and to compare the test with volumetric fluid balance method with respect to its ability to detect fluid overload.
Historical cohort study (Canadian Task Force classification II-1).
Tertiary endoscopy center.
Eighty-six women who underwent resectoscopic surgery between 1999 and 2004 at our center.
The volumetric fluid balance method was used to evaluate glycine absorption (glycine deficit) during the surgery. A flexometallic ruler was placed on the left cheek of the patient between 2 fixed points: the midpoint of the philtrum and a point on the mastoid prominence, and this distance (philtrum-mastoid prominence distance) was measured at the beginning of every 3 minutes during, and at the end of the procedure.
Eighty-six patients were divided into 2 groups: Group A, which included patients with absorption less than 1000 mL as measured by the volumetric method; and Group B, which included patients with absorption of 1000 mL or more. The results of the parotid area sign test in the 2 groups were compared. The 2 groups were comparable with respect to the age, weight, preoperative measured philtrum-mastoid prominence distance, and hospital stay. The median (and average absolute deviation) operating time in group A (15 minutes [and 6.79]; range 8-60 minutes; 95% CI of the median, 15-20 minutes) was significantly lower than the median (and average absolute deviation) operating time in group B (25 minutes [and 8.96]; range 9-60 minutes; 95% CI of the median, 20-25 minutes; p <.001). The mean postoperative philtrum-mastoid prominence distance measured in patients of group A (14.23 +/- 0.396 cm [range 14-16 cm, 95% CI 14.10-14.36 cm]) was significantly lower than that in group B [14.76 +/- 0.622 cm (range 14-17 cm, 95% CI 14.58-15.12 cm]; p <.001). By paired t test, the change in the philtrum-mastoid prominence distance after surgery as compared with the value before surgery in each patient was found to be insignificant in group A (p =.86). However, it was found to be significant in group B (p <.001). The increase in the measured philtrum-mastoid prominence distance (i.e., postoperative measurement minus the preoperative measurement) in each patient after surgery was significantly more in group B (mean +/- SD, 0.54 +/- 0.362 cm [range 0-2 cm, 95% CI 0.43-0.65 cm]) than that in group A (mean +/- SD, 0.03 +/- 0.091 cm [range 0-0.4 cm, 95% CI 0.008-0.06 cm]; p <.001). The correlation coefficient for the increase in the philtrum-mastoid prominence distance as the glycine deficit increased in the 2 groups considered together was significant (r = 0.937, p <.01). The partial regression coefficient b value for the effect of duration of surgery while controlling for the effect of fluid deficit was 0.008 (p <.001), and the b value for the effect of fluid deficit while controlling for the effect of duration of surgery was 0.437 (p <.001). The regression coefficient r value (0.727) for the goodness of the fit of the regression line to the data sets was also significant (p <.001). The sensitivity of the test with respect to the volumetric fluid balance is 97.8% (95% CI, 87.28%-99.88%) and specificity is 92.3% (95% CI, 78.03%-97.99%). The negative predictive value is 97.30% (95% CI, 84.19%-99.85%) and positive predictive value is 93.87 (95% CI, 82.13%-98.40%). The conventional positive likelihood ratio for the test is 12.72 (95% CI 4.28-37.77). The conventional negative likelihood ratio is 0.023 (95% CI 0.003-0.16).
The parotid area sign is a simple, effective, and easy-to-perform test (in real time continuously) that requires minimal equipment or training. It supplements the volumetric fluid balance method in the detection of fluid overload (1.5% glycine) during resectoscopic surgery. It may also enable us to detect fluid overload when volumetric fluid balance method fails to detect extraneous losses caused by spillage.
描述用于评估经尿道电切镜手术中液体吸收情况的临床测试——腮腺区体征,并将该测试与容量性液体平衡法在检测液体超负荷能力方面进行比较。
历史性队列研究(加拿大工作组分类II-1)。
三级内镜中心。
1999年至2004年在本中心接受经尿道电切镜手术的86名女性。
采用容量性液体平衡法评估手术期间甘氨酸吸收情况(甘氨酸缺失量)。在患者左脸颊两个固定点之间放置一个可弯曲金属尺:人中中点和乳突突出点,在手术过程中每3分钟开始时以及手术结束时测量此距离(人中-乳突突出距离)。
86例患者分为两组:A组,通过容量法测量吸收量小于1000 mL的患者;B组,吸收量为1000 mL或更多的患者。比较两组腮腺区体征测试结果。两组在年龄、体重、术前测量的人中-乳突突出距离和住院时间方面具有可比性。A组的中位(及平均绝对偏差)手术时间(15分钟[及6.79];范围8 - 60分钟;中位值的95%置信区间,15 - 20分钟)显著低于B组的中位(及平均绝对偏差)手术时间(25分钟[及8.96];范围9 - 60分钟;中位值的95%置信区间,20 - 25分钟;p <.001)。A组患者术后测量的平均人中-乳突突出距离(14.23±0.396 cm[范围14 - 16 cm,95%置信区间14.10 - 14.36 cm])显著低于B组[14.76±0.622 cm(范围14 - 17 cm,95%置信区间14.58 - 15.12 cm];p <.001)。通过配对t检验,发现A组中每位患者术后人中-乳突突出距离与术前值相比的变化无统计学意义(p =.86)。然而,在B组中发现具有统计学意义(p <.001)。B组中每位患者术后测量的人中-乳突突出距离增加量(即术后测量值减去术前测量值)(平均±标准差,0.54±0.362 cm[范围0 - 2 cm,95%置信区间0.43 - 0.65 cm])显著高于A组(平均±标准差,0.03±0.091 cm[范围0 - 0.4 cm,95%置信区间0.008 - 0.06 cm];p <.001)。将两组综合考虑时,人中-乳突突出距离增加量与甘氨酸缺失量增加之间的相关系数具有统计学意义(r = 0.937,p <.01)。在控制液体缺失影响的情况下,手术持续时间影响的偏回归系数b值为0.008(p <.001),在控制手术持续时间影响的情况下,液体缺失影响的b值为0.437(p <.001)。回归线与数据集拟合优度的回归系数r值(0.727)也具有统计学意义(p <.001)。该测试相对于容量性液体平衡的敏感性为97.8%(95%置信区间,87.28% - 99.88%),特异性为92.3%(95%置信区间,78.03% - 97.99%)。阴性预测值为97.30%(95%置信区间,84.19% - 99.85%),阳性预测值为93.87(95%置信区间,82.13% - 98.40%)。该测试的传统阳性似然比为12.72(95%置信区间4.28 - 37.77)。传统阴性似然比为0.023(95%置信区间0.003 - 0.16)。
腮腺区体征是一种简单、有效且易于实施(可实时连续进行)的测试,所需设备或培训极少。它在经尿道电切镜手术中检测液体超负荷(1.5%甘氨酸)方面补充了容量性液体平衡法。当容量性液体平衡法未能检测到因渗漏导致的额外液体丢失时,它也可能使我们能够检测到液体超负荷情况。