Objective: To explore the therapeutic effect and mechanism of integrated traditional Chinese and western medicine (TCM-WM) in treating ectopic pregnancy (EP). Methods: Seventy-eight patients suffering from unruptured ...Objective: To explore the therapeutic effect and mechanism of integrated traditional Chinese and western medicine (TCM-WM) in treating ectopic pregnancy (EP). Methods: Seventy-eight patients suffering from unruptured EP were divided into two groups at random in proportion of roughly 2∶1, Group Ⅰ(n=50) was treated with methotrexate (MTX) plus Ectopic Pregnancy No.2 (EP2), a Chinese medicinal decoction, Group Ⅱ (n=28) was treated with MTX alone for control. Results:In Group Ⅰ, the nonsurgical cure rate, involving side tubal patency rate and intrauterine pregnancy rate, were 98.0%, 88.0% and 80.0% respectively, the three parameters were all higher than those in Group Ⅱ (75.0%, 46.4% and 42.9% respectively). Moreover, the EP recurrence rate in Group Ⅰ was lower than that in Group Ⅱ (4.0% vs 14.2%), the serum β-hCG normalizing time and total disappearance time of EP mass in Group Ⅰ (25.0±7.8 days and 1.2±0.7 months) were shorter than those in Group Ⅱ (31.9±6.7 days and 5.6±3.7 months), also showing significant difference (P<0.05 and P<0.01 respectively). After being treated by EP2 decoction for 4-8 weeks, the hemorrheological parameters in Group Ⅰ were improved more markedly than those in Group Ⅱ. Conclusion: The TCM-WM treatment (MTX plus EP2) could effectively increase nonsurgical cure rate, tubal patency rate and intrauterine pregnancy rate, decrease EP recurrence rate, and reduce the serum β-hCG normalizing time and the total disappearance time of EP mass in treating EP.展开更多
目的:观察宫外孕Ⅱ号方联合米非司酮治疗宫外孕的临床疗效。方法:将2012年4月—2015年1月就诊于本院的68例宫外孕患者随机分为对照组和观察组各34例。对照组患者口服米非司酮,每次1片,日2次,观察组患者则加用自拟宫外孕Ⅱ号方内服治之,...目的:观察宫外孕Ⅱ号方联合米非司酮治疗宫外孕的临床疗效。方法:将2012年4月—2015年1月就诊于本院的68例宫外孕患者随机分为对照组和观察组各34例。对照组患者口服米非司酮,每次1片,日2次,观察组患者则加用自拟宫外孕Ⅱ号方内服治之,日1剂,两组均连用10 d。监测治疗前后血人绒毛膜促性腺激素(blood human chorionic gonadotropin,HCG)水平变化情况,记录孕酮(progesterone,P)恢复至正常的时间以及盆腔包块消失的时间,用SF-36生存质量量表评估患者治疗前后生存质量的变化,计算有效率,观察不良反应。结果:对照组有效率为67.7%,较观察组有效率91.2%明显降低,差异有统计学意义(P<0.05);观察组患者经治疗后的HCG水平(213.32±47.82)U·L-1明显低于对照组的水平(562.23±81.64)U·L-1,且HCG、P恢复至正常的时间及盆腔包块消失的时间(11.26±8.37)d、(9.15±3.24)d、(14.16±6.39)d明显低于对照组患者的时间(24.35±11.69)d、(13.55±5.41)d、(30.56±9.48)d,差异有统计学意义(P<0.05);与治疗前相比患者生存质量存在不同程度地提高,以观察组患者提高更为突出,生存质量评分较对照组患者更高,差异有统计学意义(P<0.05);观察组不良反应率为11.8%,对照组不良反应率为35.3%,差异有统计学意义(P<0.05)。结论:宫外孕Ⅱ号方联合米非司酮治疗宫外孕疗效确切,不良反应少。展开更多
文摘Objective: To explore the therapeutic effect and mechanism of integrated traditional Chinese and western medicine (TCM-WM) in treating ectopic pregnancy (EP). Methods: Seventy-eight patients suffering from unruptured EP were divided into two groups at random in proportion of roughly 2∶1, Group Ⅰ(n=50) was treated with methotrexate (MTX) plus Ectopic Pregnancy No.2 (EP2), a Chinese medicinal decoction, Group Ⅱ (n=28) was treated with MTX alone for control. Results:In Group Ⅰ, the nonsurgical cure rate, involving side tubal patency rate and intrauterine pregnancy rate, were 98.0%, 88.0% and 80.0% respectively, the three parameters were all higher than those in Group Ⅱ (75.0%, 46.4% and 42.9% respectively). Moreover, the EP recurrence rate in Group Ⅰ was lower than that in Group Ⅱ (4.0% vs 14.2%), the serum β-hCG normalizing time and total disappearance time of EP mass in Group Ⅰ (25.0±7.8 days and 1.2±0.7 months) were shorter than those in Group Ⅱ (31.9±6.7 days and 5.6±3.7 months), also showing significant difference (P<0.05 and P<0.01 respectively). After being treated by EP2 decoction for 4-8 weeks, the hemorrheological parameters in Group Ⅰ were improved more markedly than those in Group Ⅱ. Conclusion: The TCM-WM treatment (MTX plus EP2) could effectively increase nonsurgical cure rate, tubal patency rate and intrauterine pregnancy rate, decrease EP recurrence rate, and reduce the serum β-hCG normalizing time and the total disappearance time of EP mass in treating EP.
文摘目的:观察宫外孕Ⅱ号方联合米非司酮治疗宫外孕的临床疗效。方法:将2012年4月—2015年1月就诊于本院的68例宫外孕患者随机分为对照组和观察组各34例。对照组患者口服米非司酮,每次1片,日2次,观察组患者则加用自拟宫外孕Ⅱ号方内服治之,日1剂,两组均连用10 d。监测治疗前后血人绒毛膜促性腺激素(blood human chorionic gonadotropin,HCG)水平变化情况,记录孕酮(progesterone,P)恢复至正常的时间以及盆腔包块消失的时间,用SF-36生存质量量表评估患者治疗前后生存质量的变化,计算有效率,观察不良反应。结果:对照组有效率为67.7%,较观察组有效率91.2%明显降低,差异有统计学意义(P<0.05);观察组患者经治疗后的HCG水平(213.32±47.82)U·L-1明显低于对照组的水平(562.23±81.64)U·L-1,且HCG、P恢复至正常的时间及盆腔包块消失的时间(11.26±8.37)d、(9.15±3.24)d、(14.16±6.39)d明显低于对照组患者的时间(24.35±11.69)d、(13.55±5.41)d、(30.56±9.48)d,差异有统计学意义(P<0.05);与治疗前相比患者生存质量存在不同程度地提高,以观察组患者提高更为突出,生存质量评分较对照组患者更高,差异有统计学意义(P<0.05);观察组不良反应率为11.8%,对照组不良反应率为35.3%,差异有统计学意义(P<0.05)。结论:宫外孕Ⅱ号方联合米非司酮治疗宫外孕疗效确切,不良反应少。