机构地区:[1]陕西中医药大学第二附属医院西咸新区中心医院产科,咸阳712000 [2]陕西中医药大学第二附属医院西咸新区中心医院妇五科,咸阳712000
出 处:《国际医药卫生导报》2024年第17期2926-2930,共5页International Medicine and Health Guidance News
基 金:陕西省教育厅专项科研计划(20JK0606)。
摘 要:目的探讨中药配合甲状腺激素治疗对妊娠期合并甲状腺功能减退症(简称“甲减”)患者血脂调节效果,以及对母婴健康的影响。方法选取陕西中医药大学第二附属医院2022年7月至2023年6月就诊的98例妊娠期合并甲减患者进行随机对照试验,通过随机数字表法分为对照组和联合组,每组各49例。对照组:年龄27~36(31.67±4.81)岁;入院体重指数(BMI)为(22.43±3.67)kg/m^(2);孕周为(19.09±1.34)周;予低剂量左甲状腺素钠片治疗,初始剂量为25μg/d,每隔4周进行复诊,如促甲状腺激素(TSH)水平未恢复正常,则根据患者耐受程度,依次将剂量调整为50~100μg/d,直到TSH水平恢复正常,共持续治疗12周。联合组:年龄29~39(32.07±5.13)岁;入院BMI为(22.19±3.28)kg/m^(2);孕周为(19.84±1.17)周;在对照组基础上联合补中温阳汤,水煎服,每日1剂,早、晚餐后分2次服用,连续服用12周。通过12周的持续治疗,观察分析两组患者的游离四碘甲状腺原氨酸(FT_(4))、TSH、甲状腺过氧化物酶自身抗体(TPOAb)阳性率、血清总胆固醇(TC)、甘油三酯(TAG)、低密度脂蛋白胆固醇(LDL-C)、母婴结局、新生儿发育水平以及临床总有效率。统计学方法采用t检验、χ^(2)检验。结果联合组临床总有效率高于对照组[85.71%(42/49)比67.35%(33/49)],差异有统计学意义(χ^(2)=4.60,P<0.05)。分娩后,联合组TSH、TPOAb水平、TPOAb阳性率均低于对照组[(1.97±0.46)IU/ml比(2.87±0.62)IU/ml、(8.12±1.47)IU/ml比(10.96±1.82)IU/ml、6.12%(3/49)比20.41%(10/49)],差异均有统计学意义(t=8.16、8.50,χ^(2)=4.35,均P<0.05);联合组血脂水平各项指标均低于对照组,差异均有统计学意义(均P<0.05)。联合组新生儿出生3个月后智力发育指数(MDI)、运动发育指数(PDI)评分均高于对照组[(86.94±5.86)分比(80.27±5.14)分、(85.72±5.15)分比(80.98±5.23)分],差异均有统计学意义(t=5.99、4.52,均P<0.05)。两组不良母婴结局发生率比较[4.08%(2/Objective To evaluate the effect of traditional Chinese medicine combined with thyroid hormone on lipid regulation and maternal and neonatal health in pregnant patients with hypothyroidism.Methods Ninety-eight pregnant women with hypothyroidism treated at Second Hospital,Shaanxi University of Traditional Chinese Medicine from July 2022 to June 2023 were selected for the randomized controlled trial,and were divided into a control group and a combination group by the random number table method,with 49 cases in each group.The control group were 27-36(31.67±4.81)years old;their body mass index at admission was(22.43±3.67)kg/m^(2);their gestational age was(19.09±1.34)weeks.The combination group were 29-39(32.07±5.13)years old;their body mass index at admission was(22.19±3.28)kg/m^(2);their gestational age was(19.84±1.17)weeks.Both groups took levothyroxine sodium tablets at an initial dosage of 25μg/d;they revisited every 4 weeks;if their level of thyroid-stimulating hormone(TSH)did not return to normal,they took the tablets 50-100μg/d according to their resistance until their TSH level was normal;they were treated for 12 weeks.In addition,the combination group took Buzhong Wenyang Tang in the morning and at night one dosage per day for 12 weeks.After 12 weeks'treatment,the free thyroxine(FT_(4)),TSH,thyroid peroxidase antibody(TPOAb)positive rates,serum total cholesterol(TC),triglycerides(TAG),low-density lipoprotein cholesterol(LDL-C),maternal and neonatal outcomes,neonatal development[assessed by the Bayley Scales of Infant Development(BSID)],and overall clinical efficacies in both groups were observed and analyzed.t andχ^(2)tests were used.Results The overall clinical efficacy in the combination group was higher than that in the control group[85.71%(42/49)vs.67.35%(33/49)],with a statistical difference(χ^(2)=4.60,P<0.05).After delivery,the levels of TSH and TPOAb and TPOAb positive rate in the combination group were lower than those in the control group[(1.97±0.46)IU/ml vs.(2.87±0.62)IU/ml,(8.12±1.47)
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