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Effect of Ligustrazine combined with levamlodipine besylate on BNP, Ang Ⅱ and pregnancy outcomes in patients with hypertensive disorders complicating pregnancy |
WANG Xuefang LU Yanqing▲ |
Department of Obstetrics, Wuwei People′s Hospital, Gansu Province, Wuwei 733000, China |
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Abstract Objective To investigate the effects of Ligustrazine combined with levamlodipine besylate on plasma brain natriuretic peptide (BNP), angiotensin Ⅱ (Ang Ⅱ) and pregnancy outcome in patients with pregnancy-induced hypertension. Methods From January 2016 to January 2018, in Wuwei People′s Hospital, 87 patients with pregnancy-induced hypertension were selected, they were divided into two groups according to whether they used Ligustrazine or not. The control group was given 25% magnesium sulfate and levamlodipine besylate based on symptomatic treatment such as reasonable diet and sedation. The observation group was treated with Ligustrazine on the basis of the control group. BPN, AngⅡ, mean arterial pressure, 24 h urinary protein level, uterine artery, and umbilical artery systolic period the ratio of maximum blood flow velocity to end-diastolic blood flow velocity (S/D), pulse index (PI), and resistance index (RI) before and after treatment were observed, adverse reactions during treatment, treatment effect after treatment 10 d were observed. Follow-up to delivery, the pregnancy outcomes of two groups were observe. Results After treatment, the levels of BNP and AngⅡ in the observation group were lower than before treatment and the control group, the differences were statistically significant (P < 0.05). After treatment, the S/D, PI and RI of the uterine artery and umbilical artery in the observation group were lower than before treatment and the control group, the differences were statistically significant (P < 0.05). The total effective rate in the observation group was higher than the control group, the difference was statistically significant (P < 0.05). The incidence rates of premature labor, cesarean section, intrapartum or postpartum hemorrhage, placental abruption, intrauterine distress and neonatal asphyxia in the observation group were lower than the control group, the differences were statistically significant (P < 0.05). No adverse reactions occurred in both groups during treatment. Conclusion Ligustrazine injection combined with levamlodipine besylate has a satisfactory therapeutic effect on gestational hypertension, reducing the expression of BNP and AngⅡ, increasing uterine and placental blood supply, and reducing the adverse outcomes of pregnancy. It is worthy of clinical promotion.
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