妊娠期高血压

Q4 Medicine Open Hypertension Journal Pub Date : 2020-01-01 DOI:10.15713/ins.johtn.0179
E. Armenia, Michael Vornovitsky
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引用次数: 1

摘要

妊娠期高血压的识别不仅对胎儿结局很重要,而且妊娠期高血压疾病也预示着女性未来心血管事件的高风险。[1]妊娠期高血压(妊娠期间首次出现的高血压)的患病率为6%;[2]此外,高达3%的育龄妇女患有慢性高血压(随着肥胖率的上升,患病率也在上升)[3]。高血压会增加妊娠期间并发症的风险,包括先兆子痫、胎儿生长受限和胎盘早剥。[3]此外,它会使孕妇面临心力衰竭(射血分数降低和保留)和右室功能障碍的风险;在以后的生活中,女性患冠状动脉疾病和心力衰竭的风险也大大增加。[4]事实上,高血压的治疗已经被证明可以降低产妇的发病率,但它并没有被证明对胎儿的结局有实质性的影响。[3]在正常妊娠中,由于全身血管扩张和周围血管阻力降低,全身血压下降。因此,许多患有轻度慢性高血压的妇女在怀孕期间可以停止服药。到目前为止,没有证据表明轻度至中度高血压的治疗可以改善胎儿或母体的结局;因此,治疗目标的指导方针仍然存在争议。[4]根据ACC/AHA指南,治疗1期高血压以预防未来心血管事件是合理的。两种经典的一线高血压控制药物在妊娠期有相对的禁忌症。血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂可导致胎儿颅骨发育不全,以及无尿和肾功能衰竭(特别是在妊娠早期)。[5]噻嗪类药物可引起新生儿黄疸、体积减少或血小板减少(尽管一项研究显示利尿剂在不良妊娠结局方面没有显著差异)。[3,6]然而,钙通道阻滞剂可用于治疗妊娠期高血压,通常被认为是一线药物。[4]研究最充分的妊娠高血压药物是-受体阻滞剂和甲基多巴。β受体阻滞剂,特别是拉贝他洛尔,经过充分研究,已被证明在怀孕期间是安全的。拉贝他洛尔对血压也有增强作用,因为它伴有α -阻断。在一些研究中,阿替洛尔已被证明与胎儿生长受限有关:尽管数据有限,但许多从业者因此避免使用阿替洛尔。[3]甲基多巴,如前所述,是孕妇使用时间最长的药物之一;它作用于中枢α受体,降低对心脏、肾脏和周围脉管系统的交感神经张力。[7]甲基多巴在怀孕期间有广泛的安全记录;然而,它对血压的影响并不大,许多女性需要第二种药物来改善控制。因此,虽然它是安全的,但它不再经常被用作一线药物。摘要
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Hypertension in Pregnancy
Identification of hypertension in pregnancy is important not only for fetal outcomes but hypertensive disease in pregnancy also portends a higher risk for future cardiovascular events in women.[1] The prevalence of gestational hypertension (hypertension that manifests for the 1st time during pregnancy) is 6%;[2] additionally, up to 3% of childbearing women have chronic hypertension (the prevalence is increasing as obesity rates go up).[3] Hypertension increases the risk of complications during pregnancy, including preeclampsia, fetal growth restriction, and abruptio placentae.[3] In addition, it puts expectant mothers at risk for heart failure (both with reduced and preserved ejection fraction) and right ventricular dysfunction; later in life, women are also at substantially increased risk of coronary artery disease and heart failure.[4] In fact, the treatment of hypertension has been shown to reduce maternal morbidity, but it has not been shown to substantially impact fetal outcomes.[3] In a normal pregnancy, systemic blood pressure drops due to systemic vasodilation and decreased peripheral vascular resistance. As a result, many women with mild chronic hypertension can stop taking medication during pregnancy. Thus far, no evidence has been found that treatment of mild-tomoderate hypertension improves fetal or maternal outcomes; therefore, guidelines for treatment goals remain controversial.[4] According to the ACC/AHA guidelines, it is reasonable to treat Stage 1 hypertension to prevent future cardiovascular events. Two of the classic first-line agents for hypertensive control have relative contraindications in pregnancy. Angiotensinconverting enzyme inhibitors and angiotensin receptor blockers can cause skull hypoplasia in the fetus, as well as anuria and renal failure (particularly in the first trimester).[5] Thiazides can cause neonatal jaundice, volume depletion, or thrombocytopenia (although one study showed no significant difference in adverse pregnancy outcomes with diuretics).[3,6] Calcium channel blockers may be used to treat hypertension in pregnancy, however, and are often considered first-line agents.[4] The most well-studied agents for hypertension in pregnancy are beta-blockers and methyldopa. Beta-blockers, particularly labetalol, are well-studied and have been shown to be safe in pregnancy. Labetalol also has an enhanced effect on blood pressure because of its concomitant alpha-blockade. In some studies, atenolol has been shown to have an association with fetal growth restriction: Although data are limited, many practitioners avoid using atenolol as a result.[3] Methyldopa, as mentioned, is one of the drugs that have been used the longest in pregnant women; it acts on a central alpha receptor, decreasing sympathetic tone to the heart, kidneys, and peripheral vasculature.[7] Methyldopa has an extensive safety record in pregnancy; however, its effect on blood pressure is only modest, and many women require a second agent for improved control. Thus, although it is safe, it is no longer frequently used as a first-line agent. Abstract
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Open Hypertension Journal
Open Hypertension Journal Medicine-Cardiology and Cardiovascular Medicine
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