{"title":"妊娠期高血压","authors":"E. Armenia, Michael Vornovitsky","doi":"10.15713/ins.johtn.0179","DOIUrl":null,"url":null,"abstract":"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","PeriodicalId":38918,"journal":{"name":"Open Hypertension Journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Hypertension in Pregnancy\",\"authors\":\"E. Armenia, Michael Vornovitsky\",\"doi\":\"10.15713/ins.johtn.0179\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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\",\"PeriodicalId\":38918,\"journal\":{\"name\":\"Open Hypertension Journal\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Open Hypertension Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15713/ins.johtn.0179\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Hypertension Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15713/ins.johtn.0179","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
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