A comprehensive review of hypertension in pregnancy

Reem Mustafa, Sana Ahmed, Anu Gupta, Rocco C Venuto, Reem Mustafa, Sana Ahmed, Anu Gupta, Rocco C Venuto

Abstract

Hypertension is the most common medical disorder encountered during pregnancy. Hypertensive disorders are one of the major causes of pregnancy-related maternal deaths in the United States. We will present a comprehensive update of the literature pertinent to hypertension in pregnancy. The paper begins by defining and classifying hypertensive disorders in pregnancy. The normal vascular and renal physiological changes which occur during pregnancy are detailed. We will summarize the intriguing aspects of pathophysiology of preeclampsia, emphasizing on recent advances in this field. The existing diagnostic tools and the tests which have been proposed for screening preeclampsia are comprehensively described. We also highlight the short- and long-term implications of preeclampsia. Finally, we review the current management guidelines, goals of treatment and describe the potential risks and benefits associated with various antihypertensive drug classes. Preeclampsia still remains an enigma, and the present management focuses on monitoring and treatment of its manifestations. We are hopeful that this in depth critique will stimulate the blossoming research in the field and assist practitioners to identify women at risk and more effectively treat affected individuals.

Figures

Figure 1
Figure 1
Relative changes in renal hemodynamics during normal human pregnancy. Dramatic changes occur in systemic hemodynamics during physiologic pregnancy. In uncomplicated pregnancy, mean arterial pressure drops, reaching its nadir between the 16th and 20th weeks of gestation. After the 20th week, mean arterial blood pressure slowly returns to close to pre-pregnancy levels at about 40-week gestation. Changes in systemic blood pressure are paralleled by a change in cardiac output which increases dramatically. The apex is reached between the 16th and 20th weeks of gestation. Plasma volume increases substantially as well but lags behinds the increased cardiac output. MAP: mean arterial pressure. CO: cardiac output.
Figure 2
Figure 2
The amount of angiotensin required to raise blood pressure by 20 mm Hg. This figure demonstrates two important findings obtained from serial observations in primiparas. Women undergoing physiologic pregnancy (■) become resistant to the pressor effect of infused angiotensin II by 14 weeks of gestation. They require significantly higher dose of angiotensin II to increase blood pressure by 20 mm of Hg. In contrast, women destined to develop preeclampsia (♦) regain their sensitivity to angiotensin II between 22–26 weeks of gestation, well before any other clinical manifestations of preeclampsia are appreciated [7].
Figure 3
Figure 3
Changes in renal function during pregnancy. Kidney function also dramatically increases during pregnancy. The rapid developing rise in renal blood flow and glomerular filtration rate were documented in careful studies undertaken in humans. These increments average between 40 and 50%. Dr. Davison and his associates found that these improvements in renal hemodynamics occurred even prior to the changes in cardiac output and plasma volume. GFR: glomerular filtration rate. ERPF: effective renal plasma flow [8].

References

    1. Roccella EJ. Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy. American Journal of Obstetrics & Gynecology. 2000;183(1):S1–S22.
    1. Lindheimer MD. Introduction, history, controversies, and definitions. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 1–24.
    1. Luft FC, Gallery EDM, Lindheimer MD. Normal and abnormal volume hemostasis. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 271–288.
    1. Simmons LA, Gillin AG, Jeremy RW. Structural and functional changes in left ventricle during normotensive and preeclamptic pregnancy. American Journal of Physiology. 2002;283(4):H1627–H1633.
    1. Abdul-Karim R, Assali NS. Pressor response to angiotensin in pregnant and nonpregnant women. American Journal of Obstetrics & Gynecology. 1961;82:246–251.
    1. Gigee W, Raab W, Schroeder G, Wagner R. Vascular reactivity and electrolytes in normal and toxemic pregnancy; pathogenic considerations and a diagnostic pre-toxemia test. The Journal of Clinical Endocrinology and Metabolism. 1956;16(9):1196–1216.
    1. Gant NF, Daley GL, Chand S, Whalley PJ, MacDonald PC. A study of angiotensin II pressor response throughout primigravid pregnancy. The Journal of Clinical Investigation. 1973;52:2682–2652.
    1. Davison JM. Overview: kidney function in pregnant women. American Journal of Kidney Diseases. 1987;9(4):248–252.
    1. Conrad KP, Gaber LW, Lindheimer MD. The kidney in normal pregnancy and preeclampsia. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 301–340.
    1. Chesley LC. Hypothesis. Hypertensive Disorders in Pregnancy. New York, NY, USA: Appleton-Century Crofts; 1978.
    1. Agarwal I, Karumanchi SA. Preeclampsia and the anti-angiogenic state. Pregnancy Hypertension. 2011;1(1):17–21.
    1. Venuto RC, Lindheimer MD. Animal models. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 171–190.
    1. Taylor RN, Davidge ST, Roberts JM. Endothelial cell dysfunction and oxidative stress. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 145–170.
    1. Maynard SE, Min JY, Merchan J, et al. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction hypertension, and proteinuria in preeclampsia. The Journal of Clinical Investigation. 2003;111(5):649–658.
    1. Kendall RL, Thomas KA. Inhibition of vascular endothelial cell growth factor activity by an endogenously encoded soluble receptor. Proceedings of the National Academy of Sciences of the United States of America. 1993;90(22):10705–10709.
    1. Karumanchi SA, Stillman IE, Lindheimer MD. Angiogenesis and preeclampsia. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 87–104.
    1. Levine RJ, Maynard SE, Qian C, et al. Circulating angiogenic factors and the risk of preeclampsia. The New England Journal of Medicine. 2004;350(7):672–683.
    1. Robinson CJ, Johnson DD, Chang EY, Armstrong DM, Wang W. Evaluation of placenta growth factor and soluble Fms-like tyrosine kinase 1 receptor levels in mild and severe preeclampsia. American Journal of Obstetrics & Gynecology. 2006;195(1):255–259.
    1. Makris A, Thornton C, Thompson J, et al. Uteroplacental ischemia results in proteinuric hypertension and elevated sFLT-1. Kidney International. 2007;71(10):977–984.
    1. Heydarian M, McCaffrey T, Florea L, et al. Novel splice variants of sFlt1 are upregulated in preeclampsia. Placenta. 2009;30(3):250–255.
    1. Garovic V. The role of angiogenic factors in the prediction and diagnosis of preeclampsia superimposed on chronic hypertension. Hypertension. 2012;59:555–557.
    1. Maynard SE, Karunamachi SA. Angiogenic factors and preeclampsia. Seminars in Nephrology. 2011;31:33–46.
    1. Gilbert JS, Gilbert SA, Arany M, Granger JP. Hypertension produced by placental ischemia in pregnant rats is associated with increased soluble endoglin expression. Hypertension. 2009;53(2):399–403.
    1. Gu Y, Lewis DF, Wang Y. Placental productions and expressions of soluble endoglin, soluble fms-like tyrosine kinase receptor-1, and placental growth factor in normal and preeclamptic pregnancies. The Journal of Clinical Endocrinology and Metabolism. 2008;93(1):260–266.
    1. Sherwood OD. Relaxin. In: Knobil E, Neill JD, Grrenwald GS, Markert CL, Pfaff DW, editors. The Physiology of Reproduction. New York, NY, USA: Raven Press; 1994. pp. 861–1008.
    1. Hisaw FL. Experimental relaxation of the public ligament of the guinea pig. Proceedings of the Society for Experimental Biology and Medicine. 1926;23:661–663.
    1. Ziel HK, Sawin CT. Frederick L. Hisaw (1891–1972) and the discovery of relaxin. Endocrinologist. 2000;10(4):215–218.
    1. St-Louis J, Massicotte G. Chronic decrease of blood pressure by rat relaxin in spontaneously hypertensive rats. Life Sciences. 1985;37(14):1351–1357.
    1. Conrad KP, Debrah DO, Novak J, Danielson LA, Shroff SG. Relaxin modifies systemic arterial resistance and compliance in conscious, nonpregnant rats. Endocrinology. 2004;145(7):3289–3296.
    1. Debrah DO, Novak J, Matthews JE, Ramirez RJ, Shroff SG, Conrad KP. Relaxin is essential for systemic vasodilation and increased global arterial compliance during early pregnancy in conscious rats. Endocrinology. 2006;147(11):5126–5131.
    1. Debrah JE, Agoulnik A, Conrad KP. Changes in arterial function by chronic relaxin infusion are mediated by the leucine rich repeat G coupled lgr7 receptor. Reproductive Sciences. 2008;57:1151–1160.
    1. Conrad KP. Emerging role of relaxin in the maternal adaptations to normal pregnancy: implications for preeclampsia. Seminars in Nephrology. 2011;31(1):15–32.
    1. Jeyabalan A, Stewart DR, McGonigal SC, Powers RW, Conrad KP. Low relaxin concentrations in the first trimester are associated with increased risk of developing preeclampsia. Reproductive Sciences. 2009;16, article 101A
    1. Wallukut G, Homuth V, Fisher T, et al. Patients with preeclampsia develop agonistic autoantibodies against the angiotensin AT1 receptor. The Journal of Clinical Investigation. 1999;103:945–952.
    1. Siddiqui AH, Irani RA, Blackwell SC, Ramin SM, Kellems RE, Xia Y. Angiotensin receptor agonistic autoantibody is highly prevalent in preeclampsia: correlation with disease severity. Hypertension. 2010;55(2):386–393.
    1. Roberts JM. Endothelial dysfunction in preeclampsia. Seminars in Reproductive Endocrinology. 1998;16:5–15.
    1. Roberts JM, Taylor RN, Musci TJ, Rodgers GM, Hubel CA, McLaughin MK. Preeclampsia: an endothelial cell disorder. American Journal of Obstetrics & Gynecology. 1989;161:1200–1204.
    1. Granger JP, LaMarca BB, Cockrell K, et al. Reduced uterine perfusion pressure (RUPP) model for studying cardiovascular-renal dysfunction in response to placental ischemia. Methods in Molecular Medicine. 2006;122:383–392.
    1. Redman CWG, Sargent IL, Roberts JM. Immunology of normal pregnancy and preeclampsia. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 129–144.
    1. Carr DB, Epplein M, Johnson CO, Easterling TR, Critchlow CW. A sister’s risk: family history as a predictor of preeclampsia. American Journal of Obstetrics & Gynecology. 2005;193(3, supplement):965–972.
    1. Carr DB, Newton KM, Utzschneider KM, et al. Preeclampsia and risk of developing subsequent diabetes preeclampsia and risk of subsequent diabetes. Hypertension in Pregnancy. 2009;28(4):435–447.
    1. Srinivas SK, Morrison AC, Andrela CM, Elovitz MA. Allelic variations in angiogenic pathway genes are associated with preeclampsia. American Journal of Obstetrics & Gynecology. 2010;202(5):445.e1–445.e11.
    1. Mütze S, Rudnik-Schöneborn S, Zerres K, Rath W. Genes and the preeclampsia syndrome. Journal of Perinatal Medicine. 2008;36(1):38–58.
    1. Tuohy JF, James DK. Pre-eclampsia and trisomy 13. British Journal of Obstetrics and Gynaecology. 1992;99(11):891–894.
    1. Lie RT, Rasmussen S, Brunborg H, Gjessing HK, Lie-Nielsen E, Irgens LM. Fetal and maternal contributions to risk of pre-eclampsia: population based study. BMJ. 1998;316(7141):1343–1347.
    1. Esplin MS, Fausett MB, Fraser A, et al. Paternal and maternal components of the predisposition to preeclampsia. The New England Journal of Medicine. 2001;344(12):867–872.
    1. Cnossen JS, Vollebregt KC, De Vrieze N, et al. Accuracy of mean arterial pressure and blood pressure measurements in predicting pre-eclampsia: systematic review and meta-analysis. BMJ. 2008;336(7653):1117–1120.
    1. Robert M, Sepandj F, Liston RM, Dooley KC. Random protein-creatinine ratio for the quantitation of proteinuria in pregnancy. Obstetrics & Gynecology. 1997;90(6):893–895.
    1. Sethuram R, Kiran TSU, Weerakkody ANA. Is the urine spot protein/creatinine ratio a valid diagnostic test for pre-eclampsia? Journal of Obstetrics and Gynaecology. 2011;31(2):128–130.
    1. Price CP, Newall RG, Boyd JC. Use of protein: creatinine ratio measurements on random urine samples for prediction of significant proteinuria: a systematic review. Clinical Chemistry. 2005;51(9):1577–1586.
    1. Rodriguez-Thompson D, Leiberman ES. Use of random urinary protein to creatinine ratio for the diagnosis of significant proteinuria during pregnancy. American Journal of Obstetrics & Gynecology. 1995;185:808–811.
    1. Moran P, Lindheimer MD, Davison JM. The renal response to preeclampsia. Seminars in Nephrology. 2004;24(6):588–595.
    1. Cnossen JS, de Ruyter-Hanhijarvi H, van der Post JA, Mol BW, Khan KS, ter Riet G. Accuracy of serum uric acid determination in predicting pre-eclampsia: a systematic review. Acta Obstetricia et Gynecologica Scandinavica. 2006;85:519–525.
    1. Thangaratinam S, Ismail KMK, Sharp S, Coomarasamy A, Khan KS. Accuracy of serum uric acid in predicting complications of pre-eclampsia: a systematic review. International Journal of Obstetrics & Gynaecology. 2006;113(4):369–378.
    1. Koopmans CM, van Pampus MG, Groen H, Aarnoudse JG, van den berg PP, Mol BW. Accuracy of serum uric acid as a predictive test for maternal complications in preeclampsia: bivariate meta-analysis and decision analysis. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2009;146(1):8–14.
    1. Laughon SK, Catov J, Powers RW, Roberts JM, Gandley RE. First trimester uric acid and adverse pregnancy outcomes. American Journal of Hypertension. 2011;24(4):489–495.
    1. Taufield PA, Ales KL, Resnick LM, et al. Hypocalciuria in preeclampsia. The New England Journal of Medicine. 1987;317(14):897–899.
    1. Dekker GA, Makovitz JW, Wallenburg HCS. Prediction of pregnancy-induced hypertensive disorders by angiotensin II sensitivity and supine pressor test. British Journal of Obstetrics and Gynaecology. 1990;97(9):817–821.
    1. Gant NF, Chand S, Worley RJ, Whalley PJ, Crosby UD, MacDonald PC. A clinical test useful for predicting the development of acute hypertension in pregnancy. American Journal of Obstetrics & Gynecology. 1974;120:1–7.
    1. Conde-Agudelo A, Romero R, Lindheimer MD. Tests to predict preeclampsia. In: Lindheimer MD, Cunningham FG, Roberts JM, editors. Chesley's Hypertensive Disorders in Pregnancy. 3rd edition. Amsterdam, The Netherlands: Elsevier; 2009. pp. 191–214.
    1. Chien PFW, Arnott N, Gordon A, Owen P, Khan KS. How useful is uterine artery Doppler flow velocimetry in the prediction of pre-eclampsia, intrauterine growth retardation and perinatal death? An overview. British Journal of Obstetrics and Gynaecology. 2000;107(2):196–208.
    1. Grill S, Rusterholz C, Zanetti-Dällenbach R, et al. Potential markers of preeclampsia—a review. Reproductive Biology and Endocrinology. 2009;7, article 70
    1. Barton JR, Sibai BM. Prediction and prevention of recurrent preeclampsia. Obstetrics & Gynecology. 2008;112(2):359–372.
    1. Stepan H, Unversucht A, Wessel N, Faber R. Predictive value of maternal angiogenic factors in second trimester pregnancies with abnormal uterine perfusion. Hypertension. 2007;49(4):818–824.
    1. Stepan H, Geipel A, Schwarz F, Kramer T, Wessel N, Faber R. Circulatory soluble endoglin and its predictive value in second trimester pregnancies with abnormal uterine perfusion. American Journal of Obstetrics & Gynecology. 2008;21:279–287.
    1. Levine RJ, Maynard SE, Qian C, et al. Circulating angiogenic factors and the risk of preeclampsia. The New England Journal of Medicine. 2004;350(7):672–683.
    1. McKeeman GC, Ardill JES, Caldwell CM, Hunter AJ, McClure N. Soluble vascular endothelial growth factor receptor-1 (sFlt-1) is increased throughout gestation in patients who have preeclampsia develop. American Journal of Obstetrics & Gynecology. 2004;191(4):1240–1246.
    1. Chaiworapongsa T, Romero R, Kim YM, et al. Plasma soluble vascular endothelial growth factor receptor-1 concentration is elevated prior to the clinical diagnosis of pre-eclampsia. Journal of Maternal-Fetal and Neonatal Medicine. 2005;17(1):3–18.
    1. Sunderji S, Gaziano E, Wothe D, et al. Automated assays for sVEGF R1 and PIGF as an aid in the diagnosis of preterm preeclampsia: a prospecttive clinical study. American Journal of Obstetrics & Gynecology. 2010;202(1):40–47.
    1. De Vivo A, Baviera G, Giordano D, et al. Endoglin, PIGF and sFlt-1 as markers for predicting preeclampsia. Acta Obstetricia et Gynecologica Scandinavica. 2008;87(8):837–842.
    1. Stepan H, Unversucht A, Wessel N, Faber R. Predictive value of maternal angiogenic factors in second trimester pregnancies with abnormal uterine perfusion. Hypertension. 2007;49(4):818–824.
    1. Widmer M, Villar J, Benigni A, Conde-Agudelo A, Karumanchi SA, Lindheimer M. Mapping the theories of preeclampsia and the role of angiogenic factors: a systematic review. Obstetrics & Gynecology. 2007;109(1):168–180.
    1. Hadker N, Garg S, Costanzo C, et al. Financial impact of a novel pre-eclampsia diagnostic test versus standard practice:a decision- analytic modeling analysis from a UK health care payer prospective. Journal of Medical Economics. 2010;13(4):728–737.
    1. Levine RJ, Lam C, Qian C, et al. Soluble endoglin and other circulating antiangiogenic factors in preeclampsia. The New England Journal of Medicine. 2006;355(10):992–1005.
    1. Robinson CJ, Johnson DD. Soluble endoglin as a second-trimester marker for preeclampsia. American Journal of Obstetrics & Gynecology. 2007;197(2):174.e1–174.e5.
    1. Maynard SE, Moore Simas TA, Bur L, Crawford SL, Solitro MJ, Meyer BA. Soluble endoglin for the prediction of preeclampsia in a high risk cohort. Hypertension in Pregnancy. 2010;29(3):330–341.
    1. Ryu HM, Lim JH, Kim SY, Park SY, Yang JH, Kim MY. Effective prediction of preeclampsia by a combined ratio of angiogenesis-related factors. Obstetrics & Gynecology. 2008;111(6):1403–1409.
    1. Thadhani R, Kisner T, Hagmann H, et al. Pilot study of extracorporeal removal of soluble fms-like tyrosine kinase 1 in preeclampsia. Circulation. 2011;124:940–950.
    1. Livingston JC, Livingston LW, Ramsey R, Mabie BC, Sibai BM. Magnesium sulfate in women with mild preeclampsia: a randomized controlled trial. Obstetrics & Gynecology. 2003;101(2):217–220.
    1. Mackay AP, Berg CJ, Atrash HK. Pregnancy-related mortality from preeclampsia and eclampsia. Obstetrics & Gynecology. 2001;97(4):533–538.
    1. Heard AR, Dekker GA, Chan A, Jacobs DJ, Vreeburg SA, Priest KR. Hypertension during pregnancy in South Australia, Part 1: pregnancy outcomes. Australian and New Zealand Journal of Obstetrics and Gynaecology. 2004;44(5):404–409.
    1. Hauth JC, Ewell MG, Levine RJ, et al. Pregnancy outcomes in healthy nulliparas who developed hypertension. Calcium for Preeclampsia Prevention Study Group. Obstetrics & Gynecology. 2000;95:24–28.
    1. Sibai BM, Mercer B, Sarinoglu C. Severe preeclampsia in the second trimester: recurrence risk and long-term prognosis. American Journal of Obstetrics & Gynecology. 1991;165(5):1408–1412.
    1. Sibai BM, El-Nazer A, Gonzalez-Ruiz A. Severe preeclampsia-eclampsia in young primigravid women: subsequent pregnancy outcome and remote prognosis. American Journal of Obstetrics & Gynecology. 1986;155(5):1011–1016.
    1. Sibai BM, Sarinoglu C, Mercer BM. Eclampsia. VII. Pregnancy outcome after eclampsia and long-term prognosis. American Journal of Obstetrics & Gynecology. 1992;166:1757–1763.
    1. Mostello D, Kallogjeri D, Tungsiripat R, Leet T. Recurrence of preeclampsia: effects of gestational age at delivery of the first pregnancy, body mass index, paternity, and interval between births. American Journal of Obstetrics & Gynecology. 2008;199(1):55.e1–55.e7.
    1. Campbell DM, MacGillivray I, Carr-Hill R. Pre-eclampsia in second pregnancy. British Journal of Obstetrics and Gynaecology. 1985;92(2):131–140.
    1. Trogstad L, Skrondal A, Stoltenberg C, Magnus P, Nesheim BI, Eskild A. Recurrence risk of preeclampsia in twin and singleton pregnancies. American Journal of Medical Genetics. 2004;126(1):41–45.
    1. Bellamy L, Casas JP, Hingorani AD, Williams DJ. Pre-eclampsia and risk of cardiovascular disease and cancer in later life: systematic review and meta-analysis. BMJ. 2007;335(7627):974–977.
    1. Lampinen KH, Rönnback M, Kaaja RJ, Groop PH. Impaired vascular dilatation in women with a history of pre-eclampsia. Journal of Hypertension. 2006;24(4):751–756.
    1. Chambers JC, Fusi L, Malik IS, Haskard DO, De Swiet M, Kooner JS. Association of maternal endothelial dysfunction with preeclampsia. JAMA. 2001;285(12):1607–1612.
    1. Agatisa PK, Ness RB, Roberts JM, Costantino JP, Kuller LH, McLaughlin MK. Impairment of endothelial function in women with a history of preeclampsia: an indicator of cardiovascular risk. American Journal of Physiology. 2004;286(4):H1389–H1393.
    1. Kaaja RJ, Pöyhönen-Alho MK. Insulin resistance and sympathetic overactivity in women. Journal of Hypertension. 2006;24(1):131–141.
    1. Kaaja RJ, Greer IA. Manifestations of chronic disease during pregnancy. JAMA. 2005;294(21):2751–2757.
    1. Vikse BE, Irgens LM, Leivestad T, Skjærven R, Iversen BM. Preeclampsia and the risk of end-stage renal disease. The New England Journal of Medicine. 2008;359(8):800–809.
    1. Aagaard-Tillery KM, Stoddard GJ, Holmgren C, et al. Preeclampsia and subsequent risk of cancer in Utah. American Journal of Obstetrics & Gynecology. 2006;195(3):691–699.
    1. Vatten LJ, Romundstad PR, Trichopoulos D, Skjærven R. Pre-eclampsia in pregnancy and subsequent risk for breast cancer. British Journal of Cancer. 2002;87(9):971–973.
    1. Mogren I, Stenlund H, Högberg U. Long-term impact of reproductive factors on the risk of cervical, endometrial, ovarian and breast cancer. Acta Oncologica. 2001;40(7):849–854.
    1. Cohn BA, Cirillo PM, Christianson RE, Van Den Berg BJ, Siiteri PK. Placental characteristics and reduced risk of maternal breast cancer. Journal of the National Cancer Institute. 2001;93(15):1133–1140.
    1. Seely EW, Ecker J. Chronic hypertension in pregnancy. The New England Journal of Medicine. 2011;365(5):439–446.
    1. Abalos E, Duley L, Steyn DW, Henderson-Smart DJ. Antihypertensive drug therapy for mild to moderate hypertension during pregnancy. Cochrane Database of Systematic Reviews. 2007;(1) Article ID CD002252.
    1. Sibai BM. Chronic hypertension in pregnancy. Obstetrics & Gynecology. 2002;100:369–377.
    1. Davis GK, Mackenzie C, Brown MA, et al. Predicting transformation from gestational hypertension to preeclampsia in clinical practice: a possible role for 24 hour ambulatory blood pressure monitoring. Hypertension in Pregnancy. 2007;26(1):77–87.
    1. Barton JR, O'Brien JM, Bergauer NK, Jacques DL, Sibai BM. Mild gestational hypertension remote from term: progression and outcome. American Journal of Obstetrics & Gynecology. 2001;184:979–983.
    1. Helewa ME, Burrows RF, Smith J, Williams K, Brain P, Rabkin SW. Report of the Canadian Hypertension Society Consensus Conference: 1. Definitions, evaluation and classification of hypertensive disorders in pregnancy. CMAJ. 1997;157(6):715–725.
    1. Magee LA. Diagnosis, evaluation and management of the hypertensive disorders of pregnancy. American Journal of Obstetrics & Gynecology. 2008;30(supplement):S1–S48.
    1. Rey E, LeLorier J, Burgess E, Lange IR, Leduc L. Report of the Canadian Hypertension Society Consensus Conference: 3. Pharmacologic treatment of hypertensive disorders in pregnancy. CMAJ. 1997;157(9):1245–1254.
    1. Podymow T, August P. Update on the use of antihypertensive drugs in pregnancy. Hypertension. 2008;51(4):960–969.
    1. Redman CW, Beilin LJ, Bonnar J. Treatment of hypertension in pregnancy with methyldopa: blood pressure control and side effects. British Journal of Obstetrics and Gynaecology. 1977;84:419–426.
    1. Montan S, Anandakumar C, Arulkumaran S, Ingemarsson I, Ratnam SS. Effects of methyldopa on uteroplacental and fetal hemodynamics in pregnancy-induced hypertension. American Journal of Obstetrics & Gynecology. 1993;168:152–156.
    1. Horvath JS, Phippard A, Korda A, Henderson-Smart DJ, Child A, Tiller DJ. Clonidine hydrochloride—a safe and effective antihypertensive agent in pregnancy. Obstetrics & Gynecology. 1985;66:634–638.
    1. Huisjes HJ, Hadders-Algra M, Touwen BCL. Is clonidine a behavioural teratogen in the human? Early Human Development. 1986;14(1):43–48.
    1. Butters L, Kennedy S, Rubin PC. Atenolol in essential hypertension during pregnancy. BMJ. 1990;301(6752):587–589.
    1. Lip GYH, Beevers M, Churchill D, Shaffer LM, Beevers DG. Effect of atenolol on birth weight. American Journal of Cardiology. 1997;79(10):1436–1438.
    1. Reynolds B, Butters L, Evans J, Adams T, Rubin PC. First year of life after the use of atenolol in pregnancy associated hypertension. Archives of Disease in Childhood. 1984;59:1061–1063.
    1. Pickles CJ, Symonds EM, Broughton Pipkin F. The fetal outcome in a randomized double-blind controlled trial of labetalol versus placebo in pregnancy-induced hypertension. British Journal of Obstetrics and Gynaecology. 1989;96:38–43.
    1. Sibai BM, Gonzalez AR, Mabie WC, Moretti M. A comparison of labetalol plus hospitalization versus hospitalization alone in the management of preeclampsia remote from term. Obstetrics & Gynecology. 1987;70:323–327.
    1. Venuto R, Burstein P, Schneider R. Pheochromocytoma: antepartum diagnosis and management with tumor resection in the puerperium. American Journal of Obstetrics & Gynecology. 1984;150:431–432.
    1. Grodski S, Jung C, Kertes P, Davies M, Banting S. Phaeochromocytoma in pregnancy. Internal Medicine Journal. 2006;36(9):604–606.
    1. Magee LA, Schick B, Donnenfeld AE, et al. The safety of calcium channel blockers in human pregnancy: a prospective, multicenter cohort study. American Journal of Obstetrics & Gynecology. 1996;174:823–828.
    1. Lindow SW, Davies N, Davey DA, Smith JA. The effect of sublingual nifedipine on uteroplacental blood flow in hypertensive pregnancy. British Journal of Obstetrics and Gynaecology. 1988;95:1276–1281.
    1. Rizzo G, Arduini D, Mancuso S, Romanini C. Effects of nifedipine on umbilical artery velocity waveforms in healthy human fetuses. Gynecologic and Obstetric Investigation. 1987;24:151–154.
    1. Impey L. Severe hypotension and fetal distress following sublingual administration of nifedipine to a patient with severe pregnancy induced hypertension at 33 weeks. British Journal of Obstetrics and Gynaecology. 1993;100:959–961.
    1. Puzey MS, Ackovic KL, Lindow SW, Gonin R. The effect of nifedipine on fetal umbilical artery Doppler waveforms in pregnancies complicated by hypertension. South African Medical Journal. 1991;79(4):192–194.
    1. Brown MA, Buddle ML, Farrell T, Davis GK. Efficacy and safety of nifedipine tablets for the acute treatment of severe hypertension in pregnancy. American Journal of Obstetrics & Gynecology. 2002;187:1046–1050.
    1. Collins R, Yusuf S, Peto R. Overview of randomised trials of diuretics in pregnancy. British Medical Journal. 1985;290(6461):17–23.
    1. Magee LA. Drugs in pregnancy. Antihypertensives. Best Practice & Research Clinical Obstetrics & Gynaecology. 2001;15:827–845.
    1. Groves TD, Corenblum B. Spironolactone therapy during human pregnancy. American Journal of Obstetrics & Gynecology. 1995;172:1655–1656.
    1. Widerlov E, Karlman I, Storsater J. Hydralazine-induced neonatal thrombocytopenia. The New England Journal of Medicine. 1980;303(21, article 1235)
    1. Magee LA, Cham C, Waterman EJ, Ohlsson A, Von Dadelszen P. Hydralazine for treatment of severe hypertension in pregnancy: meta-analysis. BMJ. 2003;327(7421):955–960.
    1. Nevo O, Thaler I, Shik V, Vortman T, Soustiel JF. The effect of isosorbide dinitrate , a donor of nitric acid, on maternal cerebral blood flow in gestational hypertension and preeclampsia. American Journal of Obstetrics & Gynecology. 2003;188:1360–1365.
    1. Wasserstrum N. Nitroprusside in preeclampsia: circulatory distress and paradoxical bradycardia. Hypertension. 1991;18(1):79–84.
    1. Bolte AC, van Geijn HP, Dekker GA. Pharmacological treatment of severe hypertension in pregnancy and the role of serotonin(2)-receptor blockers. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2001;95:22–36.
    1. Steyn DW, Odendaal HJ. Serotonin antagonism and serotonin antagonists in pregnancy: role of ketanserin. Obstetrical & Gynecological Survey. 2000;55:582–589.
    1. Pryde PG, Sedman AB, Nugent CE, Barr M. Angiotensin-converting enzyme inhibitor fetopathy. Journal of the American Society of Nephrology. 1993;3(9):1575–1582.
    1. Buttar HS. An overview of the influence of ACE inhibitors on fetal-placental circulation and perinatal development. Molecular and Cellular Biochemistry. 1997;176(1-2):61–71.
    1. Cooper WO, Hernandez-Diaz S, Arbogast PG, et al. Major congenital malformations after first-trimester exposure to ACE inhibitors. The New England Journal of Medicine. 2006;354(23):2443–2451.
    1. Tan LK, De Swiet M. The management of postpartum hypertension. International Journal of Obstetrics & Gynaecology. 2002;109(7):733–736.
    1. Makris A, Thornton C, Hennessy A. Postpartum hypertension and nonsteroidal analgesia. American Journal of Obstetrics & Gynecology. 2004;190:577–578.
    1. Atkinson H, Begg EJ. Concentrations of beta-blocking drugs in human milk. Journal of Pediatrics. 1990;116(1, article 156)
    1. White WB. Management of hypertension during lactation. Hypertension. 1984;6(3):297–300.
    1. Ehrenkranz RA, Ackerman BA, Hulse JD. Nifedipine transfer into human milk. Journal of Pediatrics. 1989;114(3):478–480.
    1. Ward RM, Bates BA, Benitz WE, et al. The transfer of drugs and other chemicals into human milk. Pediatrics. 2001;108(3):776–789.

Source: PubMed

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