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Physiological Changes in Cardiovascular System during Normal Pregnancy: A Review
This article was originally published by Thieme Medical and Scientific Publishers Private Ltd. and was migrated to Scientific Scholar after the change of Publisher; therefore Scientific Scholar has no control over the quality or content of this article.
Abstract
Abstract
Pregnancy is a complex biological process associated with changes in physiologic functions of the body. Dramatic changes take place in the cardiovascular physiology leading to gradual adaptation of these changes by the body of the pregnant woman. Cardiac output increases during pregnancy to 30 to 50% above the prepregnant levels. The increase in cardiac output occurs due to increase in stroke volume initially during gestation and later by increase in heart rate. These changes in cardiac output are attributed to either neurohumoral factors such as estrogen and progesterone or placental factors. Maternal body position affects cardiac output with highest in kneel-chest and left lateral positions. Along with these changes, variations in heart rate, blood pressure, and blood volume are observed following a specific pattern of change during pregnancy. Hence, it is necessary to understand the cardiovascular changes during pregnancy to interpret, predict, and diagnose any cardiac disease efficiently.
Keywords
cardiac output
cardiovascular adaptations
neuro humoral factors
pregnancy
Introduction
The term pregnancy is derived from the Latin words pre- meaning before and -gnatus meaning birth. It is the period from the time of fertilization to birth. It is a complex biological process that utilizes several resources of the mother as a result leading to widespread effects on the body of the pregnant woman. Pregnancy is a special physiologic condition that enables study of various bodily adaptations in normal individuals. Immediately after conception, growth of the fetus occurs tremendously by each week with changes in several systems to cause adaptation of the maternal body to the growing fetus.1 Changes occur in anatomical and physiologic parameters to protect the mother and support the growing fetus only to return to the prepregnant levels after the birth of the baby. One of the systems that changes remarkably during pregnancy is the cardiovascular system. These changes are necessary for a successful pregnancy outcome. To meet the increased metabolic needs of the tissues of the mother and the increasing demands of the growing fetus, blood flow to various organs increases. Metabolic shifts serve largely to support fetal demands and maximize maternal efficiency.2 3 4 5 Increasing blood flow is kept intact by the uninterrupted cardiac contractions to provide the required nutrients and oxygen. Hence, the metabolic needs of the heart rise and depend on continuous energy supply.6 Observations by Lindhard in 1915 that cardiac output (CO) increases during pregnancy formed the basis for subsequent work in circulatory physiology in pregnant woman. Structural changes occur in the heart with lateral and upward shift of cardiac apex to fourth intercostal space. Increased volume and shift of the heart provide more dullness over precordial region. Such alterations often lead to presence of systolic flow-type murmur commonly seen in pregnancy. Risk assessment for estimation of maternal and offspring risk is necessary and may be done through prepregnancy counseling and stratified as per the principles of modified World Health Organization (WHO) classification of maternal cardiovascular risk.7
Cardiovascular Physiology of the Heart
Cardiac Output during Pregnancy
Dramatic changes occur in CO early during pregnancy, starting in the first trimester and reaching peak by fifth month of gestation and continuing till delivery.8 Literature suggests an increase of 30 to 35% in CO over and above the nonpregnant levels. An increase in CO was demonstrated as early as 1949, but the cause for the increase was not clearly established whether it was due to increase in contractility of the heart or due to increased stroke volume (SV) caused by increased end diastolic volume.9 It is also not clear as per literature the precise time of peaking of CO during gestation. However, studies have shown that CO shows a peak anytime between 25 and 30 weeks.10 Several studies have shown that it is necessary to maintain a stable CO from the second trimester of pregnancy, which is achieved by increase in heart rate (HR) and decrease in SV10 11 12 13 14 15 16 (Fig. 1). A steady CO is seen from 24 weeks of gestation with a small decrease closer to term.15 Increased CO during the last trimester has not been projected sufficiently as a variety of studies are available showing a decrease, no change, or an increase, and have been mostly attributed to subjective adaptations of the mother during pregnancy along with interference by anthropometric variables of the mother and positioning of the body.13, 16 17 18 19 20 21 22 23 24 25 26 Studies have also shown that this increased CO is likely to be enhanced in subsequent pregnancies.27 The changes in CO are attributed to either neurohumoral factors such as estrogen and progesterone or placental factors.28 Placenta behaving as a functional arteriovenous (AV) fistula leads to an increase in maternal HR too. As early as eighth week of gestation, the CO rises by 20%, the possible mechanism associated being peripheral vasodilatation. Factors mediating this vasodilatation are synthesis of nitric oxide by endothelium and prostaglandins, leading to a fall in systemic vascular resistance and further increase in CO to almost 40%.16 An increase in SV and an increase in HR are the main contributors for this mechanism. Relaxin produced by corpus luteum is found to have an effect in reducing the total peripheral resistance, thereby increasing CO and systemic arterial compliance.28 29 30 Though the proportion of CO to various organs remains similar to the prepregnant levels in the first trimester, due to the absolute increase in CO with advancing pregnancy, blood flow to all organs such as the uterus, breasts, kidneys, skin, brain, and heart increases by 50%. There is a combination of increased preload, increased contractility and reduced afterload due to fall in systemic vascular resistance, all contributing to increased CO to nearly 50%, thereby increasing the efficiency of the heart.19 There is an increase in coronary blood flow as coronary arteries become sensitive to stress-induced vasodilation. Venous return increases dramatically during pregnancy. Mean circulatory pressure that is an important determinant of venous return increases during pregnancy and resistance to venous return decreases.

Fig. 1 Comparison of cardiac output and stroke volume in different trimesters of pregnancy.
Maternal Body Position and Cardiac Output
Studies on normal pregnant women have shown the CO to be highest in knee-chest and left lateral positions and less in standing and supine positions. The fall in supine position is attributed to the compression of the enlarged uterus on the inferior vena cava reducing the venous return, sometimes completely occluding it toward term and is more common after 24 weeks of gestation and earlier in twin pregnancies. However, a small percentage of women only experience the symptoms associated with supine hypotension during pregnancy. Understanding the benefits of posture-related effects of blood pressure on the body would help if a pregnant woman suffers from cardiac arrest requiring successful resuscitation.20 21 31
Heart Rate Variations during Pregnancy
Heart rate is found to increase progressively till the end of pregnancy reaching its peak in the third trimester (Figs. 2, 3). About 25% change in heart from the baseline values has been noted.25 27 32 There is an increase in sympathetic activity during pregnancy that explains the increase in HR.32 A possible explanation for sympathetic overactivity is that it occurs as a compensatory mechanism to peripheral vasodilatation, increased secretion of estradiol-stimulating nitric oxide synthesis leading to β-adrenergic–mediated vasodilatation.33 The heart adjusts to higher fluid load by increasing the HR rather than increasing the end-diastolic volume, thereby increasing the CO. Echocardiography could not document any increase in end diastolic volume with increasing gestational age.34 However, there is an increase in left ventricular wall thickness and left ventricular mass during pregnancy, causing a concentric left ventricular remodeling due to additional circulatory needs during pregnancy.35 Commonly, a physiologic third heart sound and a cervical venous hum may be heard during pregnancy and need to be interpreted with caution being signs of systolic heart failure and patent ductus arteriosus, respectively.

Fig. 2 Heart rate changes with gestational age.

Fig. 3 Changes in mean heart rate with gestational age.
Changes in Blood Pressure during Pregnancy
With fall in vascular resistance caused by progesterone-mediated smooth muscle relaxation, blood pressure also falls up to midterm and then gradually rises.36 37 The combination of increased CO with fall in blood pressure is associated with reduced systemic vascular resistance.38 39 Overall vascular resistance is lower than prepregnant levels. Because nitric oxide is the main mediator for smooth muscle relaxation and fall in resistance, parallelly, there appears to be reduced response of vessels to vasoconstrictor agents as well.40 Overall, there is a fall in blood pressure by 5 to 10 mm Hg, with most of the fall occurring in the early part of pregnancy.39 41 42 Hence, the hemodynamic changes occurring during pregnancy should be compared with prepregnant values rather than early pregnancy period as many changes would have already taken place. The fall in blood pressure is seen in both systolic and diastolic blood pressures with the fall more prominent in diastolic blood pressure (Figs. 4, 5). Some recent studies have shown that there is a progressive increase in blood pressure with gestation and that the increase is related to their body mass index.43 Obese and overweight women are seen to have higher blood pressure when compared with normal-weight women during early pregnancy, and this difference sustains throughout pregnancy.44 Variations in systolic and diastolic blood pressures and mean arterial pressure are observed in women across continents probably due to a subjective variation in other factors such as nutrition and anthropometric data.31 45 46 47

Fig. 4 Mean systolic (SBP) and diastolic blood pressures (DBP) during pregnancy.

Fig. 5 Changes in mean arterial pressures with gestation.
Changes in Blood Volume during Pregnancy
One of the hallmarks of pregnancy is a significant expansion of the blood volume, particularly in the first trimester and progressively later on.48 49 50 On an average, the plasma volume increases by 40% along with an increase in erythropoiesis. Placental lactogen plays an important role in enhancing erythropoiesis by stimulating the production of erythropoietin. A condition of hemodilution occurs leading to physiologic anemia due to slight increase in plasma volume above the red cell mass. Though blood volume and SV increase, pulmonary capillary wedge pressure does not increase. Along with a fall in systemic vascular resistance, there is also a decline in the pulmonary vascular resistance.51 The combined effect of reduced colloid osmotic pressure with no significant increase in pulmonary capillary wedge pressure makes a pregnant woman susceptible to pulmonary edema. Hence, caution should be exercised while giving fluids to a pregnant woman to prevent any increase in preload that would precipitate pulmonary edema.52
Changes in Electrocardiogram during Pregnancy
Alteration in structure and function of the heart often leads to occurrence of systolic murmur during pregnancy. However, to label a pregnant woman with a diagnosis of heart disease, it is necessary to look for ECG changes that exceed normal variations during pregnancy.52 Changes occur in arrangement of chest organs, sympathohormonal changes, left ventricular dimension alteration based on hemodynamic requirements during pregnancy, all of which bring about changes in ECG. Left-axis deviation, occurrence of Q-wave, and T-wave abnormalities are common findings in ECG recordings during pregnancy. However, interpretation of these changes needs to be done with caution, though several times, these changes are seen as minor and temporary.
Understanding the physiologic changes during pregnancy is necessary to avoid any misinterpretation of these changes as pathologic processes. A systematic evaluation of hemodynamic changes during pregnancy is necessary. Any electrical changes in the heart should be evaluated cautiously due to large and subjective variations occurring during pregnancy. The cardiovascular changes are by and large temporary and reversible reverting back to the prepregnant levels within few weeks of delivery.
References
- Crit Rev Clin Lab Sci. 1997;34(01):67-139.Clinical biochemistry of pregnancy.
- [Google Scholar]
- Am J Clin Nutr. 2000;71(05):1218S-1225S. Suppl)Physiology of pregnancy and nutrient metabolism.
- [Google Scholar]
- Annu Rev Nutr. 2006;26:271-291.Maternal obesity, metabolism, and pregnancy outcomes.
- [Google Scholar]
- Diabetes Metab Res Rev. 2003;19(04):259-270.Intermediate metabolism in normal pregnancy and in gestational diabetes.
- [Google Scholar]
- Clin Obstet Gynecol. 2007;50(04):938-948.Metabolic changes in pregnancy.
- [Google Scholar]
- Physiol Rev. 2005;85(03):1093-1129.Myocardial substrate metabolism in the normal and failing heart.
- [Google Scholar]
- Eur Heart J. 2018;39(34):3165-3241.2018 ESC guidelines for the management of cardiovascular diseases during pregnancy.
- [Google Scholar]
- Br Heart J. 1992;68(06):540-543.Adaptation of the maternal heart in pregnancy.
- [Google Scholar]
- Clin Med Insights Cardiol. 2016;10:157-162.Echocardiographic assessment of cardiac changes during normal pregnancy among Nigerians.
- [Google Scholar]
- Am J Physiol. 1989;256:H1060-H1065. (4 Pt 2)Serial study of factors influencing changes in cardiac output during human pregnancy.
- [Google Scholar]
- BJOG. 2007;114(05):576-581.Haemodynamic changes in the second half of pregnancy: a longitudinal, noninvasive study with thoracic electrical bioimpedance.
- [Google Scholar]
- Cardiovasc J Afr. 2011;22(02):71-75.Cardiovascular and electrocardiographic changes in Nigerians with a normal pregnancy.
- [Google Scholar]
- Am J Obstet Gynecol. 1994;170(03):849-856.A longitudinal study of cardiac output in normal human pregnancy.
- [Google Scholar]
- Acta Obstet Gynecol Scand. 1993;72(02):103-110.Atrial natriuretic peptide (ANP) decrease during normal pregnancy as related to hemodynamic changes and volume regulation.
- [Google Scholar]
- Obstet Gynecol. 1999;94(06):978-984.Maternal central hemodynamics in hypertensive disorders of pregnancy.
- [Google Scholar]
- Obstet Gynecol. 1996;87(02):310-318.Cardiac output in normal pregnancy: a critical review.
- [Google Scholar]
- Obstet Gynecol. 2004;104(01):20-29.Echocardiographic assessment of cardiovascular hemodynamics in normal pregnancy.
- [Google Scholar]
- Circulation. 2014;130(12):1003-1008.Cardiovascular physiology of pregnancy.
- [Google Scholar]
- Am J Obstet Gynecol. 1993;169(06):1382-1392.Early pregnancy changes in hemodynamics and volume homeostasis are consecutive adjustments triggered by a primary fall in systemic vascular tone.
- [Google Scholar]
- J Obstet Gynaecol Br Commonw. 1967;74(03):319-328.A study of cardiac output at rest throughout pregnancy.
- [Google Scholar]
- Obstet Gynecol. 1996;88(01):40-46.A longitudinal study of maternal hemodynamics during normal pregnancy.
- [Google Scholar]
- Obstet Gynecol. 1990;76(06):1061-1069.Maternal hemodynamics in normal and preeclamptic pregnancies: a longitudinal study.
- [Google Scholar]
- Scand J Clin Lab Invest. 1982;42(06):513-520.Cardiac output in normal pregnancy measured by impedance cardiography.
- [Google Scholar]
- Eur J Obstet Gynecol Reprod Biol. 1996;70(02):117-122.Serial changes in cardiac output during normal pregnancy: a Doppler ultrasound study.
- [Google Scholar]
- Eur J Obstet Gynecol Reprod Biol. 1981;12(04):215-224.A longitudinal study of cardiovascular dynamic changes throughout pregnancy.
- [Google Scholar]
- IJRCOG. 2016;5(01):84-89.Role of echocardiography for assessment of cardiovascular haemodynamics during pregnancy.
- [Google Scholar]
- Am J Cardiol. 1997;80(11):1469-1473.Cardiovascular function before, during, and after the first and subsequent pregnancies.
- [Google Scholar]
- Circulation. 2002;106(03):292-295.Is the pregnancy hormone relaxin also a vasodilator peptide secreted by the heart?
- [Google Scholar]
- Am J Physiol Regul Integr Comp Physiol. 2004;287(02):R250-R261.Emerging role of relaxin in renal and cardiovascular function.
- [Google Scholar]
- Lancet. 1969;2:879-881. 7626Cardiovascular dynamics in women receiving oral contraceptive therapy.
- [Google Scholar]
- BJOG. 2001;108(04):344-352.Cardiovascular function in pregnancy: effects of posture.
- [Google Scholar]
- J Hypertens. 2014;32(04):849-856.A longitudinal study of maternal cardiovascular function from preconception to the postpartum period.
- [Google Scholar]
- J Physiol. 2012;590(15):3535-3543.Sympathetic activation during early pregnancy in humans.
- [Google Scholar]
- Am J Cardiol. 1978;41(04):655-660.Continuous ventricular dimensions in man during supine exercise and recovery. An echocardiographic study.
- [Google Scholar]
- Ultrasound Obstet Gynecol. 2017;50(06):683-696.Cardiac remodeling in normotensive pregnancy and in pregnancy complicated by hypertension: systematic review and meta-analysis.
- [Google Scholar]
- Am J Obstet Gynecol. 1985;151(02):191-196.A prospective study of blood pressure in pregnancy: prediction of preeclampsia.
- [Google Scholar]
- Am J Obstet Gynecol. 1976;125(04):509-513.Studies on blood pressure during pregnancy. I. Influence of parity and age.
- [Google Scholar]
- Am J Physiol Heart Circ Physiol. 2007;293(04):H2479-H2486.Role of nitric oxide in the coupling of myocardial oxygen consumption and coronary vascular dynamics during pregnancy in the dog.
- [Google Scholar]
- Circulation. 1997;95(10):2407-2415.Serial assessment of the cardiovascular system in normal pregnancy. Role of arterial compliance and pulsatile arterial load.
- [Google Scholar]
- J Clin Invest. 1973;52(11):2682-2689.A study of angiotensin II pressor response throughout primigravid pregnancy.
- [Google Scholar]
- Arq Bras Cardiol. 2015;104(04):284-291.Blood pressure variation throughout pregnancy according to early gestational BMI: a Brazilian cohort.
- [Google Scholar]
- J Hypertens. 2011;29(04):763-768.Mid-trimester blood pressure drop in normal pregnancy: myth or reality?
- [Google Scholar]
- J Hypertens. 2012;30(02):342-350.Changes in blood pressure during healthy pregnancy: a longitudinal cohort study.
- [Google Scholar]
- Ann Epidemiol. 2005;15(07):475-482.The risk of preeclampsia rises with increasing prepregnancy body mass index.
- [Google Scholar]
- Int J Med Public Health. 2014;4(04):441-445.A study on cardiac autonomic modulation during pregnancy by non-invasive heart rate variability measurement.
- [Google Scholar]
- Internet J Health.. 2009;9(02):4.Cardiopulmonary changes in pregnant women in Sabon-Gari local government area, of Kaduna state, Nigeria.
- [Google Scholar]
- Eur Heart J. 2011;32(24):3088-3097.Blood pressure tracking during pregnancy and the risk of gestational hypertensive disorders: the Generation R Study.
- [Google Scholar]
- Ultrasound Obstet Gynecol. 2017;49(02):177-187.Physiological adaptation of maternal plasma volume during pregnancy: a systematic review and meta-analysis.
- [Google Scholar]
- Am J Obstet Gynecol. 1972;112(03):440-450.Plasma and red cell volumes during pregnancy.
- [Google Scholar]
- Best Pract Res Clin Obstet Gynaecol. 2015;29(05):671-684.Haematological problems in obstetrics.
- [Google Scholar]
- Cardiovasc J Afr. 2016;27(02):89-94.Physiological changes in pregnancy.
- [Google Scholar]
- J Clin Diagn Res. 2014;8(09):BC17-BC21.Electrocardiographic QRS axis, Q wave and T-wave changes in 2nd and 3rd trimester of normal pregnancy.
- [Google Scholar]