| Literature DB >> 36132229 |
Umme Salma1, Ahmed Baker A Alshaikh1, Muhannad Faleh Alanazi2, Basil Mohammed Alomair3, Mubarak Alruwaili3, Raed Alruwaili3.
Abstract
Pregnancy-related cardiovascular disease with stroke remains a considerable source of higher maternal morbidity and mortality occurs in periods of pregnancy, delivery, and postpartum. It is essential to counsel the mother before pregnancy by an expert cardiologist and obstetric team to discuss any event related to preexistent cardiac or past preeclampsia for estimation of maternal and fetal risks. In pregnancy, the cardiac state includes hypertensive disorders, ischemic heart disease, valvular disease, and postpartum stroke. The incidence of stroke is increasing in pregnancy, particularly in postpartum, and its strong relationship with hypertensive disorders of pregnancy (preeclampsia). The combined cardiologist and obstetrics team requires during pregnancy mainly due to the approach to the management of a cardiac disease that subsequently prevents stroke postpartum. Therefore, a general perception of cardiac disease during pregnancy, delivery, and postpartum should be a core knowledge extent for all cardiovascular and clinicians. Many studies provided linked that deregulation of microRNAs (miRNAs) in maternal circulation and placenta tissue may development of pregnancy complications including preeclampsia considered a diagnostic marker. The desire of this review provides a detailed outline of current knowledge and dealing in this field with strength on the physiological changes during pregnancy.Entities:
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Year: 2022 PMID: 36132229 PMCID: PMC9484966 DOI: 10.1155/2022/5260085
Source DB: PubMed Journal: Oxid Med Cell Longev ISSN: 1942-0994 Impact factor: 7.310
Figure 1Physiological change in pregnancy.
Figure 2Advance maternal age has an impact on cardiac adaptation in pregnancy considered to have cardiac complications.
Figure 3Flowchart of cardiac events during pregnancy.
Management strategies of cardiac disease and stroke in pregnancy.
| Hypertensive disorder of pregnancy (HDP) | Ischemic heart disease in pregnancy (IHD) | Vulvar heart disease in pregnancy | Stroke in pregnancy |
|---|---|---|---|
| Precounseling to avoid pregnancy until control of hypertension or during pregnancy advise following below | Prepregnant council to delay pregnancy after treatment of IHD. If unexpected pregnant, then the following management | Pregnancy should be avoided in severe mitral and aortic valve disease. If unexpected pregnant, then the following management | Precounseling to control hypertension who has a previous history of preeclampsia |
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| Investigation | |||
| Urine test for proteinuria. | Positive stress ECG, MRI, and exercise testing evidence for IHD and recommendation coronary angiography, if clinically indicated. | Clinical and ECG knowledge are required sequentially for a pregnant woman to know the condition of valvular heart disease. The percutaneous valve intervention is the best treatment for those who are not responding to the medical therapy. | MRI images are considered an optimal modality during pregnancy, in case of missing timely taken MRI, then angiography CT and also perfusion CT can be chosen as a guide for proper interventional therapies. |
| Ophthalmoscopic examination. | |||
| Blood values | |||
| USG | |||
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| Risk factors | |||
| Hypertension, obesity, and family history of diabetes | Hypertension and preeclampsia are strongly associated with AMI. | Rheumatic fever is a most common | Preeclampsia, eclampsia |
| Mechanical heart valves | |||
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| Pregnancy management | |||
| Close follow-up | Close follow-up | Close follow-up | Closely monitoring. Common drugs used: labetalol, atenolol, methyldopa, nifedipine, warfarin, and heparin (low molecular weight), and direct oral anticoagulants. |
| Medical therapy: Nifedipine, methyldopa, labetalol, and hydralazine | Medical therapy: antiplatelet therapy, nitrates, beta-blockers, inotropes, and oxygen | Medical therapy for heart failure or arrhythmias | |
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| Delivery | |||
| Vaginal delivery with control of hypertension | Normal vaginal delivery unless cardiac and obstetrician indication. Continuous maternal cardiac monitoring. Continuous electronic fetal monitoring. Emergency cesarean section prior to cardiac surgery if needed. | If possible, vaginal delivery is preferred. Cesarean section is chosen when there is risk to the mother or fetus. Early delivery for clinical and hemodynamic worsening. | Vaginal delivery is the best approach if there is no obstetric contraindication. |
| Emergency cesarean section if required | |||
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| Complication | |||
| Stroke, hypertension, and cardiac disease are responsible for the development of preeclampsia or eclampsia during pregnancy and also in postpartum | Cardiac arrest, heart failure, and ventricular tachycardia | Pulmonary edema, atrial arrhythmias, stroke, and heart failure | Reversible cerebral vasoconstriction syndrome can cause both ischemic and hemorrhagic stroke and the risk of cerebral venous sinus thrombosis (CVST). Long-term disability |
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| Follow-up | |||
| The utility of subclinical vascular measurements, such as cerebral or peripheral vasomotor reactivity, carotid intimal medial thickness, coronary calcification, or clinical and biochemical biomarkers, is needed to identify women with a history of preeclampsia at increased risk of future stroke. | Maternal cardiac monitoring for at least 48 hours after delivery | Hemodynamic monitoring at least 24 hours postpartum | Counseling and cardiovascular screening of women who have a past history of preeclampsia. As well as correction of the other vascular risk factors. |
Figure 4Long-term and short-term effects of a pregnant mother with cardiac disease and stroke.
The imaging modalities in pregnancy.
| Imagines modality | Imaging finding | Indications |
|---|---|---|
| Electrocardiography | The interpretation of ECG the heart rotates to the left with a 15–20° leftward axis deviation in most women in pregnancy. | Finding structural heart diseases |
| Echocardiography | Usually, some changes occur in echo parameters during pregnancy such as an increase in valve gradient, changes in the thickness of the LV wall, and dilation of the chamber quite mild. | Delivery of the status for the structures and functions of the heart |
| Chest radiography | Diagnostic cardiovascular radiographic examination | The condition of the heart, lungs, airways, blood vessels, and the bones of the spine and chest showing by images |
| Computed tomography | The X-rays reveal the images of the part of the body obtained in the various orthogonal plane. | Anomalous coronary artery and aortic dissection |
| Magnetic resonance imaging | Any abnormality of fetus | Congenital heart disease, aortic disease, and stroke |
| Cerebral edema, ischemia, and hemorrhage | ||
| Ultrasonography | Fetal heart rate, fetal position, and fetal presentation | The initial procedure for monitoring fetal well-being in pregnancy |
Figure 5(a) In a woman, in 18 weeks of her 2nd pregnancy, the magnetic resonance appears bicuspid aortic valve (arrow) showing moderately enlarged ascending aorta up to 4.75 cm [28]. (b) Posteroanterior chest radiographs in a 22-year-old woman during and post pregnancy. At 36 weeks, the first radiograph was taken which showed an enlarged cardiac silhouette and engorged pulmonary vasculature (arrows) with apical redistribution [29]. (c) This is a case of a 24-week pregnant woman at her 30-year-old along subarachnoid hemorrhage due to eclampsia complication. Axial FLAIR MR image shows the presence of subarachnoid blood in the right posterior frontal and parietal sulci (short arrows) and subtle edema covering the underlying cortex (long arrows) [30]. (d) Peripartum cardiomyopathy showed in a pregnant woman by chest radiography [31].
Figure 6Mechanism of action of circulating miRNAs.
The different expressions of the miRNA in preeclampsia and stroke.
| MicroRNAs | Preeclampsia | Source | Stroke | Source |
|---|---|---|---|---|
| miR-145 | ↑ | Human maternal plasma | ↑ | Tissue/rat |
| miR-21 | ↑ | Human maternal plasma | ↑ | Tissue/rat |
| miR-210 | ↑ | Human placenta | ↓ | Human blood |
| miR-26a | ↑ | Human maternal plasma | ↓ | Tissue, blood/rat |
| miR-26b | ↑ | Human maternal plasma | ↓ | Tissue, blood/rat |
| miR-328 | ↓ | Human placenta | ↓ | Tissue, blood/rat |
| miR-29b | ↑ | Primary human umbilical vein endothelial cells | ↑ | Tissue, blood/rat |
| miR-204 | ↑ | Human placenta | ↑ | Tissue/rat |
| miR-23a | ↑ | Human maternal plasma | ↑ | Tissue, blood/rat |
| miR-335 | ↑ | Human placenta | ↓ | Tissue/rat |
| miR-150 | ↓ | Human placenta | ↑ | Tissue, blood/rat |
| miR-126 | ↓ | Human placenta | ↓ | Human blood |
| miR-155 | ↑ | Human placenta | ↓ | Tissue, blood/rat |
| miR-451 | ↓ | Human maternal plasma | ↑ | Tissue, blood/rat |
| miR-107 | ↓ | Human maternal plasma | ↑ | Tissue, blood/rat |
| miR-185 | ↓ | Human maternal plasma | ↑ | Tissue, blood/rat |