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Sudden cardiac arrest and death in pregnancy

Sudden cardiac arrest and death in pregnancy
Literature review current through: Jan 2024.
This topic last updated: Apr 10, 2023.

INTRODUCTION — Sudden cardiac arrest (SCA) in pregnancy affects two patients: the mother and the fetus. Depending on availability, management of these patients demands a rapid multidisciplinary approach, including anesthesiology, cardiology, obstetrics, neonatology, and sometimes cardiothoracic surgery [1].

Basic and advanced cardiac life support algorithms should be implemented; however, the physiologic and anatomic changes of pregnancy require some modifications to these protocols (algorithm 1). Randomized trials of approaches to management of pregnant patients with SCA are lacking; therefore, recommendations for these modifications are based on expert opinion and data from small case series and small cohort studies involving patients with SCA during cesarean birth.

This topic will focus on management of SCA during pregnancy. Management of SCA in nonpregnant populations is reviewed separately:

(See "Overview of sudden cardiac arrest and sudden cardiac death".)

(See "Supportive data for advanced cardiac life support in adults with sudden cardiac arrest".)

(See "Advanced cardiac life support (ACLS) in adults".)

(See "Pathophysiology and etiology of sudden cardiac arrest".)

(See "Therapies of uncertain benefit in basic and advanced cardiac life support".)

(See "Approach to sudden cardiac arrest in the absence of apparent structural heart disease".)

TERMINOLOGY — Sudden cardiac arrest (SCA) refers to the "sudden cessation of organized cardiac activity so that the victim becomes unresponsive, with no normal breathing and no signs of circulation" [2]. The event is referred to as SCA if an intervention (eg, defibrillation) or spontaneous reversion restores circulation. The event is called sudden cardiac death if the patient dies. The term SCA will be used in this topic to describe both fatal and nonfatal cardiac arrest.

SCA is further subdivided according to cardiac or noncardiac origin. Cardiac origin is assumed if another noncardiac cause is unlikely. Noncardiac causes include hemorrhage, sepsis, anesthetic- and medication-related complications, massive pulmonary embolism, vascular collapse (eg, anaphylaxis, amniotic fluid embolism), and trauma. The obstetric literature generally combines cardiac and noncardiac causes under the umbrella term "sudden cardiac death." This likely results in significant variability in reported cases and in the specific etiologies for sudden death.

The American College of Cardiology/American Heart Association Task Force provided a revised definition of sudden cardiac arrest in its 2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death, which are reviewed separately [2] (see "Overview of sudden cardiac arrest and sudden cardiac death", section on 'Definitions'). The European Society of Cardiology guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death published definitions in 2015 [3].

IDENTIFYING HIGH-RISK PATIENTS

Preconception and early pregnancy — Risk assessment to identify those patients at increased risk of cardiac complications during pregnancy is advisable, given that cardiac disease is the leading etiology of maternal death. Ideally, risk assessment is performed prior to conception and/or at the time of the initial prenatal evaluation to allow for prepregnancy counseling and for advance multidisciplinary team planning before birth to optimize outcomes [4,5].

Patients with a positive history should be referred to a cardiologist for further evaluation if they are not already under such care. Pregnancy risk indexes (eg, modified World Health Organization [mWHO] classification, Cardiac Disease in Pregnancy study [CARPREG], ZAHARA) have been developed for risk stratification of patients with preexisting heart disease. The indexes are described in detail separately. (See "Pregnancy in women with congenital heart disease: General principles", section on 'Maternal cardiovascular risk assessment'.)

Risk assessment involves performing a history/physical examination to identify signs and symptoms of heart disease and medical disorders that may affect cardiac function, obtaining any personal or family history of congenital or acquired cardiovascular disease, and reviewing any available patient-specific data (eg, electrocardiogram, echocardiography, stress testing).

A history of prior arrhythmias, systemic or pulmonary ventricular dysfunction, and prolonged QRS intervals have been identified as risk factors for SCA during pregnancy [3,6]. Risk factors for SCA in the general population should also be considered, and these include hypertension, cigarette smoking, obesity, diabetes mellitus, and a family history of premature coronary heart disease or myocardial infarction. Of note, in a study of the American Heart Association's Get with the Guidelines Resuscitation voluntary registry, which included 462 in-hospital maternal SCAs, approximately one-third had no preexisting conditions or physiologic disorders before the arrest; respiratory insufficiency (36.1 percent) and hypotension/hypoperfusion (33.3 percent) were the most common antecedent conditions [7]. (See "Overview of sudden cardiac arrest and sudden cardiac death", section on 'Risk factors'.)

Late pregnancy — Patients who were considered low risk for SCA when presenting for prenatal care and in early pregnancy become high risk if they develop pregnancy-related complications, such as amniotic fluid embolism, cardiomyopathy of pregnancy, postpartum hemorrhage, preeclampsia with severe features, or complications related to anesthesia for delivery. (See 'Etiology' below.)

PREVALENCE — In the United States, the prevalence of SCA is 13.4 events per 100,000 delivery hospitalizations (1 in 9000), based on data from the National Inpatient Sample (2017 to 2019) [8]. SCA was disproportionately more likely to occur in patients who were older, non-Hispanic Black, enrolled in Medicare or Medicaid, or had underlying medical conditions. Acute respiratory distress syndrome was the most common co-occurring diagnosis (present in 56 percent of cases), and mechanical ventilation was the most common intervention (present in 53.2 percent of cases). This study also demonstrated that health care disparities play a significant role in the occurrence of in-hospital maternal cardiac arrests. Women with a diagnosis of cardiac arrest were older, more likely to be non-Hispanic black, more likely to have underlying medical conditions (such as chronic hypertension, diabetes, smoking, asthma, renal disease, mental health disorders, and acquired heart disease), and less likely to have private health insurance.

PATHOPHYSIOLOGY — Arrhythmias due to either cardiomyopathy or a channelopathy are the most common mechanism of SCA in young individuals [9-15]. SCA can occur unpredictably in a predisposed patient or may arise as a result of a combination of a vulnerable substrate (such as preexisting congenital heart disease, valvular disease, cardiomyopathy, or a genetic predisposition to arrhythmias) along with triggers such as hemodynamic shifts, myocardial ischemia, plaque rupture (or coronary dissection), thrombosis, electrolyte abnormalities, and proarrhythmic medications. (See "Pathophysiology and etiology of sudden cardiac arrest".)

The physiologic changes of pregnancy can unmask underlying cardiac disease, increasing the propensity for adverse events. For example, increased progesterone levels can lead to biochemical remodeling in vessel walls that magnify shear forces leading to dissection and rupture. In some otherwise healthy patients, SCA occurs as a complication of a pulmonary embolism, severe hemorrhage, or amniotic fluid embolism.

ETIOLOGY

Overview — SCA may be related to conditions unique to pregnancy or etiologies found in the nonpregnant state (table 1). Frequencies by etiology are difficult to summarize because of differences in classification systems.

Two representative large studies are described below:

A review of the most common causes of SCA in pregnant patients in the United States and United Kingdom reported [16]:

Pulmonary embolism (29 percent)

Hemorrhage (17 percent)

Sepsis (13 percent)

Peripartum cardiomyopathy (8 percent)

Stroke (5 percent)

Preeclampsia/eclampsia (2.8 percent)

Complications related to anesthesia (eg, difficult or failed intubation, local anesthetic toxicity, aspiration, high neuraxial block; 2 percent)

Amniotic fluid embolism, myocardial infarction, preexisting cardiac disease (congenital, acquired, cardiomyopathy), and trauma were additional major causes of cardiac arrest, but the frequencies were not reported.

The distribution of maternal SCA (n = 4843) from the United States National Inpatient Sample from 1998 to 2011 is shown in the table (table 2) [17].

More recent series have reported high prevalences of overweight/obesity (over 60 percent) and complications of obstetric anesthesia (24 percent) in pregnant patients with SCA [18,19].

A through H mnemonic — The following A through H mnemonic was devised by the American Heart Association to help providers remember causes of SCA that should be considered in pregnant patients [20]:

A – Anesthetic complications, accident/trauma

B – Bleeding

C – Cardiac

D – Drugs

E – Embolic causes

F – Fever

G – General including hypoxia, electrolyte disturbances

H – Hypertension

Role of congenital heart disease — Congenital heart disease is the most common form of heart disease complicating pregnancy in the western world [21,22]. While most patients with congenital heart disease tolerate pregnancy well, an increasing number have moderate or complex forms of congenital heart disease and are at higher risk of pregnancy complications, including an increased risk of SCA [23]. Those patients at highest risk include those with cyanotic congenital heart disease, severe pulmonary artery hypertension, complex congenital heart disease with sequelae (eg, heart failure or significant valvular disease), congenital heart disease with history of malignant arrhythmia, Marfan syndrome, and prior Fontan procedure. (See "Anesthesia for labor and delivery in high-risk heart disease: Specific lesions".)

Data on SCA risk in patients with congenital heart disease are limited.

Data from the Registry Of Pregnancy And Cardiac disease (ROPAC) included 5739 pregnant patients of whom 57 percent had congenital heart disease, 29 percent had valvular heart disease, 8 percent had cardiomyopathy (including pregnancy-induced), and 1.6 percent had ischemic heart disease [24]. Maternal death occurred in 34 (0.6 percent); the underlying cardiac lesions were valvular heart disease (17), congenital heart disease (8), cardiomyopathy (5), and pulmonary hypertension (4). Two deaths were due to SCA, but the underlying cardiac lesion was not stated.

In a series of 1938 pregnant patients of whom 1235 (64 percent) had congenital heart disease, 14 had a cardiac death or arrest and approximately half of these patients had congenital heart disease; most of the remainder had cardiomyopathy [25].

RAPID OVERVIEW OF RESUSCITATION — Resuscitation involves the following maneuvers and interventions, which are performed simultaneously, not sequentially:

Call a "maternal" code blue, which should include a multidisciplinary team (adult resuscitation, anesthesia, obstetrics, neonatology). Obstetric and neonatal teams do not typically respond to an "adult code blue," so specific and early notification of these teams is critical.

If the uterus is at or above the umbilicus, manually displace the uterus laterally and to the left (ie, left uterine displacement) to minimize aortocaval compression [26]. (See 'Avoiding aortocaval compression' below.)

Initiate high-quality chest compression (at least 100 compressions per minute but not more than 120, compressing the chest at least 5 cm [2 inches] but no more than 6 cm [2.5 inches] with each downstroke) and ventilation (two ventilations of approximately 350 to 500 mL after every 30 compressions for patients without an advanced airway and with a uterus above the umbilicus [a larger ventilatory volume, 600 mL, is used if the uterus is below the umbilicus]) using standard hand placement for chest compression [27]. (See "Adult basic life support (BLS) for health care providers", section on 'Performance of excellent chest compressions' and "Adult basic life support (BLS) for health care providers", section on 'Ventilations'.)

Do not delay usual measures such as defibrillation and administration of medications. (See "Adult basic life support (BLS) for health care providers", section on 'Defibrillation' and "Advanced cardiac life support (ACLS) in adults".)

Place intravenous access above the diaphragm.

Assume the patient has a difficult airway. (See "Airway management for the pregnant patient".)

Estimate the gestational age of the fetus. (See 'Determining gestational age' below.)

Use end-tidal carbon dioxide monitoring to determine the presence of return of spontaneous circulation, which reduces interruptions in cardiopulmonary resuscitation (CPR) by obviating the need for pulse checks. Although an end-tidal CO2 level >10 mmHg may correlate with return of spontaneous circulation, it is not predictive of survival or long-term outcome [20]. (See "Adult basic life support (BLS) for health care providers", section on 'Pulse checks and rhythm analysis'.)

A dedicated timer should alert the entire resuscitative team when four minutes have elapsed after the onset of a maternal cardiac arrest. If there is no return of spontaneous circulation with the usual resuscitation measures and the uterine fundus is at or above the umbilicus, at four minutes begin perimortem cesarean (also called resuscitative hysterotomy [28]), and complete delivery of the newborn by five minutes following SCA. In pregnant patients, delivery early in the resuscitation process is a key intervention for improving success rates. (Perimortem cesarean birth can be defined as a cesarean birth after CPR has been initiated [29].) (See 'Delivery as part of the resuscitation process' below.)

After 15 minutes of unsuccessful resuscitation, initiate direct cardiac massage if appropriate resources and personnel are available [30,31]. Thoracotomy and open chest massage are particularly effective for patients with chest trauma, tension pneumothorax, massive pulmonary embolism, pericardial tamponade, and chest or spine deformities. Thoracotomy may also facilitate treatment of the underlying cause of the arrest (eg, removal of pericardial fluid/thrombus in cardiac arrest due to pericardial tamponade). (See 'Imaging' below.)

Evaluate need to institute extracorporeal life support [30]. (See 'Imaging' below and 'Extracorporeal life support' below.)

Continue resuscitation measures until all resources and attempts have been exhausted. This will vary depending on the clinical circumstances and resources of the facility. (See "Advanced cardiac life support (ACLS) in adults", section on 'Termination of resuscitative efforts'.)

Simultaneously, factors causing or contributing to cardiac arrest should be treated promptly (eg, bleeding/disseminated intravascular coagulation, electrolyte abnormalities, tamponade, hypothermia, hypovolemia, hypoxia, hypermagnesemia, myocardial infarction, poisoning, embolism [pulmonary, amniotic fluid, coronary], anaphylaxis, tension pneumothorax, anesthesia complications, aortic dissection). Treatment of these disorders is reviewed in separate topic reviews.

RESUSCITATION PROCEDURES — The sequence for resuscitation in adults is well-described separately. (See "Advanced cardiac life support (ACLS) in adults".)

Specific issues in pregnant patients are described below and in the algorithm (algorithm 1). Resuscitation involves concurrent interventions.

Airway management — Active airway management is the initial consideration. Intubation by an qualified provider is recommended due to the risk of aspiration and difficulty in providing adequate ventilation without securing the airway. Both intubation and bag mask ventilation can be more difficult in the late stages of pregnancy due to narrowing of upper airways (particularly in the third trimester) and decreased thoracic compliance. Back-up airway procedures, including supraglottic airway devices (eg, laryngeal mask airway) and cricothyrotomy, may be required in some cases.

Pregnant patients are at increased risk of rapidly developing hypoxemia because of decreased functional residual capacity and increased oxygen consumption as well as increased intrapulmonary shunting [32-36]. Bag-mask ventilation (8 to 10 breaths/minute) with 100 percent oxygen (two-handed, >15 L/minute) and suctioning the airway are critical before intubation in a pregnant patient to avoid desaturation. (See "Airway management for the pregnant patient".)

Intubation via video or direct laryngoscopy and 100 percent oxygen is performed using a smaller sized endotracheal tube (0.5 to 1.0 mm less in internal diameter compared with that used for nonpregnant women). Endotracheal tube placement should be verified using capnography.

Cricoid pressure during laryngoscopy, once universally recommended, is no longer used because of lack of evidence of benefit and its ability to make both intubation and placement of a supraglottic airway more difficult. Cricoid pressure for the purpose of preventing aspiration of gastric contents, which we do not recommend, is distinct from external laryngeal manipulation, which can be undertaken by the intubator to attempt to improve glottic view during laryngoscopy, particularly direct laryngoscopy. (See "Carbon dioxide monitoring (capnography)".)

Supraglottic airway devices, such as the laryngeal mask airway, should be considered if unable to intubate [37]. No more than two attempts with either direct laryngoscopy or videolaryngoscopy before insertion of a supraglottic device are recommended [20].

A large uterus (fundus above the umbilicus) that elevates the diaphragm may increase resistance to ventilation. In these patients, lower ventilation volumes (350 to 500 mL) are used compared with nonpregnant females (600 mL). Ventilation during cardiopulmonary resuscitation (CPR) should allow the chest to rise but not cause overinflation, which will further decrease thoracic compliance and increase intrathoracic pressure, impeding venous return to the heart.

Hyperventilation has adverse effects and should be avoided in any patient undergoing resuscitation. In pregnancy, nonphysiologic respiratory alkalosis (normal pregnancy is associated with mild respiratory alkalosis) can cause uterine vasoconstriction, which can lead to fetal hypoxia and acidosis [38]. (See "Advanced cardiac life support (ACLS) in adults", section on 'Airway management'.)

Chest compressions — High-quality chest compressions (at least 100 compressions per minute but not more than 120, compressing the chest at least 5 cm [2 inches] but no more than 6 cm [2.5 inches] with each downstroke) are the cornerstone of the resuscitation process. The 2015 American Heart Association (AHA) guideline on SCA in pregnancy recommends the same hand position for and performance of chest compressions in pregnant and nonpregnant adults because of an absence of data supporting a different approach in pregnancy [20]. This position is the center of the chest over the lower (caudad) portion of the sternum.

Previous AHA guidelines suggested a more cephalad hand position in pregnancy to adjust for elevation of the diaphragm by the gravid uterus. The updated guideline was based, in part, on a magnetic resonance imaging study that showed no significant vertical displacement of the heart in the third trimester of pregnancy relative to the nonpregnant state [27]. (See "Adult basic life support (BLS) for health care providers", section on 'Performance of excellent chest compressions'.)

The maternal position during chest compression is supine, with manual uterine displacement. (See 'Avoiding aortocaval compression' below.)

Intravenous access — Intravenous access should be established above the diaphragm since drugs administered via the femoral vein may not reach the maternal heart until the fetus is delivered. Access to an antecubital vein with two 14-gauge catheters can be as effective as central line catheters for volume replacement but these do not allow hemodynamic monitoring [30].

In the absence of intravenous access, rapid intraosseous access can be achieved in a few seconds using commercially available kits.

If neither intravenous nor intraosseous access is possible, the endotracheal tube can be used to administer certain medications including lidocaine, atropine, naloxone, and epinephrine. (See "Advanced cardiac life support (ACLS) in adults", section on 'Management of specific arrhythmias'.)

Avoiding aortocaval compression — We suggest manual uterine displacement to avoid aortocaval compression and to preserve supine positioning of the upper torso for optimal chest compression vector forces. A hand is used to apply maximal leftward push to the right upper border of the uterus to achieve displacement of approximately 1.5 inches from the midline (avoid pushing the uterus downward) [39]. However, if manual uterine displacement is not possible, then the operating room table should be tilted or pillows, a wood or foam resuscitation wedge (eg, Cardiff wedge), or rolled up towels or blankets should be placed under the patient to achieve a tilt of no more than 30 degrees [40].

Left lateral uterine displacement is necessary in the pregnant patient with fundal height at, or above, the umbilicus to minimize aortocaval compression (supine hypotensive syndrome), optimize venous return (preload), and generate adequate stroke volume during CPR. Our preference for manual uterine displacement is based on a randomized trial that compared manual uterine displacement versus operating room table tilt during cesarean birth and demonstrated significantly fewer episodes of hypotension and a lower ephedrine requirement in the manual displacement group [39]. In addition, manual displacement of the uterus allows the patient's upper torso to remain supine, which enables application of maximum resuscitative force for effective chest compressions, improves airway and intravenous access, and improves access for defibrillation. The inferiority of maternal tilt compared with the supine position was demonstrated in a study that used a calibrated force transducer to assess the maximum chest compression force generated at various angles of inclination in late pregnancy [40]. The maximum resuscitative force (expressed as percent body weight) was 67 percent in the supine position and decreased to 36 percent in the full lateral position. An angle of 27 degrees appeared to be the optimal angle in late pregnancy but achieved only 80 percent of the force generated in the supine position.

Defibrillation — Management of ventricular arrhythmias may require defibrillation. The right defibrillator pad/paddle is placed on the superior-anterior chest below the right clavicle, and the left defibrillator pad/paddle is placed on the inferior-lateral chest below the edge of the left breast [2].

The physiologic changes of pregnancy, including increases in blood volume and decreases in functional residual capacity, do not appear to alter transthoracic impedance or transmyocardial current [41]. Therefore, current energy requirements for adult defibrillation are appropriate for use in pregnant patients (biphasic shock 120 to 200 joules with subsequent increase in energy output if the first shock is ineffective) [20].

Before delivering the countershock, remove fetal monitoring equipment to prevent electrocution injury to the patient or rescuers. This risk is theoretical and of greatest concern when the fetus has scalp electrodes. Fetal monitors also detract from the resuscitation priorities determined by maternal status and maternal responses to resuscitative interventions. (See "Basic principles and technique of external electrical cardioversion and defibrillation".)

If a pacemaker or implantable cardioverter defibrillator is present, defibrillation is still appropriate. The external pads/paddles are placed at least one inch away from these devices.

In a study of AHA's Get with the Guidelines Resuscitation voluntary registry, which included 462 in-hospital maternal SCAs, 76.4 percent of patients had a nonshockable first documented pulseless rhythm (pulseless electrical activity: 50.8 percent; asystole: 25.6 percent) [7]. The remainder had a shockable rhythm (11.7 percent: 6.5 percent ventricular fibrillation and 5.2 percent pulseless ventricular tachycardia) or unknown rhythm (11.9 percent). Return of spontaneous circulation occurred in 73.6 percent of patients. In this cohort, the presenting rhythms are suggestive of potentially reversible clinical etiologies, such as hemorrhage, hypoxemia, thromboembolism, exposure to toxins, and electrolyte/acid/base disturbances.

Determining gestational age — In pregnant patients, determining gestational age is critical as the likelihood of neonatal viability is a factor in decision making. If the prenatal record or a corroborating family member is not available, physical examination can aid in estimating the gestational age. The formula for estimating gestational age by physical examination is:

Distance from the top of the symphysis pubis to the top of the fundus (cm) = gestational age (weeks)

The top of the uterine fundus is generally at the level of the umbilicus by 20 weeks of gestation in a singleton pregnancy. Uterine size correlates with gestational age but can be misleading in some situations, such as when there is a multiple gestation, large fibroids, severe oligohydramnios (decreased amniotic fluid volume), polyhydramnios (increased amniotic fluid volume), or maternal obesity.

Ultrasound is a reliable method for gestational age assessment but may not be possible due to time and logistical constraints during maternal assessment and resuscitation. (See "Prenatal assessment of gestational age, date of delivery, and fetal weight" and "Preterm birth: Definitions of prematurity, epidemiology, and risk factors for infant mortality" and "Periviable birth (limit of viability)".)

Fetal heart rate monitoring — In general, the status of the mother should guide management during the resuscitation process; if the status of the mother is poor and deteriorating, the status of the fetus will be further compromised. Therefore, fetal heart rate monitoring is not recommended during the resuscitation process.

If CPR is successful and the mother becomes hemodynamically stable, fetal heart rate monitors can be applied to assess the status of a fetus who is at a potentially viable gestational age. Intervention (in utero resuscitation measures, delivery) for an abnormal fetal heart rate pattern depends on maternal- and fetal-specific factors. (See "Intrapartum fetal heart rate monitoring: Overview".)

Delivery as part of the resuscitation process — The AHA and others recommend cesarean birth if spontaneous circulation has not returned within four minutes of maternal cardiorespiratory collapse [20,42,43]. Ideally, perimortem cesarean (ie, resuscitative hysterotomy) should be initiated within four minutes, and delivery of the newborn should be completed within five minutes (known as the "four-minute rule" or the "five-minute rule"). Perimortem operative vaginal birth using forceps or vacuum is appropriate if delivery can be achieved within this time frame [20]. To achieve this time frame, operative vaginal birth needs to be performed at the location of the SCA, which is often not an operating or birthing room [29,44].

The rationale for this approach is based on case reports, small case series, and experimental data showing [26,45-51]:

Irreversible brain damage can occur in nonpregnant individuals after four to six minutes of anoxia.

Pregnant patients become anoxic sooner than nonpregnant females because of decreased functional residual capacity.

If the uterine fundus is at or above the umbilicus, ineffective resuscitation efforts may become effective when the uterus is no longer gravid and potentially causing aortocaval compression. Sudden substantial improvement in hemodynamics with a return of pulse and blood pressure immediately after perimortem cesarean birth has been observed [29,52-55]. (See 'Minimum gestational age' below.)

Intact fetal survival diminishes as the time between maternal death and delivery lengthens. (See 'Evidence for the five-minute rule' below.)

Despite implementation of maneuvers to ameliorate aortocaval compression, CPR may not restore spontaneous circulation or provide adequate cardiac output. Blood flow during CPR is produced by mechanical compression of the heart between the sternum and the spine and phasic fluctuations in intrathoracic pressure. Despite appropriate use of leftward uterine displacement, the mechanical effects of the gravid uterus can decrease venous return from the inferior vena cava, obstruct blood flow through the abdominal aorta, and diminish thoracic compliance, all of which contribute to unsuccessful CPR [56]. Without restoration of cardiac output, both mother and fetus are at risk for hypoxia and eventually anoxia, especially when interruption of normal cardiac and respiratory function persists beyond four minutes [57]. Although it may be counterintuitive to operate on a hemodynamically unstable patient, cesarean birth may be lifesaving for both mother and fetus in this situation. Cardiac output peaks immediately after birth as the evacuated uterus contracts and blood from myometrial veins is autotransfused into the systemic venous system [58]. Also, the contracted uterus lifts off the vena cava, resulting in greater venous blood return to the heart, which increases stroke volume. However, unusual or ongoing blood loss during and immediately after birth can counteract these effects.

Practically, the goal of delivering the newborn within five minutes has been difficult to achieve [59,60]. In a literature review including 57 perimortem cesarean births with time to delivery information, the time was <5 minutes in 4 cases, <10 minutes in 18 cases, and <15 minutes in 32 cases [60]. Only perimortem cesarean birth within 10 minutes and in-hospital arrest were predictive of maternal survival. The reviewers believed perimortem cesarean birth was beneficial for one-third of mothers and was not harmful in any case. Overall neonatal survival was 64 percent (42/66) in singleton pregnancies with a potentially viable fetus delivered by perimortem cesarean birth; neonatal survival was attributed to perimortem cesarean birth in half of these cases. Only in-hospital arrest was predictive of neonatal survival. The mean time from arrest to delivery for newborn survivors was 14±11 minutes versus 22±13 minutes for newborn nonsurvivors.

While acknowledging that both maternal and neonatal injury-free survival rates diminish steadily as the time interval from maternal arrest to birth increases, the American College of Obstetricians and Gynecologists has opined that, even if delivery does not occur within four to five minutes, perimortem cesarean (resuscitative hysterotomy) still may be beneficial and should be considered [61].

Evidence for the five-minute rule — Although there have been no controlled clinical trials in this area, a review of case reports of perimortem cesarean birth from 1900 to 1985 suggested that normal neonatal neurologic outcome was most likely when delivery was completed within five minutes of maternal SCA. In this review, 42 of 42 newborns delivered within 5 minutes had a normal neurologic outcome compared with 7 of 8 newborns delivered within 6 to 10 minutes, 6 of 7 newborns delivered within 11 to 15 minutes, 0 of 1 newborn delivered between 16 and 20 minutes, and 1 of 3 newborns delivered within 21 to 25 minutes [49].

The authors' subsequent evaluation of perimortem cesarean cases reported from 1985 to 2004 noted the procedure was associated with spontaneous return of maternal circulation or improvement in maternal hemodynamic status in 12 of 20 cases, particularly when the delivery was completed within five minutes of maternal SCA [48]. No case of perimortem cesarean birth resulted in deterioration of the maternal condition, although these case reports were highly subject to reporting bias. Similarly, neonatal outcomes were best when delivery was completed within 5 minutes; 9 of 12 neonates delivered within this time frame had a normal neurologic outcome (neonatal outcome was not reported for 3 neonates), 2 of 6 neonates born from 6 to 15 minutes after maternal cardiac arrest had normal outcomes (1 neonatal outcome was not reported), and 4 of 7 neonates delivered after 15 minutes of maternal arrest had normal outcomes.

Additional features favoring neonatal survival include absence of sustained prearrest maternal hypoxia, minimal or no signs of fetal distress before maternal cardiac arrest, aggressive and effective resuscitative efforts for the mother, and neonatal intensive care unit on site of the emergency cesarean birth.

Minimum gestational age — The minimum gestational age for perimortem cesarean birth is controversial. Although physiologically aortocaval compression begins as early as 20 weeks, there is some imprecision within the range of 20 to 24 weeks [26]. Neonatal viability is also an imprecise assessment as it is uncertain which extremely preterm neonates, particularly those born at 23 and 24 weeks of gestation, have a reasonable chance of survival without severe deficits. Most centers would provide full neonatal support to newborns at least 24 weeks of gestation, and some centers provide this level of care to newborns greater than 220/7ths weeks of gestation [62]. (See "Periviable birth (limit of viability)".)

Given these variables, perimortem hysterotomy is a reasonable option for pregnancies ≥20 weeks of gestation/uterine size at or above the umbilicus to relieve aortocaval compression and facilitate return of spontaneous circulation regardless of fetal status (alive or demised) [30,48]. If the fetus is alive, there may be a neonatal benefit from perimortem hysterotomy at >22 to 24 weeks of gestation.

Delivery issues

High-quality chest compressions should be continued without interruption until return of spontaneous circulation.

Operative vaginal birth with forceps or vacuum is appropriate if the cervix is fully dilated, the fetus is at a low station, and delivery can be accomplished within five minutes of maternal cardiorespiratory collapse.

Cesarean birth is performed if the fetus cannot be delivered within five minutes vaginally.

Location – Transporting the patient to an operating room is not a priority [44]. An emergency cesarean delivery kit (eg, preloaded scalpel, sutures, needle holders, towel clips, retractors, forceps, scissors, suction tube, sponges, Kelly clamps, uterine pack, equipment for neonatal care/resuscitation) should be part of the resuscitation cart in patient care areas that commonly serve pregnant patients or such carts should be transported to the location of the pregnant patient who has arrested.

Consent – In the United States, there are no published reports of physician liability for performing perimortem cesarean birth without consent following maternal cardiac arrest [16].

Broad spectrum antibiotics are administered to decrease the risk of postpartum infection. (See "Cesarean birth: Preoperative planning and patient preparation", section on 'Antibiotic prophylaxis'.)

Technical points – We suggest a vertical skin incision to provide fast entry, adequate uterine exposure, and access to the diaphragm, which may be useful for further resuscitative interventions. (See 'Selected clinical scenarios' below.)

Bleeding may be minimal during the procedure due to hypoperfusion. Extraction of the placenta and closure of the hysterotomy are important steps to prevent subsequent hemorrhage when hemodynamic stability is eventually restored. (See "Cesarean birth: Surgical technique".)

Oxytocin is given routinely after vaginal or cesarean birth to reduce maternal blood loss and the risk of postpartum hemorrhage. We suggest a continuous intravenous infusion of a dilute oxytocin solution (eg, 20 milliunits/minute) to maintain firm uterine tone. Intramyometrial administration of 10 units oxytocin is an effective alternative to intravenous infusion.

Intravenous bolus injection of oxytocin should be avoided because of the risk for significant hypotension, cardiovascular collapse, and death. (See "Management of the third stage of labor: Prophylactic pharmacotherapy to minimize hemorrhage", section on 'Oxytocin'.)

Use of medications for resuscitation during pregnancy — All medications (including amiodarone) used for treatment of SCA in the nonpregnant patient are used for the pregnant patient and at the same doses. Given the lethality of SCA, the benefits from use of potentially lifesaving drugs outweigh any known or possible fetal risks.

Epinephrine (1 mg intravenous push every three to five minutes) is recommended in patients with asystole. (See "Supportive data for advanced cardiac life support in adults with sudden cardiac arrest", section on 'Epinephrine'.)

Magnesium sulfate is commonly used in obstetrics for a variety of indications (prevention of eclamptic seizures, fetal neuroprotection before preterm birth, tocolysis). If magnesium toxicity is suspected, magnesium sulfate infusion should be discontinued, and calcium chloride (10 mL of a 10 percent solution) or calcium gluconate (10 to 30 mL of a 10 percent solution) should be given intravenously or intraosseously early in the resuscitation process. (See "Preeclampsia: Intrapartum and postpartum management and long-term prognosis", section on 'Antidote'.)

Advanced cardiac life support (ACLS) guidelines do not recommend routine use of sodium bicarbonate during CPR, but it may be useful in life-threatening hyperkalemia or tricyclic antidepressant overdose. (See "Therapies of uncertain benefit in basic and advanced cardiac life support".)

However, if neither of these conditions is known or strongly suspected to be present, bicarbonate is not indicated and may worsen fetal acidosis. Since bicarbonate crosses the placenta very slowly, overcorrection of maternal acidosis will lead to pooling of carbon dioxide in the fetal compartment [31].

Arrhythmias are difficult to control, especially those resulting from bupivacaine toxicity. Amiodarone, a primary drug in the ACLS arrhythmia treatment algorithm, is the favored treatment for severe bupivacaine-induced arrhythmias; administration of the local anesthetic lidocaine to treat local anesthetic toxicity is not indicated as it has had equivocal success [63]. The arrhythmias are often refractory to therapy; emergency cardiopulmonary bypass may be lifesaving until the drug dissociates from cardiac tissue [64].

Early administration of a 20 percent lipid emulsion (conventional soybean oil-based, such as Intralipid) is an important component in resuscitation of local anesthetic-induced cardiotoxicity. This therapy, which theoretically acts as a lipid sink that binds lipid-soluble local anesthetics (eg, bupivacaine), has rapidly gained acceptance [65] since the first case reports documenting its efficacy were published in 2006 [66,67].

Lipid rescue should be initiated at the first signs of severe systemic local anesthetic toxicity while the airway is being secured. An intravenous bolus of 1.5 mL/kg lean body mass of 20 percent lipid emulsion is given over one minute, followed by an infusion of 0.25 mL/kg/minute until at least 10 minutes following successful achievement of circulatory stability. If circulatory stability is not obtained within five minutes, a second 1.5 mL/kg bolus may be administered, followed by an infusion of 0.5 mL/kg/minute. The maximum total cumulative dose of lipid is 10 mL/kg over 30 minutes [68]. (See "Local anesthetic systemic toxicity", section on 'Lipid rescue'.)

Although the anesthetic propofol is formulated as a 10 percent lipid emulsion, it should not be used for lipid rescue since the dose needed to treat local anesthetic toxicity would result in massive hypotension that may counteract any positive effect.

Checklists — The American Society of Regional Anesthesia and Pain Medicine has published a checklist for treatment of local anesthetic systemic toxicity [69]. A consensus statement by the Society for Obstetric Anesthesia and Perinatology on the management of SCA during pregnancy encouraged the use of checklists to improve team performance [37]. Maternal resuscitation guidelines from the AHA also encourage institutions to create and utilize checklists during obstetric crises and to institute mock code drills of maternal SCA.

IMAGING — Transesophageal echocardiography (TEE) and cardiopulmonary limited ultrasound examination (CLUE) are quick, portable, and reliable means of identifying potential causes of hemodynamic collapse during labor and delivery, such as pericardial effusion/tamponade and ventricular failure [70-76]. CLUE is more convenient and does not require interruption of ventilation if the patient has not yet been intubated.

TEE requires getting a probe and machine and stopping respiratory support during intubation of the esophagus with the TEE probe. After the patient has been intubated, the TEE probe can be inserted without interrupting ventilation. TEE can detect previously unrecognized cardiac conditions and is helpful for placement of venous and arterial cannulae for extracorporeal membrane oxygenation and placement of intraaortic balloon counterpulsation. TEE can also be utilized to assess the effects of intraaortic balloon counterpulsation and inotropic agents [77].

SELECTED CLINICAL SCENARIOS

Failure to respond to initial procedures — The following interventions may be appropriate for patients with SCA who fail to respond to standard resuscitative measures:

Direct cardiac massage – After 15 minutes of unsuccessful closed chest cardiopulmonary resuscitation (CPR), direct cardiac massage via thoracotomy or through the diaphragm (if the abdomen is open) can be implemented [78]. Direct cardiac massage results in near normal systemic perfusion throughout the compression cycle and with higher cranial and myocardial flow than achieved with external chest compressions of conventional CPR [79].

Intraaortic balloon pump, cardiopulmonary bypass, and extracorporeal membrane oxygenation – Intraaortic balloon pump, cardiopulmonary bypass, and extracorporeal membrane oxygenation have been used to treat patients with cardiovascular collapse, including those with pulmonary embolism, local anesthetic toxicity, recreational drug use such as cocaine, amniotic fluid embolism, and pulseless electrical activity. Case reports have described successful resuscitation using cardiopulmonary bypass intraoperatively during cesarean birth and postpartum in patients with amniotic fluid embolism and pulmonary embolism [70,80]. However, use of this technology is hampered by the preparation time required to institute the intervention. (See "Extracorporeal life support in adults in the intensive care unit: Overview" and "Amniotic fluid embolism".)

Extracorporeal life support — Extracorporeal life support (ECLS) uses a portable pump oxygenator outside of the cardiac operating room to provide extracorporeal membrane oxygenation (ECMO) in the ICU setting. There are two types of ECMO: venoarterial (VA) and venovenous (VV). Both provide respiratory support, but only VA ECMO provides hemodynamic support. Percutaneous cannulation is frequently utilized, rather than requiring surgical access. (See "Extracorporeal life support in adults in the intensive care unit: Overview".)

Extracorporeal cardiopulmonary resuscitation (ECPR) refers to utilization of VA ECMO as an adjunct to CPR for patients in cardiac arrest. ECLS and ECPR require expert multidisciplinary teams, specialized equipment, and "setup time," and are often only available at major medical centers. Significant improvements in technology have resulted in increasing utilization of ECLS and ECPR [81]. In a systematic review including 358 patients receiving ECLS during the peripartum period, overall 30-day survival was 75.4 percent [82]. Acute respiratory distress syndrome (ARDS) was the most common indication for ECLS, accounting for 49.4 percent. Cardiac failure accounted for 18.7 percent of cases. Cardiac arrest accounted for 15.9 percent, with a survival rate of 87.7 percent. Cardiac arrest was the indication for ECLS in 8.6 percent of cases with antepartum cardiac arrest and in 56.6 percent of cases of immediate postpartum ECLS. Fetal outcomes were reported in 68 cases where the mother was pregnant at the time the ECLS was initiated, including 36 deliveries performed in mothers on ECLS. Overall fetal survival was 64.7 percent with preterm birth occurring in 48.5 percent and neonatal ICU (NICU) admission in 27.9 percent. Maternal complications of ECLS included bleeding and intracranial neurologic morbidity, but the neurologically intact survival in this study was 78.9 percent.

There are no specific guidelines for the use of ECLS in pregnancy, but this review suggests that ECLS (including ECPR) can be considered in "catastrophic cardiopulmonary conditions." Identifying pregnant patients with acute cardiopulmonary decompensation and initiating ECLS prior to frank cardiac arrest may be beneficial, but has not been studied. The utility of ECPR is being studied in ongoing clinical trials, but pregnancy is an exclusion criterion for each of these trials [83]. More data are required in this area.  

ST elevation myocardial infarction — For pregnant patients with ST elevation myocardial infarction, percutaneous coronary intervention is the preferred reperfusion strategy since fibrinolytics are relatively contraindicated in pregnancy [84]. ST elevation myocardial infarction in pregnant patients may be secondary to coronary artery dissection; coronary artery catheterization is required for diagnosis and management. (See "Acute myocardial infarction and pregnancy" and "Spontaneous coronary artery dissection".)

Massive pulmonary embolism and ischemic stroke — Successful systemic thrombolysis has been reported for massive pulmonary embolism and for ischemic stroke during pregnancy [85]. If systemic thrombolysis is utilized, excessive bleeding may complicate imminent cesarean birth or the postoperative course of patients who recently gave birth. Transfusion of blood products should be anticipated: In one review of postpartum systemic thrombolytic therapy, blood transfusion was necessary in 12 of 13 cases, a large amount of blood was required for transfusion in 7 of these 12 cases, and laparotomy was eventually required to control bleeding in 5 of the 12 cases (including 3 hysterectomies) [86]. Severe bleeding was most common in patients who had a cesarean birth, and laparotomy was only necessary in patients who had a cesarean birth. Management of pulmonary embolism and ischemic stroke, including thrombolysis, is discussed separately. (See "Treatment, prognosis, and follow-up of acute pulmonary embolism in adults" and "Approach to thrombolytic (fibrinolytic) therapy in acute pulmonary embolism: Patient selection and administration" and "Initial assessment and management of acute stroke" and "Approach to reperfusion therapy for acute ischemic stroke".)

POSTARREST CARE — In the absence of the need for chest compression, the patient should be placed at 90 degrees left lateral tilt to avoid aortocaval compression, which can also occur postpartum since the uterus remains enlarged [20].

Core temperature lability is associated with increased mortality after in-hospital cardiac arrest. Hyperthermia should be avoided [87]. It is unclear whether therapeutic hypothermia is beneficial. The American Heart Association recommends avoiding routine use of therapeutic hypothermia because in undelivered patients it may not be safe for the fetus (pregnant patients have been excluded from trials on therapeutic hypothermia) and in postpartum patients it may impair coagulation and contribute to bleeding complications [20]. However, the induction of mild to moderate hypothermia (target temperature 32 to 34°C [89.6 to 93.2°F] for 24 hours) may be beneficial in comatose pregnant patients and has been used successfully in this setting [88,89]. It should also be considered in patients not following commands or showing purposeful movements following resuscitation from cardiac arrest. Temperature issues are discussed in more detail separately. (See "Initial assessment and management of the adult post-cardiac arrest patient", section on 'Temperature management'.)

In the hypothermic undelivered patient, the fetal heart rate may have a low baseline (90 to 100 beats per minute) with diminished variability [90]. Absent variability and fetal heart decelerations suggest deterioration in the fetal status; delivery should be considered if the fetus is at a viable gestational age.

OUTCOME — SCA in pregnant patients is associated with high maternal and fetal fatality rates (31.4 and 9 percent, respectively, in one large study [8]). Approximately 12 percent of maternal survivors and 21 percent of neonatal survivors had poor neurologic outcomes (cerebral performance category 3/4) in one such study [60]. Although there is a high risk of maternal mortality after cardiac arrest, in-hospital survival appears to be higher than that for nonpregnant, reproductive-age females [91,92]. This may be due to differences between the two groups in clinical risk factors and/or differences in intensity of patient monitoring among various hospital units.

Maternal and neonatal survival depends on several factors, including the underlying etiology for the arrest, pre-arrest hypotension/hypoperfusion, maternal location at the time of the arrest (out-of-hospital versus in-hospital; delivery suite versus other in-hospital sites [eg, ICU]), speed of resuscitative efforts, the skills and resources of the health care providers, and comorbidities (eg, disseminated intravascular coagulation without or with transfusion) [59,93,94]. A high survival rate in series with a high proportion of anesthetic complications may be due to the opportunity for immediate resuscitation in the operating room or labor and delivery room by skilled personnel with appropriate resources [95] and the possibility of better prearrest maternal condition.

SOCIETY GUIDELINE LINKS — Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Basic and advanced cardiac life support in adults" and "Society guideline links: Cardiac arrest in adults".)

SUMMARY AND RECOMMENDATIONS

Causes – The A through H mnemonic is useful as a reminder of the causes of sudden cardiac arrest (SCA) in pregnant patients (see 'Etiology' above):

A – Anesthetic complications, accident/trauma

B – Bleeding

C – Cardiac

D – Drugs

E – Embolic causes

F – Fever

G – General including hypoxia, electrolyte disturbances

H – Hypertension

Key resuscitation principles – Key principles for resuscitation of pregnant patients are (algorithm 1) (see 'Rapid overview of resuscitation' above):

Code blue – Call a maternal code blue, which should include a multidisciplinary team.

Uterine displacement – If the uterus is above the umbilicus, displace it off aortocaval vessels. We suggest manually displacing the uterus laterally to the patient's left rather than tilting the entire patient (Grade 2C). A hand is used to apply maximal leftward push to the right upper border of the uterus to achieve displacement of approximately 1.5 inches from the midline. Leave the upper torso supine. (See 'Avoiding aortocaval compression' above.)

Oxygenation – Assume a difficult airway. Bag-mask ventilation with 100 percent oxygen and suctioning of the airway are critical before intubation in a pregnant patient. Oxygenate well to avoid desaturation and avoid respiratory alkalosis; ventilation volumes may need to be lower than in nonpregnant females if the uterus is very large. (See 'Airway management' above.)

Chest compression – Place hands for chest compression at the same location, and perform compressions in the same way as in nonpregnant adults. (See 'Chest compressions' above.)

Defibrillation and medication management – Do not delay usual measures such as defibrillation and the administration of medications. Energy requirements for adult defibrillation are the same as in nonpregnant females. All medications at the same doses for treatment of cardiopulmonary arrest in the nonpregnant patient are used for the pregnant patient. (See 'Defibrillation' above and 'Use of medications for resuscitation during pregnancy' above.)

Resuscitative newborn delivery at four minutes

-Designate a dedicated timer to notify the resuscitation team when four minutes have elapsed after the onset of a maternal cardiac arrest. (See 'Delivery as part of the resuscitation process' above.)

-If there is no return of spontaneous circulation with the usual resuscitation measures and the uterine fundus is at or beyond the umbilicus, we agree with the American Heart Association guidelines that recommend expeditious perimortem cesarean birth (resuscitative hysterotomy) (Grade 1C). Ideally, the cesarean should be started at four minutes following cardiac arrest and delivery of the newborn completed by five minutes following the arrest. Delivery early in the resuscitation process is a key intervention for improving success rates in pregnant patients.

-Operative vaginal birth using forceps or vacuum is appropriate if the neonate can be delivered within five minutes of maternal cardiorespiratory collapse (eg, if the head is on the perineum). (See 'Delivery as part of the resuscitation process' above.)

-Perform delivery (cesarean or vaginal) at the site of resuscitation. (See 'Delivery issues' above.)

Role of postarrest hypothermia – Postarrest, induction of mild to moderate hypothermia (target temperature 32 to 34°C [89.6 to 93.2°F] for 24 hours) is reasonable in patients who are comatose or not following commands or showing purposeful movements following resuscitation. It is not used routinely because in undelivered patients it may not be safe for the fetus and in postpartum patients it may impair coagulation and contribute to bleeding complications. (See 'Postarrest care' above.)

Prognosis – Cardiac arrest in pregnant patients is associated with high maternal and neonatal fatality rates. Survival of the mother and neonate depends on several factors, including the underlying etiology for the arrest, maternal location at the time of the arrest (out-of-hospital versus in-hospital, location in hospital), speed of resuscitative efforts, and the skills and resources of the health care providers. (See 'Outcome' above.)

  1. Zelop CM, Grimes EP. Cardiopulmonary Resuscitation in Pregnancy. In: The textbook of Emergency Cardiovascular Care and CPR, Field JM, Kudenchuk PJ, O'Connor RE (Eds), Wolters Kluwer, Philadelphia 2009. p.538.
  2. Al-Khatib SM, Stevenson WG, Ackerman MJ, et al. 2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society. Circulation 2018; 138:e272.
  3. Priori SG, Blomström-Lundqvist C, Mazzanti A, et al. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC). Eur Heart J 2015; 36:2793.
  4. Regitz-Zagrosek V, Roos-Hesselink JW, Bauersachs J, et al. 2018 ESC Clinical Practice Guidelines for the management of cardiovascular diseases during pregnancy. Eur Heart J 2018.
  5. Creanga AA, Syverson C, Seed K, Callaghan WM. Pregnancy-Related Mortality in the United States, 2011-2013. Obstet Gynecol 2017; 130:366.
  6. Brickner ME. Cardiovascular management in pregnancy: congenital heart disease. Circulation 2014; 130:273.
  7. Zelop CM, Einav S, Mhyre JM, et al. Characteristics and outcomes of maternal cardiac arrest: A descriptive analysis of Get with the guidelines data. Resuscitation 2018; 132:17.
  8. Ford ND, DeSisto CL, Galang RR, et al. Cardiac Arrest During Delivery Hospitalization : A Cohort Study. Ann Intern Med 2023; 176:472.
  9. Eckart RE, Shry EA, Burke AP, et al. Sudden death in young adults: an autopsy-based series of a population undergoing active surveillance. J Am Coll Cardiol 2011; 58:1254.
  10. Topaz O, Edwards JE. Pathologic features of sudden death in children, adolescents, and young adults. Chest 1985; 87:476.
  11. Drory Y, Turetz Y, Hiss Y, et al. Sudden unexpected death in persons less than 40 years of age. Am J Cardiol 1991; 68:1388.
  12. Puranik R, Chow CK, Duflou JA, et al. Sudden death in the young. Heart Rhythm 2005; 2:1277.
  13. di Gioia CR, Autore C, Romeo DM, et al. Sudden cardiac death in younger adults: autopsy diagnosis as a tool for preventive medicine. Hum Pathol 2006; 37:794.
  14. Pilmer CM, Porter B, Kirsh JA, et al. Scope and nature of sudden cardiac death before age 40 in Ontario: a report from the cardiac death advisory committee of the office of the chief coroner. Heart Rhythm 2013; 10:517.
  15. de Noronha SV, Behr ER, Papadakis M, et al. The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths. Europace 2014; 16:899.
  16. Suresh MS, LaToya Mason C, Munnur U. Cardiopulmonary resuscitation and the parturient. Best Pract Res Clin Obstet Gynaecol 2010; 24:383.
  17. Mhyre JM, Tsen LC, Einav S, et al. Cardiac arrest during hospitalization for delivery in the United States, 1998-2011. Anesthesiology 2014; 120:810.
  18. Krexi D, Sheppard MN. Cardiovascular causes of maternal sudden death. Sudden arrhythmic death syndrome is leading cause in UK. Eur J Obstet Gynecol Reprod Biol 2017; 212:155.
  19. Beckett VA, Knight M, Sharpe P. The CAPS Study: incidence, management and outcomes of cardiac arrest in pregnancy in the UK: a prospective, descriptive study. BJOG 2017.
  20. Jeejeebhoy FM, Zelop CM, Lipman S, et al. Cardiac Arrest in Pregnancy: A Scientific Statement From the American Heart Association. Circulation 2015; 132:1747.
  21. Roos-Hesselink JW, Ruys TP, Stein JI, et al. Outcome of pregnancy in patients with structural or ischaemic heart disease: results of a registry of the European Society of Cardiology. Eur Heart J 2013; 34:657.
  22. Siu SC, Sermer M, Colman JM, et al. Prospective multicenter study of pregnancy outcomes in women with heart disease. Circulation 2001; 104:515.
  23. Silka MJ, Hardy BG, Menashe VD, Morris CD. A population-based prospective evaluation of risk of sudden cardiac death after operation for common congenital heart defects. J Am Coll Cardiol 1998; 32:245.
  24. Roos-Hesselink J, Baris L, Johnson M, et al. Pregnancy outcomes in women with cardiovascular disease: evolving trends over 10 years in the ESC Registry Of Pregnancy And Cardiac disease (ROPAC). Eur Heart J 2019; 40:3848.
  25. Silversides CK, Grewal J, Mason J, et al. Pregnancy Outcomes in Women With Heart Disease: The CARPREG II Study. J Am Coll Cardiol 2018; 71:2419.
  26. Ueland K, Novy MJ, Peterson EN, Metcalfe J. Maternal cardiovascular dynamics. IV. The influence of gestational age on the maternal cardiovascular response to posture and exercise. Am J Obstet Gynecol 1969; 104:856.
  27. Holmes S, Kirkpatrick ID, Zelop CM, Jassal DS. MRI evaluation of maternal cardiac displacement in pregnancy: implications for cardiopulmonary resuscitation. Am J Obstet Gynecol 2015; 213:401.e1.
  28. Rose CH, Faksh A, Traynor KD, et al. Challenging the 4- to 5-minute rule: from perimortem cesarean to resuscitative hysterotomy. Am J Obstet Gynecol 2015; 213:653.
  29. Dijkman A, Huisman CM, Smit M, et al. Cardiac arrest in pregnancy: increasing use of perimortem caesarean section due to emergency skills training? BJOG 2010; 117:282.
  30. Johnson MD, Luppi CJ, Over DC. Cardiopulmonary Resuscitation. In: Obstetric Anesthesia and Uncommon problems, Gambling, DR, Douglas, MJ (Eds), Saunders, Philadelphia 1998. p.51.
  31. Doan-Wiggins L. Resuscitation of the pregnant patient suffering death. In: Cardiac Arrest: the science and practice of resuscitation medicine, Turrentine MA, Braems G, Ramirez MM (Eds), Williams and Wilkins, Philadelphia 1997. p.812.
  32. Pernoll ML, Metcalfe J, Schlenker TL, et al. Oxygen consumption at rest and during exercise in pregnancy. Respir Physiol 1975; 25:285.
  33. Baldwin GR, Moorthi DS, Whelton JA, MacDonnell KF. New lung functions and pregnancy. Am J Obstet Gynecol 1977; 127:235.
  34. Hankins GD, Harvey CJ, Clark SL, et al. The effects of maternal position and cardiac output on intrapulmonary shunt in normal third-trimester pregnancy. Obstet Gynecol 1996; 88:327.
  35. Cheun JK, Choi KT. Arterial oxygen desaturation rate following obstructive apnea in parturients. J Korean Med Sci 1992; 7:6.
  36. Andersen GJ, James GB, Mathers NP, et al. The maternal oxygen tension and acid-base status during pregnancy. J Obstet Gynaecol Br Commonw 1969; 76:16.
  37. Lipman S, Cohen S, Einav S, et al. The Society for Obstetric Anesthesia and Perinatology consensus statement on the management of cardiac arrest in pregnancy. Anesth Analg 2014; 118:1003.
  38. Levinson G, Shnider SM, DeLorimier AA, Steffenson JL. Effects of maternal hyperventilation on uterine blood flow and fetal oxygenation and acid-base status. Anesthesiology 1974; 40:340.
  39. Kundra P, Khanna S, Habeebullah S, Ravishankar M. Manual displacement of the uterus during Caesarean section. Anaesthesia 2007; 62:460.
  40. Rees GA, Willis BA. Resuscitation in late pregnancy. Anaesthesia 1988; 43:347.
  41. Nanson J, Elcock D, Williams M, Deakin CD. Do physiological changes in pregnancy change defibrillation energy requirements? Br J Anaesth 2001; 87:237.
  42. Soar J, Perkins GD, Abbas G, et al. European Resuscitation Council Guidelines for Resuscitation 2010 Section 8. Cardiac arrest in special circumstances: Electrolyte abnormalities, poisoning, drowning, accidental hypothermia, hyperthermia, asthma, anaphylaxis, cardiac surgery, trauma, pregnancy, electrocution. Resuscitation 2010; 81:1400.
  43. Chu J, Johnston TA, Geoghegan J, Royal College of Obstetricians and Gynaecologists. Maternal Collapse in Pregnancy and the Puerperium: Green-top Guideline No. 56. BJOG 2020; 127:e14.
  44. Lipman S, Daniels K, Cohen SE, Carvalho B. Labor room setting compared with the operating room for simulated perimortem cesarean delivery: a randomized controlled trial. Obstet Gynecol 2011; 118:1090.
  45. O'Connor RL, Sevarino FB. Cardiopulmonary arrest in the pregnant patient: a report of a successful resuscitation. J Clin Anesth 1994; 6:66.
  46. Cordero DR, Toffle RC, McCauley CS. Cardiopulmonary arrest in pregnancy: the role of caesarean section in the resuscitative protocol. W V Med J 1992; 88:402.
  47. DePace NL, Betesh JS, Kotler MN. 'Postmortem' cesarean section with recovery of both mother and offspring. JAMA 1982; 248:971.
  48. Katz V, Balderston K, DeFreest M. Perimortem cesarean delivery: were our assumptions correct? Am J Obstet Gynecol 2005; 192:1916.
  49. Katz VL, Dotters DJ, Droegemueller W. Perimortem cesarean delivery. Obstet Gynecol 1986; 68:571.
  50. KERR MG. THE MECHANICAL EFFECTS OF THE GRAVID UTERUS IN LATE PREGNANCY. J Obstet Gynaecol Br Commonw 1965; 72:513.
  51. Eldridge AJ, Ford R. Perimortem caesarean deliveries. Int J Obstet Anesth 2016; 27:46.
  52. Cardosi RJ, Porter KB. Cesarean delivery of twins during maternal cardiopulmonary arrest. Obstet Gynecol 1998; 92:695.
  53. Finegold H, Darwich A, Romeo R, et al. Successful resuscitation after maternal cardiac arrest by immediate cesarean section in the labor room. Anesthesiology 2002; 96:1278.
  54. Oates S, Williams GL, Rees GA. Cardiopulmonary resuscitation in late pregnancy. BMJ 1988; 297:404.
  55. Parker J, Balis N, Chester S, Adey D. Cardiopulmonary arrest in pregnancy: successful resuscitation of mother and infant following immediate caesarean section in labour ward. Aust N Z J Obstet Gynaecol 1996; 36:207.
  56. Troiano NH. Cardiopulmonary resuscitation of the pregnant woman. J Perinat Neonatal Nurs 1989; 3:1.
  57. Dildy GA, Clark SL. Cardiac arrest during pregnancy. Obstet Gynecol Clin North Am 1995; 22:303.
  58. Ram M, Lavie A, Lev S, et al. Cardiac hemodynamics before, during and after elective cesarean section under spinal anesthesia in low-risk women. J Perinatol 2017; 37:793.
  59. Baghirzada L, Balki M. Maternal cardiac arrest in a tertiary care centre during 1989-2011: a case series. Can J Anaesth 2013; 60:1077.
  60. Einav S, Kaufman N, Sela HY. Maternal cardiac arrest and perimortem caesarean delivery: evidence or expert-based? Resuscitation 2012; 83:1191.
  61. ACOG Practice Bulletin No. 211: Critical Care in Pregnancy. Obstet Gynecol 2019; 133:e303.
  62. Tyson JE, Parikh NA, Langer J, et al. Intensive care for extreme prematurity--moving beyond gestational age. N Engl J Med 2008; 358:1672.
  63. Weinberg GL. Current concepts in resuscitation of patients with local anesthetic cardiac toxicity. Reg Anesth Pain Med 2002; 27:568.
  64. Soltesz EG, van Pelt F, Byrne JG. Emergent cardiopulmonary bypass for bupivacaine cardiotoxicity. J Cardiothorac Vasc Anesth 2003; 17:357.
  65. Picard J, Ward SC, Zumpe R, et al. Guidelines and the adoption of 'lipid rescue' therapy for local anaesthetic toxicity. Anaesthesia 2009; 64:122.
  66. Rosenblatt MA, Abel M, Fischer GW, et al. Successful use of a 20% lipid emulsion to resuscitate a patient after a presumed bupivacaine-related cardiac arrest. Anesthesiology 2006; 105:217.
  67. Litz RJ, Popp M, Stehr SN, Koch T. Successful resuscitation of a patient with ropivacaine-induced asystole after axillary plexus block using lipid infusion. Anaesthesia 2006; 61:800.
  68. Weinberg GL. Treatment of local anesthetic systemic toxicity (LAST). Reg Anesth Pain Med 2010; 35:188.
  69. Neal JM, Woodward CM, Harrison TK. The American Society of Regional Anesthesia and Pain Medicine Checklist for Managing Local Anesthetic Systemic Toxicity: 2017 Version. Reg Anesth Pain Med 2018; 43:150.
  70. Stanten RD, Iverson LI, Daugharty TM, et al. Amniotic fluid embolism causing catastrophic pulmonary vasoconstriction: diagnosis by transesophageal echocardiogram and treatment by cardiopulmonary bypass. Obstet Gynecol 2003; 102:496.
  71. Katz J, Shear TD, Murphy GS, et al. Cardiovascular Collapse in the Pregnant Patient, Rescue Transesophageal Echocardiography and Open Heart Surgery. J Cardiothorac Vasc Anesth 2017; 31:203.
  72. James CF, Feinglass NG, Menke DM, et al. Massive amniotic fluid embolism: diagnosis aided by emergency transesophageal echocardiography. Int J Obstet Anesth 2004; 13:279.
  73. Burrage PS, Shernan SK, Tsen LC, et al. Emergent transesophageal echocardiography in hemodynamically unstable obstetric patients. Int J Obstet Anesth 2015; 24:131.
  74. Ashford EJ, Klimkina O, Hassan ZU, et al. Transesophageal echocardiography monitoring in the delivery of a preeclamptic parturient with severe left ventricular noncompaction. J Clin Anesth 2014; 26:490.
  75. Kapoor PM, Goyal S, Irpachi K, Smita B. Importance of transesophageal echocardiography in peripartum cardiomyopathy undergoing lower section cesarean section under regional anesthesia. J Anaesthesiol Clin Pharmacol 2014; 30:427.
  76. Ortner CM, Krishnamoorthy V, Neethling E, et al. Point-of-Care Ultrasound Abnormalities in Late-Onset Severe Preeclampsia: Prevalence and Association With Serum Albumin and Brain Natriuretic Peptide. Anesth Analg 2019; 128:1208.
  77. Ecker JL, Solt K, Fitzsimons MG, MacGillivray TE. Case records of the Massachusetts General Hospital. Case 40-2012. A 43-year-old woman with cardiorespiratory arrest after a cesarean section. N Engl J Med 2012; 367:2528.
  78. Lee RV, Rodgers BD, White LM, Harvey RC. Cardiopulmonary resuscitation of pregnant women. Am J Med 1986; 81:311.
  79. Babbs CF. Hemodynamic mechanisms in CPR: a theoretical rationale for resuscitative thoracotomy in non-traumatic cardiac arrest. Resuscitation 1987; 15:37.
  80. Marty AT, Hilton FL, Spear RK, Greyson B. Postcesarean pulmonary embolism, sustained cardiopulmonary resuscitation, embolectomy, and near-death experience. Obstet Gynecol 2005; 106:1153.
  81. ELSO Live Registry Dashboard of ECMO Patient Data. Extracorporeal Life Support Organization. Available at: https://www.elso.org/Registry/ELSOLiveRegistryDashboard.aspx (Accessed on October 05, 2022).
  82. Naoum EE, Chalupka A, Haft J, et al. Extracorporeal Life Support in Pregnancy: A Systematic Review. J Am Heart Assoc 2020; 9:e016072.
  83. Kalra R, Kosmopoulos M, Goslar T, et al. Extracorporeal cardiopulmonary resuscitation for cardiac arrest. Curr Opin Crit Care 2020; 26:228.
  84. ECC Committee, Subcommittees and Task Forces of the American Heart Association. 2005 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 2005; 112:IV1.
  85. Holden EL, Ranu H, Sheth A, et al. Thrombolysis for massive pulmonary embolism in pregnancy--a report of three cases and follow up over a two year period. Thromb Res 2011; 127:58.
  86. Akazawa M, Nishida M. Thrombolysis with intravenous recombinant tissue plasminogen activator during early postpartum period: a review of the literature. Acta Obstet Gynecol Scand 2017; 96:529.
  87. Nielsen N, Wetterslev J, Cronberg T, et al. Targeted temperature management at 33°C versus 36°C after cardiac arrest. N Engl J Med 2013; 369:2197.
  88. Rittenberger JC, Kelly E, Jang D, et al. Successful outcome utilizing hypothermia after cardiac arrest in pregnancy: a case report. Crit Care Med 2008; 36:1354.
  89. Chauhan A, Musunuru H, Donnino M, et al. The use of therapeutic hypothermia after cardiac arrest in a pregnant patient. Ann Emerg Med 2012; 60:786.
  90. Aboud E, Neales K. The effect of maternal hypothermia on the fetal heart rate. Int J Gynaecol Obstet 1999; 66:163.
  91. Mogos MF, Salemi JL, Spooner KK, et al. Differences in Mortality Between Pregnant and Nonpregnant Women After Cardiopulmonary Resuscitation. Obstet Gynecol 2016; 128:880.
  92. Lavecchia M, Abenhaim HA. Cardiopulmonary resuscitation of pregnant women in the emergency department. Resuscitation 2015; 91:104.
  93. Cantwell R, Clutton-Brock T, Cooper G, et al. Saving Mothers' Lives: Reviewing maternal deaths to make motherhood safer: 2006-2008. The Eighth Report of the Confidential Enquiries into Maternal Deaths in the United Kingdom. BJOG 2011; 118 Suppl 1:1.
  94. Zelop CM, Shaw RE, Edelson DP, et al. Factors associated with non-survival from in-hospital maternal cardiac arrest: An analysis of Get With The Guidelines® (GWTG) data. Resuscitation 2021; 164:40.
  95. Balki M, Liu S, León JA, Baghirzada L. Epidemiology of Cardiac Arrest During Hospitalization for Delivery in Canada: A Nationwide Study. Anesth Analg 2017; 124:890.
Topic 14184 Version 48.0

References

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