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Anesthetic andPerioperative
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Management
2
Abstract
To provide safe anesthesia for mother and
fetus following goals should be reached: (1)
optimization and maintenance of normal
maternal physiological function, (2) optimization and maintenance of uteroplacental
blood ow and oxygen delivery, (3) avoidance of unwanted drug effects on the fetus,
(4) avoidance of stimulating the myometrium
(oxytocic effects), (5) avoidance of maternal
awareness during general anesthesia, and (6)
use of regional anesthesia, if possible.
Sugammadex rapidly reverses neuromuscular blockade without fetal harm. Antibiotics
and thromboprophylaxis are the most common medications administered for acute
abdomen during pregnancy. Antibiotics
should be administered according to the FDA
drug classes. Anesthetic management is challenging in patients with abdominal trauma or
polytrauma when in addition to hemorrhagic
shock, there are problems with the patient’s
airway management. Preoperative and postoperative fetal monitoring is essential for
early recognition of fetal distress, inuencing the timing and type of combined obstetric
and surgical intervention.
2.1 Anesthetic Management
Before discussing anesthesiologic issues related
to the acute abdomen during pregnancy, it is
important to stress that a delay in indicating and
performing necessary surgery leads to worse
maternal and fetal outcomes.
A pregnant woman should never be denied
medically necessary surgery or have that surgery delayed regardless of trimester because
this can adversely affect the pregnant woman
and her fetus. (ACOG 2019 [1])
To provide safe anesthesia for the mother and
fetus, following goals should be reached:
• optimization and maintenance of normal
maternal physiological function,
• optimization and maintenance of uteroplacen-
tal blood ow and oxygen delivery,
• avoidance of unwanted drug effects on the
fetus,
• avoidance of stimulating the myometrium
(oxytocic effects),
• avoidance of maternal awareness during gen-
eral anesthesia,
• use of regional anesthesia, if possible.
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023
G. Augustin, Acute Abdomen During Pregnancy, https://doi.org/10.1007/978-3-031-26021-6_2
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2.1.1 Anesthetic Medications
2.1.1.1 General Anesthesia
Anesthetic concerns in the pregnant patient
include two major categories: teratogenicity of
the anesthetic agents and maternal physiological
changes resulting fromanesthetic agents.
Therefore, strategies to minimize maternal and
fetal exposure to anesthetics are essential
(Table2.1).
The teratogenicity of anesthetic agents,
resulting in fetal chromosomal damage or carcinogenesis, is minimal. Any morbidity to the
fetus is considered primarily from the underlying disease, not the anesthetic agent [2, 3].
There is no increased rate of congenital anomalies with different types of anesthesia used in
surgery during pregnancy [4, 5]. In a consensus
statement published in the New England Journal
of Medicine in 2000, no anesthetic agents were
listed as denitively causative of fetal malformations [6]. Although without clinical teratogenic outcomes, thetheoretical risk should not
be completely disregarded. Many agree that surgery during the rst trimester, the period of
organogenesis, should be avoided if not emergent [3, 7, 8]. Table2.2 shows the list of common anesthetic drugs and their classication per
FDA category.
Several points should be stressed when considering the possible teratogenicity of various
anesthetic agents. First, the background incidence of congenital anomalies in humans is
approximately 3%. Second, physiologic derangements such as hypoxemia, hypercarbia, stress,
and hypotension may be teratogenic. These problems can occur during anesthesia and surgery and
sometimes exist preoperatively [10].
No currently used anesthetic agents have
been shown to have any teratogenic effects
in humans when using standard concentra-
tions at any gestational age. (ACOG 2019
[1])
Table 2.1 Strategies to minimize patient exposure to and dose and duration of anesthetics
Type of surgery Anesthetic technique Suggested modication/recommendation
Obstetric Neuraxial (epidural or spinal) utilizing
local anesthetics±opioids
Non-obstetric (non-emergent) Neuraxial as above (if applicable) or None
General anesthesia utilizing inhalational
agents
Non-obstetric (emergent) General anesthesia utilizing inhalational
agents
Fetal procedures Local anesthesia No change
Neuraxial anesthesia No change
IV sedative—hypnotic—propofol <3h duration—no change
IV sedative—Midazolam Consider IV opioids (fentanyl or
General anesthesia with inhalational
agents
General anesthesia with increased
concentration of inhalational agents for
uterine relaxation
Reproduced with permission from [9]
IV intravenous
a
Atosiban is not approved for use in the USA by the FDA
b
Nitroglycerin is difcult to titrate to effect, may result in intractable hypotension and/or pulmonary edema
None
<3h duration—No change
>3h durations—consider deferring until
postpartum
Limit times:
(a) Between induction and start of
surgery and
(b) Between end of surgery and end
of anesthesia
>3h duration—discuss risk/benet
remifentanil) or IV dexmedetomidine
<3h duration—no change
>3h duration—discuss risk/benet
Consider supplementing with
magnesium sulfate, Atosibana or
Nitroglycerinb for intraoperative
tocolysis

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Table 2.2 The placental transfer characteristics of commonly used anesthetic drugs
Placental
Drug Properties
Induction agents
Thiopental Highly lipid soluble, weak
acid
Propofol Lipid soluble +++ Transient depression of Apgar score and
Ketamine Weak base ++++ F/M ratio 1.26 occurs within 2min of
Inhalation agents
Volatile anesthetics Highly lipid soluble; low
molecular weight
Nitrous oxide ++ Possible diffusion hypoxia in neonate
Opioids
Morphine Less lipid soluble; but low
protein-binding
Fentanyl Lipid soluble +++
Pethidine Only 50% plasma protein
bound
Remifentanil + No adverse fetal effects as rapidly
Naloxone +++ Though short-term safety of naloxone is
Benzodiazepine Highly lipid soluble ++ More neonatal depression, midazolam—
NM blockers Large molecules; poorly lipid
soluble; highly ionized
Anticholinergics
Atropine Lipid soluble; tertiary amine ++
Glycopyrrolate Fully ionized; quaternary
ammonium compound
Neostigmine Quaternary ammonium
compound; but a small
molecule
Local anesthetics
Lignocaine Less lipid soluble; low
protein binding
Bupivacaine;
ropivacaine
Reproduced with permission from [10] under the CC BY 3.0
F/M fetal/maternal, NM neuromuscular
Highly lipid soluble; but high
protein binding
transfer Remarks
+++ Quickly cleared by neonate after delivery
neurobehavioral effects in neonate
intravenous bolus
+++ Greater sedative effect on neonate if
dose-delivery interval is prolonged
++
++ Prolonged neonatal depression due to
increased half-life of meperidine and its
metabolite—normeperidine
metabolized by fetus
well documented, it should be used only in
cases of absolute or relative maternal
opioid overdose
less placental transfer than diazepam
− No signicant clinical effects on fetus
−
+++ May cause fetal bradycardia; hence it is
better to add atropine to neostigmine in
incidental surgery during pregnancy
++ Can accumulate in the fetus due to “ion
trapping” if the fetus becomes acidotic
++
19
The drugs crossing the placenta may be categorized into three types. In type 1 (e.g., thiopental),
the complete transfer occurs with equilibrating
maternal and fetal blood concentrations. In type 2
(e.g., ketamine), the drug reaches a higher concentration in fetal blood than maternal blood. Only a
minimal amount reaches the fetal blood in type 3
(e.g., succinylcholine).
Sugammadex encapsulates rocuronium and
vecuronium molecules, aminosteroid agents
commonly used in general anesthesia [11]. The
combination of rocuronium and sugammadex for
rapid-sequence induction combines rapid onset
and rapid reversal of neuromuscular blockades
with avoidance of severe side effects. It is a very
comfortable combination during Cesarean section (CS) [12]. Although the impact of pregnancy
on the volume of distribution of sugammadex is
unknown, the effectiveness of rocuronium block
reversal following 2 or 4mg/kg sugammadex has

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been conrmed [13]. Rapid neuromuscular
blockade reversal is conrmed in myasthenia
gravis patients during CS [14].
There is concern about sugammadex’s ability
to encapsulate progesterone and reduce progesterone levels. Interaction with hormonal contraceptives raises the question of the adverse effects
of sugammadex administration on the maintenance of the rst trimester of pregnancy. A study
on rats in the rst trimester of pregnancy did not
babies are healthy, without congenital abnormalities [16]. Sugammadex’s effects on female reproductive function, pregnancy, and puerperium are
presented in Table2.3.
Magnesium sulfate is used to prevent uterine
contractions and preterm labor (see Sect. 4.6.2.1),
enhancing the effect of rocuronium. It does not
signicantly affect the efcacy of sugammadexin, reversing rocuronium-induced neuromuscular blockade [18].
show adverse effects. They did not affect the successful completion of pregnancy without stillbirth or miscarriage [15]. In a case series of
pregnant patients undergoing non-obstetric surgery, all fetuses showed good vitality in the cardiotocogram performed after the procedure. All
Table 2.3 Effects of Sugammadex on female reproductive function, pregnancy, delivery, and lactation [17]
Context Current evidence Research gaps
Women of reproductive
potential
Maintenance of early
pregnancy
Maternal–fetal placental
transfer
Fetal effects Primary cell cultures: Sugammadex alone in
Cesarean delivery Sugammadex reversal of rocuronium is reported
Lactating women Single preclinical study (unpublished)
In vitro studies (unpublished) indicate that
sugammadex binds progesterone, theoretically
reducing hormone levels to an extent that is
equivalent to missing dose(s) of hormonal
contraception (oral, IUD, injectable). This has
prompted manufacturer to recommend barrier
contraception for 1week following sugammadex
exposure
Single preclinical study: high-dose sugammadex
(30mg/kg) administered to rst trimester
pregnant rats failed to reduce endogenous
progesterone levels or alter live birth or stillbirth
rates
Large molecular mass and polarization in
aqueous solution predict limited placental
transfer
clinically relevant concentrations has been
reported to promote neuronal apoptosis in
primary cultures, possibly due to oxidative stress
from depletion of neuronal cholesterol
Mice: No neuronal apoptosis (healthy, mature
blood–brain barrier is impermeable to
sugammadex). Sugammadex combined with
sevourane, which disrupts blood–barrier
integrity, results in greater degree of neuronal
apoptosis than sevourane alone
to be safe and effective in parturients at the end
of CD surgery. This includes patients with
profound NMB (1 posttetanic twitch) reversed
with 4mg/kg (actual body weight)
demonstrated peak sugammadex milk levels
30min after maternal administration in postnatal
rats without detectable adverse effects on offspring
2.1.1.2 Sedation andSpinal Anesthesia
Sedation in pregnancy has always been a challenge
to anesthetists. During ERCP in pregnant patients,
sedation could have side effects from the maternal
prone position. Therefore, fetal and maternal moni-
Actual clinical risk of unintended
pregnancy due to contraceptive
failure after sexual intercourse
without barrier contraception
following sugammadex exposure is
unknown
No human evidence
No evidence regarding placental
transfer
Limited preclinical evidence. No
human evidence
Effectiveness of sugammadex rescue
reversal in cannot intubate/cannot
ventilate after 1–1.2mg/kg
rocuronium (rapid sequence
induction) has not been established
or reported
No evidence exists regarding the
presence of sugammadex in human
breast milk

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toring is mandatory [19, 20]. Following electrocardiography, noninvasive blood pressure
measurement, pulse oximetry, and fetal heart rate
monitoring (FHR) devices are applied. Insufation
of oxygen at a ow rate of 6L/min is maintained
throughout the procedure. The patients are placed in
a left lateral to a prone position. Fetal shielding is
accomplished with a lead apron placed between the
radiation source and the patient. Although there is
no proof of human teratogenicity for anesthetic
drugs, inhaled or local, all agents administered during pregnancy must be used with caution and vigilance. Currently, the best options are propofol,
midazolam, and fentanyl. Propofol is preferred as a
short-acting agent because it can be titrated easily
and has a good recovery, with a low incidence of
nausea and vomiting. Alternatively, midazolam can
be used because of its specic amnesic and anxiolytic properties. The analgesic component of this
sedation regimen is opioids. All drugs are given in
incremental doses to prevent hemodynamic and
respiratory changes in the mother and fetus during
the procedure. The most commonly conscious sedation is achieved and maintained with intravenous
midazolam 3–5 mg and duodenal hypomotility
induced by hyoscine-N-butylbromide 20mg [21].
In utero human exposure to anesthetic or
sedative drugs has no effect on the developing brain, and no animal data support an
effect with exposures less than 3h. (ACOG
Committee opinion 2019 [1])
Spinal anesthesia is widely used for
CS.Although safe, nausea, vomiting, and hypotension are frequent after spinal anesthesia
despite prehydration and left uterus displacement [22]. This is attributed to the greater aortocaval compression and greater cephalad spread
of sensory blockade by an enlarged uterus. MRI
shows a gestation-related reduction in cerebrospinal uid volume and dural sac surface area
associated with the engorged veins in the epidural space [23]. The question is whether spinal
anesthesia is effective in conditions with
increased intra- abdominal pressure (IAP).
Whether spinal local anesthetic spread in pregnant patients shows the association between
pre-incision IAP and maximum sensory block
levels is unclear [24, 25].
With an inguinal hernia, severe postoperative
complications are lower under local anesthesia,
including fewer postoperative analgesic requirements and fewer micturition problems [26].
Operating under general anesthesia in emergency
settings is better due to possible unexpected
intraoperative ndings.
2.1.2 Airway Management
Airway management becomes particularly problematic due to the physiologic changes during
pregnancy. Increased oxygen consumption and
mechanical displacement of the abdominal
organs cause the pregnant patient to increase
minute ventilation, primarily through a 30–40%
increase in tidal volume [27]. A compensatory
respiratory alkalosis with a PaCO2 from 30 to
35 mmHg develops. End-tidal CO2 monitoring
should be used intraoperatively.
The success of regional anesthesia in this population owes its popularity mainly to the airway
complications that general anesthesia entails.
Airway complications are more prevalent in a
parturient receiving general anesthesia than those
having regional techniques [28]. Unique issuesfor the gravid patient in airway management are:
• increased risk of aspiration due to delayed
gastric emptying and decreased lower esopha-
geal sphincter tone in combination with
increased intra-abdominal pressure,
• despite the safety of rapid-sequence intuba-
tion in pregnancy, because of lower serum
pseudocholinesterase levels in pregnancy,
using a lower dose of succinylcholine during
induction is recommended,
• both depolarizing and nondepolarizing muscle
relaxants cross the placenta. Effects of these
drugs on CTG pattern and fetal activity might
lead to a falsely non-reassuring tracing and
non-indicated intervention.

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A nasogastric tube inserted in a semiconscious or unconscious, injured pregnant
woman prevents aspiration of gastric contents [29].
Additionally, vascular engorgement of the
respiratory tract during pregnancy may lead to
tracheal intubation difculties. Edema in the airways leads to friable tissues, increased potential
for bleeding, and the necessity to use smallersized endotracheal tubes in the parturient [30].
Because decreased lower esophageal sphincter
pressure and delayed gastric emptying in pregnancy can cause an increased risk of aspiration,
cricoid pressure prevents aspiration during intubation [31]. Therefore, rapid-sequence intubation
is preferred for the parturient facing an emergent
abdominal operation with a full stomach [30].
Also, the underlying cause of acute abdomen,
Fig. 2.1 Left lateral tilt relieves pressure on inferior vena
cava in pregnant women
intraoperative strategy, and possible intraoperative complications mandates general anesthesia.
Other compounding airway issues include
weight gain, increased breast size, decreased functional residual capacity, increased oxygen consumption, and the potential for aortal and venocaval
compression in the supine position during intubation. These issues may lead to rapid desaturation,
potentially lower cardiac output, placental-fetal
compromise, and asphyxia during delayed attempts
2.1.2.1 Diaphragmatic Hernia
The affected side is placed uppermost if a herniais approached through a thoracotomy [32].
Mediastinal shift, which compromises venous
return and collapse of the lower lung, may be
worsened by positional compression from the
herniated dilated viscera. A rapid-sequence
induction is indicated because the patient is at
risk of pulmonary aspiration.
at securing the parturient’s airway. In addition to
these physiologic changes, disease-induced hypotension should be treated initially with aggressive
intravenous uid resuscitation. If possible, the
patient should be placed in the left lateral decubitus
positionto decompress the inferior vena cava to
increase venous return (Fig. 2.1). Trendelenburg
positioning can also increase the venous return in
the hypotensive patient [2].
General endotracheal anesthesia is preferred
for CS to manage acute abdomen and early postoperative period. General anesthesia allows
greater hemodynamic control and facilitates
management of the acid-base status, especially in
patients receiving epoprostenol for CVVH in
acute pancreatitis during pregnancy.
Anticoagulation is better titrated, including heparin in sepsis. Postoperative ventilatory support in
ICU permits the resolution of acidosis.
lation may be advantageous with atraumatic diaphragmatic hernia to expand the atelectatic lung,
increase functional residual capacity, and deliver
high oxygen concentrations. Lung ventilation
must be undertaken with low tidal volume or low
airway pressure until the abdominal contents have
been removed from the chest or until a thoracotomy has been performed. Cardiovascular collapse
might occur during positive-pressure ventilation.
The re-expanded lung previously compressed by
herniated viscera may shift mediastinal structures,
and venous return may be impeded [33, 34].
Increased pleural pressure from mechanical ventilation is transmitted to the abdomen. It results in
an increased upward displacement of the viscera
toward the diaphragm and may worsen cardiovascular collapse [34]. A surgeon must be ready to
operate before ventilation is begun [33].
2 Anesthetic andPerioperative Management
General anesthesia and positive-pressure venti-

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Premedication with an H2 antagonist, metoclopramide, and sodium citrate is usual. Rapid- sequence
induction with fentanyl, thiopentone, and suxamethonium is followed by inserting a right-sided endobronchial tube. Anesthesia is maintained with
enurane in oxygen and nitrous oxide and neuromuscular blockade with pancuronium [35]. On the
other hand, delaying a decision to insert a doublelumen tube may have advantages. First, it may not
be necessary if a simple laparotomy sufces; placing
double- lumen tubes is often difcult, especially during rapid-sequence induction. Second, changing
tubes intraoperatively allows surgical manipulation
of the stomach directly, combined with a nasogastric
tube, to ensure the abdominal stomach is empty
before a double-lumen tube placement. Head-up tilt
also reduces the risk of regurgitation from the
abdominal or thoracic stomach [35].
Normal changes of pregnancy include
increased cardiac output,which reaches its highest value after delivery due to blood transfer from
the uterus into the systemic circulation and venacaval compression release [36]. Diaphragmatic
hernia is associated with intrathoracic pressure
augmentation. It reduces venous return, increases
right and left ventricular afterload, and decreases
cardiac output. Thus, perioperative hemodynamic monitoring of patients with diaphragmatic
hernia could improve uid management.
Although a pulmonary artery catheter is an
invasive procedure, it is a gold standard for measuring cardiac output and pressures directly [37].
2.1.2.2 Abdominal Trauma
The literature on pregnant trauma victims’ obstetric, anesthetic, and surgical management is limited [38]. Pregnant trauma victims present a
unique spectrum of challenges to the trauma
healthcare team. The diagnosis may be unknown
at exploration, as may be the nature and extent of
the further procedures. Pregnancy may not always
be known to the healthcare team (at the scene of
transportation accidents, emergency room, or
operating room), complicating the situation.
Pregnancy must always be suspected (until
proven otherwise) in female trauma
patients of childbearing age [38].
Vasopressors, rarely indicated in trauma
patients, should be avoided unless necessary
because of the risk of decreasing uterine blood
ow.
If vasopressors are required, ephedrine
should be the rst choice. It preserves the
uterine blood ow, but there should be no
hesitation in using other vasopressors when
necessary.
Head andNeck Injury
Women in late pregnancy have difcult airways.
Mallampati class 4 airway (with only the hard
palate visible and with no view of the soft palate
or uvula) increased by 34% between 12 and
38 weeks [39]. The additional fact that these
patients have sustained trauma and will likely be
in cervical collars compounds is an already difcult situation [40]. If there is uncertainty about
the integrity of the cervical spine, direct laryngoscopy should be avoided, and beroptic (awake
beroptic) intubation of the trachea, if feasible
(time constraints or equipment availability),
should be considered [41]. If direct laryngoscopy
is deemed necessary, an “inline stabilization” of
the head and neck by an assistant to prevent
extension and rotation of the cervical spine is
indicated. If awake, beroptic tracheal intubation
is chosen. Analgesic and sedative drug titration
maintains continual meaningful verbal communication between the anesthesiologist and the
patient.
Respiratory depression and aspiration of stomach contents with local anesthesia are less likely if
the patient remains awake and alert. Also, a rational, alert mother minimizes the risk of neonatal
depression. In patients in anesthesia, nasogastric
decompression after intubation reduces the risk of
aspiration. Midazolam is the recommended benzodiazepine. However, it is highly unionized and
lipophilic, and the feto- maternal ratio is 0.76 at
15–20 min after maternal administration.
However, unlike other benzodiazepines, the ratio
falls rapidly. No adverse fetal effects have been
reported [42]. Trauma victims with a GCS ≤8

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usually require intubation and mechanical ventilation for intracranial pressure and airway control.
However, trauma victims with “good” GCS can
“talk and deteriorate/die” following a traumatic
head injury, particularly an injury associated with
loss of consciousness. Delayed deterioration
occurs within 48h from the initial insult.
The succinylcholine-induced ICP increase
has been a concern in the past. With an urgent
need to secure an airway in a head-injured pregnant trauma victim, succinylcholine is an appropriate and safe drug. All the intravenous
anesthetic agents (except ketamine) cause some
degree of vasoconstriction and therefore decrease
cerebral blood ow. The inhaled agents have
some cerebral vasodilatory effect; however, their
administration is usually consistent with acceptable ICP levels [43].
Spinal Cord Injury
The anesthetic management of a spinal cord injury
in pregnancy depends upon the lesion’s site, extent,
and duration. Complete cord transection is usually
associated with cardiovascular instability due to
neurogenic shock in the acute phase or subsequent
autonomic hyperreexia. In the latter case, epidural analgesia blocks afferent pathways, reducing
the stimuli and causing paroxysmal sympathetic
activity. Parasympathetic pathways are intact, and
life-threatening bradycardia can occur.
Intravascular volume status can be difcult to
assess and manage, particularly in acute injury.
Intravenous uid therapy is best guided by central
venous pressure monitoring. Attention to the
patient’s position and the compression of pelvic
venous structures by the gravid uterus distinguish
between postural hypotension and volume depletion. Maternal hypotension must be avoided to
maintain uterine blood ow and avoid secondary
ischemic damage in the evolving cord lesion.
Irrespective of the chosen method of anesthesia,
preoperative and postoperative neurological ndings should be documented.
If radiological evidence suggests that the
neurological decit is caused by edema, the
principal anesthetic concern was to avoid secondary (irreversible) cord damage in the
mother and enable timely delivery in case of
acute fetal compromise. If the patient has a
normal airway and, other than the cervical collar, there are no reasons for anticipating difculties with intubation, general anesthesia with
inline neck stabilization during intubation is
the most appropriate [44].
2.1.2.3 Increased Intra-Abdominal
Pressure
Increased IAP(see Chap. 3) is transmitted to the
thoracic cage (on average50%), which diminishes lung compliance, decreases functional
residual capacity, and increases ventilation/perfusion mismatch [45]. In critically ill pregnant
women, abdominal compartment syndrome manifests in several ways. Ventilation becomes
increasingly difcult, resulting in increased peak
and plateau alveolar pressures, hypercapnia,
hypoxia, and increased risk of ventilatorassociated lung injury because of the high pressures needed to drive ventilation [46].
2.1.2.4 Acute Appendicitis
Pregnant patients with AA, compared to nonpregnant, have similar occurrences of all specic
complications except pneumonia, which occurred
more frequently in pregnant women (0.7% vs.
0.2%, p = 0.004). All cases of postoperative
pneumonia were observed in women who underwent general endotracheal anesthesia [47].
2.1.2.5 Uterine Rupture
With a UR diagnosis, the mother’s immediate
stabilization and delivery of the fetus are imperative. After securing the airway and adequate oxygen delivery, careful and immediate correction of
hypovolemia is mandatory. Patients should have
multiple, preferably large-bore, intravenous catheters with vigorous uid resuscitation. With complete and extensive UR with fetal extrusion into
the peritoneal cavity and vaginal bleeding, ergometrine may be administered to control bleeding
from the rent and the placental site during preparation for laparotomy.
The use of prophylactic antibiotics is controversial. Some state that they have no value [48],
while others recommend their use [49] because
23% had intraperitoneal sepsis at the time of

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laparotomy [50]. Partly it depends on the quantity of blood loss. Hypovolemic shock may lead
to the translocation of gram-negative bacteria
from the ischemic bowel to the bloodstream,
complicating the presentation with endotoxemia and septic shock [51]. Hemorrhagic shock
increases the incidence of wound infections.
Most survived mothers had a mean blood loss
of >2000mL [52–54]. Blood loss depends on
the trimester of UR and uterotonics or prostaglandins for labor induction. These medications
can decrease the amount of blood loss [55].
At least 1000mL of packed red blood cells
or blood transfusions should be available
[53, 54, 56].
2.1.3 Intraoperative CO2 Monitoring
During laparoscopy, intraoperative CO2 monitoring by capnography should be used in the pregnant
patient
(Level III).
Fetal acidosis with insufation has not been
documented in the human fetus, but concerns
over the potentially detrimental effects of acidosis have led to the recommendation of maternal
CO2 monitoring [57, 58]. Initially, there was a
debate over maternal blood gas monitoring of
arterial carbon dioxide (PaCO2) versus end-tidal
carbon dioxide (ETCO2) monitoring. However,
the less invasive capnography adequately reects
maternal acid-base status in humans [59]. The
safety and efcacy of ETCO2 measurements in
pregnant women [60–62]make routine blood gas
monitoring unnecessary.
2.1.4 Extracorporeal Membranous
Oxygenation
2.1.4.1 Considerations inPregnancy
Extracorporeal membranous oxygenation
(ECMO) is the last resuscitation treatment for
patients with refractory shock. It is a complex
technique for providing life support in severe
but potentially reversible respiratory failure.
The technique oxygenates the blood outside the
body, obviating the need for gas exchange in the
lungs and, if necessary, provides cardiovascular
support. General indications for ECMO are:
• Severe acute respiratory failure with an
expected mortality rate of 80% based on physiological variables,
• Reversible respiratory failure,
• Spontaneous circulation not returning because
of cardiac arrest or refractory ventricular
brillation after 10min CPR,
• Systolic blood pressure cannot be maintained
at >70mmHg and inotropic score (IS) >60μg/
kg/min, and intra-aortic balloon pump support
(IS, μg/kg/min = dopamine + dobutamine
+15 × milrinone +100 × epinephrine
+100 × norepinephrine
+100×isoprotenolol).
ECMO therapy may be benecial during preg-
nancy or early puerperium in H1N1-related
hypoxemia [63, 64], ARDS from various causes
[65], and peripartum cardiomyopathy [66].
Venovenous ECMO is indicated for hypoxemic
respiratory failure, hypercarbic respiratory failure, respiratory failure in lung transplant, bronchopleural stulas, pulmonary air leaks, or
complex airway management. In venovenous
ECMO, no cardiac support is provided, as
opposed to venoarterial extracorporeal membrane oxygenation [65].
2.1.4.2 Amniotic Fluid Embolism
See Sect. 25.3.6.6. A total of 20 ECMO cases of
amniotic uid embolism from 1986 to 2019 were
published [67]. Extracorporeal therapies consisted
of venoarterial ECMO (11 cases), venovenous
ECMO (3 cases), and cardiopulmonary bypass (3
cases, including 2 older cases). Extracorporeal
therapies were started after delivery and were continued for a median of 48h. The length of ICU stay
ranged from 7 to 59days. Maternal and neonatal
survival was 85%. Maternal hemorrhage complicated 69% of cases, with a few patients requiring
more than 10 red blood cell transfusions [67].

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2 Anesthetic andPerioperative Management
Although not strongly recommended, from 2020,
ECMO for amniotic uid embolism is included in
the treatment guidelines— “persistent hemodynamic instability despite medical management or
need for prolonged CPR may require consideration for VA ECMO” [68]. Postpartum hemorrhage or DIC should not be considered absolute
contraindication [67].
2.1.4.3 Maternal Trauma
A single case of successful ECMO therapy for
maternal chest trauma has been reported [69].
2.2 Perioperative Medications
Interests of both the mother and the fetus must be
considered in therapy during pregnancy. Usually,
these interests do not conict because what is
good for the mother is generally good for the
fetus. Sometimes maternal therapy must be modied to substitute alternative but safer therapy
because of the concerns about drug teratogenicity
(e.g., replacing a H2 receptor antagonist for misoprostol, an abortifacient that is contraindicated
during pregnancy) [70, 71]. Rarely, the maternal
and fetal interests are opposed, as in chemotherapy for maternal cancer. This therapy is potentially life-saving to the mother but life-threatening
to the fetus [72]. These conicts raise signicant
medical, legal, and ethical issues.
There are many categories of drugs that could
have deleterious effects on a fetus, and detailed
elaboration is out of the scope of this book. There
are three main categories of medications used in
these patients: (1) anesthetic medications (see
Sect. 2.1.1), (2) prophylactic, and (3) therapeutic.
All teratogenic drugs generally determine a specic pattern or single malformation during a sensitive gestation period with a dose-dependent effect.
2.2.1 Antibiotics
The US Food and Drug Administration has categorized all antibiotics according to the risks associated with their use in pregnancy. Two categories
are important:
• category A: studies in pregnant women do not
demonstrate any risks to the mother or fetus,
• category B: while animal studies show no risk,
human studies are inadequate,or animal toxicity has been noted, but the studies on humans
show no risk.
There are no antibiotics in category A.FDA
Class B antibiotics should be administered when
the acute abdomen is highly suspected or found
(at least 30–60 min before skin incision) in all
patients (administered to 94% of patients in the
literature) [73].
2.2.1.1 Acute Appendicitis
Recommended antibiotics are second-generation cephalosporins (FDA Class B), comprising
60% of all antibiotic classes used during pregnancy for acute appendicitis (AA) [74].
Cephalosporins and metronidazole are indicated
for gangrenous or perforated AA [75].
Metronidazole use in pregnant patients is still
controversial, with a recommendation against
its use during the rst trimester of pregnancy.
However, there is no increase in teratogenic risk
when used in recommended doses regardless of
the trimester [76, 77]. The duration of antibiotic
therapy should be discontinued as early as possible. A single preoperative dose is adequate
with normal appendix or phlegmonous AA [78].
Even operation without antibiotic therapy for
phlegmonous AA is sufcient in the nonpregnant population. Therefore, for apregnant
patient with high suspicion of AA, the time from
admission to the operation should be short as
possible.
2.2.1.2 Acute Cholecystitis
Penicillins and second-generation cephalosporins are most commonly used. The rst-line treatments are ampicillin and sulbactam or cefoxitin/
cefuroxime. There is no consensus on the duration of antibiotic use in pregnancy.
Recommendations from the general population
can be applied: (1) to use antibiotics until the
patient becomes afebrile and without leukocytosis or elevated CRP, or (2) single dose or 24-h
therapy in organ occupying infection [78].
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