Acute Abdomen in Pregnancy 2

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    Acute Abdomen in Pregnancy

    Kate Pettit, MS III

    June 18, 2007

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    The Most Important Equation

    + +

    =

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    10-14 yrs

    15-19 yrs

    20-24 yrs

    25-29 yrs

    30-34 yrs

    35-39 yrs

    40-44 yrs

    45-54 yrs

    0 20 40 60 80 100 120 140

    c

    How old are your prospective

    pregnant patients?

    CDC 2004

    Live Births per 1,000 Women

    Avg Age

    at First

    Birth inUS:

    25.1 yrs

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    DDx of Abdominal Pain in

    Pregnancy

    Divided into three categories:

    1) Conditions incidental to pregnancy

    2) Conditions associated withpregnancy

    3) Conditions due to pregnancy

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    Conditions Incidental to Pregnancy

    Acute appendicitis

    Acute pancreatitis

    Peptic ulcer

    Gastroenteritis

    Hepatitis

    Bowel obstruction Bowel Perforation

    Herniation

    Meckels Diverticulitis

    Toxic megacolon

    Pancreatic pseudocyst

    Ovarian cyst rupture

    Adnexal torsion

    Ureteral calculus

    Rupture of renal pelvis Ureteral obstruction SMA syndrome Thrombosis/infarction Ruptured visceral artery

    aneurysm Pneumonia Pulmonary embolus Intraperitoneal hemorrhage Splenic rupture

    Abdominal trauma Acute intermittent porphyria Diabetic ketoacidosis

    Sickle Cell Disease

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    Conditions Due to Pregnancy

    Ectopic pregnancy Septic abortion with peritonitis Acute urinary retention due to retroverted uterus Round ligament pain

    Torsion of pedunculated myoma Placental abruption Placenta percreta HELLP Syndrome

    Acute Fatty Liver of Pregnancy Uterine rupture Chorioamionitis

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    Ectopic Pregnancy

    Classic Symptoms Abdominal pain Amennorrhea Vaginal Bleeding

    Diagnosis Transvaginal U/S (TVS)

    Presence of a truegestational sac at 4.5 to 5wks is the 1st sign of IUP.

    Cardiac activity is firstdetected at 5.5 to 6 weeks.

    Serum quantitative HCG Absence of an intrauterine

    gestational sac at hCGconcentrations >1500-2000IU/L suggests an ectopic ornonviable intrauterinepregnancy

    Management Option of medical vs surgical

    management if pt is hemodynamicallystable and no rupture has occurred.

    Emergent surgical management ifrupture has occurred and/or patient ishemodynamically unstable

    Prognosis

    Ruptured ectopic pregnancies accountfor 4- 10 percent of all pregnancyrelated deaths.

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    HELLP SyndromeHemolysis Elevated Liver Enzymes Low Platelets

    Incidence: 1 in 1K pregnancies Timing: Majority diagnosed at

    28-36 wks Labs:Plts,AST/ALT,indirect bili,haptoglobin,schistocytes on peripheral

    Smear Management:

    Emergent delivery forpregnancies > 34 weeks,nonreassuring fetal status,severe maternal disease(multiorgan dysfunction, DIC,

    liver infarction or hemorrhage,ARF, or abruptio placenta) Delayed delivery in stable

    pregnancies 140/90) 85

    RUQ/Epigastric pain 40-90

    Nausea/Vomiting 29-84

    Headache 33-60

    Visual changes 10-20

    Jaundice 5

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    Acute Fatty Liver of Pregnancy

    Incidence: Rare (1 in 7K 16K deliveries)Timing: 2nd half of pregnancy (usually 3rd tri)

    Sxs: N/V (75%), epigastric abdominal pain

    (50%), anorexia, jaundice +/- signs of pre-eclampsiaLabs:PT,PTT,AST/ALT,Cr,glucose, +/-WBC, +/-Plts

    Tx: Maternal stabilization (glucose infusion,reversal of coagulopathy) and emergentdelivery

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    Definition of Acute Abdomen

    Stedman's Medical Dictionary, 27th

    Edition defines acute abdomen as "any

    serious acute intra-abdominal condition

    attended by pain, tenderness, andmuscular rigidity, and for which

    emergency surgery must be

    considered.

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    Epidemiology

    Incidence of acute abdomen duringpregnancy is 1 in 500-635

    # 1 Acute Appendicitis

    # 2 Acute Cholecystitis

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    Challenges of Diagnosis

    Symptoms Nausea, vomiting, and abdominal pain are common

    in the normal obstetric population. N/V are mostcommon in weeks 4-16.

    Physical Exam Expanding uterus dislocates other intraabdominal

    organs.

    Labs Leukocytosis (10-20K) and anemia are common in

    normal pregnancies and thus, not as predictive ofinfection or blood loss.

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    Which conditions require urgent

    surgical management in pregnancy?

    Trauma

    Acute appendicitis

    Intestinal obstructionPerforated duodenal ulcer

    Spontaneous visceral rupture

    Ectopic pregnancyOvarian or uterine torsion

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    Timing of Surgery

    1st trimester (wks 1-12)12% SAb rate

    2

    nd

    trimester (wks 13-26)0 - 5.6% SAb rate5% rate of preterm labor

    3

    rd

    trimester (wks 27-40)30-40% rate of preterm labor

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    Imaging Options

    U/S: No known adverse effects.

    X-ray: Presence of adverse effects

    depends on total radiation dose.

    CT: Presence of adverse effects

    depends on total radiation dose.

    MRI: No known adverse effects.ERCP: Only recommended for

    therapeutic use, not for routine imaging.

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    Radiation during pregnancy

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    Use of ERCP in PregnancyAmerican Society for Gastrointestinal Endoscopy Guidelines

    ERCP should only be used when therapeutic intervention is intended(usually for biliary pancreatitis, choledocholithiasis, or cholangitis).

    Several studies have confirmed the safety of ERCP in pregnancy.

    With precautions, fetal exposure is well below the 5- to 10-rad level. Kahaleh et al. reported an estimated fetal radiation exposure of 40 mrads

    (range 1-180 mrad).

    Precautions for reducing radiation exposure: Lead shields placed under the pelvis and lower abdomen, remembering that

    the x-ray beam originates from beneath the pt. Use of brief ''snapshots'' of fluoroscopy to confirm cannula position and CBD. Minimize total fluoroscopy time.

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    Reducing Radiation in Pregnancy

    X-ray: PA exposures lowersthe radiation dose by 2 to 4mrad compared with thetraditional AP exposuresbecause the uterus is located

    in an anterior pelvic position. CT: Narrow collimation and

    wide pitch (the patient movesthrough the scanner at afaster rate) results in aslightly reduced image

    quality, but provides a largereduction in radiationexposure.

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    Sequelae of Radiation in Pregnancy

    May cause failure of implantation,malformation, growth retardation,CNS abnormalities, or fetal loss.

    Exposure

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    Childhood Leukemia and Radiation

    The background rate of leukemia in

    children is about 3.6 per 10,000.

    Exposure to one or two rad increases

    this rate to 5 per 10,000.

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    Use of contrast in pregnancy

    Iodinated contrast: Crosses the placenta Can produce transient effects on the developing fetal thyroid

    gland, although clinical sequelae from brief exposures havenot been reported.

    May be used when indicated. Gadolinium:

    Crosses the placenta. Because of limited experience with this agent, gadolinium is

    currently not recommended for use in the pregnant patientunless the potential benefit justifies the potential risk to thefetus.

    Animal studies have shown an risk of spontaneousabortion and skeletal and visceral anomalies.

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    MRI as an imaging modality

    MechanismElectromagnetic field induced changes in

    proton spin

    Theoretical risks to fetus Induction of local electric fields and currents

    Radiofrequency radiation results in heating

    of tissue

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    American College of Radiology

    Paper on MRI Safety

    MRI should only be used in pregnancy when:

    The information requested from the study

    cannot be obtained from nonionizing

    means.The information is needed to care for the pt

    and fetus during pregnancy.

    The ordering MD does not feel it is prudentto delay diagnosis until after pregnancy.

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    MRI in Pregnancy

    No studies have shown adverse effects on the

    fetus or the outcome of the pregnancy.

    However, arbitrarily MRI is NOT usually

    performed in the 1st trimester 2/2 to this beingthe period of organogenesis.

    When MRI is used, informed consent must

    include the possibility that a previously

    undiagnosed fetal abnormality may be found.

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    "No single diagnosticprocedure results in a

    radiation dose that threatens

    the well-being of the

    developing embryo and fetus."

    -- American College ofRadiology

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    Appendicitis

    #1 Cause of Acute Abdomen

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    Appendicitis

    Accounts for 25% of the operative

    indications for non-obstetric surgery

    antepartum.

    Appendicitis is NOT more common

    during pregnancy.

    Incidence is approximately equal in all

    three trimesters.

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    Signs and Symptoms

    RLQ pain: Most reliable sx Anorexia and vomiting: Not sensitive

    nor specific.

    Direct RLQ tenderness: ~100%

    Rebound tenderness: 55-75% of pts Abdominal muscle rigidity: 50-65% of

    pts

    Psoas sign: Observed less frequently.

    All findings are less common in 3rdtrimester due to laxity of abdominal wall

    muscles.

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    Adler Sign

    If the point of maximal tenderness shifts

    medially with repositioning on the left

    lateral side, the etiology is generally

    adnexal or uterine (vs appendiceal).

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    Appendiceal Location

    Historically, many referenceshave reported appendicealdisplacement.

    In 2003, a study by Hodjati et

    al showed that pregnancy didNOT change appendiceallocation.

    Degree of displacement, ifany, is likely due to different

    extents of cecal fixation.

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    Laboratory Evaluation

    WBC: Absolute number not reliable

    given leukocytosis of pregnancy.

    Differential: levels of band cells can

    be reliable indication of infection.

    U/A: Caution as 20% of pts have pyuria

    or hematuria with appendicitis due to

    extraluminal irritation of the ureter (rather

    than due to a UTI).

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    1st Line Imaging for Appendicitis

    Graded compression U/S

    80% sensitive: non-perforating appendicitis

    28% sensitive: perforated appendicitis

    3rd trimester accuracy is lower due to

    technical difficulties.

    * Doris et al (meta-analysis).

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    2nd Line Imaging for Appendicitis

    CT

    94% sensitivity

    94% specificity

    MRI

    Up to 100%

    sensitivity*

    96% specificity*No known adverse

    effects on fetus, but

    cost and availabilitymay be prohibitive.

    Fielding and Chin (2006).*Values are from small study of 45 pregnant pts.

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    Risks for Mother and Fetus

    66% risk of perforation if surgery delayed by >24 hrsfrom presentation.

    Negative laparotomy rates of up to 35% areconsidered acceptable in the pregnant population (vs15% in non-pregnant population).

    Non-perforated appendix Fetal mortality of 1.5%

    Perforated appendix Fetal mortality of 20-35% Maternal mortality of 1% 83% risk of preterm contractions due to localized peritonitis.

    In all cases, the rate of premature delivery is highestin the 1st week post-op.

    Augustin and Majerovic

    (2006).

    R d ti f Diff

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    Recommendations for Diffuse

    Peritonitis

    1) IV Cefuroxime, ampicillin, metronidazole,

    and oxygen pre-operatively.

    2) Immediate C-section can be considered,

    depending on gestational age of fetus.

    3) Preoperative intubation and ventilation in

    cases of fetal hypoxia.

    Augustin and Majerovic

    (2006).

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    Acute Cholecystitis

    # 2 Cause of Acute Abdomen

    P th h i l

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    Pathophysiology:

    Hormones and biliary disease

    Estrogen in pregnancy

    cholesterol synthesis,hepatic

    cholesterol uptake,catabolism of

    cholesterol to bile acidsBile supersaturation & cholesterol stones

    Progesterone in pregnancy

    bile stasis and GB contraction inresponse to CCK

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    Epidemiology

    Cholelithiasis is the cause of

    cholecystitis in pregnant pts in 90% of

    cases

    Incidence of cholelithiasis in pregnancy

    is 3.5-10%

    Only 30-40% of pregnant pts with

    gallstones are symptomatic

    Augustin and Majerovic(2006).

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    Presentation and Diagnosis

    Symptoms:Basically identical in

    pregnant and non-pregnant pts

    Labs:Bilirubin, +/-Transaminases,

    Alkaline phosphatase is non-specific

    as it is normally in pregnancy

    Imaging: U/S has an accuracy of 95-

    98% of detecting acute cholecystitis andcholedocolithiasis

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    Initial Management of Cholecystitis

    IV hydration

    Bowel rest

    Pain controlAntibiotics

    Fetal monitoring

    Nasogastric decompression if necessary

    S rgical Management of

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    Surgical Management of

    Cholecystitis

    Cholecystectomy is now recommended as theprimary treatment for cholecystitis because of: Recurrence rate during pregnancy of 44-92%,

    depending on date of 1st presentation Reduced use of medications Shorter hospital stay and fewer hospitalizations Elimination of risk of subsequent gallstone

    pancreatitis

    Minimizing development of potentially life-threatening complications such as perforation,sepsis, and peritonitis

    Augustin and Majerovic(2006).

    Other Indications for Cholecystectomy

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    Other Indications for Cholecystectomy

    During pregnancy

    Choledocolithiasis (after ERCP)

    Gallstone Pancreatitis

    Recurrent symptomatic cholelithiasis Several studies have found the incidence of SAb, preterm

    labor, or premature delivery to be higher in pts treated non-operatively than in those undergoing cholecystectomy.

    However, noprospective trial has been done to determine thebest management for recurrent biliary colic.

    Curet (2000).

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    Laparotomy vs Laparoscopy?

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    Choosing Surgical Technique

    Laparotomy Currently considered 1st

    line approach. Always preferred

    approach when diffuseperitonitis is present, asit is associated with alower complication ratethan laparoscopy in thissetting.

    Laparoscopy First offered in 1991 for

    pregnant patients forappendectomy andcholecystectomy.

    Many new studies showthis technique to be safein pregnancy for routineappendicitis, especiallyduring the 2nd trimester.

    Can help r/o salpingitis,adnexal mass, orectopic pregnancy whendx is uncertain.

    ecommen a ons o mprove

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    ecommen a ons o mprovesafety of laparoscopy during

    pregnancy1) Obstetrical consultation should be obtained preoperatively.2) When possible, operative intervention should be deferred until

    2nd trimester.

    3) Procedure should be performed with pt in supine, left lateraldecubitus position and degree of reverse Trendelenburgshould be minimized.

    4) Open Hasson technique should be used to prevent puncture ofuterus.

    5) Pneumoperitoneum pressures should be minimized to 8-12mm Hg with maximum 15 mm Hg.

    6) Administration of tocolytic agents and perioperative monitoringof fetal heart tones should be considered.

    7) Pneumatic compression devices should always be used asboth pneumoperitoneum and the condition of pregnancy are arisk for venous stasis.

    Halkik et al (2006).

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    Optimizing Delivery

    *Understanding what the consulting

    obstetrician is doing for your patients*

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    Use of Tocolytics for Preterm Labor

    PurposeDelay delivery so that corticosteroids can be

    administered.

    Prolong pregnancy when there are underlying,self-limited causes of labor, such as

    pyelonephritis or abdominal surgery, that are

    unlikely to cause recurrent PTL.

    Use is limited to

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    Types of Tocolytics I

    Terbutaline (Beta-2 agonist)Mechanism: Agonist at myometrium causing

    relaxationMeta-analysis showed # of births within

    subsequent 48 hrs but no change in # of birthswithin subsequent 7 days

    Magnesium sulfateMechanism: Unknown, likely competes with

    calcium reducing myometrial contractility

    Cochrane review concluded that this drug did notsignificantly reduce the proportion of womendelivering within 48 hrs.

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    Types of Tocolytics II

    Nifedipine (Calcium channel blocker)Mechanism: Directly blocks influx of Ca ions

    Meta-analysis showed # of births within 48 hrs

    as compared to terbutaline as well as

    # of birthswithin subsequent 7 days.

    Indomethacin (Cyclooxygenase inhibitor)Mechanism: Blocks production of prostaglandins

    Small studies indicate effectiveness for prolongingtime to delivery

    Use of corticosteroids to improve

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    Use of corticosteroids to improve

    fetal outcomes in premature delivery

    Administration: Two doses of 12 mg betamethasone IM given 24

    hrs apart. Benefit of therapy is initially observed 18 hrs after

    the first dose with maximal benefit 48 hrs after thefirst dose.

    Benefits include reduction in the incidence of: Neonatal respiratory distress syndrome

    Intraventricular hemorrhage Necrotizing enterocolitisMortality

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    Steroids and peritonitis?

    Glycocorticosteroids administered during the

    initial phase of experimental diffuse peritonitis

    display favorable action decreasing animal

    mortality rate regardless of the dose. However,glycocorticosteroids given in the developed

    septic syndrome decrease the pro-

    inflammatory cytokine serum concentration

    regardless of the dose, still not affecting theanimal mortality rate.

    Modzelewski et al (2002).

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    References

    Acute Fatty Liver of Pregnancy. Up-to-date. Augustin, G and M Majerovic. Non-obstetrical acute abdomen during pregnancy. European

    J of Obstetrics, Gynecology, and Reproductive Biology 2006; 131: 4-12. Brooks et al. The Pregnant Surgical Patient. ACS Surgery: Principles and Practice. Curet, MJ. Special problems in laparascopic surgery: previous abdominal surgery, obesity,

    and pregnancy. Surg Clinic North Am 2000; 80: 1093-1110. Ectopic Pregnancy. Up-to-date. Fielding, JR and BM Chin. Magnetic Resonance Imaging of Abdominal Pain during

    Pregnancy. Top Magn Resonance Imaging 2006; 17: 409-416. Halkic et al. Laparascopic management of appendicitis and symptomatic cholelithiasis during

    pregnancy. Langenbacks Arch Surg 2006; 391: 467-471. HELLP Syndrome. Up-to-date. Inhibition of preterm labor. Up-to-date. Kahaleh et al. Safety and efficacy of ERCP in pregnancy. Gastrointestinal Endoscopy 2004;

    60: 287-292. Modzelewski et al. Tests for the usefulness of glucocorticosteroids in treatment of

    experimental peritonitis. Pol Merkur Lekarski 2002; 69: 228-231. Murray et al. Diagnosis and treatment of ectopic pregnancy.CMAJ 2005; 73: 905. Pedrosa et al. MR Imaging of Acute Right Lower Quadrant Pain in Pregnant and

    Nonpregnant Patients. Radiographics 2007; 27: 721-753.

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