Ch 10 Infections Diseases in Pregnancy Flashcards

1
Q

asymptomatic bacteriuria is screened for as part of routine pregnant care and is associatd with significant risk in pregnancy

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2
Q

prevalence of ASB >100,000 colonies in culture ranges from 2-11%

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3
Q

women with abs are 20-30 fold increased risk of developing acute pyelonephritis during pregnancy \

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4
Q

abs in pregnancy is further associated with low birth weight infants and PTL

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5
Q

urinalysis might be positive for leukocyte esterase, nitrates, or hematuria, and the urine sediment will have elevated wbcs and bacteria.

nitrates are sensitive and specific to gram - negative bacteria.

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6
Q

ecoli accounts for > 80% of all ASB and UTI

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7
Q

treatment of ASB is usually with
amoxicillin, nitrofurantoin
trimethoprim/sulfamethoxazole
or cephalexint

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8
Q

because ASB may persist, a test of cure culture should be obtained 2 weeks after completion of therapy

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9
Q

wbc casts are highly associated with pyelonephritis. onset of symptoms is often abrupt and fever is universally present

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10
Q

in adddition to treating infection, in patients with dysuria or bladder pain, pyridium which is concetrated in the urine acts as a local anesthetic to reduce the pain, is commonly used for symptomatic relief.

patients should be counseled that pyridium will cause the urine to turn bright orange

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11
Q

most common complication of lower UTI is ascending infection to the kidneys, or pyelonephritis.

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12
Q

pyelonephritis is characterized by fever, chills, flank pain, dysuria, urgency, and frequency. it is sometimes associated with nausea and vomiting. oh PE, fever and costovertebral angle tenderness are often present.
lab abnormalities:
pyuria
bacteriuria
elevated WBC
WBC casts (highly associated with pyelonephritis)

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13
Q

pyelo a risk factor for preterm labor and particularly serious associated maternal complications including septic shock and ARDS. up to 20% of pregnant women with acute pyelonephritis develop multiorgan system involvement secondary to endotoxemia, resulting in sepsis.

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14
Q

GBS refers to beta hemolygic gram-positive bacteria streptococcus agalactiae and is commonly responsible for UTIs, chorioamnionitis, and endomyometritis during pregnancy. it is also a major pathogen in neonatal sepsis which has severe implications.
mortality rate with GBS is 2-50%women with hx of GBS UTI or a history of previous infant with GBS disease should be treated independent of screening

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15
Q

gbs only good for 5 weeks

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16
Q

chorioamnionitis is infection of memebranes and amnioti fluid surrounding the fetus. frequently associated with preterm and prolonged ROM but can also occur without ROM

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17
Q

herpes simplex virus serious infection with significant morbidity and mortality

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18
Q

hsv2 clasically causes genital herpes,

primary infections are astymptomatic in 50% of patients and are responsible for approx 90% of neonatal herpes. risk of transmission to neonate with primary outbreak is 20-50%risk of transmission with recurrent herpes with active lesions is approx 1%.

latent infection occurs after a primary infection. virus resides in the dorsal root ganglion and peripheral nerves can shed virus symptomatically / asymptomatically

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19
Q

ideal method of testing for genital herpes is through scraping of the lesions and sending for viral detection through PCR. virial culture is less sensitive than PCR, and additional assays are less specific.

antibody detection techniques include use of serologic tests to detect presence of antibodies to etiehr hsv2 or hsv1.

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20
Q

varicella zoster virus -highly contagious dna herpes virus transmitted by respiratory droplets / close contact and causes the disease chicken pox

it can later reactive to cause herpes zoster / shingles

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21
Q

vzv causes svereal symdromes relevant to pregnancy including

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maternal varicella pneumonia
congenital varicella syndrome
neonatal varicella infection

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22
Q

vav pneumonia in pregnancy is a risk factor for maternal mortality

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23
Q

congenital varicella predominantly when mothers are infected between 8-20 weeks of gestation. congenital varicella syndrome is characterized by

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skin scarring
limb hypoplasia
chorioretinitis
microcephaly
30% mortality in 1st year of life.
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24
Q

maternal infection in 3rd trimester, virus can cross the placenta and infant has insufficient cell-mediated immunity to prevent hematogenous dissemination of virus and cause neonatal varicella.
neonatal VZV is associated with high neonatal dealth rate.

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25
Q

infants of mothers who develop varicella disease within 5 days before delivery or 2 days after should also receive varicella zoster immunoglobulin VZIG and / or treatment with antiviral agents such as acyclovir / valacyclovir

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26
Q

maternal herpes zoster, recurrent VZV outbreaks is NOT associated with congenital anomalies / neonatal varicella

A

recurrent VZV outbreaks is NOT associated with congenital anomalies / neonatal varicella

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27
Q

if a susceptible pregnant patient is exposed to someone with varicella, she should be treated within 72-96 hours with one of two agents to prevent active infection

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varicella zoster immune globulin variZIG is recommended for postexposure prophylaxis, and nay woman who has exposure without a history of chicken pox or history of vaccination should be treated ( up to 10 days after exposure)

alternative method of prophylaxis is to administer oral acyclovir 800mg five times daily x 7 days.
oral valtrex 1000mg tid x 7 days

patients with pneumonia, encephalitis, disseminated infection and immunsuppressed should be hospitalized and treated with IV acyclovir

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28
Q

parovirus b19 is a dna virus that causes erythema infectiosum (5th disease) a common childhood illness.

virus transmiteed by repiratory droplets and infected blood products. in pregnancy, virus transmitted transplacentally in about 35% of women.

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29
Q

low grade fever, malaise, myalgias, arthralgias, red macular “slapped cheek” facial rash.. in pregnancy, vertical transmission of virus is associated with severe sequelae and fetal death. 1st trimester infections have been associated with miscarriage, whereas emid trimester and later infections associated with fetal hydrops

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30
Q

if parovirus exposure suspected in the mother, acute infection can be diagnosed by check parovirus IGM and IgG levels. if IGM is negative and igG is positive, then patient has prior immunity and is protected against a second infection. If Igm and igg are both negative, patient does not have acute infection but is susceptible to future infections. in patients with strong exposure history and negative igm and igg, serum viral pcr should be considered because igm response takes 10 days.

if studies indicate acute paraovirus infection ( + igm and + or - igg), beyond 20 weeks, GA, fetus should undergo serial ultrasounds for 12 and up to 20 weeks after maternal infection

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31
Q

a more precise way to detect evolving fetal anemia is to use doppler velocimetry to examine the peak systolic velocity of the middle cerebral artery (“MCA).

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doppler velocimetry to examine the peak systolic velocity of the middle cerebral artery (“MCA).

32
Q

increases in peack systolic velocity are associated with

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fetal anemia

33
Q

cytomegalovirus most common cause of congenital viral infection.

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34
Q

most sensitive and specific test for diagnosing congenital cmv infection is the identification of CMV in amniotic fluid by either culture of PCR>

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35
Q

pricnipal sonographic findings suggestive of serious fetal injury are microcephaly, ventriculomegaly, intercerebral calcification, fetal hydrops, growth restriction , and oligohydramnios. less common findings include fetal heart block, echogenic bowel, meconium peritonitis, renal dysplasia, ascites, and pleural effusions. fetuses that demonstrate abnormalities, particularly if they involve cns, generally have a much poorer prognosis

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36
Q

CMV most common congenital infection, 1-2% of all neonates, and is the leading cause of congenital hearing loss.

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37
Q

infants who are symptomatic can develop cytomegalic inclusion disease manifested by a constellation of findings, including hepatomegaly, splenomegaly, thrombocytopenia, jaundice, cerebral calcifications, chorioretinitis, and interstitial pneumonitis. t

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38
Q

30% of severely infected infants die, and 80% of survivors have severe neurologic morbility such as mental retardation, sensorineural hearing loss, and neuromusclular disorder

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39
Q

currently there is no treatment or prophylaxis for the disease

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40
Q

Rubella “ german measles” rate of congenital infection sharpy declines with advancing GA, so that very few fetuses are affected if infection occurs after 18 weeks

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41
Q

4 most common amomalies associated with congeital rubella syndrome are deafness, eye defects, such as cataracts, or reinopathy CNS, and cardiac malformations

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42
Q

cd4 measurements, viral load measurements, baseline blood counts, liver and renal function tests, and drug resistance should be tested at the initial visit, and is recommended that tests repeated every 3 months during pregnancy

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43
Q

hiv + pregnant women should receive indicated vaccines if not previously faccinated including
hep a
hep b
pneumococcal vaccines.

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44
Q

gonococcal infections associated with pelvic inflammatory disease in early pregnancy, as well as preterm delivery, PPROM, and puerpal infections throughout pregnancy duration.

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45
Q
untreated endocervical gonorrhea and perinatal complcations includes:
PROM
preterm delivery
chorioamnionitis
neonatal sepsis
maternal postpartum sepsis
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46
Q

chlamydial infection during pregnancy associated with several adverse maternal outcomes, including preterm delivery, premature rupture of membranes, low birth weight, and neonatal death. untreated chlamydia include neonatal conjunctivitis or pneumonia or both.

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47
Q

prevalence of chlamydia 11%. many authorities recommend that all pregnant women be screened in the first prenatal visit. if high risk, recheck 3rd trimester.

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48
Q

in order to confirm an active hepatitis B infection, hepatitis B core antibody and hepatitis B surface antibody IgM and IgG should also be checked. patients with chronic hepatitis B are
+ for Hbsag and positive for IgM aB to the core antigen.
acutely/ chronically infection may or may not be positive for hepatitis B E antigen

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49
Q

approximately 90%of mothers who are positive for both surface antigen and the E antigen transmit infection.

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50
Q

syphilis
primary syphyilis is characterized by painless chancre.
2nd ary syphilis characterized by systemic rash, muscle sores, fatigue and myalgias.
tertiary / latent syphilis characterized by long dorman phase followed by systemic organ dysfunction including paralysis, blindness, and dementia.

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51
Q

all pregnant women screened for VDRL test or RPR test. if positive, a titer is sent.
all positive results must be confirmed with fluorescent treponemal antibody absorption FTA -ABS because there are false positives with both RPR and VDRL.
systemic lupus erythematosus and antiphospholipid antibody syndrome can cause false + rpr.

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52
Q

primary syphilis - one dose of 2.4units of benzathine penicillin G
however if
secondary syphilis/ latent syphilis, patient will require weekly treatments of 2.4million units of benzathine penicillin G for 3 consecutive weeks

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53
Q

toxoplasma gonddi is a common protozoan parasite that can be found in humans and domestic animals.
domestic cats are the only host for the oocyst.

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54
Q

symptomiatic BV associated with preterm delivery. treatment in pregnancy consists of oral metronidazole for 7 days

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55
Q

chorioamnionitis/ triple I is diagnosed by maternal fever with uterine tenderness, elevated maternal WBC count and fetal tachycardia.

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56
Q

ciprofloxacin has been associated with renal anomalies in the fetus, particularly in 1st trimester exposure

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renal anomalies.

this med is generally not given in pregnancy. amoxicillin and keflex are thought to be safe in pregnancy; both are category B which means there were no adverse outcomes in animal reproduction studies

57
Q

pyelonephritis has significant morbidity during pregnancy and is associated with high rates of ICU admission and acute respiratory distress syndrome (ARDS).

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58
Q
diagnosis of chorioamnionitis - maternal fever of greater than 39degrees C and at least one of the following signs:
elevated maternal WBC count
maternal tacycardia
uterine tenderness
fetal tachycardia
and foul smelling amniotic fluid.
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59
Q

gold standard for dx of chorioamnionitis is culture of amnioc fluid which can be obtained via amniocentesis.

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60
Q

most common organism that causes chorioamnionitis is polymicrobial infection of rectovaginal organisms

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61
Q

parovirus b19 causes erythema infectiosum 5th disease

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classified with low grade fever and red macular rash giving the “slapped cheek” appearance and usually resolves with minimal intervention.

62
Q

acute parovirus infections may be transmitted through placenta to fetus. 1s trimester infections habe been associated with miscarriage, but midtrimester and later infections are associated with fetal anemia and hydrops.

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63
Q

currently, doppler ultrasound to examine peak systolic velocity of the MCA is frequently used to identify fetal anemia

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doppler ultrasound to examine peak systolic velocity of the MCA is frequently used to identify fetal anemia

64
Q

currently, doppler ultrasound to examine peak systolic velocity of the MCA is frequently used to identify fetal anemia

A

doppler ultrasound to examine peak systolic velocity of the MCA is frequently used to identify fetal anemia

65
Q

parovirus b19 causes fetal anemia by bone marrow suppression. severe anemia can lead to high output cardiac failure, hydrops and fetal death.

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66
Q

antiretroviral therapy recommended for all HIV + patients regardless of viral load of CD4 level.

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67
Q

currently, antiretroviral therapy in pregnancy includes a 3 drug regimen generally started preconception or at tim eof HIV diagnosis

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68
Q

3 drug cART regiment of zdv, lamivudine, and lopinavir/ritonavir

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69
Q

c/s delivery has been shown to lower transmission rates by 2/3 compared with vaginal delivery in patients on no therapy and particularly without onset of labor / rom in the setting of high viral load.

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70
Q

however, in women with VL < 1,000 copies/ mL there is no additional benefit of cs delivery vs vaginal delivery in hiv perinatal transmission. therefore, c/s delivery should be considered in HIV infected pregnant women with viral loads > 1,000 copies/ mL and without long standing onset of labor / rom

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