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INFECTIONS DURINGPREGNANCY
TYPES
⚫BACTERIAL INFECTION
⚫VIRAL INFECTIONS
⚫FUNGAL INFECTIONS
⚫PARASITIC AND PROTOZOAL INFECTIONS
BACTERIAL INFECTIONS
GROUP B STREPTOCOCCAL INFECTION (GBS)
Organism
⚫Streptococcus agalactiae
Risk factors
Risk factors for early onset neonatal GBS include:
⚫Positive prenatal culture for GBS this pregnancy
⚫Preterm birth of less than 37 weeks of gestation
⚫PROM for longer than 18 hours.
⚫Intrapartum maternal fever greater than 38°C
screening
Management
The CDC recommends intrapartum antimicrobial
prophylaxis for
⚫Preterm labour before 37 weeks of gestation
⚫Duration of ruptured membranes longer than 18
hours.
⚫Intrapartum temperature greater than 100.4°F
⚫pencillin G
⚫Ampicillin.
⚫Cefazolin .
TUBERCULOSIS IN PREGNANCY
Risk factors for TB
⚫Positive family history or past history
⚫Low socioeconomic status
⚫Area with high prevalence of tuberculosis
⚫HIV infection
⚫Alcohol addiction
⚫Intravenous drug abuse.
Clinical features:
⚫Cough
⚫Weight loss
⚫Sleep sweats
⚫Evening pyrexia
⚫Malaise and
⚫Fatigue
⚫enlarged lymph nodes or pleural rub
Diagnosis:
⚫Tuberculin skin test
⚫X- ray chest
⚫Early morning sputum (3 samples) for acid- fast
bacilli
⚫Gastric washings
⚫Diagnostic bronchoscopy
⚫Extra pulmonary sites- lymph nodes, bones ( rare in
pregnancy).
Effect of pregnancy on pulmonary
TB
⚫ Pregnancy does not worsen the clinical
course of TB.
Effect of TB on pregnancy
⚫The fertility rate is low
⚫a higher incidence of toxaemia, Preterm labour PPH
and difficult labour in pregnant patients suffering
from TB.
⚫the maternal and fetal prognosis is good and
therapeutic abortion is not necessary except in a
patient with multidrug resistance.
Effect on the mother
⚫Pregnancy may worsen the maternal outcome in
drug resistant patients. Medical termination of
pregnancy may be considered in selected cases.
Effects on the fetus
⚫Effective chemotherapy has reduced the
incidence of low birth weight.
⚫ Streptomycin use was associated with
congenital deafness.
Treatment
⚫Rifampicin
⚫isoniazid
⚫Ethambutol
⚫Pyrazinamide
⚫Newer anti-tubercular drugs include clofazimine,
ciprofloxacin, ofloxacin, amikacin, clarithromycin
and azithromycin.
Obstetric management:
⚫In pregnancy
⚫In labour
⚫Breast feeding
⚫Contraception
BACTERIAL VAGINOSIS
BACTERIAL VAGINOSIS
Organism-
⚫Gardnerella vaginalis, Mobiluncus, Mycoplasmas
hominis, Prevotella, and Atopobium vaginae.
Transmission
⚫sexual intercourse, hormonal changes, pregnancy,
antibiotic administration, or use of nonoxynol-9
spermicidal products, douching.
Signs and symptoms
⚫Thin, gray or white
homogeneous vaginal
discharge.
⚫Increased vaginal discharge
odor (fishy) after intercourse.
⚫Alkaline pH (> 4.5); bacterial
vaginosis does not cause vaginal
itching or dysuria.
Treatment
symptomatic
metronidazole (Flagyl), 500 mg orally twice daily for
7 days .
Asymptomatic
⚫asymptomatic pregnant patients with antibiotics for
bacterial vaginosis to prevent pre term labour.
Effect on pregnancy outcome
⚫spontaneous abortion, premature rupture of
membranes and pre term labour.
⚫chorioamnionitis and postpartum endometritis.
⚫May cause neonatal septicemia.
CANDIDIASIS
CANDIDIASIS
Organism:
⚫Candida albicans, Candida tropicalis
Transmission
⚫cause vaginal pH to be more alkaline and high
estrogen levels causing increased production of
vaginal glycogen.
Signs and symptoms
⚫Vaginal and vulvar irritation (erythematous and
edematous)
⚫Pruritic, white, curd like vaginal discharge
⚫Yeasty odor
⚫Dysuria
⚫Dyspareunia
Screening
⚫Saline or KOH wet mount microscopically examined:
shows hyphae, pseudohyphae and budding yeast
⚫Usually pH lower than 4.7
⚫Whiff test absent amine (fishy) odor
Treatment in pregnancy
⚫Use an antifungal, intravaginal agent such as
butoconazole, clotrimazole, miconazole or
terconazole
⚫Sitz baths
LEPROSY (HENSEN DISEASE) IN
PREGNANCY
⚫mycobacterium leprae
⚫With established leprosy, there is chance of
exacerbation of the lesions during pregnancy.
⚫However, the baby should be separated from the
infected mother, immediately after delivery.
⚫When the disease becomes quiescent and non-
infectious, the baby may be given to the mother.
⚫Dapsone and Clofazimine appear safe in pregnancy..
GONORRHOEA
GONORRHOEA
Organism:
⚫Neisseria gonorrhoeae
Transmission:
⚫ Gonorrhea is transmitted by close sexual
contact. The incubation period is 3 to 5 days.
Signs and symptoms
⚫Vaginal discharge: may be profuse purulent and
yellow green
⚫Itching or swelling of vulva
⚫Dysuria
⚫Dyspareunia
⚫Joint and tendon pain
⚫Anal discharge, discomfort and pain with rectal
infection.
Screening
⚫Molecular diagnostics .
⚫Endocervical culture
Treatment in Pregnancy
⚫cefixime, 400 mg orally, or one dose of Ceftriaxone,
125 mg intramuscularly.
⚫Sexual partners within the preceding 60 days should
be identified, examined, cultured and treated.
Effect on pregnancy outcome
⚫It can affect pregnancy outcome in any trimester,
causing chorioamnionitis, pre term delivery, PROM,
IUGR or postpartum sepsis.
⚫If the organism is present at the time of delivery, the
greatest neonatal risk is gonococcal ophthalmia,
which can cause blindness.
SYPHILIS
SYPHILIS
⚫Syphilis is a sexually transmitted disease caused by
Treponema pallidum.
Signs and symptoms
⚫Incubation- 10 to 90 days
⚫Primary syphilis
Stage one is evident by a chancre, which is highly
infectious, painless, round ulcerated sore that does
not get better fast. It may last 3 to 6 weeks.
Secondary syphilis:
⚫evident by a maculopapular rash
⚫This rash usually exhibited between 1 week and 3
months after primary chancre. It typically clears in
2-6 weeks but can last upto one year.
⚫Other manifestations include wart like genital
growth, lymphadenopathy, fever, sore throat, patchy
hair loss, head ache weight loss, muscle aches and
tiredness.
Latent syphilis:
⚫Stage three is usually asymptomatic. The spirochete
goes to hiding for 5 to 20 years. The patient is
seroactive during this stage.
⚫During the first year of this stage, the patient is
infectious.
⚫Tertiary syphilis:
⚫The fourth stage is remanifestation of the disease. It
slowly destroys the heart eyes, brain, CNS, and
occasionally the liver, bones and skin.
Investigations:
⚫Serological test- VDRL
⚫fluorescent treponemal antibody absorption test
(FTA- ABS)
⚫Treponema pallidum micro –haemagglutination
(MHA- TP) test which are specific.
Treatment
For Mother:
⚫For primary and secondary syphilis(<I year
duration): Benzathine penicillin 2.4 million units
intramuscularly single dose.
⚫When the duration is more than 1 year- Benzathine
penicillin 2.4 million units intramuscularly weekly
for 3 doses is given.
⚫For Baby:
⚫Positive serological reaction with a single
intramuscular dose of penicillin G 50,000 units per
kg body weight.
⚫Infected baby with positive serological reaction- (1)
isolation with mother (2) IM administration of
aqueous procaine penicillin G 50,000 units per kg
body weight each day for 10 days.
URINARY TRACT INFECTIONS
URINARY TRACT INFECTIONS
⚫Asymptomatic bacteriuria
⚫Cystitis
⚫Pyelonephritis
⚫Organism:
⚫E.coli, klebsiella pneumonia, proteus species in
recurrent UTI. Less frequent gram positive causative
organism includes group B streptococci, enterococci
and staphylococci.
Transmission:
⚫ sexual intercourse and improper wiping after
defecation.
Signs and symptoms
⚫Urinary frequency
⚫Urinary urgency
⚫Dysuria
⚫Hesitancy and dribbling
⚫Suprapubic tenderness
⚫Gross hematuria
⚫Accompanying symptoms with pyelonephritis
usually are chills, fever, and backpain with
costovertebral angle tenderness.
Screening
⚫Microscopic examination shows WBC, bacteria may
or may not be present.
⚫Dip urine may be positive for nitrates and leukocyte
esterase
⚫Clean catch midstream specimen for culture and
sensitivity.
Treatment in pregnancy for
asymptomatic bacteriuria and acute
cystitis:
⚫antibiotic therapy for asymptomatic bacteruria is
effective in lowering the risk of pyelonephritis and
preterm labour. Usually 7-10 day course is preferred
Treatment in pregnancy for
pyelonephritis:
⚫The usual treatment is amoxicillin clavulanate(
augmentin) 875 mg bd for 7-10 days
⚫Cephalosporin
Effect on pregnancy outcome
⚫The endotoxins released from gram negative bacteria
may stimulate the production of prostaglandins and
thus cause preterm labour.
VIRAL INFECTIONS IN
PREGNANCY
AIDS
⚫Organism:
⚫the HIV organism is a retrovirus of the lentivirus
family that has an affinity for the T- lymphocytes,
macrophages and monocytes.
Transmission
⚫infected blood or body secretions of semen or vaginal
fluid.
⚫unprotected sexual activity
⚫sharing of contaminated needles.
⚫Pediatric HIV primarily results from perinatal or
breast feeding transmission
Immunopathogenesis
⚫leads to slow but progressive destruction of T cells
⚫The incubation period is about 1 to 3 weeks.
⚫After a peak viral load there is gradual fall
⚫more destruction of host cells  progressive
immunosupression  opportunistic infections and
cancers
Clinical presentation:
⚫fever, malaise, headache, sore throat,
lymphadenopathy and maculopapular rash.
⚫constitutional symptoms like weight loss,
lymphadenopathy or protracted diarrhea.
⚫multiple opportunistic infections with candida,
tuberculosis, pnemocystitis, and others
Diagnosis:
⚫enzyme immunoassay
⚫Western blot test or immunofluroscence assay
Management:
⚫Prenatal care
⚫Voluntary serological testing for HIV
⚫Counseling
⚫assessed by – CD4+ T lymphocyte counts and HIV
RNA at every 3 to 4 months interval
⚫Highly active antiretroviral therapy(HAART)
(1)Nucleoside reverse transcriptase inhibitors
(Zidovudine, Zalcitabine, Lamivudine, Stavudine)
(2)Nonnucleoside reverse transcriptase inhibitors
(Nevirapine, Delavirdine) (3) Protease inhibitors
(Indinavir, Saquinavir, Ritonavir) (4) Entry
inhibitors (Efavirenz).
⚫Intrapartum care
⚫Zidovudine is given IV infusion starting at the onset
of labour or 4 hours before caesaren section. Loading
dose 2 mg/kg/hr until cord clamping is done.
⚫Amniotomy and oxytocin augmentation for vaginal
delivery should be avoided whenever possible.
⚫Elective caesarean delivery is recommended at 38
weeks of women receiving HAART
⚫Postpartum care
⚫Breast feeding
⚫Zidovudine syrup- 2mg/kg, is given to the neonate 4
times daily for first 6 weeks of life.
TORCH INFECTIONS
⚫Toxoplasmosis
⚫This is a systemic infection caused by the protozoan
Toxoplasma gondii
Consequences of fetal infection
⚫The classic triad of hydrocephalus, intracranial
calcification and chorioretinitis.
⚫The common manifestations are mental retardation,
seizure disorder, hepatosplenomegaly and central
nervous system (CNS) involvement.
Management
⚫Prenatal counselling
⚫Prevention
⚫Medications: Pyrimethamine and sulphadiazine
plus folinic acid.
Rubella
⚫RNA toga virus
⚫spread by nasopharyngeal droplets, with an
incubation period of 14- 21 days.
⚫A disease prodrome of malaise, fever, headache,
conjunctivitis and pharyngitis, lasting 1-5 days,
precedes the classic manifestations of widespread
pink/red maculopapular rash and generalized
lymphadenopathy.
Effect of maternal infection on the fetus
and newborn
⚫Spontaneous abortion
⚫Congenital rubella syndrome causing symmetric
IUGR, congenital heart disease, hepato-
splenomegaly and thrombocytopenic purpura.
⚫CNS manifestations include deafness, eye lesions
such as congenital cataract, retinopathy,
microphthalmia, microcephaly, pan-encephalitis,
brain calcification and psychomotor disorders.
Management
⚫Immunization of all adult women.
⚫Education of parents about the dangers of rubella
infection.
⚫All pregnant women should be screened for rubella
antibodies at the first prenatal visit.
Cyto megalo virus
⚫It is a double stranded DNA virus that belongs to the
herpes virus family. Humans are the only known
hosts of this virus.
Transmission
⚫CMV is transmitted through blood via transfusion or
transplacental route commonly and droplet
infection. Body fluids: semen, vaginal secretions,
saliva, urine, breast milk (rare), organ transplant and
rarely through direct contact.
Effect of maternal infection on the fetus
and the newborn
⚫About 15% of the infants are symptomatic
non-immune hydrops,
hepatosplenomegaly, CNS
symmetric
sequeale
IUGR,
like
chorioretinitis, microcephaly, hydrocephaly and
calcifications.
⚫ Almost 85% of infants are asymptomatic
Management
⚫Prenatal counselling is highly recommended.
⚫Drugs such as ganciclovir, forcarnet and cidoforvir.
Herpes simplex virus
⚫simplex virus is a member of the herpes virus family.
It is a DNA virus
Transmission
⚫Transmission is through intimate mucocutaneous
contact. It is one of the most contagious sexually
transmitted diseases (STDs).
Significance:
⚫Spontaneous abortion
⚫Intra uterine growth retardation
⚫Fetal death
⚫Preterm labour
⚫Neonatal infection
⚫Neonatal herpes
Management
⚫Acyclovir administered 200mg, four times daily for
14 days.
⚫Topical application of acyclovir cream
⚫Severe infections : IV administration of Acyclovir 5
mg/kg body weight/ 8 hourly for 5 days.
HEPATITIS B
⚫The virus is transmitted by parenteral route,
sexual contact, and vertical transmission and also
through breast milk.
Maternal infection
⚫The acute infection is manifested by flu like illness as
malaise, anorexia, nausea and vomiting. There may
be arthralgia and skin rash.
Diagnosis
⚫Diagnosis is confirmed by serological detection of
HBsAg (denote high infectivity) and antibody to
hepatitis B core antigen (HBcAg).
Management
⚫Rest
⚫Isolation
⚫Nutrition
⚫Drugs
⚫Prevention of complications
HUMAN PAPILLOMA VIRUS ( HPV)
⚫Condylomata acuminate
Effect in pregnancy
⚫can grow more rapidly during pregnancy and are
located over the genital tract and the perineal
regions.
⚫ They can grow so large as to cause dystocia and
severe hemorrhage when disruption occurs during
vaginal delivery.
Management
⚫Excisions of the lesions by cautery or use of
cryosurgery
PARASITIC AND PROTOZOAL
INFESTATIONS
⚫MALARIA
Effects of malaria on the mother
⚫Anaemia
⚫Hypoglycemia
⚫Metabolic acidosis
⚫Jaundice due to hepatic dysfunction
⚫Renal failure- due to block of renal micro circulation
⚫Pulmonary edema and respiratory distress
⚫Convulsions and coma- cerebral malaria
Effects on the fetus
⚫Abortion
⚫Preterm labor
⚫Pre maturity
⚫IUGR
⚫IUFD
Management
⚫Prevention from mosquito bites using mosquito nets
and repellents.
⚫Prophylaxis with chloroquine ( 300mg base) orally
once a week
INTESTINAL WORMS
CHLAMYDIA
⚫Organism:
⚫Chlamydia trachomatis
NURSING MANAGEMENT
⚫Primary prevention of STI
⚫Secondary prevention
⚫Tertiary prevention
Nursing diagnosis
⚫Acute pain related to excoriation from scratching
pruritic areas, ulcerations etc.
⚫Impaired skin integrity related to presence of skin
infections.
⚫Risk for complications, IUGR; spontaneous abortion;
PROM; preterm labour and fetal death related to
presence of STDs or other infections.
⚫Risk for fetal or neonatal infections, fetal
malformations and anomalies related to
complications of maternal TORCH or STDs.
⚫ Sexual dysfunction or ineffective sexuality patterns
related to perineal discomfort and prescribed abstinence
during treatment.
⚫ Self esteem disturbance related to the diagnosis of
sexually transmitted disease.
⚫ Ineffective coping related to diagnosis of STDs.
⚫ Knowledge deficit related to disease condition, mode of
transmission, fetal outcome, possible treatment
opportunities etc.
⚫ Fear and anxiety related to the possible fetal outcome
secondary to the infections.
THANK YOU……

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