2. CONTENTS
• INTRODUCTION
• SCREENING FOR TORCH INFECTION
• CLINICAL FEATURES OF TORCH INFECTION
• APPOROACH TO INFANT WITH SUSPECTED
INTRAUTERINE INFECTION
• SUMMARY OF MANAGEMENTS
3. INTRODUCTION
• The original concept of the TORCH perinatal
infections was to group five infections with
similar presentations, including rash and
ocular findings.
These five infections are:
●Toxoplasmosis
●Other (syphilis)
●Rubella
●Cytomegalovirus (CMV)
●Herpes simplex virus (HSV)
Epps RE, Pittelkow MR, Su WP. TORCH syndrome. Semin Dermatol 1995; 14:179.
4. Incidence
• World wide incidence of TORCH varies it is up to
10% of congenital infection.
• Incidence in india the specific IgM antibodies
were found to be positive 1
– 19.4% cases for toxoplasmosis
– 30.4% cases for the Rubella virus
– 34.7%cases for CMV
– 33.5%for the HSV-2 infections.
• Incidence in nepal the seropositivity for T.
gondii was 50%, rubella virus 50%, HSV-2 33.3%,
and CMV 8.3% in pregnancy.2
1.Sen MR, Shukla BN, Tuhina B. Prevalence of Serum Antibodies to TORCH Infection in and Around
Varanasi, Northern India. J Clin Diagn Res. 2012 Nov;6(9):1483-5
5. TOXOPLASMOSIS
• Caused by protozoan – Toxoplasma gondii
Domestic cat is the definitive host with infections
via:
– Ingestion of cysts (meats, garden products) Contact
with oocysts in feces.
• Congenital Toxoplasmosis
– United States – 1 in 1000 to 1 in 10000 Primary
maternal infection in pregnancy
– 1 in 3 risk of fetal infection
– Infection rate higher with infection in 3rd trimester
– Fetal death higher with infection in 1st trimester
American Academy of Pediatrics. Toxoplasma gondii Infections. In: The Red Book 2006, 27th
Ed. p.666
6. • The incidence of prenatal infection resulting in
birth of a newborn with congenital
toxoplasmosis
– United State -0.8 per 10,000 live births
– France -10 per 10,000 live births
– Globally 3rd
of population is affected.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
8. Clinical features-Maternal
• maternal symptoms in immunocompetent
– Fatigue
– Fever
– Headache
– muscle pain
– maculopapular rash
– posterior cervical lymphadenopathy.
• In immunocompromised.
– Encephalitis
– Retinochoroiditis
– mass lesions
• Four fold increase in preterm delivery rate.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
9. Clinical features
• estimated the risk to be 15 percent at 13
weeks,44 percent at 26 weeks, and 71
percent at 36 weeks. 1
• Asymptomatic at birth in 70% - 90%
• Symptoms become apparent later in life
• Classic Triad
– Chorioretinitis *
– Hydrocephalus
– Intracranial calcifications
• Consequences of intrauterine meningo-
encephalitis
• Initially asymptomatic infants are still at
high risk of developing abnormalities,
especially chorioretinitis
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
10. Screening
• Prenatal testing with varied sensitivity not
useful for screening
• Routine neonatal screening with IgM testing
implemented in some areas
• Identifies infected asymptomatic infants who
– may benefit from therapy
Guerina NG et al., Neonatal screening and early treatment for congenital Toxoplasma gondii
infection. The New England Regional Toxoplasma Working Group. NEJM 1994; 330:1858
11. diagnosis
• Serology
• DNA PCR sensitivity is 81-88%.
• Histology
• Isolation of toxoplasma gondii-91-94%.
• Usg finding of congenital infection
– Intracranial calcifications
– Hydrocephaly
– Liver calcifications
– Ascites
– Placental thickening
– Hyperechoic bowel
– Growth restriction
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill publication,
2014 pp 1255.
Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk ,
2011, pp-556.
12. Management
Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk , 2011, pp-556.
13. Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk , 2011, pp-556.
14. Syphilis
• Nickname “lues” came from the Latin lues venereum, which means
“disease,” “sickness,” or “pestilence,” and originally was loosely
applied to any venereal disease.
• Caused by – Treponema pallidium(spirochete)
• Incidence of syphilis
• Worldwide- 10.6 million cases of syphilis
• In Nepal - 2.5-19.3 % (STD/AIDS Conselling and Training Services, Family Health International, USAID. Kathmandu FSW Seroprevalence Study. 2000)
• In USA-
– 0.9 case per 100,000 persons in 2012
– 9-percent decrease from 2010
Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk , 2011, pp-556.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill publication, 2014 pp 1255.
15. • Transmitted via sexual contact.
• Placental transmission as early as 6wks gestation
– Typically occurs during second half
– Mother with primary or secondary syphilis more likely to
transmit than latent disease
• The incubation period averages 3 weeks—3 to 90 days—
depending on host factors and innoculum size.
• These are associated with the highest spirochete loads and
transmission rates of up to 30 to 50 percent.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
16. Clinical manifestation
Primary Syphillis- Chancre, 2 to 8week period
Secondary syphilis develop after 4 to 10 week of infection
– dermatological abnormalities - 90 percent of women.
– A diffuse macular rash plantar and palmar target like lesions,
patchy alopecia, and mucous patches may be seen.
– Condylomata lata are flesh-colored papules and nodules
found on the perineum and perianal area.
– constitutional symptoms
– Up to 40 percent will have cerebrospinal fluid abnormalities,
although only 1 to 2 percent will develop clinically apparent
aseptic meningitis.
– Hepatitis, nephropathy, ocular changes, anterior uveitis,
and periostitis may also develop.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
17. Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
18. • Latent syphilis develops when primary or secondary syphilis is
not treated.
– reactive serological testing
– resolved clinical manifestations.
• Early latent syphilis is latent disease acquired within
the preceding 12 months.
• Disease diagnosed beyond 12 months is either late
latent syphilis or latent syphilis of unknown duration.
• Tertiary or late syphilis
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
19. Clinical features
• Fetal:
– Stillbirth
– Neonatal death
– Hydrops fetalis
• Intrauterine death in 25%
• Perinatal mortality in 25-30% if untreated
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
20. Diagnosis
• Direct microscopic examination.
• Usg features of congenital syphilis.
• Serological examination.
– VDRL
– RPR
– TPHA
– FTA-abs
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
21. Management
Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk , 2011, pp-556.
22. Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk , 2011, pp-556.
24. Rubella
• Another name: German
measles or third disease
• Caused by : RNA virus
• Rubella infection in the first
trimester, however, poses
significant risk for abortion and
severe congenital
malformations.
• The incubation period is 12 to
23 days.
25.
26. Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition, elsevier , uk , 2011, pp-556.
27. Diagnosis
• Rubella may be isolated from the urine, blood, nasopharynx,
and cerebrospinal fluid for up to 2 weeks after rash onset.
• Serology
– Specific IgG, IgM
– If no confirmed IgG avidity test is to be done.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
28. Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition,
elsevier , uk , 2011, pp-556.
29. Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition,
elsevier , uk , 2011, pp-556.
30. CMV
• CMV, a DNA virus, is a member of the herpes family of
viruses, which causes a number of infectious syndromes in
humans.
• Three disease states are particularly important:
– intrauterine
– neonatal infection
– immunocompromised patient.
• 0.2 to 2.5 percent of all neonates
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
31. • The virus is secreted into all body fluids, and person-
to-person contact with viral-laden saliva, semen,
urine, blood, and nasopharyngeal and cervical
secretions can transmit infection.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
32. Spectrum of infection
• Intrapartum – From Cervical and Vaginal Secretions
– 2% to 28% of seropositive pregnant women shed CMV
– Approximately 50% of exposed infants become infected
– Develop clinical signs of CMV disease at about 4 to 6 weeks
of age.
• Postpartum period – Breast Feeding
– 9% to 88% of seropositive women shed CMV into their milk.
– 50% to 60% of infants become infected.
– Show no significant clinical signs (re-activation disease)
• Blood Transfusions
– 2 -20% from unscreened or unfiltered blood
Stehel EK and Sanchez PJ. Cytomegalovirus Infection in the Fetus and Neonate. NeoReviews
2005;6;e38-e45
33. Infant outcome following cytomegalovirus (CMV)
maternal infection in pregnancy.
Dk james , infection in pregnancy in High Risk Pregnancy Management Option, 4th
edition,
elsevier , uk , 2011, pp-556.
34. diagnosis
• Serology
– CMV IgG, CMV IgM
– CMV IgM is not useful ?
– CMV IgG Avidity test should be done
• DNA PCR
• Neuclic Acid Amplification test
– Sensitivities range from 70 to 99 percent and depend on
amniocentesis timing
• Usg finding of congenital CMV infections
– Findings include microcephaly, ventriculomegaly, and cerebral
calcifications; ascites, hepatomegaly, splenomegaly, and
hyperechoic bowel; hydrops; and oligohydramnios
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
35. Clinical features
• Most infections are asymptomatic, but 10 to 15 percent of
infected adults have a mononucleosis-like syndrome
characterized by
– Fever
– Pharyngitis
– Lymphadenopathy
– polyarthritis.
• Immunocompromised women may develop
– Myocarditis
– Pneumonitis
– Hepatitis
– retinitis,
– Gastroenteritis
– meningoencephalitis.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
36. • Recurrent maternal infection infects the fetus in only
0.15 to 1 percent of cases.
• A review of nine studies of CMV vertical transmission
rates reported
– first-trimester 36 percent
– second-trimester 40 percent
– third-trimester 65 percent
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
38. Munro SC et al., Diagnosis of and Screening for CMV infection in Pregnant Women. J. Clin Micro
2005; 43 (9); 4713-4718
39.
40. Management
• The management of the immunocompetent
pregnant woman with primary or recurrent CMV
is limited to symptomatic treatment.
• Counseling for continuation or termination
– pregnancy termination may be an option for some.
• Ganciclovir
• No vaccine available till now.
• Avoid primary infection to mother.
• Encourage maintain personal hygiene.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
41. Herpes Simplex Virus
• Genital herpes simplex virus infection is one of the most
common sexually transmitted diseases.
• DNA Virus
• Two type
– HSV 1
– HSV 2
• Type 1 is responsible for most nongenital infections.
However, more than half of new cases of genital herpes in
adolescents and young adults are caused by HSV-1
infection.
• Type 2 HSV is recovered almost exclusively from the genital
tract and is usually transmitted by sexual contact. Most
recurrences—greater than 90 percent—are secondary to
HSV-2.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
42. • Neonatal transmission is by three routes:
– Intrauterine in 5 percent.
– Peripartum in 85 percent.
– Postnatal in 10 percent.
• The overall transmission rate is 1 in 3200 to 1 in
30,000 births depending on the population
studied.
• Infants born to women who acquire genital HSV
near the time of delivery have a 30- to 50-
percent risk of infection.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
43. Clinical features
• First episode primary infection describes cases in which HSV-
1 or -2 is isolated from genital secretions in the absence of
HSV-1 or -2 antibodies.
• First episode nonprimary infection is diagnosed when HSV is
isolated in women who have only the other serum HSV-type
antibody present.
• Reactivation disease is characterized by isolation of HSV-1 or
-2 from the genital tract in women with the same serotype
antibodies.
• Asymptomatic viral shedding is defined by HSV as detected
by culture or PCR in the absence of clinical findings.
• Most infected women shed virus intermittently, and most
HSV transmission to a partner occurs during periods of
asymptomatic viral shedding.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
44. First-episode primary genital herpes simplex virus
infection. On the left labium majora and mons, both
vesicles and ulcers are seen.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
45. Fetal features
• Most are asymptomatic at birth
• 3 patterns of -equal frequency
with symptoms between birth
and 4wks:
– Skin, eyes, mouth (SEM)
– CNS disease
– Disseminated disease (present
earliest)
• Initial manifestations very
nonspecific with skin lesions
NOT necessarily present
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
46. Diagnosis
• Cell culture and PCR
• Serology- HSV glycoproteins G1 and G2
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
48. Varicella Zoster
• Herpes virus family, DNA virus.
• If infection occurs in first trimester 4.9% risk of congenital
varicella .
• Congenital Syndrome
-Limb hypoplasia
-Ocular abnormalities
-CNS abnormalities ( convulsive disorders ).
-Dermatomal scarring
• Serology (IgG and IgM).
• Screening: Routine screening generally not recommended.
• Prevention: If pregnant woman (with no history of previous
chickenpox) is exposed, perform STAT Varicella IgG.
• Exposed neonate should receive VZ IG prophylaxis.
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
49. Parvovirus
• Human parvovirus B19 (DNA virus)
- erythema infectiosum in childhood
- chronic arthropathy
- chronic bone marrow failure (immunodefic)
- aplastic crisis (Sickle disaease)
• Incubation 4-14 days
• Respiratory droplet spread
• High fever, “Slapped cheek syndrome’
non specific rash, no symptoms
Hydrops (anaemia, myocarditis)
Cunninghams , Infectious Disease in williams obstetrics 24th
edition, newyork , macgraw hill
publication, 2014 pp 1255.
50.
51. Take home message
• Serology is not useful in TORCH infection
• Routine screening is not recommended in
every type of TORCH infection , screening
should recommended in endemic areas.
• In our context we routinely do VDRL for
syphilis.
• Prevention Is better than cure.
Infections acquired in utero or during the birth process are a significant cause of fetal and neonatal mortality and an important contributor to early and later childhood morbidity.
The use of serologic tests for demonstration of specific antibody
to T. gondii in maternal blood is the initial and primary
method of diagnosis. IgG antibodies usually appear within
1 to 2 weeks of acquisition of an infection, peak within 1 to
2 months, decline at various rates, and usually persist for life.
The most common methods of measurement of IgG include
the Sabin-Feldman dye test, the ELISA, the immunofluorescence
assay (IFA), and the modified direct agglutination
test.IgM antibodies, conversely, may appear earlier and
decline more rapidly than IgG antibodies. They are measured
by ELISA, IFA, and the immunosorbent agglutination
assay.
Sensitivity of the VDRL and RPR tests are estimated to be 78-86% for detecting primary syphilis, 100% for detecting secondary syphilis, and 95-98% for detecting tertiary syphilis. Specificity ranges from 85-99% and may be reduced in individuals who have coexisting conditions (ie, collagen vascular disease, pregnancy, intravenous drug use, advanced malignancy, tuberculosis, malaria, viral and rickettsial diseases)
FTA-ABS is commonly used as a confirmatory test following positive VDRL or RPR test findings. FTA-ABS has a sensitivity of 84% for detecting primary syphilis infection and almost 100% sensitivity for detecting syphilis infection in other stages. Its specificity is 96%.[19]
When dark-field microscopy is not available, direct immunofluorescence staining of fixed smears (direct fluorescent antibody T pallidum [DFA-TP]) is an option. Both procedures detect the causative organism at a rate of approximately 85-92%.
2.administered for 6 weeks to neonates with symptomatic central nervous system disease prevents hearing deterioration at 6 months and possibly later