Download Risks associated with toxoplasmosis during pregnancy

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

African trypanosomiasis wikipedia , lookup

Herpes simplex wikipedia , lookup

Microbicides for sexually transmitted diseases wikipedia , lookup

Hookworm infection wikipedia , lookup

Dirofilaria immitis wikipedia , lookup

Schistosomiasis wikipedia , lookup

Sexually transmitted infection wikipedia , lookup

Chickenpox wikipedia , lookup

Trichinosis wikipedia , lookup

Coccidioidomycosis wikipedia , lookup

Human cytomegalovirus wikipedia , lookup

Sarcocystis wikipedia , lookup

Hepatitis C wikipedia , lookup

Hospital-acquired infection wikipedia , lookup

Hepatitis B wikipedia , lookup

Oesophagostomum wikipedia , lookup

Neonatal infection wikipedia , lookup

Toxoplasma gondii wikipedia , lookup

Toxoplasmosis wikipedia , lookup

Transcript
CONSULTATION DRAFT
7.6 Toxoplasmosis
There is limited evidence to support screening for toxoplasmosis during pregnancy. As infection may be
transmitted to the baby during pregnancy, the focus is on providing women with advice about how to
avoid sources of toxoplasmosis.
7.6.1
Background
Toxoplasmosis, which is caused by the parasite Toxoplasma gondii, is usually asymptomatic and selflimiting. Symptoms when they occur include swollen lymph nodes, muscle aches and pains and fever.
When women who have not previously been exposed to the parasite (eg are non-immune) become
infected during pregnancy, the infection can be transmitted to the baby (Di Mario et al 2009). The
likelihood of a woman acquiring a primary infection during pregnancy varies, depending on local
prevalence (Pappas et al 2009):
•
low prevalence: the potential for a woman to become infected is low but if she is infected during
pregnancy it will most likely be a primary infection; and
•
high prevalence: primary infection during pregnancy is unlikely due to previous exposure.
Toxoplasmosis infection can be acquired by (Di Mario et al 2009):
•
eating raw or insufficiently cooked meat;
•
not washing hands thoroughly after handling raw meat or gardening;
•
contact with cat faeces (directly or indirectly through the soil or cat litter); or
•
contact with contaminated raw vegetables or fruits.
Prevalence and incidence
In Australia, primary infection with toxoplasmosis during pregnancy is rare (Gilbert 2002) although it is
estimated that between 60% and 80% of Australians are non-immune (Pappas et al 2009).
•
Country of origin: The prevalence of immunity to toxoplasmosis is high in Latin America, parts of
Eastern/Central Europe, the Middle East, parts of South-East Asia and Africa. There is a trend
towards lower prevalence of immunity in many European countries and the United States (Pappas
et al 2009).
•
Congenital toxoplasmosis: The incidence of congenital toxoplasmosis has been reported to range
from 0.03/1,000 live births in England and Wales (Gilbert et al 2006) to 0.3/1,000 live births in southeastern Brazil (Carvalheiro et al 2005).
Risks associated with toxoplasmosis during pregnancy
•
Mother-to-child transmission rates have been reported to range from 11.3% (Ricci et al 2003) to 18.5%
(Varella et al 2009). The risk of transmission increases with gestational age (from 5% at 12 weeks to
80% just before birth) (Dunn et al 1999). However, babies infected early in pregnancy have a greater
risk of congenital abnormalities (Di Mario et al 2009).
•
Congenital toxoplasmosis has been associated with stillbirth, intracranial abnormalities and/or
developmental delay, ocular inflammation (Gilbert et al 2006) and impaired hearing (Andrade et al
2008; Brown et al 2009). In a prospective cohort study (n=620), babies with congenital toxoplasmosis
had lower gestational age but there was no significant association with low birth weight or small for
gestational age (Freeman et al 2005).
CONSULTATION DRAFT
7.6.2
Screening for toxoplasmosis
Summary of the evidence
The evidence on the benefits to women and babies of screening for toxoplasmosis is limited and
inconclusive. Routine screening for toxoplasmosis during pregnancy is not recommended in the United
Kingdom (NICE 2008).
Diagnostic accuracy of tests
Screening tests for toxoplasmosis aim to identify whether maternal infection is acute or chronic. Studies
have compared a range of tests for IgG and IgM antibodies and IgG avidity (Petersen et al 2005; Thalib et
al 2005; Flori et al 2008; Bobic et al 2009; Kasper et al 2009; Lachaud et al 2009; Elyasi et al 2010; Wallon et al 2010;
Jost et al 2011; Lesle et al 2011; Robert-Gangneux et al 2011; Yamada et al 2011). There is great heterogeneity
between the studies, making it difficult to comment on the predictive and diagnostic accuracy of one
test over another. Studies into the timing of screening are limited and inconclusive (Gilbert & Gras 2003).
No evidence on the cost-effectiveness of screening for toxoplasmosis was identified.
Harms and benefits of screening
No high-level evidence on the harms and benefits of screening for toxoplasmosis was identified. A
narrative review found that psychological consequences of screening included parental anxiety due
to false positive results and uncertainties related to prognosis of children with an antenatal diagnosis of
congenital toxoplasmosis (Khoshnood et al 2007).
Recommendation 18
Grade C
Do not routinely offer screening for toxoplasmosis to pregnant women.
Availability of safe and effective treatments
Spiramycin and sulphonamide medications have been used to treat toxoplasmosis with the aim of
reducing mother-to-child transmission and the severity of fetal infection (Peyron et al 2010).
A systematic review (Thiébaut et al 2007) found weak evidence for an association between early
maternal treatment and reduced risk of congenital toxoplasmosis. A subsequent review (Peyron et al
2010) concluded that despite the large number of studies performed, it is still not known whether
treatment of pregnant women with presumed toxoplasmosis reduces the transmission of T. gondii.
While some studies have reported a lack of symptoms among babies whose mothers were treated
during pregnancy (Berrebi et al 2007; 2010; Cortina-Borja et al 2010), current research is inadequate to assess
whether the possible benefits outweigh the potential harm to the baby from treatment (Peyron et al
2010).
7.6.3
Discussing toxoplasmosis
There is suggestive evidence that women may have low levels of knowledge about the risks associated
with T. gondii (Ferguson et al 2011) and that health education approaches may help reduce risk of
congenital toxoplasmosis (Gollub et al 2008).
Recommendation 19
Grade C
Advise pregnant women about measures to avoid toxoplasmosis infection such as:
•
washing hands before handling food;
•
thoroughly washing all fruit and vegetables, including ready-prepared salads, before eating;
•
thoroughly cooking raw meat and ready-prepared chilled meals;
•
wearing gloves and thoroughly washing hands after handling soil and gardening; and
•
avoiding cat faeces in cat litter or in soil.
CONSULTATION DRAFT
7.6.4
Practice summary: toxoplasmosis
When: Early in pregnancy.
Who: Midwife; GP; obstetrician; Aboriginal and Torres Strait Islander Health Practitioner; Aboriginal and
Torres Strait Islander Health Worker; multicultural health worker.
Discuss sources of toxoplasmosis: Explain that becoming infected with toxoplasmosis during
pregnancy can lead to the infection being transmitted to the baby so it is important to take
measures to avoid infection.
Take a holistic approach: Women who are originally from an area of low prevalence are at risk of
primary infection if they travel to countries where toxoplasmosis is highly prevalent.
Document and follow-up: If a woman is tested for toxoplasmosis, tell her the results and note them in
her antenatal record. Have a system in place so that women who become infected with
toxoplasmosis during pregnancy are given ongoing follow-up and information.
7.6.5
Resources
SA Perinatal Practice Guidelines Workgroup (2004; reviewed 2010) Chapter 53 Toxoplasmosis in pregnancy. In: South
Australian Perinatal Practice Guidelines. Adelaide: SA Health.
http://www.health.sa.gov.au/ppg/Default.aspx?PageContentID=742&tabid=35
7.6.6
References
Andrade GM, Resende LM, Goulart EM et al (2008) Hearing loss in congenital toxoplasmosis detected by newborn
screening. Braz J Otorhinolaryngol 74(1): 21–28.
Antoniou M, Tzouvali H, Sifakis S et al (2007) Toxoplasmosis in pregnant women in Crete. Parassitol 49(4): 231–33.
Berrébi A, Assouline C, Bessières M-H et al (2010) Long-term outcome of children with congenital toxoplasmosis. Am J
Obstet Gynecol 203(552): e1–6.
Berrebi A, Bardou M, Bessieres MHl et al (2007) Outcome for children infected with congenital toxoplasmosis in the
first trimester and with normal ultrasound findings: a study of 36 cases. Eur J Obstet Gynecol Reprod Biol 135:
53–57.
Bobic B, Klun I, Vujanic M et al (2009) Comparative evaluation of three commercial Toxoplasma-specific IgG
antibody avidity tests and significance in different clinical settings. J Med Microbiol 58(Pt 3): 358–64.
Brown ED, Chau JK, Atashband S et al (2009) A systematic review of neonatal toxoplasmosis exposure and
sensorineural hearing loss. Int J Pediatr Otorhinolaryngol 73(5): 707–11.
Carvalheiro CG, Mussi-Pinhata MM, Yamamoto AY et al (2005) Incidence of congenital toxoplasmosis estimated by
neonatal screening: relevance of diagnostic confirmation in asymptomatic newborn infants. Epidemiol
Infect 133(3): 485–91.
Cortina-Borja, M, Tan, H. K, Wallon, M et al (2010) Prenatal treatment for serious neurological sequelae of congenital
toxoplasmosis: An observational prospective cohort study. PLoS Med 7(10): e1000351.
Di Mario S, Basevi V, Gagliotti C et al (2009) Prenatal education for congenital toxoplasmosis. Cochrane Database
Syst Rev 2009, Issue 1. Art. No.: CD006171. DOI: 10.1002/14651858.CD006171.pub2.
Dunn D, Wallon M, Peyron F et al (1999) Mother-to-child transmission of toxoplasmosis: risk estimates for clinical
counselling. Lancet 353(9167): 1829–33.
Elyasi H, Babaie J, Fricker-Hidalgo H et al (2010) Use of dense granule antigen GRA6 in an immunoglobulin G avidity
test to exclude acute Toxoplasma gondii infection during pregnancy. Clin Vaccine Immunol 17(9): 1349–5
Ferguson W, Mayne P, Cafferkey M et al (2011) Lack of awareness of risk factors for primary toxoplasmosis in
pregnancy. Irish J Med Sci 180(4): 807–11.
Flori P, Bellete B, Crampe C et al (2008) A technique for dating toxoplasmosis in pregnancy and comparison with the
Vidas anti-toxoplasma IgG avidity test. Clin Microbiol Infect 14(3): 242–49.
Freeman K, Oakley L, Pollak A et al (2005) Association between congenital toxoplasmosis and preterm birth, low
birthweight and small for gestational age birth. BJOG 112(1): 31–37.
Gilbert R & Gras L (2003) Effect of timing and type of treatment on the risk of mother to child transmission of
Toxoplasma gondii. BJOG 110(2): 112–20.
Gilbert R, Tan HK, Cliffe S et al (2006) Symptomatic toxoplasma infection due to congenital and postnatally acquired
infection. Arch Dis Childhood 91(6): 495–98.
Gollub EL, Leroy V, Gilbert R et al (2008) Effectiveness of health education on Toxoplasma-related knowledge,
behaviour, and risk of seroconversion in pregnancy. Eur J Obstet Gynecol Reprod Biol 136(2): 137–45.
Jost C, Touafek F, Fekkar A et al (2011) Utility of immunoblotting for early diagnosis of toxoplasmosis seroconversion in
pregnant women. Clin Vaccine Immunol 18(11): 1908–12.
CONSULTATION DRAFT
Kasper DC, Prusa AR, Hayde M et al (2009) Evaluation of the Vitros ECiQ immunodiagnostic system for detection of
anti-Toxoplasma immunoglobulin G and immunoglobulin M antibodies for confirmatory testing for acute
Toxoplasma gondii infection in pregnant women. J Clin Microbiol 47(1): 164–67.
Khoshnood B, De Vigan C, Goffinet F et al (2007) Prenatal screening and diagnosis of congenital toxoplasmosis: a
review of safety issues and psychological consequences for women who undergo screening. Prenatal Diag
27(5): 395–403.
Lachaud L, Calas O, Picot MC et al (2009) Value of 2 IgG avidity commercial tests used alone or in association to
date toxoplasmosis contamination. Diag Microbiol Infect Dis 64(3): 267–74.
Lesle F, Touafek F, Fekkar A et al (2011) Discrepancies between a new highly sensitive Toxoplasma gondii ELISA assay
and other reagents: Interest of Toxo IgG Western blot. Eur J CLin Microbiol Infect Dis 30(10): 1207–12.
McQuillan GM, Kruszon-Moran D, Kottiri BJ et al (2004) Racial and Ethnic Differences in the Seroprevalence of 6
Infectious Diseases in the United States: Data From NHANES III, 1988-1994. Am J Public Health 94:1952–58.
Pappas G, Roussos N, Falagas ME (2009) Toxoplasmosis snapshots: global status of Toxoplasma gondii
seroprevalence and implications for pregnancy and congenital toxoplasmosis. Int J Parasitol 39(12): 1385–
94.
Petersen E, Borobio MV, Guy E et al (2005) European multicenter study of the LIAISON automated diagnostic system
for determination of Toxoplasma gondii-specific immunoglobulin G (IgG) and IgM and the IgG avidity
index. J Clin Microbiol 43(4): 1570–74.
Peyron F, Wallon M, Liou C et al (1999) [2006] Treatments for toxoplasmosis in pregnancy. Cochrane Database Syst
Rev 1999, Issue 3. Art. No.: CD001684. DOI: 10.1002/14651858.CD001684.
Ricci M, Pentimalli H, Thaller R et al (2003) Screening and prevention of congenital toxoplasmosis: an effectiveness
study in a population with a high infection rate. J Matern-Fetal Neonat Med 14(6): 398–403.
Robert-Gangneux F, Gangneux JP, Vu N et al (2011) High level of soluble HLA-G in amniotic fluid is correlated with
congenital transmission of Toxoplasma gondii. Clin Immun 138(2): 129–34.
Thalib L, Gras L, Romand S et al (2005) Prediction of congenital toxoplasmosis by polymerase chain reaction analysis
of amniotic fluid. BJOG 112(5): 567–74.
Thiébaut R, Leproust S, Chêne G et al (2007) Effectiveness of prenatal treatment for congenital toxoplasmosis: a
meta-analysis of individual patients' data. Lancet 369(9556): 115–22.
Varella IS, Canti ICT, Santos BR et al (2009) Prevalence of acute toxoplasmosis infection among 41,112 pregnant
women and the mother-to-child transmission rate in a public hospital in South Brazil. Mem Inst Oswaldo Cruz
104(2): 383–88.
Vaz RS, Thomaz-Soccol V, Sumikawa E et al (2010) Serological prevalence of Toxoplasma gondii antibodies in
pregnant women from Southern Brazil. Parasitol Res 106(3): 661–65.
Wallon M, Franck J, Thulliez P et al (2010) Accuracy of real-time polymerase chain reaction for toxoplasma gondii in
amniotic fluid. Obstet Gynecol 115(4): 727–33.
Yamada H, Nishikawa A, Yamamoto T et al (2011) Prospective study of congenital toxoplasmosis screening with use
of IgG avidity and multiplex nested PCR methods. J Clin Microbiol 49(7): 2552–56.
Year H, Filisetti D, Bastien P et al (2009) Multicenter comparative evaluation of five commercial methods for
toxoplasma DNA extraction from amniotic fluid. J Clin Microbiol 47(12): 3881–86.