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1.
Mem Inst Oswaldo Cruz ; 104(2): 389-92, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19430670

ABSTRACT

The aim of this study was to determine the incidence of congenital toxoplasmosis (CT) and to assess the performances of prenatal and neonatal diagnoses. From 1994-2005, in Toulouse University Hospital, France, amniocentesis was performed on 352 pregnant women who were infected during pregnancy. All women were treated with spiramycin and pyrimethamine-sulfadoxine when prenatal diagnosis was positive. Among the 275 foetuses with follow-up, 66 (24%) were infected. The transmission rates of Toxoplasma gondii were 7%, 24% and 59% in the first, second and third trimesters, respectively. The sensitivity and specificity of PCR on amniotic fluid (AF) were 91% and 99.5%, respectively. One case was diagnosed by mouse inoculation with AF and six cases were diagnosed by neonatal or postnatal screening. The sensitivity and specificity of PCR on placentas were 52% and 99%, respectively. The sensitivity of tests for the detection of specific IgA and IgM in cord blood was 53% and 64%, respectively, and specificity values were 91% and 92%. In conclusion, PCR performed on AF had the highest levels of sensitivity and specificity for the diagnosis of CT. This permits an early diagnosis of most cases and should be recommended.


Subject(s)
Pregnancy Complications, Parasitic/diagnosis , Toxoplasma , Toxoplasmosis, Congenital/diagnosis , Amniocentesis , Animals , Antibodies, Protozoan/blood , DNA, Protozoan/analysis , Drug Combinations , Enzyme-Linked Immunosorbent Assay , Female , France/epidemiology , Hospitals, University , Humans , Immunoglobulin A/blood , Immunoglobulin G/blood , Incidence , Infant, Newborn , Polymerase Chain Reaction , Predictive Value of Tests , Pregnancy , Pregnancy Complications, Parasitic/epidemiology , Prenatal Diagnosis , Pyrimethamine/therapeutic use , Sensitivity and Specificity , Spiramycin/therapeutic use , Sulfadoxine/therapeutic use , Toxoplasma/genetics , Toxoplasma/immunology , Toxoplasmosis, Congenital/drug therapy , Toxoplasmosis, Congenital/epidemiology
2.
Mem. Inst. Oswaldo Cruz ; 104(2): 389-392, Mar. 2009. tab
Article in English | LILACS | ID: lil-533534

ABSTRACT

The aim of this study was to determine the incidence of congenital toxoplasmosis (CT) and to assess the performances of prenatal and neonatal diagnoses. From 1994-2005, in Toulouse University Hospital, France, amniocentesis was performed on 352 pregnant women who were infected during pregnancy. All women were treated with spiramycin and pyrimethamine-sulfadoxine when prenatal diagnosis was positive. Among the 275 foetuses with follow-up, 66 (24 percent) were infected. The transmission rates of Toxoplasma gondii were 7 percent, 24 percent and 59 percent in the first, second and third trimesters, respectively. The sensitivity and specificity of PCR on amniotic fluid (AF) were 91 percent and 99.5 percent, respectively. One case was diagnosed by mouse inoculation with AF and six cases were diagnosed by neonatal or postnatal screening. The sensitivity and specificity of PCR on placentas were 52 percent and 99 percent, respectively. The sensitivity of tests for the detection of specific IgA and IgM in cord blood was 53 percent and 64 percent, respectively, and specificity values were 91 percent and 92 percent. In conclusion, PCR performed on AF had the highest levels of sensitivity and specificity for the diagnosis of CT. This permits an early diagnosis of most cases and should be recommended.


Subject(s)
Animals , Female , Humans , Infant, Newborn , Pregnancy , Pregnancy Complications, Parasitic/diagnosis , Toxoplasma , Toxoplasmosis, Congenital/diagnosis , Amniocentesis , Antibodies, Protozoan/blood , DNA, Protozoan/analysis , Drug Combinations , Enzyme-Linked Immunosorbent Assay , France/epidemiology , Hospitals, University , Incidence , Immunoglobulin A/blood , Immunoglobulin G/blood , Polymerase Chain Reaction , Predictive Value of Tests , Prenatal Diagnosis , Pregnancy Complications, Parasitic/epidemiology , Pyrimethamine/therapeutic use , Sensitivity and Specificity , Spiramycin/therapeutic use , Sulfadoxine/therapeutic use , Toxoplasma/genetics , Toxoplasma/immunology , Toxoplasmosis, Congenital/drug therapy , Toxoplasmosis, Congenital/epidemiology
3.
J Pediatr ; 131(6): 857-62, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9427890

ABSTRACT

We studied the propagation and the impact of zidovudine prevention on the human immunodeficiency virus-1 transmission rate from infected mothers to their infants in the French nationwide prospective cohort. Infection was diagnosed in the children on the basis of at least two positive human immunodeficiency virus-1 polymerase chain reaction tests, culture, or both. The transmission rate among treated women was compared with that among untreated women during the same period and with that among women enrolled in the cohort since 1986. The impact of zidovudine was analyzed according to the women's clinical and biologic characteristics, the mode of delivery, and use of zidovudine therapy before the pregnancy. Nearly 90% of women were treated as soon as the second half of 1994. In 1994 and 1995, 80% of mother-child pairs received at least one of the three phases of preventive treatment. Among the 663 mothers enrolled during these 2 years, only six refused the treatment. Zidovudine treatment was associated with a reduction in the transmission rate of nearly two-thirds, from 14% +/- 6% to 5% +/- 2% (p < 0.01). The degree of reduction was not influenced by the maternal CD4+ cell count or p24 antigenemia at delivery. Zidovudine treatment of the mother before the pregnancy considerably reduced the impact of preventive therapy; the transmission rate was significantly higher among pretreated mothers (20% versus 5%, p < 0.01) even after adjusting for maternal CD4+ cell count. Zidovudine prevention is now widely used in France and has had a major impact on the epidemiology of mother-child human immunodeficiency virus transmission. This justifies a policy of offering human immunodeficiency virus screening to all women before or shortly after the diagnosis of pregnancy.


Subject(s)
Acquired Immunodeficiency Syndrome/prevention & control , Anti-HIV Agents/therapeutic use , HIV Seropositivity/drug therapy , HIV Seropositivity/transmission , HIV-1 , Infectious Disease Transmission, Vertical/prevention & control , Pregnancy Complications, Infectious/drug therapy , Zidovudine/therapeutic use , Acquired Immunodeficiency Syndrome/epidemiology , Cohort Studies , Confidence Intervals , Female , France/epidemiology , HIV Seropositivity/immunology , Humans , Infant, Newborn , Multivariate Analysis , Odds Ratio , Pregnancy , Pregnancy Complications, Infectious/immunology , Prospective Studies , Risk Assessment
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