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1.
Viruses ; 13(6)2021 05 26.
Article in English | MEDLINE | ID: mdl-34073492

ABSTRACT

The current coronavirus pandemic has affected, in a short time, various and different areas of medicine. Among these, the obstetric field has certainly been touched in full, and the knowledge of the mechanisms potentially responsible for placental damage from SARS-CoV-2 occupy a certain importance. Here we present here a rare case of dichorionic twins born at 30 weeks and 4 days of amenorrhea, one of whom died in the first few hours of life after placental damages potentially related to SARS-CoV-2. We also propose a brief review of the current literature giving ample emphasis to similar cases described.


Subject(s)
COVID-19/complications , Placenta/pathology , Pregnancy Complications, Infectious/virology , SARS-CoV-2/pathogenicity , Adult , COVID-19/diagnosis , COVID-19/transmission , COVID-19/virology , Female , Humans , Infant, Newborn , Infectious Disease Transmission, Vertical , Male , Obstetric Labor Complications/virology , Placenta/virology , Pregnancy , Pregnancy Complications, Infectious/diagnosis , Pregnancy Outcome , Pregnancy, Twin , SARS-CoV-2/isolation & purification
2.
Bull Exp Biol Med ; 160(1): 88-90, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26601834

ABSTRACT

Scrapings from the cervical canals and uterine cavities of females with a history of miscarriages, pathological deliveries, and stillbirths were tested for the cytomegalovirus DNA. The incidence of the agent in the females with a history of gestosis and abnormal deliveries was significantly higher than in females without anamnesis of this kind. Parenchymatous organs of stillborn neonates and animals dead during the first month of life were studied. This analysis and studies of the umbilical cords and placentas showed generalized cytomegalovirus infection in 22% dead animals, which objectively proved intrauterine infection.


Subject(s)
Abortion, Veterinary/virology , Cytomegalovirus Infections/veterinary , Cytomegalovirus/isolation & purification , Pregnancy Complications, Infectious/veterinary , Primate Diseases/mortality , Stillbirth/veterinary , Abortion, Veterinary/etiology , Animal Husbandry , Animals , Animals, Newborn , Causality , Cervix Uteri/virology , Chlorocebus aethiops , Cytomegalovirus Infections/mortality , DNA, Viral/analysis , Female , Macaca , Male , Obstetric Labor Complications/veterinary , Obstetric Labor Complications/virology , Papio , Placenta/virology , Pregnancy , Pregnancy Complications, Infectious/virology , Russia/epidemiology , Umbilical Cord/virology , Urethra/virology , Uterus/virology , Viscera/virology
3.
J Coll Physicians Surg Pak ; 21(6): 356-9, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21711992

ABSTRACT

OBJECTIVE: To evaluate adverse pregnancy outcome in HIV infected women who received highly active antiretroviral therapy (HAART) from early pregnancy compared with untreated-maternal HIV infection. STUDY DESIGN: A cohort study. PLACE AND DURATION OF STUDY: Antenatal clinic, University of Benin Teaching Hospital, Nigeria, from January 2008 to June 2009. METHODOLOGY: Two hundred and forty nine HIV infected women who had intrapartum care constituted the study population. Unbooked HIV positive pregnant women, who had not received antiretroviral drugs during the antenatal period but received nevirapine in labour, referred to as untreated-maternal HIV infection, were compared with women who received HAART early in pregnancy. Outcome measures of interest were obstetric complications and perinatal outcome proportion. RESULTS: Intrauterine growth restriction (IUGR) (20.5% vs. 6.3%, p = 0.003), pre-term birth (25.0% vs. 9.8%, p = 0.005) and caesarean delivery (45.5% vs. 29.8%, p = 0.04) were significantly higher among women with untreated-HIV infection in pregnancy compared with women who received HAART from early pregnancy. Untreated maternal HIV-infection was associated with higher frequency of birth weight less than 2500g, 5-minutes Apgar score less than 7 and admission into neonatal unit (p < 0.05). Women with primary education were significantly higher in the group with untreated maternal HIV infection (27.3% vs. 12.7%, p = 0.003). CONCLUSION: Untreated maternal HIV-infection in pregnancy may be associated with adverse pregnancy outcome. HIV positive women with low level of education utilise PMTCT services suboptimally. This information is important for programmes designed to increase access to PMTCT services including HAART from early pregnancy.


Subject(s)
Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , Infectious Disease Transmission, Vertical/prevention & control , Obstetric Labor Complications/epidemiology , Pregnancy Complications, Infectious/drug therapy , Pregnancy Outcome , Adult , Antiretroviral Therapy, Highly Active , Apgar Score , Cesarean Section , Chi-Square Distribution , Cohort Studies , Educational Status , Female , Fetal Growth Retardation/virology , HIV Infections/complications , HIV Infections/transmission , Humans , Infant, Low Birth Weight , Infant, Newborn , Maternal Welfare , Nevirapine/therapeutic use , Obstetric Labor Complications/virology , Post-Exposure Prophylaxis , Pregnancy , Pregnancy Complications, Infectious/virology , Premature Birth/epidemiology , Premature Birth/virology , Prenatal Diagnosis , Retrospective Studies , Statistics as Topic
4.
J Reprod Med ; 52(6): 539-40, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17694976

ABSTRACT

BACKGROUND: Despite the tremendous advances made in the management of genital herpes, neonatal herpes has not been completely eradicated. In addition, the time from the onset of symptoms in the neonate to the diagnosis of herpes and institution of antiviral medication has remained unchanged in the past 20 years. CASE: Neonatal herpes infection resulted from primary, first-episode peripartum genital herpes in the mother. Due to a high index of suspicion, herpes testing was performed on the infant and neonatal herpes diagnosed. Subsequently, the mother developed evidence of primary herpes infection. CONCLUSION: This case report illustrates the problems with current management strategies for prevention of neonatal herpes.


Subject(s)
Herpes Simplex/complications , Herpes Simplex/transmission , Infectious Disease Transmission, Vertical , Obstetric Labor Complications/virology , Pregnancy Complications, Infectious/virology , Acyclovir/therapeutic use , Adolescent , Antiviral Agents/therapeutic use , Female , Herpes Simplex/drug therapy , Humans , Infant, Newborn , Infant, Newborn, Diseases , Pregnancy
5.
J Acquir Immune Defic Syndr ; 35(2): 151-4, 2004 Feb 01.
Article in English | MEDLINE | ID: mdl-14722447

ABSTRACT

For HIV-infected women who have not received antiretroviral treatment or transmission prophylaxis in pregnancy, starting antiretrovirals in labor or soon after birth can still decrease the risk of perinatal transmission. There is, therefore, potential benefit in conducting rapid HIV testing in labor, but hospitals are seldom prepared to conduct such testing. We compared protocols for rapid HIV testing at 2 hospitals to determine what proportion of women had results back early enough to intervene if results had been positive. Hospital A initially used HIV enzyme-linked immunosorbent assays (ELISAs) and changed to using rapid tests (eg, Single Use Diagnostic System [SUDS]); hospital B used only the SUDS. With use of the SUDS in hospital A, results were reported more quickly than with the ELISA protocol in the same hospital (P < 0.0001). Comparing use of the SUDS in the 2 hospitals, test results were available more quickly in hospital A than hospital B (P < 0.05), which resulted in hospital A having more results reported prior to delivery (64% vs. 38%, P < 0.05) and within 12 hours postdelivery (94% vs. 73%, P < 0.05). If HIV testing in labor is to have its maximum effect on decreasing the risk of perinatal HIV transmission, hospitals need to institute rapid HIV testing, but protocols must ensure that results are available as quickly as possible.


Subject(s)
Acquired Immunodeficiency Syndrome/diagnosis , HIV Infections/diagnosis , HIV/isolation & purification , Obstetric Labor Complications/virology , Enzyme-Linked Immunosorbent Assay , Female , Humans , Infant, Newborn , Infectious Disease Transmission, Vertical/prevention & control , Obstetric Labor Complications/diagnosis , Postpartum Period , Pregnancy , Pregnancy Complications, Infectious/diagnosis , Pregnancy Complications, Infectious/virology , Time Factors
6.
Obstet Gynecol ; 102(6): 1396-403, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14662233

ABSTRACT

OBJECTIVE: Genital herpes simplex virus (HSV) infection is one of the most common viral sexually transmitted diseases in the United States. Perinatal transmission of the virus to the fetus or neonate is a major concern in affected pregnancies. Our objective was to systematically review published data to estimate the effect of prophylactic acyclovir provided to pregnant women near term on the rate of recurrent genital herpes at delivery; the number of cesarean deliveries performed for clinical HSV recurrences or prodromal symptoms; and the prevalence of HSV virologic detection at delivery. DATA SOURCES: Our search included MEDLINE (1966-March 2003), LILACS, EMBASE, conference proceedings, abstracts from scientific forums and bibliographies of published articles with the following medical headings: acyclovir, pregnancy, Herpes viridae, and Herpesviridae. METHODS OF STUDY SELECTION: Prospectively designed criteria included randomized, clinical trials detailing the use of acyclovir in pregnancy for women with HSV published in either abstract or article form. Five trials with a total enrollment of 799 patients were included in the analysis. TABULATION, INTEGRATION, AND RESULTS: The studies were reviewed independently by three of the authors. With RevMan software, a fixed-effects model was used to calculate a summary odds ratio (OR) comparing the effect of treatment with placebo. Acyclovir prophylaxis beginning at 36 weeks' gestation was effective in reducing clinical HSV recurrences at the time of delivery (OR 0.25; 95% confidence interval [95% CI] 0.15, 0.40), cesarean deliveries for clinical recurrence genital herpes (OR 0.30; 95% CI 0.13, 0.67), total HSV detection at delivery (OR 0.11; 95% CI 0.04, 0.31), and asymptomatic HSV shedding at delivery (OR 0.09; 95% CI 0.02, 0.39). CONCLUSION: The results of this meta-analysis indicate that prophylactic acyclovir beginning at 36 weeks' gestation reduces the risk of clinical HSV recurrence at delivery, cesarean delivery for recurrent genital herpes, and the risk of HSV viral shedding at delivery.


Subject(s)
Acyclovir/therapeutic use , Antiviral Agents/therapeutic use , Herpes Simplex/prevention & control , Obstetric Labor Complications/prevention & control , Obstetric Labor Complications/virology , Female , Humans , Pregnancy , Prospective Studies , Randomized Controlled Trials as Topic , Recurrence
7.
Int J Gynaecol Obstet ; 82(1): 17-23, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12834937

ABSTRACT

OBJECTIVES: To determine the effects of duration of ruptured membranes (DRM) and duration of labor in HIV transmission. METHODS: A retrospective cohort study of 366 HIV-infected pregnant women and their infants analyzed the effects of these two variables; the cut-off point for transmission increase was estimated using a ROC curve. A multivariate analysis was performed with the most important risk factors according to the literature: maternal age, lymphocyte count, use of invasive procedures during gestation, antiretroviral treatment during pregnancy and labor, mode of delivery, newborn weight, DRM, labor duration, and the interaction of these last two factors. RESULTS: The cut-off points were estimated at 6 h for DRM and at 5 h for labor duration. A lymphocyte count below 500 cells/ml, use of invasive procedures, use of antiretroviral treatment during pregnancy and interaction between DRM, and labor duration remained significant in perinatal HIV transmission (P<0.05). CONCLUSIONS: An increased DRM increased perinatal HIV transmission when it was associated with prolonged labor.


Subject(s)
Fetal Membranes, Premature Rupture/complications , HIV Infections/transmission , Infectious Disease Transmission, Vertical , Obstetric Labor Complications/virology , Cohort Studies , Female , HIV Infections/etiology , Humans , Infant, Newborn , Pregnancy , Retrospective Studies , Risk Factors , Time Factors
9.
Arch Pediatr ; 2(2): 169-72, 1995 Feb.
Article in French | MEDLINE | ID: mdl-7735451

ABSTRACT

HIV infection in children is mainly the result of a mother-to-child transmission. The contamination during pregnancy is well known but intrapartum vertical transmission may also occur through ascending infection, blood exchange between mother and child, or direct contact with vaginal or cervical secretions. In addition HIV can be transmitted via breast milk. The reported rates of vertical transmission are highly variable: 14.4% in a European study, 18.3% in a French survey, 20 to 25% in the USA, 35 to 50% in Africa. It is unclear whether such a large variation of the rate of transmission is due to methodological differences or to different distributions of risk factors in the populations. There are some known predictive factors of HIV transmission such as low CD4 cells count, positive p24 antigenaemia and elevated concentrations of virus. The role of other factors is still debated: prematurity, virus (CMV, HTLV-1, HVB, HVC), C section prior labour, rupture of membranes. The prevention of HIV infection in infants is mainly based on contra-indication of pregnancy in infected women, desinfection of the vagina at the beginning of labour, early protection of the newborn by avoiding skin lesions and immediate washing, preventive treatment by zidovudin during pregnancy.


Subject(s)
HIV Infections/transmission , Infectious Disease Transmission, Vertical , Pregnancy Complications, Infectious , Female , HIV Infections/prevention & control , Humans , Infant, Newborn , Maternal-Fetal Exchange , Milk, Human/virology , Obstetric Labor Complications/prevention & control , Obstetric Labor Complications/virology , Pregnancy , Risk Factors
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