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1.
Microvasc Res ; 141: 104343, 2022 05.
Article in English | MEDLINE | ID: mdl-35151722

ABSTRACT

BACKGROUND: Microvascular remodeling is one major responsible for vascular adaptation in pregnancy, still it is not routinely evaluated in the obstetric field. This pilot study aimed to explore the role of nailfold capillaroscopy (NCV) in detecting microvascular changes during normal pregnancy. METHODS: A population of 30 healthy pregnant women was longitudinally followed performing clinical assessment and NVC evaluation at each trimester and post-partum. Thirty non-pregnant age-matched healthy women having received at least two NVCs with a minimum 9 to 12-month interval were selected as controls. All NVC images were evaluated by a qualitative and semi-quantitative assessment using current standardised approach. Statistical analyses were conducted to assess NVC trend throughout gestation and its possible association with pregnancy course. RESULTS: A progressive significant increase of NVC neoangiogenesis and a specular reduction in capillary dilations was observed during pregnancy (p < 0.05). These variations were not found in age-matched controls, who showed stable NVC parameters over a similar time frame (p < 0.05). Additionally, a significant inverse correlation was found between NVC neoangiogenesis rate and maternal systemic BP (rho = -0.72, p < 0.005). CONCLUSION: This first comprehensive longitudinal NVC evaluation during normal pregnancy reports significant but physiological microvascular variations throughout gestation, suggesting NVC as a safe and promising technique for further investigate and define patterns of microvascular changes also in pathological pregnancies.


Subject(s)
Microscopic Angioscopy , Scleroderma, Systemic , Capillaries/diagnostic imaging , Capillaries/pathology , Female , Humans , Microscopic Angioscopy/methods , Nails/blood supply , Pilot Projects , Pregnancy , Scleroderma, Systemic/pathology
2.
Ital J Pediatr ; 47(1): 69, 2021 Mar 23.
Article in English | MEDLINE | ID: mdl-33757559

ABSTRACT

BACKGROUND: Natalizumab is a monoclonal antibody approved for the treatment of patients with relapsing-remitting multiple sclerosis. According to the current clinical recommendations, its use during pregnancy should be carefully evaluated only in women with highly active disease who plan a pregnancy or have an unplanned pregnancy, after accurate counseling about eventual maternal disease relapse due to therapy suspension. CASE PRESENTATION: This brief case report describes a case of documented anemia that we observed in a newborn whose mother with relapsing-remitting multiple sclerosis was treated with an extended dosing protocol of natalizumab throughout pregnancy. The newborn received the infusion of erythropoietin every seven days from the fortieth day of life; subsequently, the status of anemia underwent clinical resolution. CONCLUSIONS: This case report confirmed that natalizumab can cause disorders of hematopoiesis, including anemia, thrombocytopenia, or pancytopenia, in newborns of patients treated during pregnancy. A multidisciplinary team, including experienced pediatricians and pediatric hematologists, has a critical role in managing newborns delivered by women, being treated with natalizumab for treating relapsing-remitting multiple sclerosis during pregnancy.


Subject(s)
Anemia, Neonatal/drug therapy , Erythropoietin/therapeutic use , Immunologic Factors/adverse effects , Maternal-Fetal Exchange , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Natalizumab/adverse effects , Anemia, Neonatal/chemically induced , Female , Humans , Infant, Newborn , Infusions, Intravenous , Pregnancy
3.
J Med Virol ; 93(3): 1758-1760, 2021 03.
Article in English | MEDLINE | ID: mdl-32841411

ABSTRACT

Data from both New York and London report a high prevalence of the asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in pregnant patients admitted for delivery, raising questions on the possible correlated dangers (ie, contacts with healthcare workers; the possible creation of an intrahospital outbreak at birth; and conflicting evidence on vertical transmission). For this study, results from SARS-CoV-2 screening via nasopharyngeal swab from maternity wards of the four hospitals of Genoa, Italy, were collected during a month of complete lockdown from 1 April to 30 April 2020. Out of 333 tested women, only 9 were symptomatic. Only one symptomatic patient (0.3%) and six asymptomatic ones (1.8%) tested positive. Out of the six positive asymptomatic patients, five were from the most disadvantaged neighborhood of the city (assessed by postal code). In conclusion, even if Italy was badly affected by coronavirus disease 2019 in the studied month, the reported prevalence of SARS-CoV-2 infections in asymptomatic pregnant patients at term was lower than the ones reported in the literature.


Subject(s)
Asymptomatic Infections/epidemiology , COVID-19/epidemiology , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/virology , Adult , COVID-19/virology , Communicable Disease Control/methods , Disease Outbreaks/statistics & numerical data , Female , Health Personnel , Hospitalization/statistics & numerical data , Humans , Infectious Disease Transmission, Vertical/statistics & numerical data , Italy/epidemiology , London/epidemiology , Mass Screening/methods , New York/epidemiology , Pregnancy , Prevalence , SARS-CoV-2/pathogenicity
4.
Medicina (Kaunas) ; 56(6)2020 Jun 22.
Article in English | MEDLINE | ID: mdl-32580461

ABSTRACT

Currently, limited data on maternal and neonatal outcomes of pregnant women with infection and pneumonia related to SARS coronavirus 2 (SARS-CoV-2) are available. Our report aims to describe a case of placental swabs positive for the molecular research on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 RNA in an asymptomatic woman with positive rhino-pharyngeal swab for SARS-CoV-2 who underwent an urgent cesarean section in our obstetrics unit. Sample collection, processing, and laboratory testing were conducted in accordance with the World Health Organization (WHO) guidance. In the next months, conclusive data on obstetrical outcomes concerning the gestational age and pregnancy comorbidity as well as the eventual maternal-fetal transmission are needed.


Subject(s)
Betacoronavirus/isolation & purification , Coronavirus Infections/diagnosis , Coronavirus Infections/transmission , Infectious Disease Transmission, Vertical , Placenta/virology , Pneumonia, Viral/diagnosis , Pneumonia, Viral/transmission , Adult , COVID-19 , Cesarean Section , Female , Humans , Pandemics , Pregnancy , SARS-CoV-2
5.
Biomed Res Int ; 2020: 9309121, 2020.
Article in English | MEDLINE | ID: mdl-32219148

ABSTRACT

BACKGROUND: Autoantibodies against apolipoprotein A-1 (anti-ApoA-1 IgG) were demonstrated to be associated with cardiovascular outcomes in several inflammatory diseases. As balanced inflammation is critical for uncomplicated pregnancy, we aimed to investigate the prevalence of anti-ApoA-1 IgG and anti-c-terminal ApoA-1 autoantibodies (Ac-terAA1 IgG) in a cohort of pregnant women and their potential relationship with threatened abortion (TA). METHODS: Between 2012 and 2014, 371 consecutive outpatient pregnant women were included in this study and followed until delivery. Anti-ApoA-1 and anti-Ac-terAA1 IgG were measured by ELISA technique on serum samples collected between the 24th and 26th week of pregnancy. Associations with TA were tested using linear regression analysis and C-statistics. RESULTS: Median age was 34 with a prevalence of the Caucasian ethnicity (90.5%). TA occurred in 10 women (2.7%). C-statistics indicated that anti-ApoA-1 and anti-Ac-terAA1 IgG levels upon study inclusion were predictive of TA (0.73, 95% confidence interval [CI] 0.69-0.78, p < 0.001 and 0.76, 95% CI 0.71-0.80, p < 0.001 and 0.76, 95% CI 0.71-0.80, p < 0.001 and 0.76, 95% CI 0.71-0.80, p < 0.001 and 0.76, 95% CI 0.71-0.80. CONCLUSION: Anti-ApoA-1 and anti-Ac-terAA1 IgG are independently associated with TA during pregnancy with an appealing NPV. The causal biological mechanisms underlying this association as well as the possible clinical relevance of these findings require further investigations.


Subject(s)
Abortion, Threatened/immunology , Apolipoprotein A-I/immunology , Autoantibodies/immunology , Abortion, Threatened/epidemiology , Adult , Biomarkers/blood , C-Reactive Protein/metabolism , Female , Humans , Immunoglobulin G/blood , Inflammation/immunology , Pregnancy , Prevalence , Risk Factors
6.
Biomed Res Int ; 2018: 1070151, 2018.
Article in English | MEDLINE | ID: mdl-30533423

ABSTRACT

Although essential for a successful pregnancy, a growing body of evidence suggests that maternal inflammation, when dysregulated, may represent a risk factor for both maternal and neonatal outcomes. Here, we assessed the accuracy of maternal C-reactive protein (CRP) concentrations at the middle phase of pregnancy in the identification of maternal adverse outcomes (MAO) until delivery. A correlation between CRP and a complicated pregnancy including both maternal and neonatal adverse outcomes has been investigated, too. In this retrospective study, conducted at the Diabetology Unit of IRCCS Ospedale Policlinico San Martino, Genoa (Italy), 380 outpatient pregnant women have been enrolled at the prenatal visit before performing a 75 g oral glucose tolerance test at 24th-26th gestational week for gestational diabetes mellitus (GDM) screening. Demographic, medical, and reproductive history has been obtained by verbal interview. Data about pregnancy and delivery have been retrieved from medical records. The median value of maternal baseline serum CRP was 3.25 µg/mL. Women experiencing MAO were older, more frequently suffering from hypertension, and showed higher CRP concentrations, with a cutoff value >1.86 µg/mL found by a ROC curve analysis to be accurately predictive for MAO. By a logistic regression analysis, serum CRP levels >1.86 µg/mL have been found to predict MAO also considering maternal age, hypertension, and GDM. Maternal CRP levels have been positively associated with overall pregnancy adverse outcomes (maternal and neonatal), too. In conclusion, in pregnant women serum levels of CRP can early recognize subjects at higher risk for maternal and neonatal complications needing a more stringent follow-up.


Subject(s)
C-Reactive Protein/metabolism , Pregnancy Complications/blood , Pregnancy Complications/diagnosis , Adult , Cohort Studies , Female , Humans , Infant, Newborn , Logistic Models , Pregnancy , Pregnancy Outcome , ROC Curve
7.
PLoS One ; 10(2): e0115992, 2015.
Article in English | MEDLINE | ID: mdl-25723556

ABSTRACT

The plant hormone abscisic acid (ABA) is present and active in humans, regulating glucose homeostasis. In normal glucose tolerant (NGT) human subjects, plasma ABA (ABAp) increases 5-fold after an oral glucose load. The aim of this study was to assess the effect of an oral glucose load on ABAp in type 2 diabetes (T2D) subjects. We chose two sub-groups of patients who underwent an oral glucose load for diagnostic purposes: i) 9 treatment-naive T2D subjects, and ii) 9 pregnant women with gestational diabetes (GDM), who underwent the glucose load before and 8-12 weeks after childbirth. Each group was compared with matched NGT controls. The increase of ABAp in response to glucose was found to be abrogated in T2D patients compared to NGT controls. A similar result was observed in the women with GDM compared to pregnant NGT controls; 8-12 weeks after childbirth, however, fasting ABAp and ABAp response to glucose were restored to normal in the GDM subjects, along with glucose tolerance. We also retrospectively compared fasting ABAp before and after bilio-pancreatic diversion (BPD) in obese, but not diabetic subjects, and in obese T2D patients, in which BPD resulted in the resolution of diabetes. Compared to pre-BPD values, basal ABAp significantly increased 1 month after BPD in T2D as well as in NGT subjects, in parallel with a reduction of fasting plasma glucose. These results indicate an impaired hyperglycemia-induced ABAp increase in T2D and in GDM and suggest a beneficial effect of elevated ABAp on glycemic control.


Subject(s)
Abscisic Acid/blood , Diabetes Mellitus, Type 2/blood , Diabetes, Gestational/blood , Adult , Aged , Blood Glucose , Case-Control Studies , Fasting , Female , Glucose Tolerance Test , Humans , Hyperglycemia/blood , Middle Aged , Pregnancy , Young Adult
8.
J Reprod Med ; 55(9-10): 423-9, 2010.
Article in English | MEDLINE | ID: mdl-21043369

ABSTRACT

OBJECTIVE: To evaluate patient satisfaction of cervical ripening using dinoprostone (PGE2) by either intravaginal gel or pessary. STUDY DESIGN: A group of 173 nulliparous women requiring cervical ripening were recruited in the study and randomized to receive either intravaginal gel (Prepidil, Upjohn, Milan, Italy [group A]) or intravaginal pessary (Propess, Ferring Pharmaceuticals, Malmö, Sweden [group B]). Before administration of PGE2 and after delivery, the patients answered a questionnaire investigating the anxiety and discomfort caused by cervical ripening. RESULTS: Of the group, 22 women did not adequately complete the questionnaire; therefore 151 women were included in the study. Before cervical ripening, anxiety and discomfort did not significantly differ between the two study groups; more patients in group A than in group B declared they would have preferred the other form of application. The intensity of pain experienced during the application of PGE2 was higher in group B than in group A. For the future opportunity to choose the application necessary for cervical ripening, more patients in group B than in group A would change the form of application. CONCLUSION: Patient satisfaction with the two forms of treatment appears to be equally good. The application of the intravaginal pessary causes more discomfort than the vaginal gel.


Subject(s)
Cervical Ripening , Dinoprostone/administration & dosage , Labor, Induced/methods , Oxytocics/administration & dosage , Patient Satisfaction , Adult , Dinoprostone/adverse effects , Female , Humans , Intrauterine Devices , Labor, Induced/adverse effects , Oxytocics/adverse effects , Pain/chemically induced , Pregnancy , Vaginal Creams, Foams, and Jellies
9.
Fertil Steril ; 90(3): 844-8, 2008 Sep.
Article in English | MEDLINE | ID: mdl-17953950

ABSTRACT

OBJECTIVE: To assess whether oral administration of 100 mg of nimesulide reduces pain during or after a hysterosalpingography (HSG) performed with disposable balloon catheters. DESIGN: Prospective, randomized, placebo-controlled study. SETTING: Reproductive Centre, Department of Obstetrics and Gynaecology, University of Genoa. PATIENT(S): Four hundred and forty patients undergoing HSG with a balloon catheter without applying a tenaculum. INTERVENTION(S): Patients were randomized to receive either 100 mg of oral nimesulide or a placebo solution 30 minutes before the HSG was performed. MAIN OUTCOME MEASURE(S): Patients recorded the degree of pain experienced during the examination, 2 hours afterward, and during the following week on a questionnaire using a 10-mm visual analogue scale (VAS). RESULT(S): Of the 331 (75.2 %) patients who returned the questionnaire, 151 had received nimesulide and 180 placebo. There was no difference in pain score between the two groups at any study point. Pain during HSG was correlated with nulliparity and tubal occlusion. Balloon inflation (cervix versus cavity) was not related to pain. CONCLUSION(S): Nimesulide does not reduce pain during or after HSG when the procedure is accomplished with a balloon catheter.


Subject(s)
Catheterization/adverse effects , Catheterization/instrumentation , Hysterosalpingography/adverse effects , Hysterosalpingography/instrumentation , Pain/etiology , Pain/prevention & control , Sulfonamides/administration & dosage , Administration, Oral , Adult , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Disposable Equipment , Female , Humans , Pain Measurement/drug effects , Placebo Effect , Treatment Outcome
10.
Eur Radiol ; 15(7): 1469-71, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15580506

ABSTRACT

We report a case of diagnostic hysterosalpingography performed using gadoteric acid (1,350 mOsm) in a patient with a prior severe generalized adverse reaction to iodinated contrast media.


Subject(s)
Contrast Media , Gadolinium , Hysterosalpingography/methods , Meglumine , Organometallic Compounds , Adult , Female , Fluoroscopy , Humans
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