Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
1.
J Clin Aesthet Dermatol ; 15(5): 19-28, 2022 May.
Article in English | MEDLINE | ID: mdl-35642229

ABSTRACT

Objective: We conducted a review of topical agents currently used in melasma, discussing their mechanism of action, efficacy, safety, and tolerability, with an update on newer treatments. Methods: A systematic review from PubMed database was performed, using PRISMA guidelines. The search was limited to English and Spanish studies that were double or single blinded, prospective, controlled or randomized clinical trials, reviews of literature, and meta-analysis studies. Results: 348 studies were analyzed; 80 papers met inclusion criteria. Triple combination (TC) therapy and hydroquinone (HQ) are still the most well-studied agents with strong evidence-based recommendation. TC therapy remains the gold standard of care based on efficacy and patient tolerability. Evidence has shown ascorbic acid, azelaic acid, glycolic acid, kojic acid, salicylic acid, and niacinamide to be effective as adjuvant therapies with minimal side effects. Tranexamic acid (TA) and cysteamine have become recent agents of interest due to their good tolerability, however more trials and studies are warranted. Less evidence exists for other topical agents, such as linoleic acid, mulberry extract oil, rucinol, 2% undecylenoyl phenylalanine, and epidermal growth factors agents. Limitations: Some studies discussed represented a low sample size, and there is an overall lack of recent studies with larger populations and long-term follow up. Conclusions: TC therapy continues to be the gold standard of care. Topical cysteamine and TA are newer options that can be incorporated as adjuvant and maintenance treatments into a patient's regimen. Cysteamine and topical TA have no known severe adverse effects. Evidence comparing other topical adjuvant treatments to HQ, maintains HQ as the gold standard of care.

2.
J Matern Fetal Neonatal Med ; 35(4): 765-769, 2022 Feb.
Article in English | MEDLINE | ID: mdl-32098548

ABSTRACT

BACKGROUND: Maternal obesity is a risk factor for multiple obstetrics complications and adverse outcomes. The objective of the study was to investigate the association between obesity (IMC >30) and fetal acidosis at birth. METHODS AND FINDINGS: This hospital-based cohort study was based on 24,307 live-born infants in which maternal body mass index (BMI) information was available and delivered in the Granada north region during 2007-2018 from data of the Hospital Medical Birth Registry. Multivariate using logistic regression was performed to assess the association between fetal acidosis and BMI, crude, and adjusted odds ratio of fetal acidosis were calculated. p < .05 was considered statistically significant. We adjusted by maternal age, parity, hypertension, diabetes, and smoking habits. In the study population of 17,167 term live births, 518 infants (3.02%) had an umbilical cord blood pH < 7.10. The obesity rate in mothers with acidosis at delivery was 12.7%, but morbid obesity rate was 2.51% (adjusted OR 1.82). CONCLUSION: This study strengthens the evidence that demonstrates that morbid obesity is an independent risk factor for fetal acidosis at birth.


Subject(s)
Acidosis , Obesity, Maternal , Acidosis/epidemiology , Acidosis/etiology , Body Mass Index , Cohort Studies , Female , Humans , Infant , Infant, Newborn , Maternal Age , Pregnancy , Risk Factors
3.
Matern Child Nutr ; 17(4): e13205, 2021 10.
Article in English | MEDLINE | ID: mdl-34036744

ABSTRACT

The aim of this study was to identify serum ferritin (SF) cut-off points (COPs) in a cohort of healthy full-term normal birth weight infants who had repeated measurements of SF and haemoglobin every 3 months during the first year of life. The study included 746 full-term infants with birth weight ≥2,500 g, having uncomplicated gestations and births. Participants received prophylactic iron supplementation (1 mg/day of iron element) from the first to the 12th month of life and did not develop anaemia during the first year of life. Two statistical methods were considered to identify COPs for low iron stores at 3, 6, 9 and 12 months of age: deviation from mean and cluster analysis. According to the K-means cluster analysis results by age and sex, COPs at 3 and 6 months for girls were 39 and 21 µg/L and for boys 23 and 11 µg/L, respectively. A single COP of 10 µg/L was identified, for girls and boys, at both 9 and 12 months. Given the physiological changes in SF concentration during the first year of life, our study identified dynamic COPs, which differed by sex in the first semester. Adequate SF COPs are necessary to identify low iron stores at an early stage of iron deficiency, which represents one of the most widespread public health problems around the world, particularly in low- and middle-income countries.


Subject(s)
Anemia, Iron-Deficiency , Ferritins , Anemia, Iron-Deficiency/epidemiology , Cohort Studies , Female , Hemoglobins , Humans , Infant , Iron/metabolism , Male
4.
J Matern Fetal Neonatal Med ; 33(18): 3056-3061, 2020 Sep.
Article in English | MEDLINE | ID: mdl-30621506

ABSTRACT

Objective: The aim of the study was to investigate whether the accuracy of ultrasound estimates of fetal weight (EFW) was dependent on maternal obesity.Study design: A prospective cross-sectional study of 1064 singleton pregnant women classified according to body mass index (BMI) into two categories: normal (BMI < 25 kg/m2, n = 863) and obese (BMI ≥ 35 kg/m2, n = 201) was conducted. EFW were calculated using Hadlock's formula, and the difference between EFW and the actual birthweight (absolute percent error) was analyzed in both groups. Spearman's correlation was used to assess the relationship between ultrasound performance (absolute error), maternal BMI, and actual birth weight.Results: Median absolute error of sonographic EFW was 5.90 and 6.47% for the normal and obese groups, respectively (p .38). A correlation between EFW and birth weight (BW) was found in both groups, r = 0.755 (p < .001) and r = 0.753 (p < .001), respectively. The correlation between absolute error, maternal BMI, and fetal birth weight was poor.Conclusions: Maternal obesity is unrelated to the accuracy of sonographic EFW, and regardless of maternal or fetal size, ultrasound is currently an accurate method of prediction for both obese and normal weight pregnant women.


Subject(s)
Obesity, Maternal , Birth Weight , Cross-Sectional Studies , Female , Fetal Weight , Gestational Age , Humans , Pregnancy , Prospective Studies , Ultrasonography , Ultrasonography, Prenatal
5.
J Matern Fetal Neonatal Med ; 33(2): 236-242, 2020 Jan.
Article in English | MEDLINE | ID: mdl-29886811

ABSTRACT

Background: Cesarean delivery (CD) is the most frequently performed surgical procedure worldwide. Trial of labor after cesarean (TOLAC) is associated with an increase in perinatal complications related to uterine rupture. However, in general, vaginal birth after cesarean (VBAC) is considered safe and women have less morbidity than those who undergo an elective repeat CD.Objective: To develop an integrated model with the best performance criteria for predicting vaginal delivery success after CD.Study design: Retrospective observational study including 2367 women who underwent a TOLAC. A predictive model using classification and regression tree modeling was constructed to predict vaginal delivery using maternal demographic, medical history, and labor predictors.Results: Vaginal delivery was best predicted by spontaneous onset of labor, estimated fetal weight <3775 g, maternal body mass index <25, previous CD as an elective or for fetal distress reasons, and interdelivery interval <2290 days. The algorithm showed a sensitivity of 75%, a specificity of 53%, and the area under the curve was 0.69.Conclusions: The classification and regression tree algorithm can be used to develop a predictive model for the success of TOLAC.


Subject(s)
Cesarean Section, Repeat/statistics & numerical data , Decision Trees , Trial of Labor , Vaginal Birth after Cesarean/statistics & numerical data , Adult , Birth Weight , Female , Humans , Infant, Newborn , Pregnancy , Retrospective Studies , Risk Assessment
6.
J Obstet Gynaecol ; 39(5): 628-632, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30932731

ABSTRACT

The aim of the study was to test if maternal obesity and being overweight are independent risk factors for rectovaginal Group B Streptococcus (GBS) colonisation in pregnancy and for early onset GBS disease in the neonate. A case-control study of 9877 deliveries was conducted. The obese gravidas were significantly more likely to be colonised by GBS when compared with non-obese gravidas (22.7% versus 17.5%, P < .001). Obese gravidas were still 33% more likely than non-obese women to test positive for GBS after adjusting for the perinatal factors (adjusted OR 1.33 [95% CI 1.12-1.56]). The risk of early onset GBS disease was not calculated due to its very low incidence. The conclusion is that maternal obesity is a significant risk factor for GBS colonisation at term. Impact statement What is already known on this subject? Group B Streptococcus (GBS) is as an important cause of perinatal mortality and morbidity if prophylaxis is not performed. Intrapartum antibiotics are given if the carrier status is positive or unknown, provided that the risk factors are present. What do the results of this study add? Maternal obesity is a significant and independent risk factor for GBS colonisation at term. What are the implications of these findings for clinical practice and/or further research? Maternal obesity may be considered as a risk factor that should be taken into account in strategies for reducing GBS disease in neonates.


Subject(s)
Obesity, Maternal/complications , Obesity, Maternal/microbiology , Pregnancy Complications/microbiology , Streptococcal Infections/epidemiology , Streptococcus agalactiae/growth & development , Adult , Body Mass Index , Case-Control Studies , Female , Gestational Age , Humans , Infant, Newborn , Infectious Disease Transmission, Vertical , Odds Ratio , Pregnancy , Pregnancy Complications, Infectious/epidemiology , Premature Birth/epidemiology , Rectum/microbiology , Risk Factors , Spain/epidemiology , Streptococcus agalactiae/isolation & purification , Vagina/microbiology
7.
Fetal Diagn Ther ; 35(1): 7-12, 2014.
Article in English | MEDLINE | ID: mdl-24335165

ABSTRACT

INTRODUCTION: The aim of this study was to examine if noninvasive fetal RhD genotyping from maternal blood cell-free fetal DNA performed in the first trimester of pregnancy is accurate enough to propose its routine application to replace usual immunoprophylaxis. MATERIAL AND METHODS: We carried out a prospective study analyzing fetal RhD genotype in 149 nonimmunized RhD-negative women with single pregnancies between 8 and 13 weeks of gestation. Fetal RhD genotype was detected by quantitative PCR targeting exons 5 and 7. The results were compared with postnatal cord blood phenotype, and discrepancy rates were calculated. RESULTS: The concordance of fetal RhD genotypes in maternal plasma and newborn D phenotypes at delivery was 98.2%, including 1 false-positive and 1 false-negative result. The specificity and sensitivity of the assay were 97.5% (95% CI 87.1-99.9) and 98.6% (95% CI 92.7-99.9), respectively, and 6.5% of the results were inconclusive. The application of this test in early pregnancy would avoid unnecessary antenatal prophylaxis in about 27% (40/143) of nonsensitized RhD-negative women. DISCUSSION: Determination of the fetal RhD status from cell-free fetal DNA in maternal plasma in the first trimester of pregnancy is feasible and highly accurate, thus allowing consideration of replacing general routine immunoprophylaxis in the cases of mothers with Rh-negative fetuses.


Subject(s)
Pregnancy Complications, Hematologic/diagnosis , Rh-Hr Blood-Group System/genetics , Female , Genotyping Techniques , Humans , Maternal Age , Maternal Serum Screening Tests , Pregnancy , Pregnancy Trimester, First , Sensitivity and Specificity
8.
Birth ; 40(4): 307-11, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24344712

ABSTRACT

BACKGROUND: To assess whether the presence of an episiotomy or spontaneous perineal trauma at the first delivery increases the risk of perineal trauma at the following one. METHODS: We studied 2,695 women who gave birth twice at Virgen de las Nieves University Hospital of Granada, Spain. All second deliveries were from 2004 to 2011 and prenatal database records were used to obtain information about the first deliveries. All births, first and second, were single, vaginal, unassisted, and in a cephalic presentation. Two groups were made as follows: Intact perineum (no perineal trauma or first-degree spontaneous tear at the first delivery) and perineal trauma (episiotomy or second-degree or higher spontaneous tear at the first delivery). Both groups were compared according to the degree of perineal trauma at the second delivery. RESULTS: Women included in the perineal trauma group were significantly older and a higher proportion was attended by a midwife with an obstetrician present in the delivery room. No differences were observed according to gestational age, epidural analgesia or fetal birth weight. Adjusting for these possible compounding factors and the year of birth, the risk of undergoing a second-degree or higher spontaneous tear at their next delivery was fivefold (adjusted OR 5.15, 95% CI 3.11-8.54), and the risk of undergoing an episiotomy in the second delivery was threefold (adjusted OR 3.20, 95% CI 2.19-4.69) for the perineal trauma group. CONCLUSION: The risk of undergoing a spontaneous perineal tear or an episiotomy in the second delivery is increased by the practice of episiotomy in the first one.


Subject(s)
Episiotomy/statistics & numerical data , Obstetric Labor Complications/etiology , Parity , Perineum/injuries , Adult , Female , Humans , Logistic Models , Obstetric Labor Complications/epidemiology , Pregnancy , Retrospective Studies , Risk Factors , Spain
9.
Twin Res Hum Genet ; 16(3): 727-31, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23545066

ABSTRACT

OBJECTIVE: To evaluate the perinatal outcome of intrauterine growth-restricted preterm twins and contribution of prematurity to morbidity and mortality. STUDY DESIGN: A case-control study of 211 preterm twins: 108 growth-restricted twins matched with 103 normal growth twins of the same gestational age. Mortality and morbidity rates were compared between groups. RESULT: Fetal and overall perinatal mortality rates of growth-restricted fetuses were higher than normal growth ones. Respiratory distress syndrome incidence was lower and neurologic sequelae incidence higher in growth-restricted twins. No differences were observed between groups with respect to neonatal mortality, low Apgar score, neonatal intensive care unit admission, periventricular hemorrhage, sepsis, jaundice, and hematologic or metabolic disorders. CONCLUSION: Adverse perinatal outcomes of preterm twins complicated with intrauterine growth restriction are represented by a higher antepartum mortality rate, but once born alive, neonatal outcomes seem to be associated only with gestational age at birth, excluding a protective effect on lung maturation and a higher risk of long-term neurologic sequelae.


Subject(s)
Fetal Growth Retardation/mortality , Case-Control Studies , Chi-Square Distribution , Confidence Intervals , Female , Gestational Age , Humans , Infant Mortality , Infant, Newborn , Infant, Premature , Odds Ratio , Pregnancy , Pregnancy Outcome , Pregnancy, Multiple , Respiratory Distress Syndrome, Newborn/mortality
10.
Arch. neurociencias ; 1(3): 186-8, jul.-sept. 1996. ilus
Article in Spanish | LILACS | ID: lil-210814

ABSTRACT

Este estudio fue llevado a cabo con el objetivo de disociar entre las acciones motoras ejercidas por la administración aguda (1, 2, 5, 10, 20, 40, 60, 80, y 100 mg/kg-1 ip) de HEPB y fenobarbital y sus efectos sobre el componente descriminativo de la memoria de reconocimiento en la rata. A dosis mayores de 20 mg/kg-1, ambos anticonvulsionantes indujeron una reducción (dosis dependiente) en el número de corridas por ensayo (en ratas entradas para recorrer un corredor de 4.2 m de longitud), así como el número de elecciones efectuadas por ensayo en un laberinto en ®T¼ (continuo al corredor) para reconocer (mediante indicios no especiales) el brazo no electrificado que contenía alimento. Sin embargo, ninguno de estos fármacos afectó el porcentaje de elecciones correctas ejecutadas en el paradigma discriminativo, aún bajo condiciones de severa incoordinación motora ejercida por dosis de 60 mg/kg-1 de fenobarbital o de 100 mg/kg-1 de HEPB. Estos datos indican que si bien, a dosis subanestésicas, los anticonvulsionantes probados no alteran la memoria de reconocimiento en la rata, la eficiencia en general que resulta de la prueba conductual para dicha memoria es efectuada por un deterioro en la actividad y coordinación motora


Subject(s)
Rats , Animals , Male , Female , Anticonvulsants/pharmacokinetics , Memory/drug effects , Motor Activity/drug effects , Phenobarbital/pharmacokinetics , Rats, Wistar/surgery
SELECTION OF CITATIONS
SEARCH DETAIL
...