Update on thrombocytopenia in pregnancy / Atualização sobre trombocitopenia na gravidez

Abstract Thrombocytopenia, defined as platelet count < 150,000mm3, is frequently diagnosed by obstetricians since this parameter is included in routine surveillance during pregnancy, with an incidence of between 7 and 12%. Therefore, decisions regarding subsequent examination and management are primordial. While most of the cases are due to physiological changes, as gestational thrombocytopenia, other causes can be related to severe conditions that can lead to fetal or maternal death. Differentiating these conditions might be challenging: they can be pregnancy-specific (pre-eclampsia/ HELLP syndrome [hemolysis, elevated liver enzymes, low platelets]), or not (immune thrombocytopenia purpura, thrombotic thrombocytopenic purpura or hemolytic uremic syndrome). Understanding the mechanisms and recognition of symptoms and signs is essential to decide an adequate line of investigation. The severity of thrombocytopenia, its etiology and gestational age dictates different treatment regimens.

Resumo Trombocitopenia, definida como uma contagem de plaquetária < 150.000mm3, é frequentemente diagnosticada pelos obstetras, uma vez que este parâmetro está incluído na vigilância de rotina durante a gravidez, com uma incidência de entre 7 e 12%. Assim, decisões relativas à avaliação e orientação subsequentes são primordiais. Embora a maioria dos casos ocorra devido a alterações fisiológicas, como a trombocitopenia gestacional, outras causas podem estar relacionadas com condições graves que podem levar à morte fetal ou materna. Distinguir entre estas entidades pode ser desafiante: elas podem ser específicas da gravidez (pré-eclâmpsia/síndrome HELLP [hemolysis, elevated liver enzymes, low platelets]) ou não (púrpura trombocitopênica imune, púrpura trombocitopênica trombótica ou síndrome hemolítico urêmico). Compreender os mecanismos e reconhecer os sinais e sintomas é essencial para decidir uma adequada linha de investigação. A severidade da trombocitopenia, a sua etiologia e a idade gestacional ditam regimes de tratamento diferentes.

Manejo de una paciente embarazada con déficit congénito de factor VII leve / Management of a pregnant patient with mild factor VII congenital deficiency

RESUMEN No hay guías específicas para el manejo de pacientes embarazadas con la deficiencia de Factor VII; no hay una correlación entre el nivel de FVII y el riesgo de hemorragia y el nivel del Factor VII aumento durante el embarazo. Presentamos un caso clínico, el manejo y las recomendaciones del consenso.

Seguimiento de gestante con síndrome de plaquetas pegajosas: primer caso comunicado en Cuba / Gestational follow-up of pregnant woman with sticky platelets syndrome: first patient reported in Cuba

El síndrome de plaquetas pegajosas es una entidad en la que se presentan hiperagregabilidad plaquetaria y manifestaciones clínicas trombóticas. Fue observada hace más de 30 años en personas jóvenes con eventos oclusivos, arteriales, venosos, miorcárdicos, cerebrales y, años más tarde, se describió en mujeres con pérdidas recurrentes de embarazos y complicaciones obstétricas. El tratamiento de elección es la aspirina, con la cual se logra revertir la hiperagregabilidad plaquetaria. Se presenta el seguimiento de una gestante con diagnóstico de síndrome de plaquetas pegajosas tipo II, con antecedentes de dos pérdidas de embarazos. Durante la gestación recibió terapia antiagregante plaquetaria y heparina de bajo peso molecular. A pesar de esta terapéutica surgieron complicaciones en el tercer trimestre de la gestación que condujeron a la interrupción temprana del embarazo. Se logró una recién nacida viva, con bajo peso, sin otras complicaciones perinatales. Actualmente la paciente se mantiene con aspirina y no ha referido eventos oclusivos. Este trabajo demuestra que la atención a estas pacientes por un equipo multidisciplinario permite obtener resultados alentadores.

Sticky platelet syndrome is an entity where patients have platelet hiperaggregability and thrombotic clinical manifestations. It was observed more than 30 years ago in young people with occlusive arterial, venous, myocardial infarctions, stroke, and later it was reported in women with recurrent pregnancy loss and obstetric complication events. The treatment of choice is aspirin which reverted platelet hyperaggregability. We present a pregnant woman diagnosed with type II sticky platelets syndrome with a history of two pregnancy loss. During this pregnancy, she received antiplatelet therapy and molecular weight heparin. Despite this therapy, complications arose in the third quarter that led to the early termination of pregnancy, but we obtained an alive underweight newborn without any perinatal complications. Currently, the patient maintains aspirin and she has no occlusive events. These results demonstrate that the care of these patients by a multidisciplinary team has successful outcome.

Talassemia beta maior e gestação na adolescência: relato de dois casos / Beta thalassemia major and pregnancy during adolescence: report of two cases

A talassemia beta maior é uma doença hematológica hereditária rara em que deficiência na síntese de cadeias globínicas beta causa anemia grave. O tratamento consiste de transfusão sanguínea e quelação de ferro. Descrevemos dois casos de adolescentes com talassemia beta maior, com gestação não planejada e início tardio de pré-natal. Uma delas apresentou piora da anemia, necessidade transfusional aumentada, restrição de crescimento fetal e senescência placentária. A outra apresentava também hipotireoidismo e baixo peso materno, e foi internada por duas ocasiões durante a gestação, por choque hemorrágico do dengue e por infecção respiratória associada a vírus influenza H1N1. Uma delas apresentou restrição de crescimento fetal e teve parto vaginal no termo complicado com hipotonia uterina. Ambas necessitaram de transfusão sanguínea no pós-parto e optaram por medroxiprogesterona como método contraceptivo subsequentemente. Esse relato ressalta a importância de orientação contraceptiva para essas mulheres e o papel do cuidado pré-natal especializado em conjunto com hematologista.

Beta thalassemia major is a rare hereditary blood disease in which impaired synthesis of beta globin chains causes severe anemia. Medical treatment consists of chronic blood transfusions and iron chelation. We describe two cases of adolescents with beta thalassemia major with unplanned pregnancies and late onset of prenatal care. One had worsening of anemia with increased transfusional requirement, fetal growth restriction, and placental senescence. The other was also diagnosed with hypothyroidism and low maternal weight, and was admitted twice during pregnancy due to dengue shock syndrome and influenza H1N1-associated respiratory infection. She also developed fetal growth restriction and underwent vaginal delivery at term complicated by uterine hypotonia. Both patients required blood transfusions after birth and chose medroxyprogesterone as a contraceptive method afterwards. This report highlights the importance of medical advice on contraceptive methods for these women and the role of a specialized prenatal follow-up in association with a hematologist.

Trombocitopenia en el embarazo: gestacional, inmune y congénita / Thrombocytopenia in pregnancy: gestational, immune and congenital

La trombocitopenia afecta hasta el 10 por ciento de todos los embarazos y es un diagnóstico común y un problema en el manejo de las pacientes, ya que puede estar relacionado con condiciones prexistentes presentes en las mujeres en edad fértil, como la trombocitopenia inmune primaria y las trombocitopenias congénitas; o con trastornos intrínsecos del embarazo, como la trombocitopenia gestacional. Se recomienda que todas las mujeres embarazadas con recuento de plaquetas por debajo de 100 x 10(9)/L sean sometidas a una evaluación por el hematólogo y el obstetra. El análisis cuidadoso del momento del inicio de la trombocitopenia asociado a las manifestaciones clínicas y las pruebas de laboratorio específicas, es indispensable para proporcionar un diagnostico apropiado y una asistencia médica materna-fetal en el momento oportuno, en preparación para el desafío homeostático...

Thrombocytopenia affects up to 10 percent of all pregnant women and is a common diagnosis and a problem in the management of patients as it may be related to preexisting conditions in women of childbearing age, such as primary immune thrombocytopenia and congenital thrombocytopenia or intrinsic disorders of pregnancy as gestational thrombocytopenia. It is recommended that all pregnant women with a platelet count below 100 x 10(9) / L should undergo an evaluation by the hematologist and the obstetrician. Careful analysis of the time of onset of thrombocytopenia associated to clinical manifestations and specific laboratory tests are essential to provide appropriate diagnosis and maternal - fetal medical care at the right time, when preparing for the homeostatic challenge...

Reflexiones médicas a propósito de un caso de tromboembolia pulmonar en el embarazo / Medical reflections on a case of pulmonary thromboembolism in pregnancy

La mortalidad materna en el mundo es aún alta. La tromboembolia pulmonar como causa de muerte ocupa el segundo lugar en países desarrollados. En Latinoamérica, la frecuencia informada es de 0.6%, lo cual contrasta con la señalada para países desarrollados (14.9%). Esta diferencia puede estar relacionada a sesgos de información. Por tal motivo se revisó la información actual del tema y presentamos un breve caso clínico de una mujer quien presentó evento de tromboembolia pulmonar en la semana 30 del embarazo; el manejo adecuado de la misma, permitió la supervivencia materna y fetal.

Maternal mortality is still high in the world. Pulmonary thromboembolism as a cause of death is the second in developed countries. The frequency of reported events in Latin-American is 0.6%, which contrasts with that reported for developed countries (14.9%). This difference may be related to information bias. A review of the current information about this topic is presented, and we report a short case of a pregnant woman who presented pulmonary thromboembolism event at 30 weeks of pregnancy. Appropriate therapy allowed maternal and fetal survival.

Influência do tipo de aleitamento materno e da presença de anemia na mãe na concentração de hemoglobina aos 6 meses de idade / Influence of breastfeeding type and maternal anemia on hemoglobin concentration in 6-month-old infants

Objetivo: Verificar a influência do tipo de aleitamento materno e da presença de anemia na mãe no nível de hemoglobina de lactentes aos 6 meses de idade. Métodos: Estudo transversal, aninhado em estudo de intervenção de base comunitária, randomizado, controlado, que objetivou aumentar a duração do aleitamento materno exclusivo nos primeiros 6 meses de vida. O estudo foi realizado em quatro cidades do estado de Pernambuco, sendo os recém-nascidos recrutados no período de março a agosto de 2001. Seis meses após o parto, avaliou-se a concentração da hemoglobina de 330 mães/lactentes e o tipo de aleitamento. A identificação dos fatores que, de modo independente, contribuíram na concentração de hemoglobina das crianças foi realizada utilizando análise de regressão linear multivariada. Resultados: O tipo de aleitamento não influenciou a concentração de hemoglobina na amostra como um todo. No entanto, ao se analisar o grupo de crianças em aleitamento exclusivo/predominante, verificou-se uma diferença significante na mediana da hemoglobina de 0,7 g/dL em detrimento das filhas de mães anêmicas. A hemoglobina materna, o tipo de piso da residência, o tipo de parto e o peso ao nascer contribuíram significantemente na variação da concentração de hemoglobina das crianças. Conclusões: Ao contrário do observado em relação ao tipo de aleitamento materno, a anemia materna exerceu influência sobre os valores de hemoglobina de lactentes aos 6 meses, mesmo quando consideradas apenas as crianças em aleitamento exclusivo/predominante, apontando para a necessidade de prevenção da anemia materna antes da concepção, durante a gravidez e na lactação.

Objective: To verify the influence of breastfeeding type and of maternal anemia on hemoglobin concentration in 6-month-old infants. Methods: This was a cross-sectional study nested in a community-based, randomized and controlled intervention study that aimed to prolong the duration of exclusive breastfeeding during the first 6 months of life. This study was conducted in four towns in the Brazilian state of Pernambuco and newborn infants were recruited from March to August of 2001. The hemoglobin concentrations of 330 mothers and infants were assayed and type of breastfeeding was assessed 6 months after delivery. Multivariate linear regression analysis was used to identify factors that independently contributed to the infants hemoglobin concentration. Results: The type of feeding had no influence on the hemoglobin concentration in the sample as a whole, however, there was a significant difference when the exclusive + predominant breastfeeding” subset of infants was analyzed, with the children of anemic mothers exhibiting a reduction of 0.7g/dL in median hemoglobin. Mothers hemoglobin level, type of flooring at home, type of delivery, and birthweight all significantly contributed to the variation in the infants hemoglobin concentration. Conclusions: In contrast with type of breastfeeding, maternal anemia did have an influence on the hemoglobin levels of 6-month-old infants, even when only children on exclusive + predominant breastfeeding” were analyzed. These findings highlight the need to prevent maternal anemia before conception, during pregnancy and throughout lactation.

Isoinmunización antikell: manejo clínico de 26 casos / Antikell alloinmunization: clinical management of 26 cases

La principal causa de anemia fetal es la isoinmunización Rh por el desarrollo de anticuerpos frente al antí-geno D. La aloinmunización antiKell es una patología poco frecuente aunque puede producir un cuadro de anemia fetal muy grave. Su incidencia relativa ha aumentado en los últimos años debido al mayor número de transfusiones sanguíneas por disminución de la isoinmunización anti-D. Presentamos 26 casos de isoin-munización antiKell controlados en el Hospital La Paz de Madrid, durante los años 2003-2009 y una revisión de la literatura.

The main cause of fetal anemia is red-cell alloimmunization. Kell alloinmunization is a rare disease, although it can produce severe fetal damages. The relative incidence of antiKell isoinmunization has increased last years due to the blood transfusions has grown also, and anti-D aloinmunization has decreased. We report twenty six cases of pregnant women with isoinmunization antikell controlled in La Paz Hospital, Madrid, between 2003-2009 and a review of the literature.

Hemolytic Disease of the Newborn Associated with Anti-Jr(a) Alloimmunization in a Twin Pregnancy: The First Case Report in Korea / 대한진단검사의학회지

Jr(a) is a high-frequency antigen found in all ethnic groups. However, the clinical significance of the anti-Jr(a) antibody has remained controversial. Most studies have reported mild hemolytic disease of the newborn and fetus (HDNF) in Jr(a)-positive patients. Recently, fatal cases of HDNF have also been reported. We report the first case of HDNF caused by anti-Jr(a) alloimmunization in twins in Korea. A 33-yr-old nulliparous woman with no history of transfusion or amniocentesis was admitted at the 32nd week of gestation because of vaginal bleeding caused by placenta previa. Anti-Jr(a) antibodies were detected in a routine laboratory examination. An emergency cesarean section was performed at the 34th week of gestation, and 2 premature infant twins were delivered. Laboratory examination showed positive direct antiglobulin test and Jr(a+) phenotype in the red blood cells and the presence of anti-Jr(a) antibodies in the serum in both neonates. The infants underwent phototherapy for neonatal jaundice; this was followed by conservative management. They showed no further complications and were discharged on the 19th postpartum day. Preparative management to ensure the availability of Jr(a-) blood, via autologous donation, and close fetal monitoring must be performed even in cases of first pregnancy in Jr(a-) women.

Detection & management of anaemia in pregnancy in an urban primary health care institution.

BACKGROUND & OBJECTIVE: In India, anaemia in pregnancy remains a major public health problem associated with increased risk of low birth weight deliveries. A study was carried out at an urban primary health institution in Delhi, to assess feasibility of screening all pregnant women attending antenatal clinic for anaemia, identifying those with moderate anaemia (haemoglobin between 5.0 - 7.9 g/dl), administering intramuscular (im) therapy to them in the out-patient department (OPD), and observing the impact on maternal haemoglobin (Hb) levels and birth weight of the infant. METHODS: In the antenatal clinic all pregnant women were screened for anaemia. Women with Hb between 5.0- 7.9 g/dl were counselled and those who were willing, were given six intramuscular injections each consisting of iron sorbitol citric acid complex containing 150 microg elemental iron, 1500 microg folic acid, 150 microg hydroxocobalamine acetate (vitamin B1)). They were followed up through pregnancy and till delivery. Birth weight of infants of women who received therapy were compared with birth weight of infants born in DCMC. RESULTS: Over 80 per cent of 3698 women who attended the antenatal clinic were anaemic; 745 (20.1%) had Hb between 5.0-7.9 g/dl. Of these, 419 women agreed to take im therapy as outpatients; 367 took all 6 injections. Metallic taste on the tongue, nausea, vomiting and pain at the injection site were the side effects reported. The mean Hb even 9 wk after completion of therapy was only 9.6 g/dl. Mean birth weight in 340 women who completed the treatment was 2.8 kg - significantly (P<0.001) higher than birth weight in women who had Hb <8.0 g/dl at the time of delivery, but lower than birth weight of infants born to non anaemic women. INTERPRETATION & CONCLUSION: In urban primary health care institutions, it is possible to screen pregnant women for anaemia, identify those with Hb between 5.0 and 7.9 g/dl and give them im therapy as outpatients. Use of a preparation with fewer and milder side effects, counselling and support of women who develop side effect may result in high compliance rates; 900 mg of elemental iron as iron sorbitol citric acid was insufficient to raise mean Hb beyond 9.6 g/dl. The dosage has to be increased to achieve optimal results in relation to maternal haemoglobin levels and birth weight.

Anemia del embarazo en la Provincia de Concepción, Chile: relación con el estado nutricional materno y el crecimiento fetal

Estudios realizados en Santiago han determinado que la anemia al inicio del embarazo es un problema de salud pública. No se conoce la situación en el resto del país. El propósito de este estudio fue establecer la prevalencia de anemia en mujeres embarazadas de la provincia de Concepción y evaluar su asociación con su estado nutricional y el crecimiento fetal de sus recién nacidos. Cumplieron con los requisitos de ingreso 1782 mujeres que iniciaron el año 2004 control prenatal en los centros de atención primaria del sistema de salud público de Concepción. La anemia se determinó con los criterios de la OMS (Hb < 11g / dl) y del Center for Disease Control de los Estados Unidos de América (CDC) (Hb < percentilo 5 para cada semana de gestación). Se comparó la presencia o ausencia de anemia con las variables independientes antropométricas maternoinfantiles, la prematurez y el puntaje Apgar del recién nacido, además de la edad, paridad, morbilidad y hábito tabáquico de la madre. Se realizó un análisis multivariado con regresión logística del posible efecto de la anemia en el crecimiento fetal. La prevalencia de anemia fue de 10,9% y de 14,5% según los criterios OMS y CDC, respectivamente. El estado nutricional de la madre se asoció significativamente con la anemia. Sin embargo, la anemia según OMS y CDC al inicio del embarazo no se asoció con el crecimiento fetal en el análisis multivariado. La anemia materna y es algo superior a la del estudio más reciente de Santiago.

Maternal anemia in Concepción province, Chile: association with maternal nutritional status and fetal growth. Previous studies in Santiago, Chile have established that anemia in the earliest stages of pregnancy is a public health issue. The situation in other parts of the country is unknown. The purpose of this study is to establish the prevalence of anemia in pregnant women in the province of Concepcion and evaluate its association with maternal nutricional status and fetal growth. The study included 1782 women with singleton pregnancies who began prenatal check-ups in 2004 at the public primary health care centers. Anemia was established using the following criteria: from WHO (Hb < 11g / dl) and from the USA Center for Disease Control (CDC) (Hb < percentile 5 for each gestational week). Anemia prevalence was compared in relation to independent study variables: maternal age, parity, morbidity and smoking habit, and mother and child anthropometry. A multivariable logistic regression model studied the possible effect of anemia on fetal growth. The prevalence of anemia was 10.9% and 14.5% using the WHO and CDC criteria, respectively. The mother’s nutritional status was significantly associated with anemia. However, anemia according to WHO and CDC criteria at the beginning of pregnancy was not significantly associated to fetal growth in the univariate and multivariate analyses. The prevalence of anemia in the province of Concepcion constitutes a public health problem that needs to be addressed and it is slightly higher to that recently observed in the county of Puente Alto, Santiago.

Trombocitopenia y embarazo / Thrombocytopenia and pregnancy

La trombocitopenia es la causa más común de sangrado en la población general, siendo también la principal causa de alteraciones de la coagulación en las pacientes obstétricas, observándose en aproximadamente el 10% de ellas. Son múltiples las causas de esta alteración, dentro de las cuales las más comunes son: trombocitopenia gestacional, trombocitopenia relacionada a preeclampsia y a enfermedades autoinmunes. La complicación anestesiológica más importante relacionada con la trombocitopenia es la producción de un hematoma peridural secundario a una anestesia neuroaxial. El objetivo de esta revisión es dar a conocer las diversas causas de trombocitopenia en pacientes embarazadas y su enfrentamiento desde el punto de vista anestesiológico.

Thrombocytopenia is the most common cause of bleeding in the general population, being also the principal cause of coagulation deficits in obstetric patients, with an incidence of 10% in this population. The most common ethiologies are: gestational thrombocytopenia, preeclampsia and autoimmune disease related thrombocytopenia. The most important anesthesiological complication in relation to thrombocytopenia is the formation of an epidural hematoma secondary to a neuraxial puncture. The objective is to review the different kinds of thrombocytopenia during pregnancy and the anesthesiological approach.

An increase of the cardiothoracic ratio leads to a diagnosis of Bart's hydrops.

BACKGROUND: Thalassemia is a common single gene disorder in Southeast Asia. a-thalassemia is a group of syndrome characterized by deficient production of the alpha-globin chain. Individuals with heterozygous alpha-thalassemia-1 are at risk of having a fetus that has Hemoglobin Bart's hydrops fetalis (Hb Bart's). Usually, when the hemoglobin electrophoresis in heterozygous alpha-thalassemia-1 is normal, the Mean Corpuscular Volume (MCV) is lowered. We report a case of increased cardiothoracic ratio that led to a diagnosis of Hb Bart's in a couple who had normal hemoglobin electrophoresis and low MCV. CASE REPORT: A 23-year-old woman, gravida 2, Para 0-0-1-0, initially presented for antenatal care at 13 weeks pregnancy. Her MCV was 67 fentolitre, DiChlorophenol-IndolPhenol (DCIP) test was negative and hemoglobin electrophoresis was normal. Her husbands MCV was 67 fentolitre, and hemoglobin electrophoresis was normal. Cardiomegaly (an increased of the cardiothoracic ratio) was detected by ultrasonogram at 25 weeks of gestation. She and her husband were comprehensively counseled after an Hb Bart's was suspected. A cordocentesis was performed and the fetal blood was tested for hemoglobin electrophoresis. The result was later known and confirmed as Hb Bart's. The couple decided to terminate the pregnancy. The induced abortion was successful and the patient was discharged on the second day after the abortion. She was well at the 4-week follow-up. CONCLUSION: A prenatal ultrasonographic screening should be conducted in couples who are suspected of being alpha-thalassemia-1 carriers when DNA study of alpha-globin gene cannot be performed. The increase of cardiothoracic ratio will help detect an early stage of Hb Bart's.

Risk of a couple having a child with severe thalassemia syndrome, prevalence in lower northern Thailand.

Thalassemia screening in pregnant women and their spouses was performed at Buddhachinaraj Provincial Hospital and 8 community hospitals in Phitsanulok; lower northern Thailand. The prevalence of thalassemic carrier state was determined of 1,198 couples. Of these, 4.8% had heterozygous alpha thalassemia-1, 1.6% had heterozygous beta thalassemia, 12.4% had heterozygous hemoglobin (Hb) E, 2.7% had homozygous Hb E and 0.25% of others had abnormal Hb. Eighteen at risk couples (1.5%) were identified. Fifteen couples were at risk for compound heterozygous Hb E / beta thalassemia and the remaining 3 were at risk for homozygous alpha thalassemia-1. Prenatal diagnosis (cordocentesis) was performed in 4 couples at risk, but no fetuses with severe thalassemic disease were detected.

Microangiopatía trombótica en adultos / Thrombotic microangiopathy in adults

Thrombotic microangiopathic hemolytic anemias include thrombotic thrombocytopenic purpura (TTP), hemolytic uremic syndrome (HUS) and pregnancy associated thrombotic microangiopathy (TMA). Eight adult patients (four males and four females) with TMA who were treated between 2003 and 2004 at the Hospital Italiano de Buenos Aires were reviewed. The average age was 40. Clinical diagnosis of TMA was made on admission in four patients. During their stay in hospital, 4 patients developed HUS characteristics, three as TTP and one presented pregnancy associated TMA. All of them revealed thrombocytopenia and microangiophatic hemolytic anemia. Renal impairment was the third most frequent characteristic at presentation. The patients with TTP revealed the most severe condition. All patients received daily plasma exchange. Immunosuppressants were also used. Four patients recovered completely, 2 passed away, one remains with renal impairment and requires hemodialysis, and a colectomy was performed on one of them. The TMA syndromes are occlusive disorders associated to platelet microvascular thrombi. Systemic and renal circulations are primarily affected. TTP/HUS might represent an overlapping spectrum of idiopathic or secondary disease. Prompt recognition and treatment are vital, because high mortality occurs due to these disorders. Among the differential diagnosis of TMA we can refer to sepsis, neoplasms, systemic vasculitis, eclampsia and others. The mainstay treatments are daily plasma exchange and infusion with fresh frozen plasma. Improving the management of these diseases is required considering their high morbidity and mortality.

Purpura trombocitopénico idiopatico y embarazo: cesarea versus parto vaginal / Idiopathic thrombocytopenic purpura and pregnancy: cesarean section versus vaginal delivery

Si bien el púrpura trombocitopénico idiomático (PTI) es una patología poco frecuente, su importancia radica en que existe una alta morbimortalidad materno-fetal durante el embarazo, el parto y el puerperio. Es en el parto donde actualmente existe mayor controversia, con respecto a que vía es más recomendable, cesárea o vía vaginal. Nuestro propósito es acortar la brecha de la duda con respecto a ésta incógnita en base a la literatura disponible actualmente tanto a nivel nacional como internacional presentando una revisión bibliográfica sobre el PTI en el embarazo dando una pequeña reseña sobre la fisiopatología de ésta, diagnóstico y tratamiento, centrándonos en la controversia sobre que vía de parto es la más indicada. Se adoptó la estrategia de búsqueda desarrollada en la revisión electrónica de bases de datos, bajo criterios definidos que permitieron identificar los estudios con mejor evidencia posible. En nuestra búsqueda se encontraron 18 trabajos que cumplieran con nuestros criterios de búsqueda. En la literatura no encontramos un trabajo prospectivo randomizado con un buen grado de evidencia y fuerza que afirme una vía por sobre otra. Los trabajos encontrados corresponden a reportes de casos y guías de expertos que recomiendan un manejo por sobre otro. Podemos concluir que la vía del parto se definiría según condiciones obstétricas y no por el nivel de plaquetas fetales encontrados. Además, algunos de los procedimientos para determinar los niveles de plaquetas estarían relacionado a un mayor riesgo de morbimortalidad que la patología base.

Thrombotic microangiopathies presenting as an obstetric emergency.

Thrombotic microangiopathies are disorders that arise due to a diffuse endothelial damage. They predominantly manifest either as thrombotic trombocytopenic purpura (TTP) or hemolytic uremic syndrome (HUS). When they arise as a complication of pregnancy and associated disorders they are associated with a high mortality and morbidity.

The prevalence and risk factors of anemia in pregnant women.

OBJECTIVE: To determine the prevalence and risk factors of anemia in pregnant women. METHOD: The pregnant women were screened with complete blood count, hemoglobin electrophoresis and serology tests for hepatitis B, syphilis and HIV. In cases of anemia, serum for iron and ferritin were investigated. Anemia was defined as a hemoglobin level less than 11.0 g/dl in the first and third trimester of pregnancy or less than 10.5 g/dl in the second trimester. Factors associated with anemia were analyzed by using student's t-test and chi-square. The statistically significant factors were tested with the use of multiple logistic regression. RESULTS: A total of 1,304 pregnant women were recruited. The prevalence of anemia was 19.2 per cent (251 cases). Classified in each trimester, the prevalence was 14.8 per cent, 20.5 per cent and 38.6 per cent in the first, second and third trimester, respectively. One hundred and sixty-one cases of anemia were available for serum iron and ferritin levels. Iron deficiency anemia, by means of serum ferritin, was detected in 32 cases (19.9%). An abnormal pattern of hemoglobin electrophoresis was detected in 367 cases (28.1%). Gestational age at first prenatal visit, abnormal hemoglobin electrophoresis and educational status were associated with anemia during pregnancy. CONCLUSION: The prevalence of anemia in pregnant women who first attended the prenatal visit was 19.2 per cent. Factors associated with anemia during pregnancy were gestational age at first prenatal visit, abnormal hemoglobin electrophoresis and educational status.

Sao os parametros hemostaticos capazes de predizer a doenca hipertensiva especifica da gravidez (DHEG)? / Are the hemostatic parameters able to predict the preeclampsia?

A DHEG esta associada a vasoconstricao generalizada e a diversas alteracoes da hemostasia. O diagnostico dessa doenca e, frequentemente, dificil de ser estabelecido, sendo muitas vezes erroneamente diagnosticada em casos de doenca renal. Desta forma, torna-se altamente desejavel a definicao de parametros hemostaticos que tenham valor preditivo para o diagnostico e prognostico da mesma. Neste estudo, foram...