Critical Care Issues in Pregnancy
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Porphyromonas Gingivalis Within Placental Villous Mesenchyme and Umbilical Cord Stroma Is Associated with Adverse Pregnancy Outcome
RESEARCH ARTICLE Porphyromonas gingivalis within Placental Villous Mesenchyme and Umbilical Cord Stroma Is Associated with Adverse Pregnancy Outcome Sizzle F. Vanterpool1,2, Jasper V. Been1,3,4, Michiel L. Houben5, Peter G. J. Nikkels6, Ronald R. De Krijger7, Luc J. I. Zimmermann1,8, Boris W. Kramer1,2,8, Ann Progulske-Fox9, Leticia Reyes9,10* 1 Department of Pediatrics, Maastricht University Medical Center, Maastricht, the Netherlands, 2 School for Mental Health and Neurosciences (MHeNS), Maastricht University, Maastricht, the Netherlands, 3 School for Public Health and Primary Care (CAPHRI), Maastricht University, Maastricht, the Netherlands, 4 Division of Neonatology, Erasmus University Medical Center–Sophia Children’s Hospital, Rotterdam, the Netherlands, 5 Department of Pediatrics, Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, the Netherlands, 6 Department of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands, 7 Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands, 8 School for Oncology and Developmental Biology (GROW), Maastricht University, Maastricht, the Netherlands, OPEN ACCESS 9 Department of Oral Biology, Center for Molecular Microbiology, University of Florida, Gainesville, Florida, Citation: Vanterpool SF, Been JV, Houben ML, United States of America, 10 Department of Pathobiological Sciences, University of Wisconsin-Madison, Nikkels PGJ, De Krijger RR, Zimmermann LJI, et al. Madison, Wisconsin, United States of America (2016) Porphyromonas gingivalis within Placental * [email protected] Villous Mesenchyme and Umbilical Cord Stroma Is Associated with Adverse Pregnancy Outcome. PLoS ONE 11(1): e0146157. doi:10.1371/journal. pone.0146157 Abstract Editor: Motohiro Komaki, Tokyo Medical and Dental University, JAPAN Intrauterine presence of Porphyromonas gingivalis (Pg), a common oral pathobiont, is impli- cated in preterm birth. -
Gestational Diabetes Insipidus, HELLP Syndrome and Eclampsia in a Twin Pregnancy: a Case Report
Journal of Perinatology (2010) 30, 144–145 r 2010 Nature Publishing Group All rights reserved. 0743-8346/10 $32 www.nature.com/jp PERINATAL/NEONATAL CASE PRESENTATION Gestational diabetes insipidus, HELLP syndrome and eclampsia in a twin pregnancy: a case report JL Woelk, RA Dombroski and PR Brezina Department of Obstetrics and Gynecology, East Carolina University, Greenville, NC, USA alanine aminotransferase, 65 U lÀ1; and lactate dehydrogenase, We report a case of eclampsia in a twin pregnancy complicated by HELLP 390 U lÀ1. A 24-h urine collection was begun to quantify proteinuria. syndrome and diabetes insipidus. This confluence of disease processes During the first night of hospitalization, the patient developed suggests that a modification of common magnesium sulfate treatment marked polyuria and polydipsia. Urine output increased to 1500 cc hÀ1 protocols may be appropriate in a certain subset of patients. by the early morning totaling 12 l for the entire night. Repeat Journal of Perinatology (2010) 30, 144–145; doi:10.1038/jp.2009.115 electrolytes were unchanged. The endocrinology service was then Keywords: diabetes insipidus ; eclampsia ; HELLP syndrome ; twin consulted for the management of presumptive DI. Therapy with the pregnancy ; magnesium sulfate administration of dDAVP (1-deamino-8-D-arginine vasopressin) orally twice daily was initiated. Serum osmolality was increased at 296 mOsm kgÀ1, and urine osmolality was decreased to 71 mOsm kgÀ1 Introduction with a specific gravity of 1.000. The 24-h urine results showed a total The association between diabetes insipidus (DI) and liver protein of 780 mg. The patient denied the previously reported dysfunction in a preeclamptic patient has been established in headaches, blurry vision and right upper quadrant pain, and her blood multiple case reports.1 This case is an important example that pressures remained 140 to 155 mmHg (systolic) and 80 to 95 mmHg illustrates how the pathophysiology of DI and the pharmacokinetics (diastolic), consistent with a diagnosis of mild preeclampsia. -
ABCDE Acronym Blood Transfusion 231 Major Trauma 234 Maternal
Cambridge University Press 978-0-521-26827-1 - Obstetric and Intrapartum Emergencies: A Practical Guide to Management Edwin Chandraharan and Sir Sabaratnam Arulkumaran Index More information Index ABCDE acronym albumin, blood plasma levels 7 arterial blood gas (ABG) 188 blood transfusion 231 allergic anaphylaxis 229 arterio-venous occlusions 166–167 major trauma 234 maternal collapse 12, 130–131 amiadarone, overdose 178 aspiration 10, 246 newborn infant 241 amniocentesis 234 aspirin 26, 180–181 resuscitation 127–131 amniotic fluid embolism 48–51 assisted reproduction 93 abdomen caesarean section 257 asthma 4, 150, 151, 152, 185 examination after trauma 234 massive haemorrhage 33 pain in pregnancy 154–160, 161 maternal collapse 10, 13, 128 atracurium, drug reactions 231 accreta, placenta 250, 252, 255 anaemia, physiological 1, 7 atrial fibrillation 205 ACE inhibitors, overdose 178 anaerobic metabolism 242 automated external defibrillator (AED) 12 acid–base analysis 104 anaesthesia. See general anaesthesia awareness under anaesthesia 215, 217 acidosis 94, 180–181, 186, 242 anal incontinence 138–139 ACTH levels 210 analgesia 11, 100, 218 barbiturates, overdose 178 activated charcoal 177, 180–181 anaphylaxis 11, 227–228, 229–231 behaviour/beliefs, psychiatric activated partial thromboplastin time antacid prophylaxis 217 emergencies 172 (APTT) 19, 21 antenatal screening, DVT 16 benign intracranial hypertension 166 activated protein C 46 antepartum haemorrhage 33, 93–94. benzodiazepines, overdose 178 Addison’s disease 208–209 See also massive -
Incidence of Eclampsia with HELLP Syndrome and Associated Mortality in Latin America
International Journal of Gynecology and Obstetrics 129 (2015) 219–222 Contents lists available at ScienceDirect International Journal of Gynecology and Obstetrics journal homepage: www.elsevier.com/locate/ijgo CLINICAL ARTICLE Incidence of eclampsia with HELLP syndrome and associated mortality in Latin America Paulino Vigil-De Gracia a,⁎, José Rojas-Suarez b, Edwin Ramos c, Osvaldo Reyes d, Jorge Collantes e, Arelys Quintero f,ErasmoHuertasg, Andrés Calle h, Eduardo Turcios i,VicenteY.Chonj a Critical Care Unit, Department of Obstetrics and Gynecology, Complejo Hospitalario de la Caja de Seguro Social, Panama City, Panama b Critical Care Unit, Clínica de Maternidad Rafael Calvo, Cartagena, Colombia c Department of Gynecology and Obstetrics, Hospital Universitario Dr Luis Razetti, Barcelona, Venezuela d Unit of Research, Department of Gynecology and Obstetrics, Hospital Santo Tomás, Panama City, Panama e Department of Gynecology and Obstetrics, Hospital Regional de Cojamarca, Cajamarca, Peru f Department of Gynecology and Obstetrics, Hospital José Domingo de Obaldía, David, Panama g Unit of Perinatology, Department of Gynecology and Obstetrics, Instituto Nacional Materno Perinatal, Lima, Peru h Department of Gynecology and Obstetrics, Hospital Carlos Andrade Marín, Quito, Ecuador i Unit of Research, Department of Gynecology and Obstetrics, Hospital Primero de Mayo de Seguridad Social, San Salvador, El Salvador j Department of Gynecology and Obstetrics, Hospital Teodoro Maldonado Carbo, Guayaquil, Ecuador article info abstract Article history: Objective: To describe the maternal outcome among women with eclampsia with and without HELLP syndrome Received 7 July 2014 (hemolysis, elevated liver enzymes, and low platelet count). Methods: A cross-sectional study of women with Received in revised form 14 November 2014 eclampsia was undertaken in 14 maternity units in Latin America between January 1 and December 31, 2012. -
Ask the Experts Amniotic Fluid Embolism Steven L. Clark, MD
Ask the Experts Questions have been written by: Amniotic Fluid Embolism Angela K. Hardyk, MD Mount Nittany Physician Group Ob/Gyn Steven L. Clark, MD State College, PA (Obstet Gynecol 2014;123:337–48) Responses have been written by: Steven L. Clark, MD Hospital Corporation of America Nashville, TN Question 1: How would you counsel a patient about a future pregnancy if she has been lucky enough to survive an amniotic fl uid embolism (AFE)? Would there be any special precautions she would need to take for her next pregnancy? Response from Dr. Clark: The available data in this area consist only of several very small series and case reports. These data suggest that the risks of recurrence are low. In addition, a pathophysiologic mechanism of disease that hinges on a maternal reaction to a specif- ic set of fetal antigens would suggest that recurrence ought to be uncommon. On the other hand, having dodged one bullet, is it really wise to spin the wheel again? My counseling goes something like this: “Available data suggest that the risk of recurrence is low, and there are a number of reports of successful pregnancy outcome after AFE survival. However, given the potential severity of AFE if it does recur, and a lack of really good data regarding risks, I advise you to undertake another pregnancy only if you are willing to accept a small risk of catastrophic outcome including death.” If a patient chooses to undertake pregnancy, I do not alter my management in any way, other than delivery in a tertiary center. -
Management of Prolonged Decelerations ▲
OBG_1106_Dildy.finalREV 10/24/06 10:05 AM Page 30 OBGMANAGEMENT Gary A. Dildy III, MD OBSTETRIC EMERGENCIES Clinical Professor, Department of Obstetrics and Gynecology, Management of Louisiana State University Health Sciences Center New Orleans prolonged decelerations Director of Site Analysis HCA Perinatal Quality Assurance Some are benign, some are pathologic but reversible, Nashville, Tenn and others are the most feared complications in obstetrics Staff Perinatologist Maternal-Fetal Medicine St. Mark’s Hospital prolonged deceleration may signal ed prolonged decelerations is based on bed- Salt Lake City, Utah danger—or reflect a perfectly nor- side clinical judgment, which inevitably will A mal fetal response to maternal sometimes be imperfect given the unpre- pelvic examination.® BecauseDowden of the Healthwide dictability Media of these decelerations.” range of possibilities, this fetal heart rate pattern justifies close attention. For exam- “Fetal bradycardia” and “prolonged ple,Copyright repetitive Forprolonged personal decelerations use may onlydeceleration” are distinct entities indicate cord compression from oligohy- In general parlance, we often use the terms dramnios. Even more troubling, a pro- “fetal bradycardia” and “prolonged decel- longed deceleration may occur for the first eration” loosely. In practice, we must dif- IN THIS ARTICLE time during the evolution of a profound ferentiate these entities because underlying catastrophe, such as amniotic fluid pathophysiologic mechanisms and clinical 3 FHR patterns: embolism or uterine rupture during vagi- management may differ substantially. What would nal birth after cesarean delivery (VBAC). The problem: Since the introduction In some circumstances, a prolonged decel- of electronic fetal monitoring (EFM) in you do? eration may be the terminus of a progres- the 1960s, numerous descriptions of FHR ❙ Complete heart sion of nonreassuring fetal heart rate patterns have been published, each slight- block (FHR) changes, and becomes the immedi- ly different from the others. -
Ante Partum Haemorrhage
Ante Partum Haemorrhage Sara Alhaddab Alanood Asiri Ante Partum Haemorrhage (APH): Bleeding in early pregnancy (first 20 weeks of gestation) causes: Affects 3-5 % of pregnancies. • - Miscarriage • Bleeding from or into the genital tract. - Ectopic pregnancy • Occurring from 20 weeks of pregnancy and prior - Molar pregnancy to the birth of the baby. - Local causes: tumor, trauma etc. Causes: Landmark of fetal viability is 20 weeks. • Placenta previa. • Placenta abruption. • Local causes (cervical or vaginal lesions, lacerations). Trauma, tumor and infections. • Unexplained (SGA, IUGR). SGA: small for gestational age. • Vasa previa. • Uterine rupture. - APH is the leading cause of prenatal and maternal morbidity and prenatal mortality (mainly prematurity). - Obstetrics hemorrhage remains one of the major causes of maternal death in the developing countries. Management: In the hospital maternity unit with facilities for resuscitation such as: Source: Essentials of Obstetrics and Gynecology. § Anesthetic support. § Blood transfusion resources. § Performing emergency operative delivery. § Multidisciplinary team including (midwifery, obstetric staff, neonatal and anesthetic). Investigations: • Tests if suspecting vasa previa are often not applicable • Tocolysis: shouldn’t be used in: v Unstable patient. v Fetal compromise. v Major APH. It’s a decision of a senior obstetrician. Senior (consultant) anesthetic care needed in high-risk hemorrhage. • Risk of PPH: patient should receive active management of 3rd stage of labor using syntometrine (in absence of high BP). Syntometrine → active uterine contraction after delivery to prevent PPH. • AntiD Ig should be given to all non sensitized RH –ve if the have APH, at least 500 IU AntiD Ig followed by a test of FMH if it is more than 40 ml of RBC additional AntiD required. -
Ophthalmic Associations in Pregnancy
CLINICAL Ophthalmic associations in pregnancy Queena Qin, Celia Chen, Sudha Cugati PREGNANCY RESULTS in various physiological variation in pregnancy.2 It normally changes in the female body, including in fades slowly after pregnancy and does the eyes. A typical pregnancy results in not need active intervention. Background A range of ocular pathology exists cardiovascular, pulmonary, metabolic, • Cornea – corneal thickness, curvature during pregnancy. Some pre-existing eye hormonal and immunological changes. and sensitivity may be altered during conditions, such as diabetic retinopathy, Hormonal changes occur, with a rise of pregnancy. Corneal thickness and can be exacerbated during pregnancy. oestrogen and progesterone levels to curvature can increase in pregnancy, Other conditions manifest for the first suppress the menstrual cycle.1 especially in the second and third time during pregnancy as a result of The eye, an end organ, undergoes trimesters, and return to normal in complications such as pre-eclampsia changes during pregnancy. Some of the postpartum period.3 Patients who and eclampsia. Early recognition and understanding of the management of these changes exacerbate pre-existing wear contact lenses may experience ophthalmic conditions is crucial. eye conditions, while other conditions intolerance to the use of contact lenses. manifest for the first time during Pregnant women should be advised Objective pregnancy. Early recognition and to delay obtaining a new prescription The aim of this article is to discuss the understanding of management of for glasses or undergoing a contact physiological and pathological changes in the eyes of pregnant women. ophthalmic conditions during pregnancy lens fitting until after delivery. Laser Pathological changes are sub-divided is crucial for the primary care physician. -
Gestational Diabetes Insipidus (GDI) Associated with Pre-Eclampsia
MOJ Women’s Health Case Report Open Access Gestational diabetes insipidus (GDI) associated with pre-eclampsia Abstract Volume 5 Issue 6 - 2017 Gestational diabetes insipidus (GDI) is a rare complication of pregnancy, usually developing in the third trimester and remitting spontaneously 4-6weeks post-partum. Afsoon Razavi, Muhammad Umair, Zehra It is mainly caused by excessive vasopressinase activity, an enzyme expressed by Tekin, Issac Sachmechi placental trophoblasts which metabolizes arginine vasopressin (AVP). The treatment Department of medicine, Icahn School of Medicine at Mount requires desmopressin. A 38year old G3P0A2 women with no significant medical Sinai/NYC Health+ Hospital/Queens, USA history was admitted to obstetrical service on 36th week of gestation due to significant malaise, anorexia, nausea, vomiting, polyuria, nocturia, and polydipsia, worsening Correspondence: Afsoon Razavi, MD, Department of in the 2weeks prior to presentation. Physical examination demonstrated decreased Medicine, Icahn School of Medicine at Mount Sinai/NYC skin turgor, hyperactive tendon reflexes and no pedal edema, and her blood pressure Health+Hospital/Queens, Diabetes center, 4th floor, Suit P-432, Pavilion building, Queens hospital center, 82-68 164th street, was 170/100mmHg, heart rate 67beats/min and weight 60kg (BMI 23.1kg/m2). Her Jamaica, New York, 11432, USA, Tel +8183843165, laboratory results a month prior to admission showed normal basic metabolic panel Email [email protected] and liver function tests. On admission she found to have urine osmolality112mOsmol/ kg (350-1000); serum osmolality 308mOsmol/kg (278-295); Urinalysis revealed Received: July 25, 2017 | Published: August 16, 2017 specific gravity less than 1005 with proteinuria. serum sodium 151mmol/L (135-145); potassium 4.1mmol/L (3.5-5.0); Cl 128mmol/L, urea 2.2 mmol/L (2.5-6.7), creatinine 1.4mg/dL, Bilirubin 1.3mg/dL, AST 1270 U/L, alkaline phosphatase, 717U/L, uric acid 10.1mg/dL and INR 1.1. -
Prioritization Changes
Oregon Health Plan Prioritized List changes Planned Out-of-hospital Birth The Health Evidence Review Commission approved the following changes to the Prioritized List of Health Services on August 13, 2020, based on the approved coverage guidance, “Planned Out-of- hospital Birth.” The changes will take effect on the Prioritized list of Health Services for the Oregon Health Plan on October 1, 2020. Changes for the Prioritized List of Health Services: GUIDELINE NOTE 153 PLANNED OUT-OF-HOSPITAL BIRTH Lines 1,2 Planned out-of-hospital birth is included on this line for pregnant women who are at low risk for adverse obstetric or birth outcomes. The high-risk conditions outlined below would either preclude coverage of planned out-of-hospital birth, necessitate a consultation, or require transfer of the mother or infant to a hospital setting. When a condition requiring transfer arises during labor, an attempt should be made to transfer the mother and/or her newborn; however, imminent fetal delivery may delay or preclude actual transfer prior to birth. Coverage of prenatal, intrapartum, and postpartum care is recommended with the performance of appropriate risk assessments (at initiation of care and throughout pregnancy and delivery) and the out- of-hospital birth attendant’s adherence to the consultation and transfer criteria as outlined below. When a high-risk condition develops that requires transfer or planned hospital birth, coverage is recommended when appropriate care is provided until the point the high-risk condition is identified. For women who have a high-risk condition requiring consultation, ongoing coverage of planned out-of- hospital birth care is recommended as long as the consulting provider’s recommendations are then appropriately managed by the out-of-hospital birth attendant in a planned out-of-hospital birth setting. -
1 Supplementary Table S2. Summary of the Results of Systematic Literature
Supplementary Table S2. Summary of the results of systematic literature review Question 1. What is the evidence that the following pre-conception (planned versus unintended pregnancy, disease activity and damage, antibody profile, lupus medications, management of flares, access to specialist services, immunization status and update) and post-conception/delivery (parenting issues, lupus medications, management of flares, access to specialist care) factors influence maternal and foetal outcomes, and thus, should be considered in pregnancy risk stratification and counselling in women with SLE or APS? 1. Women with SLE 1.1. Pre-conception factors associated maternal outcomes Factor/predictor Outcome(s) and example(s) of effect size Best study References design1 Active/flaring SLE (before Active/flaring SLE during pregnancy. SLE flares during the pre-gestation period had OR 4 1-21 or at conception) 5.1 for flare during pregnancy; previous (within 6 months before conception) organ involvement predicted same organ involvement during pregnancy (especially haematological, renal, skin, serological activity); SLE flares during the pre-gestation period had OR 5.1 for development of flare during pregnancy; SLEDAI ≥4 at conception had sensitivity 64% and specificity 75% for SLE exacerbation during pregnancy; remission during the 6-month period prior to conception is associated with lower odds for flare during pregnancy Organ damage. Pre-gestational SLE activity (SLAM-R index) correlates with post-partum 5 22 damage accrual Pregnancy-induced hypertension, (pre-)eclampsia/HELLP. Positive correlation with 4 12 14 21 23 pre-conception SLEDAI; active SLE within 4 months before conception was associated with pregnancy-induced hypertension (25% versus 11%) Adverse maternal outcome (composite outcome or death). -
Amnioinfusion
Review Article Indian Journal of Obstetrics and Gynecology Volume 7 Number 4 (Part - II), October – December 2019 DOI: http://dx.doi.org/10.21088/ijog.2321.1636.7419.12 Amnioinfusion Alka Patil1, Sayli Thavare2, Bhagyashree Badade3 How to cite this article: Alka Patil, Sayli Thavare, Bhagyashree Badade. Amnioinfusion. Indian J Obstet Gynecol. 2019;7(4)(Part-II):641–644. 1Professor and Head, 2,3Junior Resident, Department of Obstetrics and Gynaecology, ACPM Medical College, Dhule, Maharashtra 424002, India. Corresponding Author: Alka Patil, Professor and Head, Department of Obstetrics and Gynaecology, ACPM Medical College, Dhule, Maharashtra 424002, India. E-mail: [email protected] Received on 20.11.2019; Accepted on 16.12.2019 Abstract potentially at risk. Oligohydramnios is one of the high-risk pregnancy, posing diagnostic challenge Amniotic fluid is a dynamic medium that plays and dilemma in management. These high-risk a significant role in fetal well-being. It is essential pregnancies should be monitored, managed during pregnancy for normal fetal growth and organ and delivered at a tertiary care center for good development. About 4% of pregnancies are complicated pregnancy outcome. by oligohydramnios. It is associated with an increased incidence of perinatal morbidity and mortality due to its Amniotic fl uid is essential for the continued well antepartum and intrapartum complications. Gerbruch being of the fetus and has following functions: and Hansman described a technique of Amnioinfusion • Shock absorber preventing hazardous to overcome these difficulties to prevent the occurrence pressure on the fetal parts of fetal lung hypoplasia in pregnancies complicated by oligohydramnios. Amnioinfusion reduces both • Prevents adhesion formation between fetal the frequency and depth of FHR deceleration.