Management of Labour and Obstructed Labour
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NUR 306- MIDWIWERY-II.Pdf
THE CATHOLIC UNIVERSITY OF EASTERN AFRICA P.O. Box 62157 A. M. E. C. E. A 00200 Nairobi - KENYA Telephone: 891601-6 Fax: 254-20-891084 MAIN EXAMINATION E-mail:[email protected] SEPTEMBER-DECEMBER 2020 TRIMESTER SCHOOL OF NURSING REGULAR PROGRAMME NUR/UNUR 306: MIDWIFERY II-LABOUR Date: DECEMBER2020 Duration: 3 Hours INSTRUCTIONS: i. All questions are compulsory ii. Indicate the answers in the answer booklet provided PART -I: MULTIPLE CHOICE QUESTIONS (MCQs) (20 MARKS): Q1.The following are two emergencies that can occur in third stage of labour: a) Cord prolapsed, foetal distress. b) Ruptured uterus ,foetal distress. c) Uterine inversion, cord pulled off. d) Cord round the neck, foetal distress. Q2 A woman in preterm labor at 30 weeks of gestation receives two 12-mg doses of betamethasone intramuscularly. The purpose of this pharmacologic treatment is to: a). Stimulate fetal surfactant production. b). Reduce maternal and fetal tachycardia associated with ritodrine administration. c). Suppress uterine contractions. d). Maintain adequate maternal respiratory effort and ventilation during magnesium sulfate therapy. Q3. Episiotomy should only be considered in case of : a) Breech, vacuum delivery, scarring from genital cutting, fetal distress. b) Primigravida, disturbed woman, genital cutting, obstructed labor. c) Obstructed labor, hypertonic contractions, multigravida, forceps delivery. Cuea/ACD/EXM/APRIL 2020/SCHOOL OF NURSING Page 1 ISO 9001:2015 Certified by the Kenya Bureau of Standards d) Primigravida, hypotonic contractions, fetal distress, genital cutting. Q4.A multiporous woman in labour tells the midwife “I feel like opening the bowels”.How should the midwife respond? a) Allow the woman to use the bedpan. -
Delivery Mode for Prolonged, Obstructed Labour Resulting in Obstetric Fistula: a Etrr Ospective Review of 4396 Women in East and Central Africa
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by eCommons@AKU eCommons@AKU Obstetrics and Gynaecology, East Africa Medical College, East Africa 12-17-2019 Delivery mode for prolonged, obstructed labour resulting in obstetric fistula: a etrr ospective review of 4396 women in East and Central Africa C. J. Ngongo T. J. Raassen L. Lombard J van Roosmalen S. Weyers See next page for additional authors Follow this and additional works at: https://ecommons.aku.edu/eastafrica_fhs_mc_obstet_gynaecol Part of the Obstetrics and Gynecology Commons Authors C. J. Ngongo, T. J. Raassen, L. Lombard, J van Roosmalen, S. Weyers, and Marleen Temmerman DOI: 10.1111/1471-0528.16047 www.bjog.org Delivery mode for prolonged, obstructed labour resulting in obstetric fistula: a retrospective review of 4396 women in East and Central Africa CJ Ngongo,a TJIP Raassen,b L Lombard,c J van Roosmalen,d,e S Weyers,f M Temmermang,h a RTI International, Seattle, WA, USA b Nairobi, Kenya c Cape Town, South Africa d Athena Institute VU University Amsterdam, Amsterdam, The Netherlands e Leiden University Medical Centre, Leiden, The Netherlands f Department of Obstetrics and Gynaecology, Ghent University Hospital, Ghent, Belgium g Centre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya h Faculty of Medicine and Health Science, Ghent University, Ghent, Belgium Correspondence: CJ Ngongo, RTI International, 119 S Main Street, Suite 220, Seattle, WA 98104, USA. Email: [email protected] Accepted 3 December 2019. Objective To evaluate the mode of delivery and stillbirth rates increase occurred at the expense of assisted vaginal delivery over time among women with obstetric fistula. -
Fetal Compromise (Acute): Management If Suspected This Document Should Be Read in Conjunction with the Disclaimer
King Edward Memorial Hospital King Edward Memorial Hospital Obstetrics & Gynaecology Obstetrics & Gynaecology CLINICAL PRACTICE GUIDELINE Fetal compromise (acute): Management if suspected This document should be read in conjunction with the Disclaimer Aim To identify suspected or actual fetal compromise and initiate early intervention to promote placental and umbilical blood flow to decrease risk of hypoxia and acidosis. Key points1 1. Fetal compromise in labour may be due to a variety of pathologies including placental insufficiency, uterine hyperstimulation, maternal hypotension, cord compression and placental abruption. Identification and management of reversible abnormalities may prevent unnecessary intervention. 2. Continuous electronic cardiotocograph (CTG) monitoring should be commenced when fetal compromise is detected at the onset of labour or develops during labour. 3. A normal CTG is associated with a low probability of fetal compromise and has the following features: Baseline rate 110-160 bpm Baseline variability 6-25 bpm Accelerations of 15 bpm for 15 seconds No decelerations. 4. The following features are unlikely to be associated with fetal compromise when occurring in isolation: Baseline rate 100-109 bpm Absence of accelerations Early decelerations Variable decelerations without complicating features. 5. The following features may be associated with significant fetal compromise and require further action (see management section on next page): Baseline fetal tachycardia >160 bpm Reduced or reducing baseline variability -
A Guide to Obstetrical Coding Production of This Document Is Made Possible by Financial Contributions from Health Canada and Provincial and Territorial Governments
ICD-10-CA | CCI A Guide to Obstetrical Coding Production of this document is made possible by financial contributions from Health Canada and provincial and territorial governments. The views expressed herein do not necessarily represent the views of Health Canada or any provincial or territorial government. Unless otherwise indicated, this product uses data provided by Canada’s provinces and territories. All rights reserved. The contents of this publication may be reproduced unaltered, in whole or in part and by any means, solely for non-commercial purposes, provided that the Canadian Institute for Health Information is properly and fully acknowledged as the copyright owner. Any reproduction or use of this publication or its contents for any commercial purpose requires the prior written authorization of the Canadian Institute for Health Information. Reproduction or use that suggests endorsement by, or affiliation with, the Canadian Institute for Health Information is prohibited. For permission or information, please contact CIHI: Canadian Institute for Health Information 495 Richmond Road, Suite 600 Ottawa, Ontario K2A 4H6 Phone: 613-241-7860 Fax: 613-241-8120 www.cihi.ca [email protected] © 2018 Canadian Institute for Health Information Cette publication est aussi disponible en français sous le titre Guide de codification des données en obstétrique. Table of contents About CIHI ................................................................................................................................. 6 Chapter 1: Introduction .............................................................................................................. -
Chapter 9 Risk Factors
Chapter 9 Risk factors 9.1 Introduction The previous chapters have all focused on adverse pregnancy and birth outcomes as risk factors for foetal loss and neonatal death. The present chapter takes the discussion and analysis one layer further to the underlying risk factors for the selected adverse pregnancy and birth outcomes themselves. These risk factors are more remote in the causal chain and include maternal factors, complications of the placenta, cord, and membranes, and birth complications. These have been referred to earlier, in Chapter 3, in the operationalisation of the conceptual model (Figure 3.6). Besides their direct effect on pregnancy/birth outcome, they are believed to affect foetal loss (i.e. spontaneous abortion and stillbirth), both directly and indirectly, and neonatal death indirectly through the intermediate outcomes (i.e. adverse pregnancy and birth outcomes). As became clear in Chapter 3, many different causes and risk factors underlie the adverse pregnancy and birth outcomes, but what appear to be main risk factors? Are these risk factors also important in regions in transition and, more specifically, in Kerala? Moreover, does the relative importance of these risk factors change during the epidemiologic transition? A region’s position within the transition could very well be reflected by its specific combination of underlying risk factors. Factors such as infections and malnutrition are likely to be important during the early of the transition, while others such as diabetes and advanced maternal age may become more significant during later stages. This could lead to a redefinition of the concepts of endogenous and exogenous mortality (see Chapter 2). -
INTRODUCTION Effect of Different Dosages of Intravaginal Misoprostol
Original Article Gynecology and Obstetrics Medical Journal of Islamic World Academy of Sciences Effect of Different Dosages of Intravaginal Misoprostol for Second Trimester Pregnancy Termination Maysoon Sharief1, Enaas S. Al-Khayat1 1Department of Gynecology and Obstetrics, College of Medicine, University of Basrah, Basrah, Iraq. ABSTRACT Miscarriage is a common complication of early pregnancy; however; curettage and dilation are considered standard methods taking care of early pregnancy failure. Misoprostol has been used as an alternative agent for termination of early pregnancy. Therefore, this study was aimed to compare the efficacy and side effects of two different intravaginal misoprostol trials for the second trimester pregnancy termination of missed miscarriage between 14 and 23 weeks. A clinical trial was carried out in Basrah Maternity & Children Hospital during the period from October 2011 to November 2012. A total of 100 women experienced missed miscarriages at 14-23 weeks of gestation were admitted for medical termination of pregnancy. Patients were divided into the following two groups: Group 1: 50 patients received 400 µg of intravaginal misoprostol/8 hours. Group 2: 50 patients received 800 µg of intravaginal misoprostol/8 hours. The patients were followed up for 24 hours. The primary outcome measure was induction-miscarriage interval; the secondary outcomes were the rate of successful miscarriage and complete miscarriage; the incidence of side effects was compared in both groups. The rates of successful termination of pregnancy in both groups 1 and 2 were 86% and 90%, respectively. The success rates of the drug in group 1 were 0%, 12%, 36%, 34%, 10%, and 4% after first, second, third, fourth, fifth, and sixth doses, respectively; whereas, the success rates in group 2 were 24%, 34%, 24%, 12%, 4%, and 0% after first, second, third, fourth, fifth, and sixth doses, respectively. -
PPH 2Nd Edn #23.Vp
43 Standard Medical Therapy for Postpartum Hemorrhage J. Unterscheider, F. Breathnach and M. Geary INTRODUCTION firm contraction of the organ. If severe haemorrhage has already set in, it is highly recommended that the drug should Failure of the uterus to contract and retract following be given by the intravenous route. For this purpose one-third childbirth has for centuries been recognized as the of the standard size ampoule may be injected or, for those most striking cause of postpartum hemorrhage (PPH) who wish accurate dosage, a special ampoule containing and complicates up to 10% of pregnancies globally. In 0.125 mg is manufactured. An effect may be looked for in less the developing world, PPH is responsible for one than one minute.’ maternal death every 7 minutes1. Another uterotonic agent, oxytocin, the hypothalamic In the 19th century, uterine atony was treated by polypeptide hormone released by the posterior pitu- intrauterine placement of various agents with the aim itary, was discovered in 1909 by Sir Henry Dale8 and of achieving a tamponade effect. ‘A lemon imperfectly synthesized in 1954 by du Vigneaud9. The develop- quartered’ or ‘a large bull’s bladder distended with ment of oxytocin constituted the first synthesis of water’ were employed for this purpose, with apparent a polypeptide hormone and gained du Vigneaud a success. Douching with vinegar or iron perchloride Nobel Prize for his work. was also reported2,3. Historically, the first uterotonic The third group of uterotonics comprises the ever- drugs were ergot alkaloids, -
OBGYN-Study-Guide-1.Pdf
OBSTETRICS PREGNANCY Physiology of Pregnancy: • CO input increases 30-50% (max 20-24 weeks) (mostly due to increase in stroke volume) • SVR anD arterial bp Decreases (likely due to increase in progesterone) o decrease in systolic blood pressure of 5 to 10 mm Hg and in diastolic blood pressure of 10 to 15 mm Hg that nadirs at week 24. • Increase tiDal volume 30-40% and total lung capacity decrease by 5% due to diaphragm • IncreaseD reD blooD cell mass • GI: nausea – due to elevations in estrogen, progesterone, hCG (resolve by 14-16 weeks) • Stomach – prolonged gastric emptying times and decreased GE sphincter tone à reflux • Kidneys increase in size anD ureters dilate during pregnancy à increaseD pyelonephritis • GFR increases by 50% in early pregnancy anD is maintaineD, RAAS increases = increase alDosterone, but no increaseD soDium bc GFR is also increaseD • RBC volume increases by 20-30%, plasma volume increases by 50% à decreased crit (dilutional anemia) • Labor can cause WBC to rise over 20 million • Pregnancy = hypercoagulable state (increase in fibrinogen anD factors VII-X); clotting and bleeding times do not change • Pregnancy = hyperestrogenic state • hCG double 48 hours during early pregnancy and reach peak at 10-12 weeks, decline to reach stead stage after week 15 • placenta produces hCG which maintains corpus luteum in early pregnancy • corpus luteum produces progesterone which maintains enDometrium • increaseD prolactin during pregnancy • elevation in T3 and T4, slight Decrease in TSH early on, but overall euthyroiD state • linea nigra, perineum, anD face skin (melasma) changes • increase carpal tunnel (median nerve compression) • increased caloric need 300cal/day during pregnancy and 500 during breastfeeding • shoulD gain 20-30 lb • increaseD caloric requirements: protein, iron, folate, calcium, other vitamins anD minerals Testing: In a patient with irregular menstrual cycles or unknown date of last menstruation, the last Date of intercourse shoulD be useD as the marker for repeating a urine pregnancy test. -