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Edited by David A. Warrell, Timothy M. Cox, John D. Firth

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Latest update

The November 2012 update sees updates to over 70 chapters, focusing on Neurology and Gastroenterology. This update also incorporates a selection of 29 Case Histories taken from related titles in the Oxford Case Histories series, linked to from related chapters. Each case includes several questions followed by detailed answers and discussion to enhance diagnostic and clinical understanding.

Neurology updates include substantial updates to key chapters and new material on a wide range of topics including spinal cord injury, autonomic nervous system disorders, and inherited neurodegenerative diseases. 

Gastroenterology updates
include extensive revisions of key chapters on liver failure and acute pancreatitis and new material on a wide range of matters, ranging from the common to the rare: including surgical treatments for colonic diverticular disease, antibody tests for immune disorders, and a revised treatment algorithm for small bowel bacterial overgrowth.

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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages and recommendations are for the non-pregnant adult who is not breastfeeding.

Contents

Hypertension in pregnancy

Chapter:
Hypertension in pregnancy
Author(s):

C.W.G. Redman

DOI:
10.1093/med/9780199204854.003.1404

In normal pregnancy the arterial pressure falls in the second half of the first trimester: systolic pressure then remains unchanged throughout pregnancy, with diastolic pressure tending to rise gradually towards its prepregnancy level in the later weeks.

Definitions, epidemiology and clinical features—(1) Pregnancy-induced hypertension (PIH), transient hypertension of pregnancy, or gestational hypertension describe new hypertension, defined as blood pressure equal to or in excess of 140/90 mmHg, which without proteinuria affects up to 10% of women after mid term (20 weeks) and resolves after delivery. (2) Pre-eclampsia, which affects 3 to 5% of pregnancies, is defined by the presence of PIH and pregnancy-induced proteinuria arising after 20 weeks gestation that both improve after delivery. Other features include (a) renal insufficiency; (b) hepatocellular dysfunction and/or severe epigastric/right upper quadrant pain; (c) neurological problems—convulsions (eclampsia), severe headaches, persistent scotomata; (d) haematological disturbances—thrombocytopenia, disseminated intravascular coagulation, haemolysis; (e) fetal growth restriction.

Differential diagnosis—the main differential diagnosis of pre-eclampsia is from chronic hypertension, which in its pure form does not share the renal, coagulation, hepatic and placental abnormalities of pre-eclampsia. The perinatal risks of chronic hypertension in pregnancy result from superimposed pre-eclampsia.

Aetiology—the cause of pre-eclampsia is unknown, but it depends upon the placenta and is characterized by diffuse maternal endothelial dysfunction and a systemic inflammatory response.

Management before pregnancy and prevention—women with no more than moderate chronic hypertension should stop antihypertensive treatment before conception. There is no good method of preventing pre-eclampsia, but low-dose aspirin may be effective in some women.

Management during pregnancy—extreme hypertension (≥160/110 mmHg), whatever the underlying cause, is as dangerous as it is in any other medical situation and demands treatment, but there is no clear reason for treating more moderate hypertension on either maternal or fetal grounds, although most centres will initiate treatment at less extreme levels of blood pressure. As far as it is known the progression of moderate pre-eclampsia is not delayed, nor is the later superimposition of pre-eclampsia on moderate chronic hypertension prevented. Key aspects of management include (1) antihypertensive agents—methyldopa is the most thoroughly tested drug for use in pregnancy: no significant adverse reactions have been observed, but because of its side effect profile labetalol and nifedipine are popular alternatives. (2) Magnesium sulphate – this should be given to prevent eclampsia (grand-mal convulsions) in women with the HELLP syndrome (haemolysis, elevated liver enzymes and low platelet counts) and those who have had one eclamptic convulsion. (3) Delivery of the baby and placenta—this is the definitive treatment for pre-eclampsia.

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