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3.
Aust N Z J Obstet Gynaecol ; 40(1): 33-7, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10870776

ABSTRACT

Essential thrombocythaemia is a rare myeloproliferative disorder that often presents with haemorrhagic or thrombotic complications. It may be detected incidentally in an asymptomatic younger adult and there are only a few case reports of essential thrombocythaemia in pregnant women. The risks posed by essential thrombocythaemia during pregnancy and its optimal management are uncertain. To determine if there is increased incidence of obstetric complications seen in women who have essential thrombocythaemia, we collected a large case series from a number of tertiary obstetric units in Australia and New Zealand. There were 30 pregnancies in 12 women who had essential thrombocythaemia. There were 17 live births (57%), 7 stillbirths (23%), 5 miscarriages (17%) and 1 ectopic (3%). Five pregnancies were complicated by placental abruption. When the outcomes of those women who received treatment with aspirin or interferon were compared to those that did not receive any treatment, there was a trend towards a higher livebirth rate (79% v. 38%, p = 0.06). Seven women were treated with aspirin and 5 had successful outcomes with no fetal complications. Four women were treated with alpha-interferon which reduced their platelet counts and all had successful outcomes with no fetal complication. These findings suggest that there is a high incidence of miscarriage, stillbirth and abruption in women with essential thrombocythaemia. Their pregnancies should be carefully monitored. Treatment with low dose aspirin and/or the use of alpha-interferon may be associated with an improved pregnancy outcome.


Subject(s)
Pregnancy Complications, Hematologic/epidemiology , Pregnancy Complications, Hematologic/therapy , Thrombocytosis/epidemiology , Thrombocytosis/therapy , Adult , Australia/epidemiology , Female , Humans , Infant, Newborn , New Zealand/epidemiology , Obstetrics/methods , Pregnancy , Pregnancy Outcome , Retrospective Studies
4.
Aust N Z J Obstet Gynaecol ; 38(2): 221-3, 1998 May.
Article in English | MEDLINE | ID: mdl-9653867

ABSTRACT

Eating disorders and the associated behavioural problems and drug abuse are uncommon in pregnancy. When they do occur they are often unrecognized because of denial but when significant may pose a risk to both the mother and her fetus. This case illustrates a number of problems that may be encountered in women with eating disorders in pregnancy, including prolonged and recurrent metabolic disturbances and diuretic abuse. In particular it illustrates the derangements of thyroid function seen in pregnant women with eating disorders and reminds us that when a cause for thyrotoxicosis remains obscure, thyroxine abuse should be considered and explored.


Subject(s)
Anorexia Nervosa/diagnosis , Pregnancy Complications/chemically induced , Substance-Related Disorders/diagnosis , Thyrotoxicosis/chemically induced , Thyroxine/adverse effects , Adult , Diagnosis, Differential , Female , Furosemide/administration & dosage , Furosemide/adverse effects , Humans , Hypokalemia/chemically induced , Hypokalemia/diagnosis , Patient Care Team , Pregnancy , Pregnancy Complications/diagnosis , Thyroid Function Tests , Thyrotoxicosis/diagnosis , Thyroxine/administration & dosage
5.
Aust N Z J Obstet Gynaecol ; 38(4): 396-8, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9890217

ABSTRACT

To assess the maternal haematological effects of betamethasone administered in late pregnancy, an automated full blood count was performed before and daily for 5 days after betamethasone in 25 women with a singleton pregnancy between 23 and 33 weeks' gestation. From a mean (+/- SD) baseline level of 11.0+/-2.2 x 10(9)/L, the total white cell count increased significantly to 13.2+/-2.9 x 10(9)/L and 13.5+/-3.1 x 10(9)/L on the first and second day after treatment respectively, returning to baseline on day 3 (p<0.0001, ANOVA). These changes represented a mean increase in the neutrophil count of 35% and a mean decrease in the lymphocyte count of 23%. While there was considerable intersubject variation in the extent of the changes, this study has quantified the leucocytosis induced by betamethasone in late pregnancy, information that may assist with the clinical evaluation of a woman at risk of preterm delivery.


Subject(s)
Betamethasone/adverse effects , Glucocorticoids/adverse effects , Leukocytosis/chemically induced , Neutropenia/chemically induced , Pregnancy/drug effects , Adult , Apoptosis/drug effects , Blood Cell Count/drug effects , Female , Humans , Pregnancy Trimester, Third
6.
Aust N Z J Obstet Gynaecol ; 35(1): 22-6, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7771993

ABSTRACT

Two cases of severe twin-twin transfusion syndrome are described. In both, serial amniocenteses were followed by resolution of the disordered inter-twin haemodynamics with 4 intact term survivors. In all reports to date of aggressive reduction with or without successful outcome, volume reduction has been dictated by subjective or semiquantitative ultrasonic estimates of liquor volume. With the use of intraamniotic pressure estimation we describe a more rational basis for the removal of these large volumes of amniotic fluid.


Subject(s)
Amniocentesis , Amniotic Fluid/physiology , Fetofetal Transfusion/complications , Polyhydramnios/therapy , Acute Disease , Adult , Female , Humans , Manometry , Polyhydramnios/etiology , Polyhydramnios/physiopathology , Pregnancy , Pregnancy Outcome , Pressure
7.
Aust N Z J Obstet Gynaecol ; 35(1): 38-41, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7771997

ABSTRACT

1. A heterogeneous group of randomized trials have been conducted using low-dose aspirin to prevent preeclampsia. The results do not support widespread use of low-dose aspirin to prevent preeclampsia. 2. On the basis of existing literature, it is reasonable to use prophylactic low-dose aspirin from early pregnancy in the following groups: (i) Women with prior fetal loss after the first trimester, with placental insufficiency (ii) Women with severe fetal growth retardation in a preceding pregnancy either due to preeclampsia or unexplained (iii) Women with severe early-onset preeclampsia in a previous pregnancy necessitating delivery at or before 32 weeks' gestation. 3. On the basis of existing literature, it is recommended that aspirin not be used in the following groups: (i) Healthy nulliparous women (ii) Women with mild chronic hypertension (iii) Women with established preeclampsia. 4. The data are sufficient to support further trials in more homogeneous select subgroups of women considered at risk of developing preeclampsia.


Subject(s)
Aspirin/therapeutic use , Pre-Eclampsia/prevention & control , Aspirin/administration & dosage , Female , Humans , Patient Selection , Pregnancy , Primary Prevention/methods , Randomized Controlled Trials as Topic
12.
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