FURTHER STUDIES ON THE EFFECT OF ORAL CONTRACEPTIVES ON ENDOCRINE FUNCTION WITH SPECIAL REFERENCE TO LUTEINISING HORMONE EXCRETION

1969 ◽  
Vol 62 (3) ◽  
pp. 477-488 ◽  
Author(s):  
A. D. Papanicolaou ◽  
A. Loraine ◽  
Margaret C. N. Jackson

ABSTRACT Serial assays of luteinising hormone (LH) and pregnanediol in urine have been performed in four women during and following long term therapy with oral contraceptives. One subject was treated with a progestogen-oestrogen mixture, another with a progestogen alone and two with a sequential regime. In three subjects there was definite evidence for the resumption of ovulation in the first post-treatment cycle; in the fourth the evidence was less clear cut. None of the patients showed suppression of urinary LH activity as a result of medication, and in all four the fiducial limits of individual assays in the treatment and post-treatment cycles overlapped to a considerable extent. One woman receiving sequential therapy showed a midcycle LH peak in the post-treatment but not in the treatment cycle. These findings are compatible with the view that long term therapy with oral contraceptives does not produce any deleterious effects on pituitary gonadotrophic function. In one subject the short term effect of chlormadinone acetate administered continuously in low dosage was investigated. The compound produced little effect on either LH or oestrogen output, but may have inhibited ovulation as judged by urinary pregnanediol assays.

1972 ◽  
Vol 17 (8) ◽  
pp. 270-274
Author(s):  
D. A. Adamopoulos ◽  
J. A. Loraine ◽  
J. Ginsburg ◽  
N. B. Loudon

Serial assays of urinary oestrogens, pregnanediol, follicle-stimulating hormone (FSH) and luteinising hormone (LH) have been performed in two women who developed amenorrhoea as a result of medication by oral contraceptives. Oestrogen levels were generally within the range normally found during the follicular phase of the menstrual cycle. However, in both subjects during part of the investigation there was a rise to midcycle levels; in the first woman this occurred spontaneously and in the second as a result of clomiphene treatment. Urinary LH activity was present in both patients throughout the study but in neither was a midcycle peak of LH output observed. The findings are compatible with the view that long term therapy by oral contraceptives may impair the cyclic release of gonadotrophins at the hypothalamic level thus resulting in amenorrhoea and anovulation.


1967 ◽  
Vol 54 (1) ◽  
pp. 96-104 ◽  
Author(s):  
E. T. Bell ◽  
A. L. Herbst ◽  
Mariamma Krishnamurti ◽  
J. A. Loraine ◽  
Eleanor Mears ◽  
...  

ABSTRACT Pituitary gonadotrophic function together with urinary steroid excretion has been studied in four women during and following long term therapy with oral contraceptives. Assays of follicle-stimulating hormone (FSH) were performed in all subjects while luteinising hormone (LH) output was measured in two. Estimations of urinary oestrogens and pregnanediol indicated absence of ovarian activity during treatment and the resumption of ovulation in the first or second post-treatment cycle. In the three women who received progestogen-oestrogen mixtures depression of FSH and LH activities during treatment was noted. In the subject receiving a progestogen alone such a depression did not occur. Following withdrawal of medication urinary FSH excretion remained similar to that during treatment while LH levels either rose or were unchanged. It is concluded that the long term effects of oral contraceptives on pituitary gonadotrophic function are variable and may depend on such factors as the composition of the tablet administered, its total dosage and the duration of therapy.


1997 ◽  
Vol 17 (03) ◽  
pp. 161-162
Author(s):  
Thomas Hyers

SummaryProblems with unfractionated heparin as an antithrombotic have led to the development of new therapeutic agents. Of these, low molecular weight heparin shows great promise and has led to out-patient therapy of DVT/PE in selected patients. Oral anticoagulants remain the choice for long-term therapy. More cost-effective ways to give oral anticoagulants are needed.


2007 ◽  
Vol 40 (05) ◽  
Author(s):  
M Kungel ◽  
A Engelhardt ◽  
T Spevakné-Göröcs ◽  
M Ebrecht ◽  
C Werner ◽  
...  

2021 ◽  
Vol 12 ◽  
pp. 204201882110011
Author(s):  
Sarah Montenez ◽  
Stéphane Moniotte ◽  
Annie Robert ◽  
Lieven Desmet ◽  
Philippe A. Lysy

Background: Amiodarone treatment is effective against various types of arrhythmias but is associated with adverse effects affecting, among other organs, thyroid function. Amiodarone-induced thyroid dysfunction was not thoroughly evaluated in children as it was in adults, yet this affection may lead to irreversible neurodevelopmental complications. Our study aimed to define the incidence and risk factors of amiodarone-induced thyroid dysfunction in children. Methods: The study was designed as an observational study with a retrospective clinical series of 152 children treated by amiodarone in the Pediatric Cardiology Unit of our center from 1990 to 2019. All patients were divided into three groups according to their thyroid status: euthyroid, AIH (amiodarone-induced hypothyroidism) or AIT (amiodarone-induced thyrotoxicosis). Patients from these three groups were compared in terms of key clinical and therapeutic features. Results: Amiodarone-induced thyroid dysfunction was present in 23% of patients. AIT (5.3%) was three times less common than AIH (17.7%), and its occurrence increased with older age ( p < 0.05), treatment dosage ( p < 0.05), treatment duration ( p < 0.05) and the number of loading doses administered ( p < 0.05). There were no distinctive clinical features between euthyroid and AIH groups. A multivariable prediction model of AIT was built, with a yield of 66.7% as positive predictive value and 96.7% as negative predictive value. Conclusion: We observed that one in five children developed amiodarone-induced thyroid dysfunction. Special attention is required for older children with a high dosage and long-term therapy and who received a large number of loading doses, since these children are at risk to develop AIT, which is more delicate to manage than AIH.


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