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Book of Medical Disorders in Pregnancy - Tintash

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Inhalation <strong>of</strong> volatile organic compounds<br />

is a particular practice <strong>of</strong> children and<br />

teenagers. A variety <strong>of</strong> other materials<br />

are also used i.e. glue, toluene, gasol<strong>in</strong>e,<br />

solvents, th<strong>in</strong>ners, and aerosols. Maternal<br />

and neonatal renal tubular acidosis,<br />

pulmonary <strong>in</strong>jury, and cardiac arrhythmias<br />

are exacerbated. Preterm delivery,<br />

<strong>in</strong>trauter<strong>in</strong>e growth retardation,<br />

and fetal death have been reported when<br />

these agents are abused dur<strong>in</strong>g pregnancy.<br />

Caffe<strong>in</strong>e:<br />

Fig14.1: Shows schematic presentation <strong>of</strong> various drugs <strong>in</strong><br />

pregnancy.<br />

Caffe<strong>in</strong>e, like theophyll<strong>in</strong>e is rapidly<br />

absorbed from the gastro<strong>in</strong>test<strong>in</strong>al tract.<br />

Its half-life is <strong>in</strong>creased two to three fold<br />

<strong>in</strong> pregnancy.<br />

It is known to cross the placenta. The<br />

average daily <strong>in</strong>take is 99 mg, and<br />

approximately 28% <strong>of</strong> pregnant women<br />

consume more than 150 mg <strong>of</strong> caffe<strong>in</strong>e<br />

per day throughout pregnancy.<br />

185<br />

There is no evidence that caffe<strong>in</strong>e <strong>in</strong>take<br />

has any adverse effect on late pregnancy<br />

outcome or fetal growth.<br />

Caffe<strong>in</strong>e <strong>in</strong>take <strong>of</strong> greater than 150<br />

mg/day <strong>in</strong>creases the risk <strong>of</strong> late first<br />

trimester and second trimester<br />

spontaneous abortion. C<strong>of</strong>fee per se may<br />

be more embryo toxic than other<br />

caffe<strong>in</strong>e sources.<br />

REFERENCE:<br />

1. Australian Drug Evaluation Committee.<br />

Medic<strong>in</strong>es <strong>in</strong> <strong>Pregnancy</strong>: An Australian<br />

Categorization <strong>of</strong> Risk. Canberra,<br />

Australia: AGPS. 1992.<br />

2. Gray J, Weaver R, Bollert J et al. The<br />

oral toxicity <strong>of</strong> cl<strong>in</strong>damyc<strong>in</strong> <strong>in</strong><br />

laboratory animals. Toxicol Appl<br />

Pharmacol 1972; 21: 516.<br />

3. Hengst VP. Investigations <strong>of</strong> the<br />

teratogenicity <strong>of</strong> daraprim<br />

(pyrimetham<strong>in</strong>e) <strong>in</strong> humans. Zentralbl<br />

Gynakol 1972; 94: 551.

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