Book of Medical Disorders in Pregnancy - Tintash
Book of Medical Disorders in Pregnancy - Tintash
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.