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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Prophylactic this <strong>in</strong>cludes rout<strong>in</strong>e<br />
adm<strong>in</strong>istration <strong>of</strong> iron dur<strong>in</strong>g pregnancy<br />
and lactation. Iron supplementation<br />
should start after the sixteenth week <strong>of</strong><br />
pregnancy <strong>in</strong> order to avoid <strong>in</strong>crease <strong>in</strong><br />
the early vomit<strong>in</strong>g <strong>of</strong> pregnancy. If the<br />
patient's <strong>in</strong>itial hemoglob<strong>in</strong> level is over<br />
90 per cent or 11 gram per cent then she<br />
requires only a s<strong>in</strong>gle dose <strong>of</strong> 200 mgm<br />
<strong>of</strong> ferrous sulphate. Each tablet <strong>of</strong> 200<br />
mgm <strong>of</strong> ferrous sulphate conta<strong>in</strong>s 60 mg<br />
<strong>of</strong> elemental iron. If the hemoglob<strong>in</strong><br />
level is less than 90 per cent she should<br />
receive 180mg. <strong>of</strong> elemental iron, which<br />
can be given daily <strong>in</strong> divided doses after<br />
meals.<br />
When ferrous sulphate or gluconate is<br />
not tolerated well by the patient, ferrous<br />
succ<strong>in</strong>ate or ferrous fumarate may be<br />
tried. A number <strong>of</strong> preparations such as<br />
fefol, feospan and autr<strong>in</strong> are available <strong>in</strong><br />
the market; some <strong>of</strong> these have been <strong>in</strong><br />
use for many decades without any side<br />
effects and therefore can be safely<br />
prescribed. Am<strong>in</strong>o-acids are an essential<br />
part <strong>of</strong> the hemoglob<strong>in</strong> molecule, there<br />
fore all pregnant women should be<br />
encouraged to dr<strong>in</strong>k milk and eat meat.<br />
Therapeutic:<br />
Iron <strong>in</strong> therapeutic doses can be<br />
adm<strong>in</strong>istered by oral, <strong>in</strong>tramuscular or<br />
<strong>in</strong>travenous route. Oral route is preferred<br />
<strong>in</strong> treatment <strong>of</strong> outdoor cases, while<br />
<strong>in</strong>tramuscular <strong>in</strong>jections are<br />
recommended <strong>in</strong> patients where rapid<br />
<strong>in</strong>crease <strong>in</strong> hemoglob<strong>in</strong> is needed.<br />
Some patients are unable to<br />
tolerate iron by mouth, they also need<br />
<strong>in</strong>tramuscular therapy. Some <strong>of</strong> the<br />
commonly used iron preparations for<br />
<strong>in</strong>tramuscular adm<strong>in</strong>istration <strong>in</strong>clude the<br />
follow<strong>in</strong>g.<br />
Iron sorbitol citric acid complex<br />
(Ject<strong>of</strong>er):<br />
This preparation conta<strong>in</strong>s 50 mg <strong>of</strong><br />
elemental iron <strong>in</strong> one milliliter solution.<br />
Each <strong>in</strong>jection <strong>of</strong> 2 ml. <strong>of</strong> Ject<strong>of</strong>er may<br />
be expected to raise the hemoglob<strong>in</strong> by<br />
about 0.3 gram per hundred milliliters <strong>of</strong><br />
blood.<br />
Imferon: Iron can also be given by<br />
<strong>in</strong>travenous route. Imferon is an iron<br />
dextran complex which is available <strong>in</strong> 5<br />
ml ampoules and conta<strong>in</strong>s 100 mg <strong>of</strong><br />
iron. In pregnant patients each 100 mg <strong>of</strong><br />
iron can raise the hemoglob<strong>in</strong> by about<br />
0.3 per cent. Total dose <strong>of</strong> iron required<br />
to meet deficiency <strong>of</strong> hemoglob<strong>in</strong> can be<br />
mathematically calculated by us<strong>in</strong>g the<br />
formula shown <strong>in</strong> table (31). This compound<br />
must not be allowed to leak<br />
outside the ve<strong>in</strong> as it is extremely irritant<br />
and can cause thrombophlebitis.<br />
The total dose <strong>of</strong> iron, as iron dextran, is<br />
mixed with 1000 ml <strong>of</strong> normal sal<strong>in</strong>e<br />
solution, 8,000 units <strong>of</strong> hepar<strong>in</strong> are<br />
added <strong>in</strong> this to discourage venous<br />
thrombosis. The drip should be run at a<br />
rate <strong>of</strong> 10 drops per m<strong>in</strong>ute for fifteen<br />
m<strong>in</strong>utes and then, at 45 drops a m<strong>in</strong>ute<br />
until the <strong>in</strong>fusion is completed, and this<br />
should take about five hours. The drip<br />
should be stopped on the slightest<br />
evidence <strong>of</strong> adverse reaction and 50<br />
mgm <strong>of</strong> Phenergan along with 100 mgm<br />
<strong>of</strong> hydrocortisone should be given to<br />
avert exacerbation <strong>of</strong> reactions.<br />
When iron is adm<strong>in</strong>istered<br />
<strong>in</strong>travenously, a shower <strong>of</strong> renal casts<br />
and leucocytes <strong>of</strong>ten appears <strong>in</strong> the<br />
maternal ur<strong>in</strong>e.<br />
Intravenous total dose iron therapy<br />
should be avoided <strong>in</strong> patients who have a<br />
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