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Blood Transfusion in the Neonatal Intensive Care Unit FREE

ROBERT W. NOVAK, MD; CLIFFORD MARTIN, MT(ASCP) SBB
Am J Dis Child. 1982;136(7):652-653. doi:10.1001/archpedi.1982.03970430084032.
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Sir.—The article by Hakanson et al (Journal 1981;135:1145-1146) recommending a "cow" technique for efficient blood use in a neonatal intensive care unit, though it presented some procedural considerations of particular value in today's climate of cost containment, suffered from serious shortcomings. Development of new patient care approaches demands consideration of their impact on the individual patient as well as the institution. In our opinion, the recommended program does not adequately consider the individual neonate.

Although multiple transfusions from a single unit are desirable and in fact practical, the approach used by the authors has several disadvantages. Both types A and O blood are used, and the units are actually placed in the nursery. This, despite the contention that great care is exercised, risks an ABO hemolytic transfusion reaction. (That most infants possess isoagglutinins was coincidentally noted in the same issue of the Journal, in an article abstracted from a

REFERENCES

Jones BB:  Iso-agglutinins in the blood of the new-born . Am J Dis Child 1981;;135:1103.
Myhre BA:  Fatalities from blood transfusions . JAMA 1980;;244:1333-1335.
 Committee on Standards, American Association of Blood Banks : Standards for Blood Banks and Transfusion Services , ed 10. Washington, DC, American Association of Blood Banks, 1981;, pp 28-29.
Code of Federal Regulations , pt 600-799. Bureau of Biologics, Food and Drug Administration, 1981;, pp 25-38.

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References

Jones BB:  Iso-agglutinins in the blood of the new-born . Am J Dis Child 1981;;135:1103.
Myhre BA:  Fatalities from blood transfusions . JAMA 1980;;244:1333-1335.
 Committee on Standards, American Association of Blood Banks : Standards for Blood Banks and Transfusion Services , ed 10. Washington, DC, American Association of Blood Banks, 1981;, pp 28-29.
Code of Federal Regulations , pt 600-799. Bureau of Biologics, Food and Drug Administration, 1981;, pp 25-38.

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