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Iowa Neonatology Handbook: Hematology
Bone Marrow Aspiration: Indications
John A. Widness, MD
Peer Review Status: Internally Peer Reviewed
- Chromosome Analysis
To obviate the need for doing an unnecessary bone marrow analysis, it is essential
to check that a prenatal chromosome analysis via CVS, amniocentesis, or cordocentesis
has not previously been done. Infants with multiple anomalies may have been
previously evaluated by Ob-Gyn and thus tested.
- Situations in which procedure may be considered:
Although a diagnosis can be made in a relatively short time (6-30 hours
vs. 48-96 hours for peripheral blood samples), the use of bone marrow
aspirations should be reserved for the diagnosis of conditions which are
considered to be incompatible with life such as Trisomy 13, 18, or Triploidy
(rarely). Accordingly, a patient with probable Down Syndrome would normally
not be a candidate. In considering bone marrow aspiration, the technical
of doing so must be considered. These include:
- The failure rate for chromosome results for bone marrow sample
is high (8-10%) relative to that of peripheral blood (<1%)
- Chromosome morphology is generally poor, not allowing for identification
of small, chromosomal rearrangements
- Even in successful cases, the yield of analyzable cells is small
increasing the risk of missing mosaicism.
While the results are pending, most situations are ones in which non-surgical
life support therapies should be offered after discussion with the medical
staff and the family.
- Who to contact:
- Weekdays before 3 pm: Prior to bone marrow aspiration, contact the
Cytogenetics Laboratory staff must be called (6-3877) so that the
necessary preparation for processing a specimen can be made. If possible,
schedule the aspiration prior to 3 pm on weekdays since specimen processing
takes approximately 2 hours.
To obtain a bone marrow specimen, the pediatric hematologist may be
consulted (beeper 339-9023) and the Bone Marrow Laboratory notified
(6-2543) if a smear of the marrow is desired. Since it is the nursery's
responsibility to provide the necessary equipment, Central Sterilizing
Service must be contacted to provide a "bone marrow aspirate
set-up tray". Delivery takes appropriately one half hour.
- Evenings or weekends: Prior to bone marrow aspiration contact the
staff geneticist on call (131-1681), and the cytogenetics lab person
on call (call the Cytogenetics Lab at 6-3877 for the recorded message
of the current beeper number, or call the long-distance beeper: 1-800-202-8098).
Do not perform the bone marrow aspiration until someone from the Cytogenetics
Laboratory has been contacted since results cannot be obtained from
the specimen if the sample is not processed within 1-2 hours.
- Procedure:
Obtain 1-3 cc of bone marrow sample in a green-top heparinized tube. Also
obtain a blood sample (2-3 cc) in a green-top tube for a chromosome analysis
in case the marrow specimen fails to yield adequate results. If there
is enough volume from a marrow sample, the specimen can be set up for
both 2 and 24 hour processing. In small aspirate samples, only the 24
hour culture will be set up. Preliminary results from banded chromosomes
will be available within six to thirty hours. The final report will be
provided in 5-10 days.
- Thrombocytopenia
Bone marrow aspiration for neonatal thrombocytopenia (platelet count <
50,000/mm3) is usually not necessary. However, in difficult or persistent
cases, it may be helpful to discuss the evaluation and treatment of this condition
with a member of the pediatric hematology division.
References
Christensen R D, Rothstein G, Anstall H B, Bybee B Granulocyte transfusions
in neonates with bacterial infection, neutropenia, and depletion of mature marrow
neutrophils. Pediatrics, 1982;70:1-6.
Cordle D G, Strauss R G (1993). Guidelines for Neonatal Transfusion Therapy
- 1993. Iowa City:UIHC Elmer L. DeGowin Memorial Blood Center, University of
Iowa Hospitals and Clinics, 1993. (reprinted in this book, pp. __ - ___).
Strauss R G. Current status of granulocyte transfusions to treat neonatal
sepsis. J Clin Apheresis 1989;5:25-29.
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