Powered Bone Marrow Biopsy Procedures Produce Larger Core Specimens, with Less Pain, in Less Time Than with Standard Manual Devices

Bone marrow sampling remains essential in the evaluation of hematopoietic and many non-hematopoietic disorders. One common limitation to these procedures is the discomfort experienced by patients. To address whether a Powered biopsy system could reduce discomfort while providing equivalent or better...

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Published inHematology reports Vol. 3; no. 1; p. e8
Main Authors Miller, Larry J., Philbeck, Thomas E., Montez, Diana F., Puga, Tatiana A., Brodie, Kim E., Cohen, Stephen C., Spadaccini, Cathy, Swords, Ronan, Brenner, Andrew J.
Format Journal Article
LanguageEnglish
Published Italy MDPI AG 01.01.2011
PAGEPress Publications
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ISSN2038-8330
2038-8322
2038-8330
DOI10.4081/hr.2011.e8

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Summary:Bone marrow sampling remains essential in the evaluation of hematopoietic and many non-hematopoietic disorders. One common limitation to these procedures is the discomfort experienced by patients. To address whether a Powered biopsy system could reduce discomfort while providing equivalent or better results, we performed a randomized trial in adult volunteers. Twenty-six subjects underwent bilateral biopsies with each device. Core samples were obtained in 66.7% of Manual insertions; 100% of Powered insertions (p = 0.002). Initial mean biopsy core lengths were 11.1 ± 4.5 mm for the Manual device; 17.0 ± 6.8 mm for the Powered device (p < 0.005). Pathology assessment for the Manual device showed a mean length of 6.1 ± 5.6 mm, width of 1.0 ± 0.7 mm, and volume of 11.0 ± 10.8 mm3. Powered device measurements were mean length of 15.3 ± 6.1 mm, width of 2.0 ± 0.3 mm, and volume of 49.1 ± 21.5 mm3 (p < 0.001). The mean time to core ejection was 86 seconds for Manual device; 47 seconds for the Powered device (p < 0.001). The mean second look overall pain score was 33.3 for the Manual device; 20.9 for the Powered (p = 0.039). We conclude that the Powered biopsy device produces superior sized specimens, with less overall pain, in less time.
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Conflicts of interest: LJM, TEP, DFM, TAP, and KEB are employees of Vidacare Corporation, the sponsor of the study and manufacturer of one of the study devices; SCC, RS, and AJB (or their organizations) have accepted research grant funds from Vidacare Corporation, the sponsor of the study and manufacturer of one of the study devices; CS has no potential conflicts of interest.
ISSN:2038-8330
2038-8322
2038-8330
DOI:10.4081/hr.2011.e8