scholarly journals 661. Futility of Bacterial Bone Marrow Cultures: Experience over a 19 Year Period

2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S386-S386
Author(s):  
Ahnika Kline ◽  
Harry Porterfield ◽  
A Zelazny

Abstract Background Bone marrow biopsies are often performed on patients with unclear diagnoses and cultures may be ordered for both routine bacterial, mycobacterial and fungal pathogens. They are performed in semi-sterile conditions and involve needle penetration through the skin, posing an increased risk of skin contamination. These cultures also require a substantial amount of laboratory personnel time. Methods Cultures collected from 2001-2020 were surveyed in the lab electronic record. We assessed the culture type (fungal, bacterial, mycobacterial), and the presence of pathogens and contaminants. An organism was deemed a contaminant if it was consistent with skin flora or listed as a contaminant in the report given to the physician. Organisms for which the role in bone marrow disease is unclear were included as possible pathogens. For questionable non-contaminant organisms, clinical significance was determined based on if patient was treated for the organism. For all bone marrow cultures, growth of the same organism within 1 month of the bone marrow specimen was surveyed to determine whether the organism would have been found by alternative methods. Results Of 483 bacterial bone marrow cultures, there were 110 (23%) positives, of which 76 (69%) were deemed contaminants. Twenty (18%) of the 76 contaminants grew in the routine bacterial culture. However, 49 (65%) contaminants grew in the AFB culture, of which 10 also grew in the bacterial culture. For the 34 non-contaminant organisms, 26 were determined to be clinically significant. Nineteen of the 26 had a matching culture (usually blood) growing the organism within 1 month. The majority of pathogens were mycobacteria (18 of the 34). Fungal organisms represented 5 cultures and 11 were bacterial. Of the 11 bacterial organisms, 1 was a Helicobacter species (grown in special media), and 4 had a matching positive blood culture. Only 4 (1% of 483) bacterial non-contaminants grew in the routine bacterial culture. Given an unknown number of true negatives, we can only conclude a positive predictive value (PPV) of 0.16 for routine bacterial cultures. Including AFB and fungal cultures, the PPV increased to 0.30. Conclusion Our findings indicate that routine bacterial bone marrow culture is unlikely to yield a novel result and is likely a poor use of lab resources. Disclosures All Authors: No reported disclosures

Endocrinology ◽  
1987 ◽  
Vol 120 (6) ◽  
pp. 2326-2333 ◽  
Author(s):  
B. R. MACDONALD ◽  
N. TAKAHASHI ◽  
L. M. MCMANUS ◽  
J. HOLAHAN, ◽  
G. R. MUNDY ◽  
...  

1979 ◽  
Author(s):  
K. L. Kellar ◽  
B. L. Evatt ◽  
C. R. McGrath ◽  
R. B. Ramsey

Liquid cultures of bone marrow cells enriched for megakaryocytes were assayed for incorporation of 3H-thymidine (3H-TdR) into acid-precipitable cell digests to determine the effect of thrombopoietin on DNA synthesis. As previously described, thrombopoietin was prepared by ammonium sulfate fractionation of pooled plasma obtained from thrombocytopenic rabbits. A control fraction was prepared from normal rabbit plasma. The thrombopoietic activity of these fractions was determined in vivo with normal rabbits as assay animals and the rate of incorporation of 75Se-selenomethionine into newly formed platelets as an index of thrombopoietic activity of the infused material. Guinea pig megakaryocytes were purified using bovine serum albumin gradients. Bone marrow cultures containing 1.5-3.0x104 cells and 31%-71% megakaryocytes were incubated 18 h in modified Dulbecco’s MEM containing 10% of the concentrated plasma fractions from either thrombocytopenic or normal rabbits. In other control cultures, 0.9% NaCl was substituted for the plasma fractions. 3H-TdR incorporation was measured after cells were incubated for 3 h with 1 μCi/ml. The protein fraction containing thrombopoietin-stimulating activity caused a 25%-31% increase in 3H-TdR incorporation over that in cultures which were incubated with the similar fraction from normal plasma and a 29% increase over the activity in control cultures to which 0.9% NaCl had been added. These data suggest that thrombopoietin stimulates DNA synthesis in megakaryocytes and that this tecnique may be useful in assaying thrombopoietin in vitro.


2000 ◽  
Vol 23 (3) ◽  
pp. 519-522 ◽  
Author(s):  
Zeni Z.C. Alfonso ◽  
Eduardo D. Forneck ◽  
Waldir F. Allebrandt ◽  
Nance B. Nardi

In addition to bone marrow and peripheral blood, stem cells also occur in human umbilical cord blood (HUCB), and there is an increasing interest in the use of this material as an alternative source for bone marrow transplantation and gene therapy. In vitro hematopoiesis has been maintained for up to 16 weeks in HUCB cultures, but the establishment of an adherent, stromal layer has consistently failed. Adherent cell precursors among mononuclear cells from HUCB were sought for in long-term cultures. Mononuclear cells obtained from cord blood after full term, normal deliveries were cultivated at different concentrations in Iscove's modified Dulbecco's medium (IMDM) with weekly feeding. An adherent layer was detected in 16 of 30 cultures, 12 of which were plated at cell concentrations higher than 2 x 10(6) cells/ml. In contrast to bone marrow cultures, in which the stroma is detected early, in most (10/16) positive cultures from HUCB the adherent layer was identified only after the fourth week of culture. The cells never reached confluence and detached from the plate approximately four weeks after detection. May-Grünwald-Giemsa staining of positive cultures revealed fibroblast- or endothelial-like adherent cells in an arrangement different from that of bone marrow stroma in 13 samples. In two of these, the adherent cells were organized into characteristic, delimited cords of cells. Unlike bone marrow cultures, fat cells were never observed in the adherent layers. A rapid development of large myeloid cells in the first week of culture was characteristic of negative cultures and these cells were maintained for up to 12 weeks. HUCB contains adherent cell precursors which occur in lower numbers than in bone marrow and may be at a different (possibly less mature) stage of differentiation.


1989 ◽  
Vol 9 (9) ◽  
pp. 3973-3981 ◽  
Author(s):  
G V Borzillo ◽  
C J Sherr

Murine long-term bone marrow cultures that support B-lymphoid-cell development were infected with a helper-free retrovirus containing the v-fms oncogene. Infection of B-lymphoid cultures resulted in the rapid clonal outgrowth of early pre-B cells, which grew to high cell densities on stromal cell feeder layers, expressed v-fms-coded glycoproteins, and underwent immunoglobulin heavy-chain gene rearrangements. Late-passage cultures gave rise to factor-independent variants that proliferated in the absence of feeder layers, developed resistance to hydrocortisone, and became tumorigenic in syngeneic mice. The v-fms oncogene therefore recapitulates known effects of the v-abl and bcr-abl oncogenes on B-lineage cells. The ability of v-fms to induce transformation of early pre-B cells in vitro underscores the capacity of oncogenic mutants of the colony-stimulating factor-1 receptor to function outside the mononuclear phagocyte lineage.


1987 ◽  
Vol 15 (6) ◽  
pp. 268-271 ◽  
Author(s):  
Jennifer Hoy ◽  
Kenneth Rolston ◽  
Roy L. Hopfer

Stem Cells ◽  
1999 ◽  
Vol 17 (6) ◽  
pp. 339-344 ◽  
Author(s):  
John Eugenes Chisi ◽  
Joanna Wdzieczak‐Bakala ◽  
Josiane Thierry ◽  
Cecile V. Briscoe ◽  
Andrew C. Riches

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