Highlights
- •This study demonstrate that the rate of unsuspected infection is high after tibial open fracture.
- •The high risk of late infection after grafting a nonunion with a standard graft is confirmed by this study.
- •An important finding of this study is the reduced rate of late infection in patients treated with early implantation of bone marrow concentrate graft.
Abstract
Introduction
Open fractures are at risk of nonunion; surgeons are reluctant to propose early standard
bone grafting after open fractures, preferring to wait in order to adequately assess
the facture status of infection. Bone marrow contains mesenchymal stem cells (MSCs)
and granulocyte and macrophage precursors identified in vitro as colony forming units-granulocyte
macrophage (CFU-GM), both of which have a prophylactic action against infection. We
therefore tested the hypothesis that early injection of bone marrow concentrate would
be useful in these fractures.
Methods
We evaluated a series of 231 patients who had received early percutaneous implantation
of bone marrow concentrate (BMC) to treat open fractures (with gap less than 10 mm)
that were Gustilo-Anderson Type II or III. The results were compared with those of
67 control (no early graft) patients and with those of 76 patients treated with an
early, standard of care, iliac bone graft. All patients were treated with external
fixation and were considered to have an aseptic fracture at the time of early grafting,
but the actual status of infection was re-assessed at the time of grafting by histology
and/or analysis of the aspirate. The bone marrow graft contained after concentration
49,758 ± 21,642 CFU-GM-derived colonies/cc and 9400 ± 1435 MSCs/cc which represents
an important increase compared to the level of CFU-GM cells and MSCs present in a
standard auto-graft. Healing was evaluated at 9 months.
Results
The rate of unsuspected infections was higher than 15% in the 3 groups. Bone union
and removal of external fixation was achieved at 9 months by 50.7% of patients in
the Control Group, by 86.8% of patients in the group with a standard bone graft, and
by 87.4% of patients in the bone marrow group. A 90% risk reduction (p = 0.005) in the need for an invasive standard bone graft to treat a nonunion and
in the risk of infection was observed when bone marrow was proposed as early injection
to the treatment of type II or type-III tibial fractures.
Conclusion
Bone marrow concentrate for early grafting in open fractures with limited gap was
efficient for healing while decreasing infection.
Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to InjuryAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- The devastating effects of tibial non-union on health-related quality of life.J Bone Joint Surg Am. 2013; 95 (Dec 18): 2170-2176
- Fracture-related infection: a consensus on definition from an international expert group.Injury. 2018; 49 (Mar): 505-510
- Morbidity of graft harvesting versus bone marrow aspiration in cell regenerative therapy.Int Orthop. 2014; 38 (Sep): 1855-1860
- Percutaneous autologous bone-marrow grafting for nonunions. Influence of the number and concentration of progenitor cells.J Bone Joint Surg Am. 2005; 87 (Jul): 1430-1437
- Fixed intramedullary nailing and percutaneous autologous concentrated bone-marrow grafting can promote bone healing in humeral-shaft fractures with delayed union.Injury. 2010; 41: 563-567
- Percutaneous autologous bone marrow injections for delayed or non-union of bones.J Orthop Surg (Hong Kong). 2013; 21: 60-64
- The effect of autologous concentrated bone marrow grafting on the healing of femoral shaft non-unions after locked intramedullary nailing.Injury. 2014; 45: S7-S13
- Cellular therapies for the treatment of non-union: the past, present and future.Injury. 2013; 44 (Jan): S46-S49https://doi.org/10.1016/S0020-1383(13)70011-1
- Progenitor cells and tissue repair: more to come?.Injury. 2016; 47 (Dec): S1-S2https://doi.org/10.1016/S0020-1383(16)30833-6
- Local transplantation of bone marrow concentrated granulocytes precursors can cure without antibiotics infected nonunion of polytraumatic patients in absence of bone defect.Int Orthop. 2016; 40 (Nov): 2331-2338
- Recombinant human bone morphogenetic protein-2: a randomized trial in open tibial fractures treated with reamed nail fixation.J Bone Joint Surg Am. 2011; 93 (May 4): 801-808https://doi.org/10.2106/JBJS.I.01763
- Single-stage treatment of infected tibial non-unions and osteomyelitis with bone marrow granulocytes precursors protecting bone graft.Int Orthop. 2018; 42 (Oct): 2443-2450
- Current Concepts Review: the management of open fractures.J Bone Joint Surg Am. 1990; 72: 299-304
- Separation of leukocytes from blood and bone marrow.Scand. J. Clin. Lab. Invest. 1968; 2T: 1-106
- Stimulation by human placental conditioned medium of hemopoietic colony formation by human marrow cells.Blood. 1977; 49: 573-583
- Supercharging allografts with mesenchymal stem cells in the operating room during hip revision.Int Orthop. 2014; 38 (Oct): 2033-2044
- Treatment of open fractures of the shaft of the tibia.J Bone Joint Surg Br. 2001; 83: 62-68
- Antibacterial effect of human mesenchymal stem cells is mediated in part from secretion of the antimicrobial peptide LL-37.Stem Cells. 2010; 28 (December): 2229-2238
- Mesenchymal stem cells augment the anti-bacterial activity of neutrophil granulocytes.PLoS ONE. 2014; 9 (Sep 19)
Article info
Publication history
Published online: December 31, 2020
Accepted:
December 14,
2020
Footnotes
This paper is part of a Supplement supported by the European Society of Tissue Regeneration in Orthopaedics and Traumatology (ESTROT).
Identification
Copyright
© 2020 Elsevier Ltd. All rights reserved.