Thrombocytosis after major lower extremity trauma: Mechanism and possible role in free flap failure

被引:32
作者
Choe, EI
Kasabian, AK
Kolker, AR
Karp, NS
Zhang, L
Bass, LS
Nardi, M
Josephson, G
Karpatkin, M
机构
[1] NYU,MED CTR,INST RECONSTRUCT PLAST SURG,NEW YORK,NY 10016
[2] NYU,MED CTR,DEPT HEMATOL,NEW YORK,NY 10016
关键词
D O I
10.1097/00000637-199605000-00010
中图分类号
R61 [外科手术学];
学科分类号
摘要
Microvascular thrombosis and free flap failure are complications of free tissue transfer for coverage of lower extremity soft-tissue and bony defects despite appropriate vessel selection and adherence to meticulous technique. Increased rates of flap failure have been associated with reconstruction performed between 3 days and 6 weeks after injury, as well as in patients with thrombocytosis. We have found that serum platelet levels rise significantly after lower extremity injury. It is our theory that a circulating mediator or cytokine is released in response to injury, inducing the thrombocytosis. Twenty-one patients with Gustilo grade IIIb and IIIc injuries were studied prospectively. Serum was collected throughout the postinjury period. Platelet count, leukocyte count, hemoglobin concentration, and hematocrit were determined. Samples were also subjected to a platelet aggregation study as well as enzyme-linked immunosorbent assay for interleukin-3, interleukin-6, interleukin-11, and granulocyte macrophage-colony-stimulating factor. Megakaryocyte growth and development factor enzyme-linked immunosorbent assay and a myleoproliferative leukemia virus-transfected cell line assay for thrombopoietin were performed. Bone marrow was studied with flow cytometric analysis. Mean initial platelet count was 196,000 per cubic millimeter. There was an initial 26% decline to 140,000 per cubic millimeter, followed by an increase to 361% of baseline on day 16. No significant variations in serum leukocyte count or hemoglobin concentration were seen. Spontaneous and induced platelet aggregation responses were normal. Interleukin-6 was detected at elevated levels. However, interleukin-3, interleukin-ll, granulocyte macrophage-colony-stimulating factor, and thrombopoietin were not measurable. Marked megakaryocytosis was seen on bone marrow analysis. Interleukin-6 may, therefore, play a role in the mechanism of thrombocytosis. We suggest that because patients with complex bony injuries of the leg experience platelet elevations that peak approximately 2 weeks after injury, microvascular free flap reconstructions should be considered high risk during this time period.
引用
收藏
页码:489 / 494
页数:6
相关论文
共 30 条
[1]  
ACLAND RD, 1990, CLIN PLAST SURG, V17, P733
[2]   AGGREGATION OF BLOOD PLATELETS BY ADENOSINE DIPHOSPHATE AND ITS REVERSAL [J].
BORN, GVR .
NATURE, 1962, 194 (4832) :927-&
[3]   MANAGEMENT OF OPEN TIBIAL FRACTURES [J].
BYRD, HS ;
SPICER, TE ;
CIERNEY, G .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1985, 76 (05) :719-728
[4]  
CARRINGTON PA, 1991, BLOOD, V77, P34
[5]   INVIVO SYNERGISM OF RECOMBINANT HUMAN INTERLEUKIN-3 AND RECOMBINANT HUMAN INTERLEUKIN-6 ON THROMBOPOIESIS IN PRIMATES [J].
GEISSLER, K ;
VALENT, P ;
BETTELHEIM, P ;
SILLABER, C ;
WAGNER, B ;
KYRLE, P ;
HINTERBERGER, W ;
LECHNER, K ;
LIEHL, E ;
MAYER, P .
BLOOD, 1992, 79 (05) :1155-1160
[6]   EARLY MICROSURGICAL RECONSTRUCTION OF COMPLEX TRAUMA OF THE EXTREMITIES [J].
GODINA, M .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1986, 78 (03) :285-292
[7]   PROBLEMS IN THE MANAGEMENT OF TYPE-III (SEVERE) OPEN FRACTURES - A NEW CLASSIFICATION OF TYPE-III OPEN FRACTURES [J].
GUSTILO, RB ;
MENDOZA, RM ;
WILLIAMS, DN .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1984, 24 (08) :742-746
[8]   NEW INSIGHTS INTO THE REGULATION OF MEGAKARYOCYTOPOIESIS BY HEMATOPOIETIC AND FIBROBLASTIC GROWTH-FACTORS AND TRANSFORMING GROWTH FACTOR-BETA-1 [J].
HAN, ZC ;
BELLUCCI, S ;
WAN, HY ;
CAEN, JP .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (01) :1-5
[9]   ANALYSIS OF 200 FREE FLAPS [J].
HARASHINA, T .
BRITISH JOURNAL OF PLASTIC SURGERY, 1988, 41 (01) :33-36
[10]  
ISHIBASHI T, 1989, BLOOD, V74, P1241