Benefits of early application of pelvic circumferential compression device to reduce bleeding in pelvic fractures

• Published in: BMC musculoskeletal disorders 2022-03, Vol.23 (1), p.203-203, Article 203
• Main Authors: Rungsinaporn, Visit, Akkarawanit, Pawin, Kongmalai, Pinkawas
• Format: Article
• Language: English
• Subjects: Blood transfusion; Evaluation; Fracture; Fractures, Bone - complications; Fractures, Bone - diagnostic imaging; Fractures, Bone - surgery; Hematocrit change; Hemorrhage; Hemorrhage - diagnostic imaging; Hemorrhage - etiology; Hemorrhage - prevention & control; Humans; Orthopedic equipment and supplies; PCCD; Pelvic binder; Pelvic Bones - diagnostic imaging; Pelvic Bones - injuries; Pelvic fracture; Pelvis; Pressure; Prevention; Retrospective Studies
• ISSN: 1471-2474; 1471-2474
• DOI: 10.1186/s12891-022-05166-3

To study of efficacy of early pelvic circumferential compression device using in patients with suspected pelvic trauma, compared with conventional stepwise approach. Traumatic injury and at least one of the following criteria are required for inclusion: loss of consciousness or a Glasgow coma score (GCS) of less than 13; systolic blood pressure less than 90 mmHg; falling from more than 6 m; injury to several important organs; and a positive pelvic compression test. Patients who satisfied the inclusion criteria for the experimental group were given an early application of a commercial pelvic sling beginning in July 2019. The control group consisted of cases who got the device after clinical or radiological confirmation of a pelvic fracture in the previous year. Gender, age, mechanism of injury, GCS, hospital stay, amount of packed red blood cell transfusion, hematocrit in emergency room, and hematocrit 24 h after application of pelvic binder were all assessed and compared. The study had a total of 30 participants, with 15 in each group. The number of packed red blood cell transfusions in the early pelvic binder group (0.80 ± 1.42) is considerably lower than in the control group (2.4 ± 2.32) (P = 0.008), although the hematocrit change is not statistically different between the groups (2.1 VS 0.7) (P = 0.191). The time it took to install a pelvic binder was considerably shorter in the early pelvic binder group (16.40 ± 5.45) than in the control group (40.40 ± 13.64) (P = 0.001). There were no problems associated to soft tissue and skin necrosis in either group of patients. The use of the PCCD for 24 h prior to clinical and radiographic confirmation has significantly reduced the rate of packed red blood cell transfusion in any pelvic fracture patient without device-related complications. The study was entered into the Thai Clinical Trials Registry ( TCTR20210809007 ).