EAST MULTICENTER STUDY PROPOSAL (Proposal forms must be completed in its entirety, incomplete forms will not be considered) GENERAL INFORMATION Study Title: Hemothorax Management and Outcomes in Blunt and Penetrating Trauma Primary investigator / Senior researcher: Jeremy Cannon, MD, SM, FACS Co-primary investigator: Mark Seamon, MD, FACS BACKGROUND AND SIGNIFICANCE Use this area to briefly (1-2 paragraphs only) outline the burden of the problem to be examined: The true incidence and outcomes of traumatic hemothorax remains unknown. The landmark study by the AAST Retained Hemothorax Study Group described the management course in these patients once a retained hemothorax has been identified. However, management during the index presentation with a hemothorax remains poorly quantified. In addition, interventions which might mitigate the progression of a hemothorax to either a retained hemothorax or empyema have not been fully characterized. Presently, the management options for primary traumatic hemothorax include observation, open tube thoracostomy, percutaneous/small-bore tube thoracostomy, or surgical drainage. To fully characterize the ideal management strategy for hemothorax following blunt or penetrating trauma, the natural history of this disease needs to be captured from initial presentation through to post-discharge follow-up. The specific aims of this multicenter study are: Primary aim: Primary aim should be succinctly stated here – single sentence ideal: We aim to fully characterize the incidence and outcomes of hemothorax management in blunt and penetrating trauma. Secondary aims: Any secondary aims should be stated here: 1 EXPERIMENTAL DESIGN/METHODS Inclusion Criteria: Any age, blunt or penetrating trauma resulting in a hemothorax of any size on initial Chest CT on the day of admission for trauma. Exclusion Criteria: None Therapeutic Interventions: Prospective observational study managed at the surgeon’s discretion with observation through the 1st follow-up visit post-discharge. Outcomes Measures: Primary Outcome: (List here) Retained hemothorax ≥ 300 mL on Chest CT obtained at any time after initial Chest CT Secondary Outcomes: (List here) Death Hospital Length of Stay Ventilator-free days in 1st 30 days of admission Glasgow Outcomes Scale-Extended SF-36 Fibrothorax Empyema Number of interventions including tube thoracostomy, VATS, thoracotomy or other procedures Variables: List the specific variables to be collected and analyzed here. For organization, it is useful to divide these into categories for consideration. Examples of categories might include: Demographics, Admission physiology, Management variables, Surgical variables, Outcomes 2 DEMOGRAPHICS Age Gender COPD/Home O2 Antiplatelets/Anticoagulants Obesity (BMI) ADMISSION PHYSIOLOGY HR Blood Pressure HCT Cr INR Base Excess Lactate INJURY CHARACTERISTICS Mechanism of injury (blunt, penetrating, both, other) Hemothorax Side Hemothorax Size (mL--measured on CT) Diaphragmatic injury Rib fractures (number, location) Flail chest ISS AIS head AIS chest AIS abdomen Pulmonary contusion MANAGEMENT Initial Management-Injury Day 1 Observation Open tube thoracostomy Percutaneous tube thoracostomy (“pigtail”) VATS Open Evacuation Estimated Hemothorax Evacuated (mL) Antibiotics used YATS used Follow-up CT Imaging Indication (abnormality on CXR, respiratory symptoms, other) Day of follow-up imaging Size of retained hemothorax or effusion, if present (mL) Other findings (PE, consolidation, pneumatocele) Management—Injury Day 2 to Discharge Successful initial management Subsequent tube (injury day) Subsequent thrombolytics (injury day) Subsequent VATS (injury day) Subsequent Thoracotomy (injury day) OUTCOMES Retained hemothorax (describe management) Death 3 Discharge (LTAC, SNF, Rehab, or Home) Hospital LOS Ventilator-free days in the first 30 Post-discharge visit x1 Post-injury day at follow-up CXR findings on post-discharge visit (if obtained) CT findings on post-discharge visit (if obtained) Empyema (describe management and cultures) Fibrothorax Glasgow Outcomes Scale-Extended (at discharge, at 1st follow-up and at 6 months) SF-36 (at 1st follow-up and at 6 months) Need for additional interventions after initial discharge Data Collection and Statistical Analysis: Outline the data collection plan and statistical analysis plan succinctly here The above data will be collected on each patient starting within 24 hours of admission and continuing through their hospital course. Follow-up data will be collected within 24 hours of their post-discharge visit. Data will be entered into a de-identified online data repository. Target enrollment is 500 patients over 2 years. Risk factors for retained hemothorax or empyema development will be assessed using univariate and multivariate analysis. Continuous variables will be compared using Student’s t-test and the Mann Whitney U test. The Chi-squared tests or Fisher’s exact test will be used to compare categorical variables. All variables with a p value <0.2 on univariate analysis will be entered into a multivariable logistic regression analysis to identify independent risk factors for retained hemothorax or empyema development. Data will be reported as adjusted odds ratios with 95 % confidence intervals. Statistical significance will be set at a p<0.05. Consent Procedures: Outline consent procedures here, if applicable. As an example for a prospective study where waiver of consent will be sought, verbiage might include: “This is a prospective observational study, designed to prospectively record data on patients who are managed according to institutional patient management protocols. Thus, waiver of informed consent is requested. Data will be recorded on a data sheet and transferred to a secured database that is devoid of patient identifiers.” This is a prospective observational stud intended to record data on patients who are managed according to institutional patient management protocols. Waiver of informed consent will be requested; however, we appreciate that some institutional IRBs may request formal consent from the patient or a legally authorized representative. Data will be recorded on a data sheet and transferred to a secured database that is devoid of patient identifiers. 4 Risk/ Benefit Analysis: Succinctly outline a risk / benefit analysis. An example of this might include: “The incidence and natural history DISEASE PROCCESS TO BE STUDIED is unknown. If the optimal timing for and type of intervention can be identified to optimize outcomes in these patients, then significant benefit will result.” The incidence and natural history of traumatic hemothorax is unknown. If the optimal timing for and type of intervention can be identified to optimize outcomes in these patients, then significant benefit will be realized by future patients. Instructions for submitting data collection tools: All data submissions should be entered through the EAST Multicenter Trial Taskforce website portal. Instructions can be found on the EAST website. The data collection sheet located under the Multicenter Trial Taskforce heading for this study can be utilized to record the data, and then the information transferred to the portal entry system. For any questions regarding this study, please contact the PI. 5 References: Include a brief listing of key references here: 1. Stiles PJ, Drake RM, Helmer SD, Bjordahl PM, Haan JM. Evaluation of chest tube administration of tissue plasminogen activator to treat retained hemothorax. Am J Surg. 2014 Jun;207(6):960-3. PubMed PMID: 24495319. 2. Kulvatunyou N, Erickson L, Vijayasekaran A, Gries L, Joseph B, Friese RF, O'Keeffe T, Tang AL, Wynne JL, Rhee P. Randomized clinical trial of pigtail catheter versus chest tube in injured patients with uncomplicated traumatic pneumothorax. Br J Surg. 2014 Jan;101(2):17-22. PMID: 24375295. 3. Kulvatunyou N, Joseph B, Friese RS, Green D, Gries L, O'Keeffe T, Tang AL, Wynne JL, Rhee P. 14 French pigtail catheters placed by surgeons to drain blood on trauma patients: is 14-Fr too small? J Trauma Acute Care Surg. 2012 Dec;73(6):1423-7. PubMed PMID: 23188235. 4. Moore FO, Duane TM, Hu CK, Fox AD, McQuay N Jr, Lieber ML, Como JJ, Haut ER, Kerwin AJ, Guillamondegui OD, Burns JB; Eastern Association for the Surgery of Trauma. Presumptive antibiotic use in tube thoracostomy for traumatic hemopneumothorax: an Eastern Association for the Surgery of Trauma practice management guideline. J Trauma Acute Care Surg. 2012 Nov;73(5 Suppl 4):S341-4. PubMed PMID: 23114491. 5. DuBose J, Inaba K, Okoye O, Demetriades D, Scalea T, O'Connor J, Menaker J, Morales C, Shiflett T, Brown C, Copwood B; AAST Retained Hemothorax Study Group. Development of posttraumatic empyema in patients with retained hemothorax: results of a prospective, observational AAST study. J Trauma Acute Care Surg. 2012 Sep;73(3):752-7. PubMed PMID: 22929504. 6. Inaba K, Lustenberger T, Recinos G, Georgiou C, Velmahos GC, Brown C, Salim A, Demetriades D, Rhee P. Does size matter? A prospective analysis of 28-32 versus 36-40 French chest tube size in trauma. J Trauma Acute Care Surg. 2012 Feb;72(2):422-7. PubMed PMID: 22327984. 7. DuBose J, Inaba K, Demetriades D, Scalea TM, O'Connor J, Menaker J, Morales C, Konstantinidis A, Shiflett A, Copwood B; AAST Retained Hemothorax Study Group. Management of post-traumatic retained hemothorax: a prospective, observational, multicenter AAST study. J Trauma Acute Care Surg. 2012 Jan;72(1):11-22; discussion 22-4; quiz 316. PubMed PMID: 22310111. 8. Smith JW, Franklin GA, Harbrecht BG,