Wounds and Injuries Clinical Trial
Official title:
Comparison of Epidural and Paracostal Catheter Placement for Pain Control After Rib Fractures
NCT number | NCT02295098 |
Other study ID # | 14-1979 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 19, 2015 |
Est. completion date | June 2017 |
Verified date | June 2018 |
Source | University of Colorado, Denver |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators plan to compare the incidence of successful placement of epidural pain catheters versus paracostal catheters for the control of pain and prevention of pulmonary complications for adult trauma patients with blunt chest wall trauma resulting in multiple rib fractures. When a trauma patient has > or = to 3 rib fractures on the same side, is being admitted to the Surgical ICU, and is encountered within 72 hours from the time of their injury, they will be eligible for the study. If they (or a proxy) choose to participate, consent will be obtained and they will randomly be assigned to receive either an epidural or paracostal catheter for pain control. The aim of the study is to determine if paracostal catheters are noninferior to epidurals for controlling pain in multisystem trauma patients. Secondarily the investigators will evaluate success and time of placement of the assigned intervention and follow the patient throughout their hospital course to compare the success of analgesia provided by each modality along with any complications and/or benefits of the two types of catheters.
Status | Completed |
Enrollment | 36 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - >/= 3 rib fractures on a single side - Admitted to the Surgical ICU - Recruited within 24 hours of admission Exclusion Criteria: - Patient allergy to local anesthetics - Patient refusal - Inability to consent for any reason - Prisoners - Age < 18 - Pregnant women (pregnancy screen performed as part of routine trauma admission labs) - Absolute contraindications for either thoracic epidural or paracostal pain catheter placement which include: 1. Localized rash or skin infection over the likely site of insertion (We never want to translocate infectious material from the skin to the epidural space or even into the soft tissue where paracostal catheters lay, although for these there is more flexibility in adjusting placement) 2. Spinal/vertebral instability/fracture including any significant vertebral body injury and 3 or more spinous process fractures near the level of desired epidural placement (transverse process fractures are not considered a contraindication) 3. History of extensive back surgery at the level of desired epidural placement 4. Severe aortic stenosis, mitral stenosis, or pulmonary hypertension 5. Inability to correct coagulopathy (to International Normalized Ratio>1.5) 6. Persistent hemodynamic instability (hypotension with Systolic Blood Pressure<90 that does not respond to initial fluid boluses and requires ongoing pressors beyond the 72 hour window for enrollment) 7. Inability to cooperate and participate in placement (if intubated and sedated, for example) or to lie in the correct position for placement (lateral decubitus for paracostal pain catheters, either sitting up or lateral decubitus for epidural placement) 8. Concern for elevated intracranial pressure (we imagine these patients will also be intubated) |
Country | Name | City | State |
---|---|---|---|
United States | Denver Health Medical Center | Denver | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Denver |
United States,
Brasel KJ, Guse CE, Layde P, Weigelt JA. Rib fractures: relationship with pneumonia and mortality. Crit Care Med. 2006 Jun;34(6):1642-6. — View Citation
Bulger EM, Arneson MA, Mock CN, Jurkovich GJ. Rib fractures in the elderly. J Trauma. 2000 Jun;48(6):1040-6; discussion 1046-7. — View Citation
Bulger EM, Edwards T, Klotz P, Jurkovich GJ. Epidural analgesia improves outcome after multiple rib fractures. Surgery. 2004 Aug;136(2):426-30. — View Citation
Carrier FM, Turgeon AF, Nicole PC, Trépanier CA, Fergusson DA, Thauvette D, Lessard MR. Effect of epidural analgesia in patients with traumatic rib fractures: a systematic review and meta-analysis of randomized controlled trials. Can J Anaesth. 2009 Mar;56(3):230-42. doi: 10.1007/s12630-009-9052-7. Epub 2009 Feb 11. Review. — View Citation
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Gebhardt R, Mehran RJ, Soliz J, Cata JP, Smallwood AK, Feeley TW. Epidural versus ON-Q local anesthetic-infiltrating catheter for post-thoracotomy pain control. J Cardiothorac Vasc Anesth. 2013 Jun;27(3):423-6. doi: 10.1053/j.jvca.2013.02.017. — View Citation
Grider JS, Mullet TW, Saha SP, Harned ME, Sloan PA. A randomized, double-blind trial comparing continuous thoracic epidural bupivacaine with and without opioid in contrast to a continuous paravertebral infusion of bupivacaine for post-thoracotomy pain. J Cardiothorac Vasc Anesth. 2012 Feb;26(1):83-9. doi: 10.1053/j.jvca.2011.09.003. Epub 2011 Nov 17. — View Citation
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Mohta M, Verma P, Saxena AK, Sethi AK, Tyagi A, Girotra G. Prospective, randomized comparison of continuous thoracic epidural and thoracic paravertebral infusion in patients with unilateral multiple fractured ribs--a pilot study. J Trauma. 2009 Apr;66(4): — View Citation
Moon MR, Luchette FA, Gibson SW, Crews J, Sudarshan G, Hurst JM, Davis K Jr, Johannigman JA, Frame SB, Fischer JE. Prospective, randomized comparison of epidural versus parenteral opioid analgesia in thoracic trauma. Ann Surg. 1999 May;229(5):684-91; discussion 691-2. — View Citation
Simon BJ, Cushman J, Barraco R, Lane V, Luchette FA, Miglietta M, Roccaforte DJ, Spector R; EAST Practice Management Guidelines Work Group. Pain management guidelines for blunt thoracic trauma. J Trauma. 2005 Nov;59(5):1256-67. — View Citation
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Truitt MS, Mooty RC, Amos J, Lorenzo M, Mangram A, Dunn E. Out with the old, in with the new: a novel approach to treating pain associated with rib fractures. World J Surg. 2010 Oct;34(10):2359-62. doi: 10.1007/s00268-010-0651-9. — View Citation
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain assessment immediately before and after catheter placement | Pain scores are assessed by nursing on an hourly basis in the ICU | within an hour before and after catheter placement | |
Secondary | successful placement of randomized intervention (paracostal vs. epidural catheter) | Within 24 hours of recruitment | ||
Secondary | Comparison of analgesic effect as measured by daily pain scores | Daily pain scores are assessed by nursing hourly in the ICU and every shift after transfer to the floor. These are measured by the Critical-Care Pain Observation Tool (CPOT). | Duration of admission up to 30 days | |
Secondary | Comparison of improvements in pulmonary function | Respiratory therapist assessment of pulmonary function (including incentive spirometry maximum, forced vital capacity, peak expiratory flow, respiratory rate and supplemental oxygen requirement) every shift will be reviewed for evidence of respiratory embarrassment. | Duration of admission up to 30 days as long as the patient remains in the ICU | |
Secondary | Comparison of improvements in maximum daily incentive spirometry | Nursing assessment of incentive spirometry every shift will be reviewed for evidence of respiratory embarrassment. | Duration of admission up to 30 days | |
Secondary | Comparison of improvements in forced vital capacity | Respiratory therapist assessment of forced vital capacity every shift will be reviewed for evidence of respiratory embarrassment. | Duration of admission up to 30 days as long as the patient remains in the ICU | |
Secondary | Comparison of improvements in peak expiratory flow | Respiratory therapist assessment of peak expiratory flow every shift will be reviewed for evidence of respiratory embarrassment. | Duration of admission up to 30 days as long as the patient remains in the ICU | |
Secondary | Number of patients in each group with pulmonary complications | All patients will be assessed daily for other evidence of respiratory embarrassment including: hypoxemia, pneumonia, empyema, need for mechanical ventilation, or readmission due to pulmonary complaints. | Duration of admission up to 30 days | |
Secondary | ICU length of stay | Duration of admission up to 30 days | ||
Secondary | Hospital length of stay | Duration of admission up to 30 days | ||
Secondary | 30-day Mortality | Duration of admission up to 30 days | ||
Secondary | Comparison of daily requirement for narcotics and other additional pain medications. | Duration of admission up to 30 days | ||
Secondary | Number of patients who had alterations in their care related to the studied interventions (paracostal vs. epidural catheters) | We will assess any possible alterations in care related to interventions (e.g., failure to mobilize, anticoagulate, etc.). | Duration of admission up to 30 days |
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