Resuscitative endovascular balloon occlusion of the aorta
SpecialtyTrauma Surgery, Vascular Surgery, Emergency Medicine, Interventional Radiology
UsesSevere hemorrhage, non-compressible torso hemorrhage, pelvic hemorrhage, obstetric hemorrhage, gastrointestinal hemorrhage.
Other optionsEmergency Thoracotomy with Aortic Cross Clamping

Resuscitative endovascular balloon occlusion of the aorta (REBOA) is a minimally invasive procedure performed during resuscitation of critically injured trauma patients. Originally developed as a less invasive alternative to emergency thoracotomy with aortic cross clamping, REBOA is performed to gain rapid control of non-compressible truncal or junctional hemorrhage.[1][2] REBOA is performed first by achieving access to the common femoral artery (CFA) and advancing a catheter within the aorta.[1] Upon successful catheter placement, an occluding balloon may be inflated either within the descending thoracic aorta (Zone 1) or infrarenal abdominal aorta (Zone 3).[1][2] REBOA stanches downstream hemorrhage and improves cardiac index, cerebral perfusion, and coronary perfusion.[1][3][4] Although REBOA does not eliminate the need for definitive hemorrhage control, it may serve as a temporizing measure during initial resuscitation.[1] Despite the benefits of REBOA, there are significant local and systemic ischemic risks.[1][5] Establishing standardized REBOA procedural indications and mitigating the risk of ischemic injury are topics of ongoing investigation.[1][4] Although this technique has been successfully deployed in adult patients, it has not yet been studied in children.[6]

Medical Uses

Traumatic Injury

Severe hemorrhagic shock caused by non-compressible traumatic injury to the torso and junctional regions remains a major cause of death among civilian and military trauma victims.[1][2][3][4] In contrast to peripheral hemorrhage caused by injury to an extremity, traumatic injuries to the torso and junctional regions are not amendable to direct pressure or tourniquet application.[1][2][4] Because non-compressible torso hemorrhages are not amendable to external interventions, these injuries account for approximately 90% of exsanguinating deaths.[4] Severe hemorrhage is managed either with vascular embolization or damage control surgical techniques such as abdominal packing or removal of non-essential organs.[2] However, in patients with severe hemorrhagic shock at risk for cardiovascular collapse, emergency thoracotomy with aortic cross clamping may be performed though outcomes are typically poor.[2][3]

REBOA Deployment

REBOA was developed as a rapidly deployable, minimally invasive alternative to emergency thoracotomy with aortic cross-clamping. Although there is no single indication criteria for the procedure, it is typically performed for patients with either blunt or penetrating traumatic injuries to the torso with severe hemorrhage refractory to blood product resuscitation.[7] REBOA is performed by gaining access to the common femoral artery and inserting a small endovascular catheter with an inflatable balloon within the aorta.[1] Upon inflation of the occluding balloon, blood flow across the descending aorta is either partially or completely obstructed which subsequently stanches downstream bleeding.[1][2][3] The adjustable catheter design of the REBOA device allows for variable positioning of the occluding balloon within the aorta based on the suspected source of bleeding.[1][2] Zone 1 positioning in the descending thoracic aorta minimizes blood flow below the diaphragm and significantly reduces bleeding within the abdomen, pelvis, and lower extremities.[2] Alternatively, Zone 3 placement within the infrarenal descending abdominal aorta reduces bleeding within the pelvis and lower extremities while preserving blood supply within the abdomen.[2] Although REBOA does not replace the need for definitive surgical management, it may act as a temporizing measure by temporarily augmenting cardiac index to preserve cerebral and myocardial perfusion.[1][3][4] Immediately following successful REBOA deployment, patients must be considered for emergent surgical intervention.[1][2][7][8]

Ongoing Investigation

The safety and efficacy of REBOA in the treatment of severe hemorrhagic shock is an area of ongoing research. Early studies reported conflicting data regarding mortality and failed to establish any clear benefit of REBOA when compared to emergency thoracotomy with aortic cross clamping.[1][2][4] However, design improvements of the REBOA device and continuously evolving patient selection criteria have subsequently improved REBOA outcomes.[1] Current literature demonstrates a survival benefit of REBOA deployment in patients with severe hemorrhagic shock who do not require cardiopulmonary resuscitation (CPR).[1] However, despite REBOA demonstrating its greatest efficacy when deployed prior to cardiovascular collapse, recent data has also shown promise when deployed during (CPR).[1] Closed cardiopulmonary compressions with the REBOA device deployed has demonstrated improved cardiac compression fraction and end-tidal CO2 when compared to emergency thoracotomy with aortic cross clamping and cardiac massage.[1] Additionally, some centers have promoted REBOA deployment in patients with hypotension at risk for progression to severe hemorrhagic shock but who do not yet meet criteria for emergency thoracotomy with aortic cross clamping.[3] The variability in REBOA outcomes likely reflects the variability in institutional patient selection and indications criteria which highlights the need for ongoing evaluation.[2]

Key Procedural Steps

Access to the common femoral artery is first achieved using ultrasound guided, open, or percutaneous technique.[1] The REBOA device is then positioned either within Zone 1 (descending thoracic aorta) or Zone 3 (infrarenal abdominal aorta) before the occluding balloon is inflated with saline.[1] Upon successful definitive hemorrhage control, the occluding balloon is slowly deflated and the patient is monitored for recurrent bleeding or metabolic derangement.[1] Finally, the REBOA sheath is removed and the patient is monitored for access site complications or potential ischemic complications.[1]

The key procedural steps of REBOA deployment are listed in the table below:

REBOA Deployment Procedure
Procedural Step Notes
1) Obtain Access to Common Femoral Artery(CFA):
  • Access to CFA is performed using standard technique.
  • Ultrasound guided access is preferred although percutaneous and open approaches are also acceptable.
2) Positioning of REBOA Balloon:
  • Zone 1 (descending thoracic aorta): 46 cm measured at CFA access site ; length measured from catheter p-tip placed at sternal notch and extended to CFA access site.
  • Zone 3 (infrarenal abdominal aorta): 28 cm measured at CFA access site ; length measured from catheter p-tip placed at xiphoid process and extended to CFA access site.
3) Inflation of REBOA Balloon:
  • Care must be taken not to over-inflate REBOA balloon as overinflation may lead to aortic injury.
  • Balloon inflation time and volume of injected saline should be recorded and documented at CFA access site.
4) Perform Definitive Hemorrhage Control:
  • Definitive hemorrhaging control must be achieved using surgical or embolization techniques.
5) Deflation of REBOA Balloon:
  • Careful monitoring of the patient's hemodynamic status is critical as a significant decrease in cardiac afterload is expected and may lead to hypotension or cardiovascular collapse.
  • Prolonged downstream ischemia may lead to reperfusion injury and metabolic derangement. REBOA balloon deflation should be coordinated between surgical and anesthesia teams to minimize uncontrolled hemodynamic shifts.
6) Removal of REBOA Sheath:
  • Steady, direct pressure should be applied for 30 minutes to CFA access site following REBOA removal.
  • Neurovascular checks should be performed in bilateral lower extremities each hour the REBOA sheath remains in place and for 24-hours following removal to assess for access site complications or vascular injury.
  • Following REBOA removal, angiography of the lower extremity or duplex ultrasound studies should be performed to confirm lower extremity vascular patency.

Potential Complications

Despite the minimally invasive nature of the REBOA device, there are significant risks associated with its use. Although occlusion of the aorta may temporarily augment cardiac index to preserve cardiac and coronary perfusion, there is a significant risk of downstream ischemia which may lead to local ischemic changes or systemic metabolic derangement.[2][3] Significant complications such as limb amputation, metabolic acidosis, and severe reperfusion injury have all been reported with REBOA use and are the subjects of ongoing research.[1][2][3] Although there is no definitive consensus within the academic or surgical communities, many centers recommend balloon occlusion times of less than 30 minutes whenever possible to minimize the risk of clinically significant ischemia.[3] Alternatively, some institutions have recommended partial aortic occlusion or intermittent balloon deflation to minimize the effect of downstream ischemia.[3] Although intermittent balloon deflation is less technically difficult to perform, partial occlusion of the aorta has been demonstrated to reduce uncontrolled hemorrhage while simultaneously limiting distal ischemia and extending safe occlusion times.[3]

Additional potential complications are listed below:

See also

References

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 Glaser J, Stigall K, Cannon J, Jensen S, Morrison JJ, Snyder S, Russo R, Manley J, Becker T, Dubose J (2020-03-30). "Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) for Hemorrhagic Shock (CPG ID:38)" (PDF). Joint Trauma System Clinical Practice Guidelines (CPG ID:38). Retrieved March 13, 2023.
  2. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Castellini G, Gianola S, Biffi A, Porcu G, Fabbri A, Ruggieri MP, et al. (August 2021). "Resuscitative endovascular balloon occlusion of the aorta (REBOA) in patients with major trauma and uncontrolled haemorrhagic shock: a systematic review with meta-analysis". World Journal of Emergency Surgery. 16 (1): 41. doi:10.1186/s13017-021-00386-9. PMC 8358549. PMID 34384452.
  3. 1 2 3 4 5 6 7 8 9 10 11 Russo RM, White JM, Baer DG (June 2021). "Partial Resuscitative Endovascular Balloon Occlusion of the Aorta: A Systematic Review of the Preclinical and Clinical Literature". The Journal of Surgical Research. 262: 101–114. doi:10.1016/j.jss.2020.12.054. PMID 33561721.
  4. 1 2 3 4 5 6 7 Borger van der Burg BL, van Dongen TT, Morrison JJ, Hedeman Joosten PP, DuBose JJ, Hörer TM, Hoencamp R (August 2018). "A systematic review and meta-analysis of the use of resuscitative endovascular balloon occlusion of the aorta in the management of major exsanguination". European Journal of Trauma and Emergency Surgery. 44 (4): 535–550. doi:10.1007/s00068-018-0959-y. PMC 6096615. PMID 29785654.
  5. ↑ Cochran C. "ISRCTN - ISRCTN16184981: The effectiveness and cost-effectiveness of Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) for trauma". www.isrctn.com. doi:10.1186/ISRCTN16184981. Retrieved 2018-02-25.
  6. ↑ Yamashiro KJ, Galganski LA, Grayson JK, Johnson MA, Beyer CA, Spruce MW, et al. (October 2020). "Resuscitative endovascular balloon occlusion of the aorta in a pediatric swine model: Is 60 minutes too long?". The Journal of Trauma and Acute Care Surgery. 89 (4): 616–622. doi:10.1097/TA.0000000000002620. PMID 32068720. S2CID 211160046.
  7. 1 2 Maiga AW, Kundi R, Morrison JJ, Spalding C, Duchesne J, Hunt J, et al. (December 2022). "Systematic review to evaluate algorithms for REBOA use in trauma and identify a consensus for patient selection". Trauma Surgery & Acute Care Open. 7 (1): e000984. doi:10.1136/tsaco-2022-000984. PMC 9791466. PMID 36578977.
  8. 1 2 3 4 Caicedo Y, Gallego LM, Clavijo HJ, Padilla-Londoño N, Gallego CN, Caicedo-Holguín I, et al. (October 2022). "Resuscitative endovascular balloon occlusion of the aorta in civilian pre-hospital care: a systematic review of the literature". European Journal of Medical Research. 27 (1): 202. doi:10.1186/s40001-022-00836-3. PMC 9575194. PMID 36253841.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.