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Anesthesia Care of the Organ Donor
Last updated: 01/08/2026
Key Points
- There are two types of organ donation: donation after brain death (DBD) and donation after circulatory death (DCD).
- Organ donor physiology deteriorates rapidly after brain death or circulatory death due to autonomic collapse, endocrine failure, and systemic inflammation, requiring aggressive, protocol-driven anesthesia and critical care optimization to preserve organ viability.
- Effective donor management focuses on maintaining hemodynamic stability, protective ventilation, temperature control, and metabolic control, and on targeted hormone therapy to maximize the number and quality of transplantable organs.
Types of Organ Donation
DBD1,2
- DBD is the most common donation pathway and involves irreversible cessation of all brain and brainstem function.
- Diagnosis must meet the following conditions: persistent coma, absence of brainstem reflexes, and apnea.
- Ancillary tests (computed tomography angiography, computed tomography perfusion, radionuclide perfusion studies, electroencephalogram) are used when the exam or apnea test cannot be completed.
- Please see the OA summary: Organ Donation: Donation After Brain Death and Donation After Cardiac Death for more details. Link
• Hemodynamic changes after brain death include:- Reflex hypertension and bradycardia (Cushing’s reflex)
- Catecholamine storm (hypertension, tachycardia, and increased afterload)
- Myocardial stunning
- Vasoplegia
- Loss of sympathetic tone
- Hypothermia
- Diabetes insipidus (DI)
- Low cortisol
- Thyroid dysfunction
DCD3
- DCD is used when patients do not meet criteria for brain death but undergo withdrawal of life-sustaining therapy (WLST) due to irreversible illness.
- Death is confirmed via cardiorespiratory criteria (cardiac arrest) and a mandatory “no-touch” standoff period following WLST.
- The transplant team cannot be involved in decisions related to patient prognosis, withdrawal of ventilatory or organ-perfusion support, or determination of death, as each would represent a conflict of interest.
- Informed consent is obtained from the patient’s legal decision maker(s), which is obtained after the decision is made to withdraw support.
- The possibility that the patient may not die or may not provide transplanted organs must be communicated to the consenter.
- Warm ischemia during the agonal phase represents the principal threat to organ viability. Therefore, the anesthetic approach focuses on non-interference with the dying process while preparing for rapid organ recovery once death is declared.
Figure 1. Comparison of DBD and DCD donation pathways.
Abbreviations: EVHP, ex vivo heart perfusion; NRP, neonatal resuscitation program
Source: Beuth J, et al. New strategies to expand and optimize heart donor pool: Ex-vivo heart perfusion and donation after circulatory death: A review of current research and future trends. Anesth Analg. 2019;128(3):406-13.
Care of the Organ Donor4-6
Hemodynamic Management
- The primary goals are to preserve end-organ perfusion, avoid tachycardia and excessive vasoconstriction, and support myocardial function.
- Maintain heart rate 60-120 bpm, mean arterial pressure (MAP) greater than 65 mmHg, central venous pressure 6-10 mmHg, and urine output 1-3 mL/kg/hr.
- Esmolol may be used to treat tachycardia or hypertension.
- Anticholinergic agents may not work for bradycardia if the vagal nerve has been compromised. Direct-acting agents such as isoproterenol is preferred.
- Avoid excessive fluid administration. Balanced crystalloids (e.g, Lactated Ringer’s, Plasma-Lyte) are preferred. If lung procurement is planned, colloids are preferred.
- DCD often requires vasopressors due to vasoplegia.
- First-line treatment is norepinephrine, followed by vasopressin (especially if DI is present).
- Myocardial stunning is common and often reversible.
- Optimize preload and afterload before excluding the heart for transplantation.
Respiratory Management
- Lung-protective ventilation strategies have been shown to improve organ yield and graft function.
- Maintain tidal volumes 6-8 mL/kg of ideal body weight (ideal body weight), positive end-expiratory pressure 5-8 cm H2O, plateau pressures less than 30 cm H2O, and PaO2 greater than 100 mmHg.
Endocrine and Hormonal Management
- DI
- DI occurs in up to 80% of donors due to posterior pituitary failure.
- Symptoms include urine output more than 3–4 mL/kg/hr, low urine osmolality, and hypernatremia.
- Treatments include vasopressin infusion or DDAVP and aggressive free-water replacement to maintain Na less than 155 mEq/L.
- Thyroid hormone dysfunction
- Low T3 levels and impaired conversion contribute to myocardial dysfunction.
- Corticosteroids
- Steroids reduce inflammatory cytokines, improve oxygenation in lung donors, and treat adrenal insufficiency.
- Methylprednisolone 15 mg/kg improves oxygenation, reduces inflammatory mediator levels, and increases the likelihood of lung procurement.
- Glucose management
- Hyperglycemia results from insulin resistance and endocrine collapse.
- Maintain glucose less than 180 mg/dL with an insulin infusion.
Temperature Regulation
- Hypothermia is common due to hypothalamic failure and peripheral vasodilation. Temperature preservation improves organ quality and reduces coagulopathy.
- Maintain core body temperature between 35.8°C and 37.8°C using forced-air warming, increased room temperature, and warmed intravenous fluids.
Coagulopathy and Hematology Management
- Maintain hemoglobin levels not less than 8 g/dL (10 or more for heart donors), platelet count greater than 50,000/µL, and international normalized ratio less than 1.5.
- Correct coagulopathy with fresh frozen plasma or cryoprecipitate to prevent intraoperative bleeding.
Infection Prophylaxis
- Administer broad-spectrum antibiotics due to the risk of ventilator-associated pneumonia and bloodstream infections.
Types of Organ Donation
Phases of Organ Procurement and Intraoperative Management5,6
- The intraoperative course of organ procurement can be divided into several phases, each associated with specific anesthetic responsibilities to preserve organ function and maintain surgical conditions.
- Initial Phase
- Spinal reflexes may cause hypertension or movement despite confirmed brain death.
- Low-dose volatile anesthetics may be used to blunt reflex hypertension and facilitate surgical exposure.
- Neuromuscular blockade may be administered to prevent spinally mediated movement.
- Maintain adequate MAP to ensure continued organ perfusion until the aortic cross-clamp.
- Aortic Cross-Clamping
- Aortic cross-clamping results in the abrupt cessation of organ blood flow and a rapid decline in venous return, MAP, and end-tidal CO2.
- This marks the shift from maintaining physiologic stability to supporting surgical conditions only.
- Cold Perfusion and Organ Preservation
- Preservation solutions (e.g., University of Wisconsin solution) are infused immediately after cross-clamping to rapidly cool organs and minimize ischemic injury.
- Hemodynamic support and ventilation are typically discontinued once cold perfusion is established.
- Anesthetic responsibilities are now focused on assisting with surgical workflow and equipment management.
References
- Kumar L. Brain death and care of the organ donor. J Anaesthesiol Clin Pharmacol. 2016;32(2):146-152. PubMed
- Smith, M. Physiologic Changes During Brain Stem Death – Lessons for Management of the Organ Donor. J Heart Lung Transplant 2004;23:S217-22. PubMed
- Reich DJ, Mulligan DC, Abt PL, et al. ASTS recommended practice guidelines for controlled donation after cardiac death organ procurement and transplantation. Am J Transplant. 2009; 9(9):2004-11. Link
- Wood KE, Becker BN, McCartney JG, et al. Care of the potential organ donor. N Engl J Med. 2004;351(26):2730-2739. PubMed
- Balogh J, Jonna S, Diaz G, et al. The role of anesthesiologists in organ donation. Transplantation Reports. 2022;7(4):100116. Link
- Brown MB, Abramowicz AE, Panzica PJ, et al. Anesthetic considerations of organ procurement after brain and cardiac death: A narrative review. Cureus. 2023;15(6):e40629. PubMed
Other References
- Walters S, Kleiman A. Organ Donation: Donation After Brain Death and Donation After Cardiac Death. OpenAnesthesia. 2023. Link
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