Free On-line Access

SPCI - Sociedade Portuguesa de Cuidados Intensivos

Revista Brasileira de Terapia Intensiva

AMIB - Associação de Medicina Intensiva Brasileira


ISSN: 0103-507X
Online ISSN: 1982-4335

Ícone Fechar

How to Cite


Westphal GA, Caldeira Filho M, Vieira KD, Zaclikevis VR, Bartz MCM, Wanzuita R, et al. Diretrizes para manutenção de múltiplos órgãos no potencial doador adulto falecido: Parte III. Recomendações órgãos específicas. Rev Bras Ter Intensiva. 2011;23(4):410-425



Special Article

Guidelines for potential multiple organ donors (adult). Part III: organ-specific recommendations

Diretrizes para manutenção de múltiplos órgãos no potencial doador adulto falecido: Parte III. Recomendações órgãos específicas

Glauco Adrieno Westphal, Milton Caldeira Filho, Kalinca Daberkow Vieira, Viviane Renata Zaclikevis, Miriam Cristine Machado Bartz, Raquel Wanzuita, Álvaro Réa-Neto, Cassiano Teixeira, Cristiano Franke, Fernando Osni Machado, Joel de Andrade, Jorge Dias de Matos, Karine Becker Gerent, Alfredo Fiorelli, Anderson Ricardo Roman Gonçalves, Ben-Hur Ferraz Neto, Fernando Suparregui Dias, Frederico Bruzzi de Carvalho, Gerson Costa, José Jesus Camargo, José Mário Meira Teles, Marcelo Maia, Marcelo Nogara, Maria Emília Coelho, Marilda Mazzali, Nazah Cherif Mohamad Youssef, Péricles Duarte, Rafael Lisboa de Souza, Rogério Fernandes, Spencer Camargo, Valter Duro Garcia

Conflicts of interest: None.

Final version: June 2011

Corresponding author:

Glauco Adrieno Westphal
Rua Oscar Schneider, 237 - Bairro Atiradores
Zip Code: 89203-040 - Joinville (SC), Brazil
Phone: (47) 3423-0303
Email: [email protected]



Brain death (BD) alters the pathophysiology of patients and may damage the kidneys, the lungs, the heart and the liver. To obtain better quality transplant organs, intensive care physicians in charge of the maintenance of deceased donors should attentively monitor these organs. Careful hemodynamic, ventilatory and bronchial clearance management minimizes the loss of kidneys and lungs. The evaluation of cardiac function and morphology supports the transplant viability assessment of the heart. The monitoring of liver function, the management of the patient's metabolic status and the evaluation of viral serology are fundamental for organ selection by the transplant teams and for the care of the transplant recipient.




The relative shortage of organ donors has lead to discussions concerning the use of borderline donors, which increases the relevance of assessing the care of potential donors.

Deceased donors often experience shock and rhabdomyolysis along with an increase in the administration of nephrotoxic drugs or radiology contrasts, which may lead to acute renal failure (C)(1)(A)(2)(D).(3) To maintain adequate function, kidneys should receive appropriate care (C).(4,5)

The lungs are particularly sensitive to the pathophysiological changes that occur with brain death and are susceptible to infective agents, inflammatory responses and cardiovascular dysfunction (D)(6)(C).(7) Judicious fluid replacement, protective ventilation, the use of bronchial hygiene physiotherapy and serial lung function studies minimize the loss of transplantable lungs (D).(6)

An assessment of the morphology and function of the donor heart are mandatory before heart transplantation (B).(8) The early correction of hemodynamic and metabolic disorders with the aim of reversing heart dysfunction increases the potential of the organ for transplantation (B).(9)

An elevated bilirubin, elevated levels of transaminases, or a positive finding by serology for B and C viruses (except if HBsAg-positive), are not absolute contraindications for the transplantation of a donor liver (C)(10-16)(A)(17)(C).(18) However, an elevation in liver enzymes may be a sign of either hypoperfusion or of the initial immunological response in the setting of subclinical viral hepatitis (C).(19)

These factors need not prevent the use of an organ for transplantation. They should, however, alert the maintenance team to act to restore adequate blood flow to the organ. The factors should also be of concern to the transplant team in reference to organ selection and to the care of the transplant recipient (C).(19)



These guidelines are aimed at contributing to the institutional coordination of organ transplantation and will provide "real world" guidelines that are appropriate in the Brazilian context for the uniform care of the deceased donor. Ultimately, this aim of this guide is to increase the quality and quantity of transplantable organs.



The Writing and Planning Committee, comprised of young intensive care physicians and intensive medicine residents, conducted an extensive literature review. From this review, they formulated questions and forwarded the questions to all of the authors of this article. These initial questions served as the starting point for receiving suggestions for the formulation of other questions and definitions.

The final questions were revised by the Executive Committee and were returned to the authors to develop the guidelines presented in this article.

The questions guided the literature review, which was conducted using the P.I.C.O. methodology where P stands for the target population, I for the intervention, C for the control or comparative group and O for the clinical outcome.

The retrieved articles were critically analyzed and categorized according to their grade of recommendation and the strength of the presented evidence in the following manner:

A: More consistent experimental or observational studies.

B: Less consistent experimental or observational studies.

C: Case reports (non-controlled studies).

D: Opinions that lack critical evaluation and are based on consensus, physiological trials or animal models.

Given the paucity of evidence from trials involving deceased donors, many of these recommendations were based on comparisons with other clinical conditions. Therefore, physiological, epidemiological and experimental analyses were used.

The seven discussion subgroups were as follows: 1) overview; 2) hemodynamic support; 3) endocrine-metabolic management; 4) mechanical ventilation and pulmonary maintenance; 5) liver maintenance; 6) renal maintenance and 7) heart maintenance. Each subgroup had a coordinator who was responsible for stimulating and guiding the discussions via email. The texts from each subgroup were organized by the Writing and Planning Committee, presented for review by the Executive Committee and were returned to each subgroup for review. The full text was provided to all panel members and discussed in a meeting held during the XIV South-Brazilian Intensive Care Medicine Congress in May 2001 at Joinville, Santa Catarina, Brazil. The coordinators presented their recommendations at the meeting and discussed the results with conference attendees. Because a large portion of the research that the recommendations were based on was poorly supported, the grade of recommendation was added based on the GRADE system (Grading of Recommendation, Assessment, Development and Evaluation). This system allowed us to classify the quality of the recommendations as STRONG (should be done), WEAK (perhaps should be done) and NONSPECIFIC (there are no advantages or disadvantages). A strong recommendation means that the benefits of an intervention outweigh the risks. A weak recommendation means that the benefits of an intervention are likely to outweigh the risks, although the evidence is weak and more research on the subject is warranted. A nonspecific recommendation means that the benefits and risks of the intervention must be assessed on a case-by-case basis. A strong recommendation should be understood as "recommended" and a weak recommendation as "suggested."

A description of the method for the collection of evidence

The primary database used for the literature review was MEDLINE, which was accessed via the PubMed service. The search was based on the P.I.C.O. methodology of structured questions. Using the MeSH interface (Medical Subject Heading), the following combinations of key words were used: (organ donor OR donor management OR brain death AND recommendation OR consensus), (organ donor OR donor management OR lung transplantation AND mechanical ventilation OR strategies of ventilation), (organ donor OR donor management OR lung transplantation AND fluid challenge OR fluid resuscitation OR positive balance), (organ donor OR donor management OR lung transplantation AND bronchoscopy OR bronchoalveolar lavage), (organ donor OR donor management OR lung transplantation AND pneumonia-ventilator associated), (organ donor OR donor management OR lung transplantation AND prevention and control), (brain-death OR organ donor AND renal donation), (renal function AND brain-death organ donation), (brain-death organ donor AND management OR kidney transplantation), (organ transplantation OR donor kidneys OR management donor kidneys), (transplantability AND liver OR hepatic AND donor), (cadaveric donor AND timing AND liver transplantation), (expanding the donor pool AND liver OR marginal donor liver AND outcome OR extended criteria donor AND MELD), (deceased cardiac donor OR non heart beating donor AND brain death donor), and (organ donors AND echocardiographic OR cardiac transplantation OR management of heart donors). The secondary databases used for the literature review included the Cochrane, Ovid and Trip databases.



What are the recommended measures to ensure the preservation of renal function?

For the maintenance of adequate renal function, which consists of a normal creatinine clearance (> 80 mL/min) and 1 to 3 mL/kg/h urinary output, we recommend a MBP≥ 65 mmHg, a CVP between 6 and 10 cm2 and diuresis at > 1 mL/kg/h in a deceased donor (C).(4,5) These parameters can be achieved with the vigorous infusion of crystalloid solutions (C).(20) Eventually, the use of excessive fluid infusion becomes of value to avoid the use of vasopressors (D).(21,22) However, no controlled or retrospective studies have been done that specifically address the ideal method of fluid replacement for deceased donors.

The aim of vigorous fluid replacement is to protect the donor kidney. However, the maintenance of renal function may jeopardize lung function and eventually render lungs inappropriate for transplantation (D).(6) A recent study analyzing the effects of restrictive fluid replacement aimed at improving lung obtention has shown that maintaining hemodynamic parameters within the minimum normal range (CVP < 6 mmhg) to prevent volume overload increased the number of available lungs without reducing the number of available kidneys. additionally, the graft quality was maintained, in contrast to the graft quality associated with more liberal fluid replacement (C).(23)

Another alternative to liberal fluid replacement is the use of catecholamines. In addition to their hemodynamic effects, catecholamines such as dopamine have been found to have an anti-inflammatory effect. In vitro dopamine reduces IL-8 and chemokine expression in the tubular cells as well as delaying the function of adhesion molecules, such as ICAM-1 and VCAM, and inducing HO-1 expression (C).(24-26) A recent study showed that the infusion of low-dose dopamine (4 µg/kg/min) after a diagnosis of brain death and until the organs were removed for transplant reduced the need for immediate post-transplant dialysis in transplant recipients without changing the graft and patient survival rates B).(27) However, high-dose dopamine (10 µg/kg/min) and/or norepinephrine may impair organ function because of the vasoconstrictive effect of these substances (D).(6)

In our review of the literature, we found no studies that addressed the association between iodine contrasts and nephrotoxicity in deceased donors. We recommend following the guidelines associated with other types of patients (D).(3)

There is no single approach that can be recommended to maintain organ perfusion (D).(28-30) A level of perfusion that is as close as possible to normal perfusion is fundamental for maintaining renal function.


- To maintain the donor's hemodynamic stability (MBP > 65 mmHg and urinary output > 1 mL/kg/h) (C)(4,5) by means of fluid replacement, vasopressor drugs and, when required, inotropic drugs (D).(6,28-30) Strong Recommendation.

- Consider the use of low-dose vasopressors such as dopamine (4 µg/kg/min) in stable subjects to reduce the need for post-transplant dialysis (B).(27) Weak Recommendation.

Are changes in creatinine and/or creatinine clearance levels in the donor organ a contraindication for renal transplant?

A baseline creatinine (Cr) of 1.5 mg/dL (D)(31) or 2 mg/dL (D)(32) is considered at the upper limits for kidneys to be considered appropriate for donation (D).(28) A donor kidney with values rising above these levels is known as an expanded-criteria kidney (ECK).

A donor kidney with a creatinine clearance (CrCl) lower than 50 mL/min alone is considered as an exclusion criterion for transplantation (D).(33) However, these kidneys may be considered for a double-renal transplant (D).(34) Some research has suggested that CrCl values between 50 and 70 mL/min in ECK donors is an indication for the use of the kidney in double-renal transplantation (B).(35) Other research has shown that the use of an ECK donor with a creatinine clearance < 100 ml/min was associated with an increased serum creatinine one year after transplantation (B).(36) CrCl < 80 ml/min in kidneys harvested from elderly donors (> 55 years) has been associated with lower rates of renal survival after transplantation (B).(37)

Acute renal failure (ARF) is not an absolute contraindication for transplantation of the donor kidney. Several reports have shown that patients with ARF due to rhabdomyolysis will come to have an acceptable creatinine clearance (C).(38) Successful case series have been reported with ARF donors (C).(1,39-41) Other authors recommend the use of a pre-implant histology assessment as a criterion for using a graft (B)(36)(C).(42) There are no controlled studies that address this subject. There may then be a bias in the studies noted above because only the positive series results were published.


- Assessing the viability of kidneys for transplant should not be based only on changes in Cr and/or CrCl (D)(33)(B)(35). Strong Recommendation.

Should serial serum creatinine measurements and creatinine clearance calculations be performed for all potential donors? How frequently should these calculation be performed?

Serum creatinine (Cr) is an indirect method used for estimating the rate of glomerular filtration. Some limitations should be considered in reference to the value of this estimation. Cr is a product of muscle metabolism and is distributed in the water volume of the body. The production rate is proportional to the subject's muscle mass. In the critically ill condition of deceased donors, rhabdomyolysis is common and leads to sudden increases in plasma creatinine levels. Conversely, the infusion of large volumes of fluid can dilute Cr and reduce the level in the plasma., The use of Jaffe's method may also interfere with the accuracy of Cr measurements.

The assessment of baseline renal function

A baseline Cr is used in the assessment of all deceased donor kidneys. Its main function is to identify pre-existing renal disease and chronic impairment of glomerular filtration. For these purposes, a baseline Cr is used to calculate the estimated creatinine clearance (CrCl) using the Cockroft-Gault formula.

CrCl is just one parameter that can be used to identify previous renal disease and a family history of renal disease. Other criteria, such as a urinalysis and sediment evaluation is mandatory to rule out glomerular disease (hematuria, proteinuria or cylindruria) or urinary tract infection.

A baseline creatinine of between 1.5 mg/dL (D)(31) and 2 mg/dL (D)(32) is the maximal tolerable level for renal transplantation. A donor kidney with values rising above these levels is known as an ECK. A Cr > 1.36 mg/dL is associated with late graft function (B).(43) Lower Cr levels in a donor organ are associated with lower Cr levels in the transplant recipient (C).(44)

Research has shown that the measurement of CrCl alone failed to strongly correlate with the measurement of renal graft outcome (C).(45) Other research has shown that CrCl > 70 mL/min was the best discriminator associated with strong renal function at 1 to 12 months after renal transplantation when compared with other scores (D).(33) A CrCl < 50 ml/min is an exclusion criterion for the use of a renal graft (D).(33) Transplant recipients of kidneys from higher CrCl donors have higher rates of graft survival, patient survival and renal function (B).(46)

Serial renal function assessment

Changes in Cr and diuresis volume are used as criteria for diagnosing acute renal injury (ARI) (C)(1)(A).(2) A deceased donor is exposed to several ARI risk factors, such as shock, rhabdomyolysis, the use of nephrotoxic drugs or radiology contrasts. In a stable setting, Cr is expected to increase daily by 1 mg/dL when glomerular filtration has ceased. However, in a critically ill patient, as previously mentioned, the increased distribution volume may underestimate the real level of variation. Patients with anuria may experience days without a significant change in Cr levels when receiving significant volume expansion because of Cr dilution. Conversely, with rhabdomyolysis, an increase in Cr may overestimate the amount of kidney damage. Additionally, the ancillary parameter of diuresis volume is higher in deceased donors due to the lack of the effects of the tubular antidiuretic hormone (ADH). These factors should be considered when assessing serial Cr measurements (C).(1)

There are no studies that suggest when serial Cr measurements should be performed in the setting of the management of the deceased donor. The Canadian Forum on Medical Management to Optimize Donor Organ Potential recommends repeating Cr measurements every 6 hours (D),(28) but this recommendation was suggested without a rationale. Changes in Cr within 48 hours are used as diagnostic criteria in ARI diagnosis (A).(2) However, a 48-hour period may not be feasible in the setting of the deceased donor.

There is no indication for the use of CrCl estimated by formulas in the setting of ARI. Its use is indicated for assessing the balance between Cr production and excretion.


- Record a baseline Cr and then repeat the measurement every 24 hours for all potential donors (D)(28)(B)(43)(C).(44) Strong Recommendation.

- Analyze the volume of diuresis and Cr variation in conjunction with the clinical conditions of all potential donors (C).(1) Strong Recommendation.

What are the indications for the use of renal ultrasonography (USG) in the assessment of potential donors?

There is no precise indication for the use of renal USG in the assessment of potential donors. The information obtained from USG is not useful (D).(28)

There may be some cases where USG could be useful. When a donor with a family history of renal disease, such as polycystic renal disease or cases of suspected chronic renal disease has an initial increase in the creatinine level, USG could be useful for assessing the size of the kidneys. When available, a total abdominal USG could be useful for ruling out neoplasms.


- Routine renal USGs are not indicated for deceased donors. The use of this test should be evaluated on a case-by-case basis (D).(13) Strong Recommendation



How should be gas exchange be monitored? Which tests should be performed? What are the ideal blood gas parameters?

Brain death releases inflammatory mediators and induces a number of hemodynamic changes. Although all solid organs are affected, the lungs are particularly sensitive to the effects of hemodynamic instability. The lungs are additionally susceptible to the effects of resuscitation efforts and changes in capillary permeability (D)(6)(C).(7) Long-term hospitalization in the ICU also exposes the lungs to infective agents. These harmful agents account for the loss of many organs and render less than 20% of multiple organ donors appropriate for transplantation (C).(47) Judicious fluid replacement, careful ventilation and serial evaluations minimize the loss of these organs (D).(6)

Routine tests and procedures for the assessment of lungs from a deceased donor include the following: pulse oxymetry, serial arterial blood gases, tracheal cannula suction, chest radiography, bronchoscopy and bronchoalveolar lavage (D).(28) Target blood gas levels for the maintenance of lungs for transplantation are as follows: SaO2 > 95% and PaO2 > 80 mmHg; or PaO2 > 300 mmHg with FiO2 of 100% and PEEP of 5 cmH2O; or PaO2/FiO2 > 300 mmHg (D).(28) Acidosis should be corrected with sodium bicarbonate or by increasing the rate of ventilation (PaCO 2 between 30 and 35 mmHg) for a pH > 7.2 (C).(48) Some studies have shown that it is possible to transplant organs from donors with more severe changes if the changes were not associated with other risk factors (C).(49-51) Blood gas measurements should be repeated at least every 6 hours and/or whenever oxymetry monitoring or ventilation parameters have changed. Some articles have shown that the rate of graft failure is higher in this group. However, other studies show no differences. This improvement should be sustained (C).(50,51) Other mandatory tests include: 1) Chest radiography: preferably with the head of the bed at 45º and with ventilation tidal volume of 12 mL/kg body weight (use this volume during the test only). Radiographic studies should be done less than 6 hours before organ extraction (C).(51) 2) A bronchoscopy should be performed as a part of the multi-organ donor assessment and for the collection of bronchoalveolar lavage fluid specimen(B).(52,53)


- Continuous pulse oxymetry monitoring, arterial blood gases every 6 hours, and chest radiography every 24 hours (D)(28) (C).(51) Strong Recommendation.

- The ideal blood gas parameters are as follows: SaO2 > 95% and PaO2 > 80 mmHg or PaO2 > 300 mmHg with FiO2 of 100% and PEEP of 5 cmH2 or PaO2/FiO2 > 300 mmHg (D).(28) Strong Recommendation.

- Even when these target values are not achieved, lung donation is not contraindicated. Strong Recommendation.

Once all of the above criteria are met, when is bronchoscopy indicated?

The respiratory management of a potential donor is frequently complicated by pulmonary injuries such as the following: neurogenic pulmonary edema, respiratory infections, pulmonary bleeding and traumatic pulmonary injury (D)(6,54,55) (C).(56) The development of atelectasis secondary to the supine position of the deceased donor, the prolonged period of mechanical ventilation and aggressive fluid resuscitation are frequent causes of hypoxemia. If these conditions are not corrected, there is up to a 30% reduction in the likelihood of the feasibility of transplanting these lungs (D).(57)

The objectives of bronchoscopy in a donor are as follows: to assess the bronchial anatomy; to evaluate and remove endobronchial foreign bodies; to identify and assess aspirated material for possible infection; and to clear secretions (D.(6,57,58) The performance of an early bronchoscopy is an important factor in the aggressive management of potential donors. Studies have shown that the performance of a bronchoscopy, along with frequent pulmonary suction (respiratory physical therapy) and pulmonary expansion ventilation techniques (using PEEP), results in a significant increase in both the quality of the donor organs and in the number of transplantable organs (D)(29)(C).(56,59-62) A bronchoscopy can be performed either by a local hospital physician or by the transplant team surgeon (D).(28) During the bronchoscopy, respiratory fluids should be collected (bronchoalveolar lavage fluid) for Gram staining and cultures with the aim of guiding eventual antibiotic therapy (D).(28,57)

In donors presenting with evidence of gas exchange abnormalities and radiographic evidence of unilateral lung injury, a therapeutic bronchoscopy may support a contralateral lung assessment with the aim of avoiding the discarding of a potential donor organ and of contributing to graft survival (D).(6,29,57,63)


- A bronchoscopy is indicated for all potential lung donors (D)(29)(C).(56,59-62) Strong Recommendation.

- If a bronchoscopy cannot be performed at the hospital of origin, clinicians should inform the team responsible for removing the organs that this test could not be performed. In these circumstances, the procedure will be performed by the organ removal team (D).(28) Strong Recommendation.

Which bronchial hygiene procedures should be used?

The aims of bronchial hygiene physiotherapy are to prevent atelectasis and to improve the pulmonary gas exchange of mechanically ventilated critically ill patients (D).(6,57) The recommended procedures are as follows: low-pressure tracheal suction (D),(28,57,58) chest percussion, postural drainage, decubitus positioning every 2 hours (D)(28) and pulmonary expansion techniques (D).(6,64) There are few studies concerning bronchial hygiene for deceased donors. Many of our recommendations are taken from the guidelines associated with other clinical conditions.

Some studies (D)(57) have recommended that tracheal suction be performed with closed suction circuits. However, recent meta-analytical research involving living critical patients failed to show any significant difference regarding the incidence of mechanical ventilation-associated pneumonia when using closed suction circuits(A).(65,66)

To reduce pulmonary aspiration, some protocols for donor management have recommended raising the head of the bed to at least 30º and to maintaining the tracheal tube balloon pressure at close to 25 cmH2O(C)(53)(D)(57)(C).(67) A semi-seated position (the head of the bed raised to between 30º and 45º) has been found to reduce the incidence of mechanical ventilation-associated pneumonia and will likely reduce the bronchial aspiration of contaminated oropharyngeal material (A).(68-70) We infer that these recommendation will have similar beneficial effects in the setting of the deceased donor. Another strategy to prevent subglottic secretions from entering the lower respiratory tract is the maintaining of optimal tracheal tube balloon pressure. Balloon pressures below 20 cmH2O have been shown to increase the risk of pneumonia while pressures above 30 cmH2O have been shown to increase the risk of ischemic tracheal injury (B).(71-73)

When potential donors develop atelectasis, especially when he atelectasis is associated with hypoxemia, postural drainage is recommended along with ventilatory alveolar recruitment and therapeutic bronchoscopy (D).(64)


- The tracheal tube should be suctioned only in the presence of tracheal secretions. Follow decubitus positioning every 2 hours (D).(28,57,58) Keep the head of the bed raised to between 30º and 45º (A).(68-70) Keep the tracheal tube balloon pressure between 20 and 30 cmH2O (B).(71-73) Strong Recommendation.

How should volume therapy be managed in a potential lung donor?

The maintenance of a potential donor includes the challenge of restoring or maintaining hemodynamic stability. Hypovolemia is a frequent occurrence and should be aggressively treated. However, fluid overload may result in pulmonary edema, which may render the donor organ unfit for transplantation (D).(74) Intravenous fluids must then be carefully monitored. This is especially important for potential lung donors. The lungs may be injured during sympathetic hyperactivity and become increasingly susceptible to pulmonary edema and capillary leakage. Although hypovolemia should be corrected, the excessive administration of fluids should be avoided. Fluid replacement should be judicious with the aim of maintaining a euvolemic status. The Lung Work Group (D)(48) recommends that a pulmonary artery catheter be inserted to assist with fluid management and to assure good tissue perfusion. Measurements obtained from the pulmonary artery will assist clinicians in maintaining a central venous pressure (CVP) of 6-8 mmHg and a pulmonary wedge pressure (PCWP) of 8-12 mmHg. Recent studies have shown that a CVP > 7 mmHg in a deceased donor, even after heart dysfunction was ruled out, was associated with a poorer clinical outcome, a prolonged period of mechanical ventilation and an increase in the rate of mortality rate for patients receiving lung transplants (C).(75) The findings of this research were additionally supported by an observational study where patients who were initially considered unacceptable as lung transplant donors became effective donors after an aggressive fluid restriction strategy (previous fluid balance: 4.1 + 1.3 L versus -1.7 + 0.8 L; p < 0.008; and previous cvp: 11.3 + 0.9 mmHg versus 6.7 + 0.4 mmHg (D).(76) However, hypovolemic deceased donors in general have more systemic inflammation and less viable transplantable organs (C).(77,78)

Although the monitoring of CVP and PCWP are recommended by some researchers, the accuracy and usefulness of the measurements remains uncertain (C).(79) Although ventricular filling pressures are the preferred method for assessing cardiovascular responsiveness, recent evidence suggests that CVP and PCWP measurements exhibit low sensitivity and specificity (C)(80)(B).(81-83) More accurate methods should be chosen to assess the variables of dynamic cardiovascular volume responsiveness (B)(81,82,84) (see the hemodynamic management section).


- Use volume expansion techniques in potential lung donors when appropriate. Avoid fluid overload (C).(78) Maintain adequate tissue perfusion to avoid the loss of potential donor organs because of hypovolemia (C).(77,78) Strong Recommendation.



Are echocardiography and/or pulmonary artery catheter (PAC) monitoring needed to assess heart transplantability?

The assessment of the morphologic and hemodynamic status of the heart is essential for heart transplant and should be performed as soon as consent is obtained for the donation (B).(8) An echocardiogram provides information concerning ventricular contractility, interventricular septum thickness, the presence of an intracardiac shunt, valve disease and, with the use of the Doppler, the flow velocity of the anterior descending coronary artery. This assessment is particularly important for donors with coronary disease risk factors (C).(85) Invasive hemodynamic monitoring with a PAC increases the number of available heart transplants as compared with donors who were not monitored with a PAC without affecting the amounts of infused fluid or the vasopressors administered (B).(9)


- An echocardiogram should be performed on all potential heart donors to assess the morphologic and functional status of the heart (B)(8) (C).(85) Strong Recommendation.

- Consider using a pulmonary artery catheter in all potential heart donors (B).(9) Weak Recommendation.

Which invasive hemodynamic monitoring methods (PAC) or echocardiographic parameters are considered ideal for assessing the donor heart?

The following factors contribute to the failure of transplanted hearts: left ventricular systolic dysfunction (an ejection fraction of less than 50%) (B);(8,86) changes in structure caused by variances in contractility (C);(85) reduced coronary flow as determined by Doppler studies (C)(85); and prolonged organ ischemia (D).(87) Both echocardiography and PAC monitoring are used to identify hearts that are suboptimal candidates for transplantation (B).(8) Echocardiographic assessment of the left ventricular ejection fraction assists in predicting which organs are viable for transplantation (B).(8) A morphological assessment assists in identifying structural changes that may preclude the use of the organ (C).(85) Hemodynamic monitoring with a PAC allows for the sequential assessment of pharmacological interventions and can assess whether circulatory changes in the a potential donor have been reversed, which improves the outcome for the heart transplant recipient (B).(9) The management of a potential donor through the use of a reanimation protocol corrects and promotes hemodynamic stability ( systolic blood pressure > 90 mmHg; wedge pressure 15 mmHg; cardiac index > 2.5 L/min/m2) and assists in the management of metabolic disorders. This protocol may reverse heart dysfunction and increase the chances of the viability of a donor organ by up to 30% D.(88,89) In a series of 49 cases of potential deceased donors with left ventricular ejection fraction (LVEF) lower than or equal to 50% who were initially considered inappropriate for transplant, the use of the animation protocol improved LVEF in 38 cases (78%), and 34 of these donor hearts were successfully transplanted (C).(90)


- The ideal parameters for the donor heart are as follows: a left ventricular ejection fraction > 50% (B);(8) no variance in structure or contractility (C);(85) a cardiac index > 2.5 L/min/m2 and a PCWP 15 mmHg (D).(88,89) Even when these target values are not achieved, heart transplantation may not be contraindicated. Strong Recommendation.

- Consider inserting a PAC to monitor efforts at attempting to reverse cardiac dysfunction (CI < 2.5 l/min/m2 and PCWP 15 mmHg) and increase the chances of increasing the viability of the donor organ (B).(8,9) Weak Recommendation.

Do increases in biomarker values contraindicate the transplantation of the donor heart?

Serum troponin levels alone should not be used as a basis for rejecting a donor heart for transplantation (D).(28)

An increase in cardiac enzymes is common in potential deceased donors. Although an increase is related to worsening myocardial dysfunction and transplant failure, it is not necessarily indicative of coronary disease. An increase in the levels of cardiac enzymes alone neither identifies coronary disease or serves as a basis for rejecting the donor heart for transplantation. An increase in cardiac enzymes should be assessed for a correlation with persistent myocardial dysfunction (D).(91)


- Transplantation of a donor heart is not contraindicated based on an increase in cardiac biomarkers alone. The variance in the biomarkers should be assessed for a correlation with persistent myocardial dysfunction (D).(91) Strong Recommendation.

In which conditions should potential heart donors undergo cineangiocoronariography?

During the last three decades, the upper age limit for donors has increased. The increased rate of mortality for patients receiving hearts from older donors has raised questions concerning donor selection (C).(92)

Overall, cineangiocoronariography should be performed on male donors greater than 45 years of age and on female donors greater than 50 years of age. Factors such as cocaine use or the atherosclerotic risk factors of hypertension, diabetes, smoking, dyslipidemia or a positive family history should be considered as an indication for performing cineangiocoronariography even in younger donors (C).(93)

Cineangiocoronariography can also be indicated when heart dysfunction is verified in donors by echocardiography or with invasive hemodynamic monitoring. It should be noted that segmental left ventricular (LV) dysfunction is frequently seen in patients with brain injuries without the presence of coronary disease (C).(93)

Because cineangiocoronariography is not widely available in Brazil, the loss of donor organs could occur if all potential donors were required to have cineangiocoronariography. When cineangiocoronariography is not available, men greater than 45 years of age and women over the age 50 should be considered as potential donors for acute high risk recipients (D).(91)

The use of "marginal" organs for transplant is acceptable, particularly for acute high risk recipients (C).(94) Even organs with mild to moderate coronary artery disease can be used for transplantation, and myocardial revascularization may be performed during or after transplantation (C).(95)


- Indications for cineangiocoronariography include the following:

Potential male donors greater than 45 years of age and female donors greater than 50 years of age. (D).(89)

Young donors with a previous history of drug abuse (i.e. cocaine) or with atherosclerotic risk factors, such as systemic arterial hypertension, diabetes mellitus, smoking, dyslipidemia or family history (D).(89)

Cineangiocoronariography should not be performed based on an increase in cardiac enzyme levels alone (C).(92) Strong Recommendation.

- The unavailability of cineangiocoronariography does not rule out the organ viability. Strong Recommendation.



Which blood chemistry variables should be monitored in liver donors? Is there any serology change which would preclude or complicate the donation of a liver?

Patients diagnosed with brain death frequently experience hydroelectrolytic disorders, particularly hypernatremia. Hypernatremia may be a predictor of primary liver graft failure. The exact mechanism for this is not known, but it is presumed to be related to hepatocyte edema and the subsequent exacerbation of the injury mediated by reperfusion. A serum sodium greater than 160 mEq/L should be corrected before explantation. However, there is no evidence that higher sodium levels contraindicate using the donor organ (C).(96-99)

Changes in potassium level should be corrected to maintain cardiovascular viability, but these changes do not impact the viability of the donor liver. No human studies have shown unfavorable outcomes for patients receiving livers from hyperkalemic donors (C).(100)

An increase in transaminases and bilirubin may be indicative of liver ischemia from hypoperfusion, or the increase may be a sign of subclinical viral hepatitis. This does not preclude the use of the donor organ for transplantation, but the transplant team should monitor the patient postoperatively for complications or for viral hepatitis (C).(19)

The measuring of transaminases, bilirubin, alkaline phosphatase, gamma-glutamyl transferase, INR (International Normalized Ratio) and prothrombin time every 6 hours is recommended with no clear rationale (D).(28,101)

Hyperglycemia is not a contraindication for liver transplantation. However, hyperglycemia can affect peri-hepatocyte osmolarity. Hypoglycemia may also impact liver neoglucogenesis and may indicate liver damage (D).(102)

A liver from an HBsAg positive donor should not be used for transplantation (C).(10-12) Other serologies are not absolutely excluded for liver explant, but the donor organ should be rated as of borderline quality. Anti-HBsAg positive donors may have their livers safely used, as the infection is not transmitted to the recipient (C).(10-13) However, there is a disease transmission risk for anti-HBc IgG positive donors (C).(14,15) The possibility of a liver transplant in this setting is dependent on the recipient's anti-Hbs status. If the recipient is anti-Hbs positive, the liver can be used because the recipient's own surface antibodies will prevent the reactivation of hepatitis B(C)(16)(A).(17) If the recipient's status is negative, antiviral drugs and immunoglobulin should be used (C).(18)

Livers from hepatitis C donors can be safely used in HCV (+) recipients. A liver biopsy should always be performed because bridging fibrosis organs should not be used (C).(18)


- Measure serum sodium, potassium and blood glucose levels at least every 6 hours (D).(28,101) Weak Recommendation.

- Measure transaminases (AST/ALT), bilirubin and APT levels at least every 24 hours (D).(28,101) Weak Recommendation.

- Maintain serum sodium below 160 mEq/L (C).(96-99) Strong Recommendation.

- Liver donation from C and B viruses positive serology potential donors (except if HBsAg positive) is not contraindicated (C).(10-12,18) Strong Recommendation.



1. Rodrigo E, Miñambres E, Piñera C, Llorca J, Fernández-Fresnedo G, Vallejo A, et al. Using RIFLE criteria to evaluate acute kidney injury in brain-deceased kidney donors. Nephrol Dial Transplant. 2010;25(5):1531-7.

2. Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG, Levin A; Acute Kidney Injury Network. Acute Kidney Injury Network: report of an initiative to improve outcomes in acute kidney injury. Crit Care. 2007;11(2):R31.

3. Prevention of contrast-induced nephropathy. [Internet]. [cited 2011 Oct 18]. Available from:

4. Zaroff JG, Rosengard BR, Armstrong WF, Babcock WD, D'Alessandro A, Dec GW, et al. Consensus conference report: maximizing use of organs recovered from the cadaver donor: cardiac recommendations, March 28-29, 2001, Crystal City, Va. Circulation. 2002;106(7):836-41.

5. Dictus C, Vienenkoetter B, Esmaeilzadeh M, Unterberg A, Ahmadi R. Critical care management of potential organ donors: our current standard. Clin Transplant. 2009;23 Suppl 21:2-9.

6. Wood KE, Becker BN, McCartney JG, D'Alessandro AM, Coursin DB. Care of the potential organ donor. N Engl J Med. 2004;351(26):2730-9.

7. Smith M. Physiologic changes during brain stem death--lessons for management of the organ donor. J Heart Lung Transplant. 2004;23(9 Suppl):S217-22.

8. Venkateswaran RV, Townend JN, Wilson IC, Mascaro JG, Bonser RS, Steeds RP. Echocardiography in the potential heart donor. Transplantation. 2010;89(7):894-901.

9. Hadjizacharia P, Salim A, Brown C, Inaba K, Chan LS, Mascarenhas A, Margulies DR. Does the use of pulmonary artery catheters increase the number of organ available for transplantation? Clin Transplant. 2010;24(1):62-6.

10. Dodson SF, Bonham CA, Geller DA, Cacciarelli TV, Rakela J, Fung JJ. Prevention of de novo hepatitis B infection in recipients of hepatic allografts from anti-HBc positive donors. Transplantation. 1999;68(7):1058-61.

11. Ho JK, Harrigan PR, Sherlock CH, Steinbrecher UP, Erb SR, Mo T, et al. Utilization of a liver allograft from a hepatitis B surface antigen positive donor. Transplantation. 2006;81(1):129-31.

12. Saab S, Chang AJ, Comulada S, Geevarghese SK, Anselmo RD, Durazo F, et al. Outcomes of hepatitis C- and hepatitis B core antibody-positive grafts in orthotopic liver transplantation. Liver Transpl. 2003;9(10):1053-61.

13. Dodson SF, Issa S, Araya V, Gayowski T, Pinna A, Eghtesad B, et al. Infectivity of hepatic allografts with antibodies to hepatitis B virus. Transplantation. 1997;64(11):1582-4.

14. Lowell JA, Howard TK, White HM, Shenoy S, Huettner PC, Brennan DC, Peters MG. Serological evidence of past hepatitis B infection in liver donor and hepatitis B infection in liver allograft. Lancet. 1995;345(8957):1084-5.

15. Wachs ME, Amend WJ, Ascher NL, Bretan PN, Emond J, Lake JR, et al. The risk of transmission of hepatitis B from HbsAg(-), HBcAb(+), HBIgM(-) organ donors. Transplantation. 1995;59(2):230-4.

16. Roque-Afonso AM, Ferray C, Samuel D, Simoneau D, Roche B, et al. Antibodies to hepatitis B surface antigen prevent viral reactivation in recipients of liver grafts from anti-HBC positive donors. Gut. 2002;50(1):95-9.

17. Cholongitas E, Papatheodoridis GV, Burroughs AK. Liver grafts from anti-hepatitis B core positive donors: a systematic review. J Hepatol. 2010;52(2):272-9.

18. Ricchiuti A, Brunati A, Mirabella S, Pierini A, Franchello A, Salizzoni M. Use of hepatitis C virus-positive grafts in liver transplantation: a single-centre experience. Transplant Proc. 2005;37(6):2569-70.

19. Miranda LEC, Macedo FIB, Fonseca Neto OCL, Lacerda CM. Use of extended criteria of donors in liver transplantation. J Bras Transplant 2007;10(3):774-8.

20. Schnuelle P, Johannes van der Woude F. Perioperative fluid management in renal transplantation: a narrative review of the literature. Transplant Int. 2006;19(12):947-59.

21. Peeters P, Vanholder R. Therapeutic interventions favorably influencing delayed and slow graft function in kidney transplantation: mission impossible? Transplantation. 2008;85(7 Suppl):S31-7.

22. Carlier M, Squifflet JP, Pirson Y, Decocq L, Gribomont B, Alexandre GP. Confirmation of the crucial role of the recipient's maximal hydration on early diuresis of the human cadaver renal allograft. Transplantation. 1983;36(4):455-6.

23. Minãmbres E, Rodrigo E, Ballesteros MA, Llorca J, Ruiz JC, Fernandez-Fresnedo G, et al. Impact of restrictive fluid balance focused to increase lung procurement on renal function after kidney transplantation. Nephrol Dial Transplant. 2010;25(7):2352-6.

24. Schnuelle P, Lorenz D, Mueller A, Trede M, Van Der Woude FJ. Donor catecholamine use reduces acute allograft rejection and improves graft survival after cadaveric renal transplantation. Kidney Int. 1999;56(2):738-46.

25. Schnuelle P, Berger S, de Bour J, Persijn G, van der Woude FJ. Effects of catecholamine application to brain-dead donors on graft survival in solid organ transplantation. Transplantation. 2001;72(3):455-63.

26. Schnuelle P, Yard BA, Braun C, Dominguez-Fernandez E, Schaub M, Birck R, et al. Impact of donor dopamine on immediate graft function after kidney transplantation. Am J Transplant. 2004;4(3):419-26.

27. Schnuelle P, Gottmann U, Hoeger S, Boesebeck D, Lauchart W, Weiss C, et al. Effects of donor pretreatment with dopamine on graft function after kidney transplantation: a randomized controlled trial. JAMA. 2009;302(10):1067-75.

28. Shemie SD, Ross H, Pagliarello J, Baker AJ, Greig PD, Brand T, Cockfield S, Keshavjee S, Nickerson P, Rao V, Guest C, Young K, Doig C; Pediatric Recommendations Group. Organ donor management in Canada: recommendations of the forum on Medical Management to Optimize Donor Organ Potential. CMAJ. 2006;174(6):S13-32.

29. Kutsogiannis JD, Pagliarello G, Doig C, Ross H, Shemie SD. Medical management to optimize donor organ potential: review of the literature. Can J Anaesth. 2006;53(8):820-30.

30. Roche AM, James MF. Fluid therapy in organ transplantation. Curr Opin Organ Transplant. 2007;12(3):281-6.

31. Merion RM, Ashby VB, Wolfe RA, Distant DA, Hulbert-Shearon TE, Metzger RA, et al. Deceased-donor characteristics and the survival benefit of kidney transplantation. JAMA. 2005;294(21):2726-33.

32. Keitel E, Michelon T, dos Santos AF, Bittar AE, Goldani JC, D'almeida Bianco P, et al. Renal transplants using expanded cadaver donor criteria. Ann Transplant. 2004;9(2):23-4.

33. Singh D, Kiberd B, Lawen J. Can the outcome of older donor kidneys in transplantation be predicted? An analysis of existing scoring systems. Clin Transplant. 2004;18(4):351-6.

34. European Best Practice Guidelines for Renal Transplantation (Part1). Produced by theEBPG Expert Group on Renal Transplantation. Cadaveric heart-beating donors. Nephrol Dial Transplant. 2000;15(Suppl 7):39.

35. Stratta RJ, Rohr MS, Sundberg AK, Armstrong G, Hairston G, Hartmann E, et al. Increased kidney transplantation utilizing expanded criteria deceased organ donors with results comparable to standard criteria donor transplant. Ann Surg. 2004;239(5):688-95; discussion 695-7.

36. Karpinski J, Lajoie G, Cattran D, Fenton S, Zaltzman J, Cardella C, Cole E. Outcome of kidney transplantation from high-risk donors is determined by both structure and function. Transplantation. 1999;67(8):1162-7.

37. Carter JT, Lee CM, Weinstein RJ, Lu AD, Dafoe DC, Alfrey EJ. Evaluation of the older cadaveric kidney donor: the impact of donor hypertension and creatinine clearance on graft performance and survival. Transplantation. 2000;70(5):765-71.

38. Greenstein SM, Moore N, McDonough P, Schechner R, Tellis V. Excellent outcome using "impaired" standard criteria donors with elevated serum creatinine. Clin Transplant. 2008;22(5):630-3.

39. Anil Kumar MS, Khan SM, Jaglan S, Heifets M, Moritz MJ, Saeed MI, et al. Successful transplantation of kidneys from deceased donors with acute renal failure: Three-year results. Transplantation. 2006;82(12):1640-5.

40. Deroure B, Kamar N, Depreneuf H, Jacquet A, Francois H, Charpentier B, et al. Expanding the criteria of renal kidneys for transplantation: use of donors with acute renal failure. Nephrol Dial Transplant. 2010;25(6):1980-6.

41. Kayler LK, Garzon P, Magliocca J, Fujita S, Kim RD, Hemming AW, et al. Outcomes and utilization of kidneys from deceased donors with acute kidney injury. Am J Transplant. 2009;9(2):367-73.

42. Lin NC, Yang AH, King KL, Wu TH, Yang WC, Loong CC. Results of kidney transplantation from high-terminal creatinine donors and the role of time-zero biopsy. Transplant Proc. 2010;42(9):3382-6.

43. Koning OH, Ploeg RJ, van Bockel JH, Groenewegen M, van der Woude FJ, Persijn GG, Hermans J. Risk factors for delayed graft function in cadaveric kidney transplantation: a prospective study of renal function and graft survival after preservation with University of Wisconsin solution in multi-organ donors. European Multicenter Study Group. Transplantation. 1997;63(11):1620-8.

44. Tian YF, Liao CH, Chen MJ. Risk factors among donor characteristics which affect graft outcome in paired kidney transplantation. Transplant Proc. 2008;40(7):2281-4.

45. Blasi-Ibanez A, Hirose R, Feiner J, Freise C, Stock PG, Roberts JP, Niemann CU. Predictors associated with terminal renal function in deceased organ donors in the intensive care unit. Anesthesiology. 2009;110(2):333-41.

46. Iordanous Y, Seymour N, Young A, Johnson J, Iansavichus AV, Cuerden MS, Gill JS, Poggio E, Garg AX; Donor Nephrectomy Outcomes Research (DONOR) Network. Recipient outcomes for expanded criteria living kidney donors: the disconnect between current evidence and practice. Am J Transplant. 2009;9(7):1558-73.

47. Association of Organ Procurement Organization. OPO voluntary survey on local organ donor and transplantation activity for 12 month totals, annual report. McLean (VA): The Association; 2000.

48. Rosengard BR, Feng S, Alfrey EJ, Zaroff JG, Emond JC, Henry ML, et al. Report of the Crystal City meeting to maximize the use of organs recovered from the cadaver donor. Am J Transplant. 2002;2(8):701-11.

49. Whiting D, Banerji A, Ross D, Levine M, Shpiner R, Lackey S, Ardehali A. Liberalization of donor criteria in lung transplantation. Am Surg. 2003;69(10):909-12.

50. Pierre AF, Sekine Y, Hutcheon MA, Waddell TK, Keshavjee SH. Marginal donor lungs: a reassessment. J Thorac Cardiovasc Surg. 2002;123(3):421-7; discussion, 427-8.

51. Lardinois D, Banysch M, Korom S, Hillinger S, Rousson V, Boehler A, et al. Extended donor lungs: eleven years experience in a consecutive series. Eur J Cardiothorac Surg. 2005;27(5):762-7.

52. Reyes KG, Mason DP, Thuita L, Nowicki ER, Murthy SC, Pettersson GB, Blackstone EH. Guidelines for donor lung selection: time for revision? Ann Thorac Surg. 2010;89(6):1756-64; discussion 1764-5.

53. Angel LF, Levine DJ, Restrepo MI, Johnson S, Sako E, Carpenter A, et al. Impact of a lung transplantation donor-management protocol on lung donation and recipient outcomes. Am J Respir Crit Care Med. 2006;174(6):710-6.

54. Wilkes DS, Egan TM, Reynolds HY. Lung transplantation: opportunities for research and clinical advancement. Am J Respir Crit Care Med.2005;172(8):944-55. Review.

55. DuBose J, Salim A. Aggressive organ donor management protocol. J Intensive Care Med. 2008;23(6):367-75. Review.

56. Venkateswaran RV, Patchell VB, Wilson IC, Mascaro JG, Thompson RD, Quinn DW, et al. Early donor management increases the retrieval rate of lungs for transplantation. Ann Thorac Surg. 2008;85(1):278-86; discussion 286.

57. Van Raemdonck D, Neyrinck A, Verleden G, Dupont L, Coosemans W, Decaluwé H, et al. Lung donor selection and management. Proc Am Thorac Soc. 2009;6(1):28-38. Review.

58. Mascia L, Mastromauro I, Viberti S, Vincenzi M, Zanello M. Management to optimize organ procurement in brain dead donors. Minerva Anestesiol. 2009;75(3):125-33.

59. Gabbay E, Williams TJ, Griffiths AP, Macfarlane LM, Kotsimbos TC, Esmore DS, Snell GI. Maximizing the utilization of donor organs offered for lung transplantation. Am J Respir Crit Care Med. 1999;160(1):265-71.

60. Botha P. Extended donor criteria in lung transplantation. Curr Opin Organ Transplant. 2009;14(2):206-10. Review.

61. Riou B, Guesde R, Jacquens Y, Duranteau R, Viars P. Fiberoptic bronchoscopy in brain-dead organ donors. Am J Respir Crit Care Med. 1994;150(2):558-60.

62. Fernandes PMP, Samano MN, Junqueira JJM, Waisberg DR, Noleto GS, Jatene FB. Lung donor profile in the state of São Paulo, Brazil, in 2006. J Bras Pneumol. 2008;34(7):497-505.

63. Puskas JD, Winton TL, Miller JD, Scavuzzo M, Patterson GA. Unilateral donor lung dysfunction does not preclude successful contralateral single lung transplantation. J Thorac Cardiovasc Surg. 1992;103(5):1015-7; discussion 1017-8.

64. Del Río F, Escudero D, De La Calle B, Gordo Vidal F, Valenín Paredes M, Ramón Núñez J. Evaluación y mantenimiento del donante pulmonar. Med Intensiva. 2009;33(1):40-9.

65. Subirana M, Solà I, Benito S. Closed tracheal suction systems versus open tracheal suction systems for mechanically ventilated adult patients. Cochane Database Syst Rev. 2007;(4):CD004581.

66. Siempos II, Vardakas KZ, Falagas ME. Closed tracheal suction systems for prevention of ventilator-associated pneumonia. Br J Anaesth. 2008;100(3):299-306.

67. Lloyd-Jones H, Wheeldon DR, Smith JA, Potter CD, Wallwork J, Large SR. An approach to the retrieval of thoracic organs for transplantation. AORN J. 1996;63(2):425-23, 425-6.

68. Muscedere J, Dodek P, Keenan S, Fowler R, Cook D, Heyland D; VAP Guidelines Committee and the Canadian Critical Care Trials Group. Comprehensive evidence-based clinical practice guidelines for ventilator-associated pneumonia: prevention. J Crit Care. 2008;23(1):126-37.

69. Li Bassi G, Torres A. Ventilator-associated pneumonia: role of positioning. Curr Opin Crit Care. 2011;17(1):57-63.

70. Alexiou VG, Lerodiakonou V, Dimopoulos G, Falagas ME. Impact of patient position on the incidence of ventilator-associated pneumonia: a meta-analysis of randomized controlled trials. J Crit Care. 2009;24(4):515-22.

71. Lorente L, Blot S, Rello J. New issues and controversies in the prevention of ventilator-associated pneumonia. Am J Respir Crit Care Med. 2010;182(7):870-6.

72. Rello J, Soñora R, Jubert P, Artigas A, Rué M, Vallés J. Pneumonia in intubated patients: role of respiratory airway care. Am J Respir Crit Care Med. 1996;154(11):111-5.

73. Wain JC Jr. Postintubation tracheal stenosis. Semin Thorac Cardiovasc Surg. 2009;21(3):284-9.

74. Tuttle-Newhall JE, Collins BH, Kuo PC, Schoeder R. Organ donation and treatment of the multi-organ donor. Curr Probl Surg. 2003;40(5):266-310.

75. Pilcher DV, Scheinkestel CD, Snell GI, Davey-Quinn A, Bailey MJ, Williams TJ. High central venous pressure is associated with prolonged mechanical ventilation and increased mortality after lung transplantation. J Thorac Cardiovasc Surg. 2005;129(4):912-8.

76. Straznicka M, Follete DM, Eisner MD, Roberts PF, Menza RL, Babcock WD. Aggressive management of lung donors classified as inacceptable: excellent recipient survival one year after transplantation. J Thorac Cardiovasc Surg. 2002;124(2):250-8.

77. Dominguez-Roldan JM, Jimenez-Gonzalez PI, Garcia-Alfaro C, Hernandez-Hazañas F, Fernandez-Hinojosa E, Bellido-Sanchez R. Electrolytic disorders, hyperosmolar states, and lactic acidosis in brain dead patients. Transplant Proc. 2005;37(5):1987-9.

78. Murugan R, Venkataraman R, Wahed AS, Elder M, Carter M, Madden NJ, Kellum JA; HIDonOR Study Investigators. Preload responsiveness is associated with increased interleukin-6 and lower organ yeld from brain-dead donors. Crit Care Med. 2009;37(8):2387-93.

79. Stoica SC, Satchithananda DK, Charman S, Sharples L, King R, Rozario C, et al. Swan-Ganz catheter assessment of donor hearts: outcome of organs with borderline hemodynamics. J Heart Lung Transplant. 2002;21(6):615-22.

80. Boldt J, Lenz M, Kumle B, Papsdorf M. Volume replacement strategies on intensive care units: results from a postal survey. Intensive Care Med. 1998;24(2):147-51.

81. Kumar A, Anel R, Bunnell E, Habet K, Zanotti S, Marshall S, et al. Pulmonary artery occlusion pressure and central venous pressure fail to predict ventricular filling volume, cardiac performance, or the response to volume infusion in normal subjects. Crit Care Med. 2004;32(3):691-9.

82. Michard F, Boussat S, Chemla D, Anguel N, Mercat A, Lecarpentier Y, et al. Relation between respiratory changes in arterial pulse pressure and fluid responsiveness in septic patients with acute circulatory failure. Am J Respir Crit Care Med. 2000;162(1):134-8.

83. Osman D, Ridel C, Ray P, Monnet X, Anguel N, Richard C, Teboul JL. Cardiac filling pressures are not appropriate to predict hemodynamic response to volume challenge. Crit Care Med. 2007;35(1):64-8.

84. Hofer CK, Müller SM, Furrer L, Klaghofer R, Genoni M, Zollinger A. Stroke volume and pulse pressure variation for prediction of fluid responsiveness in patients undergoing off-pump coronary artery bypass grafting. Chest. 2005;128(2):848-54.

85. Hashimoto S, Kato TS, komamura K, Hanatani A, Niwaya K, Funatsu T, et al. Utility of echocardiographic evaluation of donor hearts upon the organ procurement for heart transplantation. J Cardiol. 2011;57(2):215-22.

86. Zaroff JG, Babcock WD, Shiboski SC. The impact of left ventricular dysfunction on cardiac donor transplant rates. J Heart Lung Transplant. 2003;22(3):334-7.

87. Fiorelli AI, Stolf NA, Pego-Fernandes PM, Oliveira Junior JL, Santos RH, Contreras CA, et al. Recommendations for use of marginal donors in heart transplantation: Brazilian Association of Organs Transplantation guideline. Transplant Proc. 2011;43(1):211-5.

88. Wheeldon DR, Potter CD, Oduro A, Wallwork J, Large SR. Transforming the "unacceptable" donor: outcomes from the adoption of a standardized donor management technique. J Heart Lung Transplant. 1995;14(4):734-42.

89. Potter CD, Wheeldon DR, Wallwork J. Functional assessment and management of heart donors: a rationale for characterization and a guide to therapy. J Heart Lung Transplant. 1995;14(1 Pt 1):59-65.

90. Zaroff JG, Babcock WD, Shiboski SC, Solinger LL, Rosengard BR. Temporal changes in left ventricular systolic function in heart donors: results of serial echocardiography. J Heart Lung Transplant. 2003;22(4):383-8.

91. Baldwin JC, Anderson JL, Boucek MM, Bristow MR, Jennings B, Ritsch ME Jr, Silverman NA. 24th Bethesda conference: Cardiac transplantation. Task Force 2: Donor guidelines. J Am Coll Cardiol. 1993;22(1):15-20.

92. Rodeheffer RJ, Naftel DC, Stevenson LW, Porter CB, Young JB, Miller LW, et al. Secular trends in cardiac transplant recipient and donor management in the United States, 1990 to 1994. A multi-institutional study. Cardiac Transplant Research Database Group. Circulation. 1996;94(11):2883-9.

93. Seiler C, Laske A, Gallino A, Turina M, Jenni R. Echocardiographic evaluation of left ventricular wall motion before and after heart transplantation. J Heart Lung Transplant. 1992;11(5):867-74.

94. Lima B, Rajagopal K, Petersen RP, Shah AS, Soule B, Felker GM, et al. Marginal cardiac allografts do not have increased primary graft dysfunction in alternate list transplantation. Circulation. 2006;114(1 Suppl):I27-32.

95. Marelli D, Laks H, Bresson S, Ardehali A, Bresson J, Esmailian F, et al. Results after transplantation using donor hearts with preexisting coronary artery disease. J Thorac Cardiovasc Surg. 2003;126(3):821-5.

96. Mangus RS, Fridell JA, Vianna RM, Milgrom ML, Chestovich P, Vandenboom C, Tector AJ. Severe hypernatremia in deceased liver donors does not impact early transplant outcome. Transplantation. 2010;90(4):438-43.

97. Totsuka E, Dodson F, Urakami A, Moras N, Ishii T, Lee MC, et al. Influence of high donor serum sodium levels on early postoperative graft function in human liver transplantation: effect of correction of donor hypernatremia. Liver Tranpl Surg. 1999;5(5):421-8.

98. González FX, Rimola A, Grande L, Antolin M, Garcia-Valdecasas JC, Fuster J, et al. Predictive factors of early postoperative graft function in human liver transplantation. Hepatology. 1994;20(3):565-73.

99. Figueras J, Busquets J, Grande L, Jaurrieta E, Perez-Ferreiroa J, Mir J, et al. The deleterious effect of donor high plasma sodium and extended preservation in liver transplantation. A multivariate analysis. Transplantation. 1996;61(3):410-3.

100. Abouna GM, Aldrete JA, Starzl TE. Changes in serum potassium and pH during clinical and experimental liver transplantation. Surgery. 1971;69(3):419-26.

101. D'Império F. Morte encefálica, cuidados ao doador de órgãos e transplante de pulmão. Rev Bras Ter Intensiva. 2007;19(1):74-84.

102. Busuttil RW, Klintmalm GB, editors. Transplantation of the liver. 2nd ed. Philadelphia: Saunders; 2005.



These guidelines are provided by the Associação de Medicina Intensiva Brasileira (AMIB) and Associação Brasileira de Transplantes de Órgãos (ABTO) was supported by SC - Transplantes - Central de Notificação Captação e Distribuição de Órgãos e Tecidos do Estado de Santa Catarina - CNCDO/SC.



Click to enlarge


Maintenance guidelines for potential multiple organ deceased donors

Coordinator: Glauco Adrieno Westphal

Executive committee

Cristiano Franke, Joel de Andrade, Jorge Dias de Matos, Milton Caldeira Filho, Fernando Osni Machado.

Writing and planning committee

Kalinca Daberkow Vieira, Miriam Cristine Machado Bartz, Raquel Wanzuita, Viviane Renata Zaclikevis.


1. Overview

Coordinator: Fernando Osni Machado

Participants: Fabiano Nagel, Gerson Costa, Luiz Henrique Melo, Nazah Cherif Mohamad Youssef, Nelson Akamine.

2. Hemodynamic support

Coordinator: Gilberto Friedman

Participants: Eliézer Silva, Glauco Adrieno Westphal, Mirela Cristine de Oliveira, Miriam Cristine Machado Bartz, Nelson Akamine, Rafael Lisboa de Souza.

3. Endocrine-metabolic management

Coordinator: Álvaro Réa-Neto

Participants: Felipe Dal-Pizzol, Maria Emília Coelho, Milton Caldeira Filho.

4. Mechanical ventilation and pulmonary maintenance

Coordinator: Cassiano Teixeira

Participants: José Jesus Camargo, José Mário Meira Teles, Péricles Duarte, Spencer Camargo.

5. Liver maintenance

Coordinator: Karine Becker Gerent

Participants: Marcelo Nogara, Rogério Fernandes.

6. Renal maintenance

Coordinator: Jorge Dias de Matos

Participants: Anderson Ricardo Roman Gonçalves, Marilda Mazzali, Valter Duro Garcia.

7. Heart maintenance

Coordinator: Cristiano Franke

Participants: Alfredo Fiorelli, Ben-Hur Ferraz Neto, Fernando Suparregui Dias, Frederico Bruzzi, Marcelo Maia.



Submission On-line

Indexed in




Associação de Medicina Intensiva Brasileira - AMIB

Rua Arminda nº 93 - 7º andar - Vila Olímpia - São Paulo, SP, Brasil - Tel./Fax: (55 11) 5089-2642 | e-mail: [email protected]

Cookie Policy

GN1 - Systems and Publications