Laboratory tests (renal function/immunological compatibility)
Blood pressure
24-h urine collection to quantify creatinine clearance and measure proteinuria
Oral glucose tolerance test and HbA1C if indicated
Metabolic workup if previous renal stones
Donor ABO typing
Complete blood count with platelet count and differential
Measurement of transaminases
Lipid profile
Complete coagulation studies
Urinalysis and culture
Electrocardiograph
Chest x-ray
Crossmatch performed
Human leukocyte antigen (HLA) typing of the donor may be done
Clinical history and physical examination
Initial interview with specific focus on renal disease and family history of renal disease
Completion of a detailed health questionnaire
Donor education and completion of evaluation of consent
Detailed history and physical examinations by transplant nephrologists and surgeons
Multiple complete vital signs
Detailed evaluation by mental health expert
Interview with independent living donor advocate
Assessment for transmissible infectious disease
Human immunodeficiency virus, hepatitis B and C
Rapid plasma reagin
Testing for tuberculosis (TB) – TB skin testing or QuantiFERON-TB Gold
Testing for Strongyloides, Trypanosoma cruzi, and West Nile virus for donors from endemic areas
Evaluation of renal anatomy with cross-sectional imaging
Age-appropriate health screening, including cancer screening
Prostate-specific antigen (recommendations based on donor age and family history)
Gynecologic examination with Papanicolaou smear
Colonoscopy
Mammogram
Pregnancy test if indicated
Echocardiography and cardiac stress testing as indicated
Pulmonary function studies and computed tomography scanning of the chest as indicated
2.3 Contraindications
General contraindications to living donation are [6] (Table 2.2):
The presence of vascular disease that precludes the arterial and venous anastomoses required for a technically successful transplant
Recent or current malignancy
Chronic illness with short life expectancy
Active substance abuse
Active infectious process
Coronary artery disease
Psychosocial factors that may hinder future adherence to medical treatment
Table 2.2
Contraindications
Absolute | Relative | |
---|---|---|
Age | Less than 18 years | Over 65 years (excluded in many programs) |
Substance abuse | Active substance abuse | Abstinence from substance abuse with documented completion of rehabilitation |
Hypertension | Multiple agents or high doses of single agents for control End-organ injury Additional strong risk factors for cardiovascular disease | Borderline or control with single agents |
Diabetes | Diabetes mellitus | Impaired glucose tolerance |
Obesity | Morbid obesity (BMI >35) or obesity (BMI >30) with comorbid conditions | Obesity |
Renal disease | Evidence of renal disease, including a reduced creatinine clearance (GFR <80 mL/min), proteinuria (>250 mg), or hematuria | Borderline creatinine clearance, microscopic hematuria |
Renal stones | Multiple or recurrent renal calculi of a metabolic condition that predisposes to the recurrence of renal calculi | Single renal stone |
Infection | HIV, hepatitis B, hepatitis C | Hepatitis B core antibody |
Cancer | Cancer, either current or treated but at significant risk for recurrence | |
Cardiovascular disease | Coronary or peripheral vascular disease Valvular heart disease | |
Renal anatomic abnormalities | Significant discrepancy in the kidney sizes | Vascular anomalies |
As per guidelines patients with previous malignancies can undergo renal transplantation after a period of 2 years. It is not needed in cases of incidental renal carcinoma, in situ carcinoma, focal neoplasm low-grade bladder cancer, or basal cell skin cancer. A waiting time of more than 2 years is necessary in cases of melanoma, breast cancer, colorectal carcinoma, and uterine carcinoma [7].
2.4 Radiologic Evaluation
The optimal imaging modality remains a matter of debate. Angiography, the classic gold standard for defining renal anatomy, is now rarely used. Currently Computerized Tomography Angiography (CTA) or Magnetic Resonance Angiography (MRA) is used to evaluate the donor kidneys, define vascular anatomy, and assess donors for other abdominal anomalies or pathology [8]. These imaging modalities are particularly important for assessing anatomic variations affecting the renal arteries, veins, or ureters (Fig. 2.1), which are an important consideration in determining the suitability of an individual for living kidney donation. In providing precise information on the anatomy of the renal vasculature and possible variants and diseases prior to surgery, CTA has reduced the risks and complications during and after renal transplantation, improving the likelihood of a successful outcome [10]. MRA is, however, considered equally accurate in defining renal anatomy and detecting incidental findings that may influence the decision about an individual’s suitability to be a living kidney donor. While MRA has the advantage of avoiding ionizing radiation and potentially nephrotoxic contrast agents, it is much less sensitive in detecting small renal or ureteral stones [9]. Ultimately the choice of imaging modality should probably be based on local imaging expertise and specific protocols.
Fig. 2.1
The CTA gives us wealth of information on the arterial anatomy. It gives us an idea about the prehilar branching, the number of vessels, and the relation of splenic vessels to the upper pole
All potential donors should have a chest x-ray.
Knowledge of the surgical techniques performed and the exclusion criteria allows radiologists to write an accurate radiological report. The radiological arterial report must include renal artery atherosclerosis, aneurysms, arteriovenous malformations and arteriovenous fistulas, dissection, thrombosis, and fibromuscular dysplasia.
The venous report should include the venous variants of the inferior vena cava (duplication, left location, etc.) and the renal veins (retroaortic, circumaortic) and the location, number, diameter, and variants of gonadal, adrenal, and lumbar veins (Fig. 2.2). A delayed topogram acquired in the excretory phase, delayed CT images, or conventional abdominal radiography must be performed to evaluate the collecting system and ureters and screen for a possible duplication anomaly [11, 12].
Fig. 2.2
The venous anatomy is also well delineated with the triple-phase contrast CTA. As depicted in this picture the relation of the renal vein with the adrenal vein and the lumbar vein is clearly seen. This is of strategic importance in surgical planning
2.5 Specific Medical Evaluations
Factors that most commonly contribute to the medical complexity of living kidney donors are age, obesity, hypertension, and psychosocial issues.
2.5.1 Age
There is a clear trend toward accepting older individuals as donors. Registry data indicate that between 2000 and 2009, the mean age of living kidney donors increased from 39.6 to 41.3 years, while the percentage of living kidney donors in the 50- to 64-year-old age range increased from 18.1 to 25%, and the percentage of donors between 18 and 34 years of age declined from 33.2 to 30.3% [13]. With respect to the impact of increasing donor age on potential complications, despite the intuitive sense that older living kidney donors might be at increased risk, several groups have reported that the perioperative risk is not increased in older living donors [14, 15].