[Frontiers in Bioscience 14, 4746-4757, January 1, 2009]

Surgical aspects of live kidney donation

Leonienke Francisca Dols1, Niels Frederik Kok1, Jan Nicolaas IJzermans1

1 Department of Surgery, Erasmus MC, Gravendijkwal 230, PO Box 2040, 3000 CA, Rotterdam, The Netherlands

TABLE OF CONTENTS

1. Abstract
2. Introduction
3. Benefits of live kidney donor transplantation
4. Innovations in live kidney donation
5. Care of the live donor
5.1. Standard care of the live donor
5.2. Improvements in imaging of the donor
5.3. Improvements in surgical technique
5.3.1. Laparoscopic donor nephrectomy
5.3.2. Hand-assisted laparoscopic donor nephrectomy
5.3.3. Retroperitoneoscopic donor nephrectomy
5.3.4. Minimally invasive open donor nephrectomy
5.3.5. Evidence-based approach in the surgical management
5.4. Improvements in perioperative care
5.5. Improvements in follow-up
6. Conclusion and future perspectives
7. Acknowledgements
8. References

1. ABSTRACT

In the early 1990s live kidney donation regained popularity to meet the demand of kidney transplantation. Significant developments in the field of live kidney donation have established live donation as the potential prime source of kidney transplants in the future. Nowadays management focuses on logistic and immunological innovations, and improvements in care of the live donor. However, a flawless surgical procedure in donors and recipients is a prerequisite for further expansion of live kidney donor transplantation. From a surgical perspective the introduction of the laparoscopic approach has been a major breakthrough. Less invasive techniques to procure live donor kidneys have been held responsible for a steep increase in the number of live donors. In addition, less invasive imaging, improvements in perioperative care, and novel insights in follow-up have all improved the care of the live donor. Live kidney donation may develop as the most promising source of renal organs since artificial kidneys, xenografts and stem cell therapy for restoring intrinsic kidney function will probably not find application on large scale in the near future.

2. INTRODUCTION

The kidney is an essential organ, which plays a pivotal role in acid/base balance, sodium/potassium balance, calcium metabolism, regulation of blood pressure, red blood cell synthesis and excretion of metabolites. A variety of renal diseases finally results in renal insufficiency.

Kidney replacement therapy consists of dialysis and kidney transplantation. Hemodialysis and peritoneal dialysis can lead to long-term survival and may bridge patients to kidney transplantation. However, the impact of dialysis on quality of life is enormous. Kidney transplantation is considered the optimal kidney replacement therapy for many patients with end-stage renal disease (1, 2).

In the early 1950s, Rene Kuss and Joseph Murray performed the first successful kidney transplantations in France and the United States respectively (3, 4). The discovery of adequate immunosuppressive therapy in the 1960s enabled deceased donor kidney transplantation, preventing risky operations performed on healthy individuals. As enough deceased donors were present at that time, live kidney donor transplantation was pushed into the background.

In the late 1980s and 1990s, a discrepancy between organ demand and supply occurred because of an increasing number of patients suffering from end-stage renal disease and a stagnating number of transplants. The average waiting time for a kidney from a deceased donor increased considerably. Mainly because of mortality and worsening condition precluded transplantation. Annually, up to twenty percent is removed from the waiting list. Increasing the number of deceased donors has failed mainly due to relatives refusing donation (5). This prompted a new interest in live donor kidney transplantation amongst other alternatives.

In the last decade, the number of transplants from live donors significantly increased in the Western World (6). The revival of live kidney donation is a result of the aforementioned gap between the demand and supply of organs. Live kidney donor transplantation has created opportunities including pre-emptive and ABO-incompatible kidney transplantation that contribute to the success of live kidney donation. The expansion of live kidney donation is only possible by continuous innovations and research in screening of the donor, perioperative care and last but not least the surgical technique. These innovations have limited the discomfort to the donor and incited live donation. In this review we will focus on current surgical issues surrounding live kidney donation.

3. BENEFITS OF LIVE KIDNEY DONOR TRANSPLANTATION

Live kidney donor transplantation renders some significant benefits over kidney transplantation from a deceased donor. First, the transplant usually starts functioning immediately following transplantation, as opposed to transplants derived from deceased donors. Ischemic damage to the allograft is minimal due to short ischemic time. This is important, as cold ischemic time is a well-known risk factor for delayed graft function (7). Second, transplant survival is significantly improved. Three-year survival rates are approximately 81 to 87 percent for living unrelated donors and 70 percent for cadaveric kidneys (8-10).Third, dialysis may be avoided by planning live donor kidney transplantation. This so-called pre-emptive kidney transplantation is gaining popularity. It reduces the costs of dialysis and the related operations needed to introduce a catheter or develop a shunt; furthermore such an approach may improve transplant function and survival (2). Current allocation guidelines impede pre-emptive kidney transplantation from a deceased donor. Fourth, live kidney donor transplantation turns emergent surgery into elective surgery and thereby improves surgical results without any doubt. Candidates for donation and transplantation can be carefully screened and the transplantation can be scheduled at a time when donor and recipient are well prepared for surgery. Finally, a higher degree of histoincompatibility may be accepted in live kidney donor transplantation because the grafts are derived from healthy donors and do not sustain significant injury during the time awaiting explantation (11). Nevertheless, kidney transplantation is a surgical procedure with risks of mortality and morbidity

4. INNOVATIONS IN LIVE KIDNEY DONATION

Live kidney donation has been fostered by immunologic maneuvers that can overcome biologic obstacles such as HLA disparity and ABO or cross-match incompatibility. In the classic, successful live kidney donor transplantations of the 1950s, the transplant was derived from an HLA identical individual, often a twin. Despite the rapid developments in immunosuppressive therapy, most transplants were derived from relatives until the early 1990s.

Nowadays transplants derived from genetically unrelated donors appear to provide excellent function and long-term survival is comparable with the survival of a graft derived from related donors (11). Awareness of the success of grafts from unrelated donors resulted in a spectacular increase of unrelated donors, in particular from spouses (12).

Among the genetically unrelated donors, the percentage of those without a direct relation to the recipient increases, including those participating in cross-over transplant programs, list-exchange programs and Good Samaritan kidney donor programs. (13, 14).

Cross-over transplantations (donor-paired exchange) intend to help recipients accompanied by a donor with a different, incompatible, blood group. This pair is coupled to one or two other pairs having the same problem of blood group incompatibility. However, the blood group of the donor of the first pair and the recipient of the second or third pair matches. So, donor A donates to recipient B, donor B donates to recipient C and donor C may donate to recipient A. Although the logistics are demanding and a sufficient pool is necessary to create combinations between pairs, these cross-over transplant programs or pair-wise donation may be highly successful (15).

List-exchange transplantation is relatively new. The live donor and the recipient have incompatible blood groups. The donor donates his kidney to a recipient waiting for an organ derived from a deceased donor. In exchange, the intended recipient, related to the live donor, receives priority on the deceased donor waitlist. List-exchange may be live saving, in particular for those recipients who do not find a compatible donor by a cross-over program or for whom transplantation across the blood group is not optional.

Good Samaritan kidney donors are also denoted as truly altruistic donors who do not have any relation to a recipient (14). The transplants of these donors are usually intended for recipients awaiting deceased donor transplantation.

An uncommon type of kidney donor is a patient whose kidney is removed for medical indication (i.e. iatrogenic ureteral lesions that could not be repaired, kidney stones). These donors/patients usually have another kidney that functions well and they do not require auto-transplantation. Donation to the organ pool may be an option.

Integration of all aforementioned practices would help to reduce the number of transplant candidates waiting. Recent calculations estimate that up to eleven percent of the transplanted kidneys may be recruited from this pool of formerly uncommon donors (16, 17).

Another innovative approach includes the transplantation of living donor renal allografts across blood group barriers (18, 19). This requires protocols to reduce and maintain anti-blood group antibodies at safe levels. Developments in immuno-absorption have resulted in good results for such transplantations (18).

5. CARE OF THE LIVE DONOR

5.1. Standard care of the live donor

The crucial aspect in live kidney donor transplantation is the potential harm to the donor. From an ethical perspective live kidney donation is only justified if the harm to the donor is limited and the potential benefit to the recipient is major. The risk for the immediate and long-term health adverse consequences to the donor is therefore very important. The Amsterdam Forum has established guidelines for the (relative) contra-indications to live kidney donation: donors must have sufficient renal function (GFR more than 80 ml/min), no hypertension (less than 140/90 mm Hg), no obesity (BMI less than 35 kg/m�), negative urine analysis for protein (less than 300mg/24 hours) and erythrocytes, no diabetes, stone disease, malignancy or urinary tract infections, a minor or no cardiovascular or pulmonary risk and smoking cessation and alcohol abstinence is obligatory (20).

A multidisciplinary approach is required to optimize quality of a live kidney donation program. Disciplines have to cooperate in the screening of donors and informing relatives without exerting pressure on potential donors. Each step in the multidisciplinary approach should be optimized. Imaging of the donor kidney should be performed without any complications and the surgical procedure, while peri-operative care should be optimally organized to minimize pain and discomfort to the donor. Advances in surgical technique have improved the comfort of the donor considerably and the risks of morbidity and mortality have been minimized. Adequate follow-up may identify donors who develop hypertension early and may also aid donors from a social perspective, for example, by advising those who struggle with their recovery or experience problems resuming work (21).

Together with the solution of more donor kidneys another problem arises. The ethical aspects concerning living unrelated transplantation are even more complicated than the medical ones due to concern of commercialization. Many people consider it unethical to pay kidney donors. In developing countries this can become a problem. People are more willingly towards donation if there is a financial reward. Some advocate for a reward for donors as renal replacement therapy is much more expensive. Others suggest that establishing controlled donor compensation programs could partly solve the shortage in organs (22-24).

5.2. Improvements in imaging of the donor

Imaging is of great importance in selecting donors. It determines the choice of the kidney to be donated. Donors with bilateral arterial stenosis, cysts, fibromuscular dysplasia or parenchymal tumors should be excluded from donation. To ensure sufficient renal function for the donor, the best-functioning kidney should be left to the donor. This requires techniques to rule out how both kidneys of the donor contribute to donor function. In addition to providing detailed information on the donor, radiological examinations should be safe, minimally invasive and the time for these investigations should be limited. In laparoscopic donor nephrectomy, tactile feedback to the surgeon, and thereby relatively easy discrimination of vessels by pulsatile movement, is lost. Therefore, especially for laparoscopy, preoperative planning has become increasingly important. The anatomy of the renal arteries must be visualized, as the presence of multiple arteries has been associated with increased complexity for removal and an increased rate of ureteral complications in the recipient (25). Traditionally, the renal anatomy was assessed by angiography with good results but significant consequences for the donor, including radiation and a short stay in the hospital. Magnetic resonance imaging (MRI) and computed tomography (CT) have both been reported as feasible alternatives (26-33). In our hospital, MRI has gradually replaced angiography as this technique does not cause radiation and, in addition, provides information on the venous anatomy (34). CT may help to determine renal split function (35).

Live kidney donors are healthy individuals who deserve the least invasive and the least time consuming imaging with the best predictive value. At present, none of the techniques encompasses all the features outlined. However, imaging with CT and MRI is less invasive than angiography, provides information on venous anatomy and the renal parenchyma, and does not require observation of the live donor in the hospital for several hours after the procedure. Further development of these techniques will contribute to selection and surgical planning.

5.3. Improvements in surgical technique

5.3.1. Laparoscopic donor nephrectomy

Traditionally, kidneys were harvested by a 15 to 25 cm flank incision that transected three layers of abdominal muscles. Resection of ribs was frequently applied to allow sufficient access to the kidney. This procedure injured the abdominal wall resulting in substantial postoperative pain, an average hospital stay of 7 days and prolonged sick leave. In the long term, some donors suffered from chronic neuralgia and incisional hernias (36).

Fortunately, renewed interest in live kidney donation occurred in an era in which minimally invasive surgery was gradually replacing conventional surgery. In 1995, Ratner and colleagues performed the first laparoscopic donor nephrectomy (37). Various alternatives to this laparoscopic approach have been presented since, including hand-assisted laparoscopic donor nephrectomy and retroperitoneoscopic donor nephrectomy. Meanwhile, the classic open approach has been refined and minimally invasive principles are more often applied in open surgery.

As described above Ratner and colleagues introduced a laparoscopic technique for live kidney donation in 1995. He used a midline incision to harvest the kidney transplant, instead of the Pfannenstiel incision we use nowadays (37). The donor is in a lateral decubitus position. The first trocar is inserted periumbilically. The abdomen is insufflated with CO2, a 30 degrees video-endoscope is introduced and three to four additional trocars are inserted (Figure 1). The right or left hemicolon is dissected from the lateral abdominal wall and mobilized medially. Gravity aids this mobilization. The kidney is located behind the hepatic or splenic flexure. The fascia of Gerota is opened and the kidney is dissected from the surrounding capsule. The renal vessels are dissected and encircled with vessel loops to facilitate identification from different directions. The venous branches of the renal vein are clipped and divided with scissors. The ureter is dissected until it crosses the gonadal vein. Then, a 5 to 8 cm horizontal suprapubic incision or Pfannenstiel incision is made as extraction site while maintaining pneumoperitoneum. An endobag is introduced via a small incision in the peritoneum. Subsequently, the ureter is clipped and divided with scissors and the renal artery and vein are divided with an endostapler. The kidney is caught with the endobag and extracted via Pfannenstiel incision. Then, the transplant is cooled down by perfusing it with a preservation solution at 4 degrees centigrade and stored on ice. This step is similar in all the techniques. The Pfannenstiel incision is sutured once the pneumoperitoneum is restored. The peritoneal cavity is checked for bleeding; the remnants of the renal vessels and the adrenal gland in particular are checked. After haemostasis is ensured, the trocars are removed under vision and the incisions are sutured.

The introduction of this technique has given rise to much discussion in the transplant society because the pneumoperitoneum, necessary to obtain vision, leads to an increased intra-abdominal pressure and thereby may affect renal perfusion with subsequent ischemia/reperfusion injury to the transplant. Recovery of transplant function would be delayed as indicated by slower declining recipient serum creatinine (38).

Subsequently, various studies have proven that there are no clinical short-term adverse effects of laparoscopic donor nephrectomy on transplant function. However, these studies either did not continuously assess renal function during the first weeks or did not adjust serum creatinine values for possible confounders at baseline (39-41). Adjusting the fluid regimen of the donor anticipates potentially adverse effects of increased pressure and decreased perfusion (40).

Three prospective studies, comparing open with laparoscopic donor nephrectomy are listed in table 1 (42-44). Several cohort studies from large volume centers in the United States have proven the feasibility and safety of the laparoscopic technique (45, 46). Leventhal et al reported a group of 500 patients with an overall rate of intra- and postoperative complications of respectively 2.8% and 3.4%. There were 9 conversions (1.8%), of which 6 were in the first 100 cases. Thirty patients experienced an intraoperative or procedure-related complication (6.0%). Only 1 recipient experienced delayed graft function, and only 1 recipient had a urological complication.

The laparoscopic live donor nephrectomy is technically more demanding than the open approach, with a prolonged learning curve (47, 48). Therefore the introduction of the laparoscopic method in small centers can be difficult.

5.3.2. Hand-assisted laparoscopic donor nephrectomy

Hand-assistance during laparoscopic donor nephrectomy requires an extraction incision that is little larger than the aforementioned extraction site for total laparoscopic donor nephrectomy. This allows one hand of the surgeon to enter the peritoneal cavity via a hand port. These hand ports allow introduction of, manipulation by, and removal of the hand of the surgeon while maintaining pneumoperitoneum. Some surgeons make a midline incision to place their hand port in an ergonomic position. The introduction of various trocars is similar to the conventional laparoscopic approach. Advantages of this technique include maintaining tactile sensation, the possibility to present tissues and the creation of surgical planes with the hand. In case of bleeding, it is easier to directly stop the bleeding manually and repair the injury. This technique contributes to a steeper learning curve for the hand-assisted method compared to the total laparoscopic approach (49). Potential disadvantages are higher costs because of the hand port, a worse ergonomic position of the surgeon during operation, a higher rate of wound infections and increased traumatic injury to the transplant as a consequence of manipulation. Literature on the pros and cons of either technique is scarce and inconclusive. Bargman and co-workers compared laparoscopic donor nephrectomy with and without hand-assistance (50). They found a statistically significant difference in the mean operative time for the two groups (200 +/- 20.8 minutes for Standard Laparoscopy vs. 219 +/- 28.3 minutes for Hand-Assisted Laparoscopy; P = 0.02). No differences were observed regarding mean estimated blood loss, warm ischemia time, length of postoperative hospital stay, intravenous analgesia or pain score on postoperative day 1 and 2. Five minor complications in the laparoscopy group and three in the hand-assisted group occurred. The mean preoperative, 1-month, and 3-month postoperative QoL scores did not differ significantly between the groups. None of the recipients required postoperative dialysis, and there was no statistical difference between the two groups in serum creatinine concentration. The authors concluded that laparoscopic and hand-assisted donor nephrectomies have similar outcomes and postoperative pain, minimal complication rates and similar impact on quality of life.

5.3.3. Retroperitoneoscopic donor nephrectomy

Retroperitoneoscopic donor nephrectomy is a modification of the technique first described by Ratner. In this technique the peritoneal cavity is not opened. The technique has been described with and without hand-assistance (51, 52). The retroperitoneal space is developed and insufflated with CO2. Several trocars are introduced (Figure 2). The peritoneal sac containing the bowel is mobilized medially. The dissection of the kidney and the renal vessels is similar to transperitoneal donor nephrectomy but the angle is different. The kidney is extracted via a muscle-splitting flank incision or a Pfannenstiel incision (51-54). The discussion to use or not to use hand-assistance is similar to the discussion about hand-assistance during the transperitoneal approach. Appropriately designed studies on this topic are lacking and the evidence is based on expert opinions. The potential advantage of the retroperitoneoscopic technique is that the peritoneum is not opened; also the descending colon and the splenocolic ligament are left intact, thereby avoiding injuries to these organs. Moreover, the angle at which the vessels are dissected may be preferable (51). The hand-assisted technique is claimed to offer advantages in the management of severe bleeding (49, 55, 56).

Wadstrom concluded from his first 75 cases that the retroperitoneoscopic hand-assisted method facilitates the procedure by enabling short operation times and significantly reducing the risks associated with endoscopic live donor nephrectomy (52). Bachman et al. concluded that retroperitoneoscopic donor nephrectomy provides comparable perioperative features, such as operation time, warm ischemia time and overall complication rate compared with open donor nephrectomy. Additionally, it does not have a negative impact on operation time of the recipient, graft ischemia and early graft function (53).

No large case series or comparative cohort studies have been published to date. In the future, the value of retroperitoneoscopic donor nephrectomy alongside the transperitoneal approaches has to be assessed. Preferably the primary endpoint should be the quality of life, with the time of the operation and complications as secondary endpoints.

5.3.4. Minimally invasive open donor nephrectomy

The introduction of laparoscopic approaches has also encouraged refinement of open approaches. Many centers have banned rib resections, replaced classic flank incisions by incisions at other, alternative sites, and currently apply principles of minimally invasive surgery including minimal tissue damage and limited access. These incisions have in common that the incision is located anterior and more medial compared to classic open incisions; the size of the incision is also smaller.

A minimal flank incision most closely correlates to the conventional flank incision. The retroperitoneal cavity is accessed with a smaller incision, varying from 7 cm in lean donors to 15 cm in obese individuals. The oblique and transverse abdominal muscles can be either divided or split. Mechanical retractors allow sufficient access with minimal skin incision. In addition, instruments also used in laparoscopic surgery, including endostaplers, may be used to maintain limited access in case of difficult anatomy i.e. multiple renal vessels. Most Dutch surgeons and urologists use the muscle-split approach when open donor nephrectomy is performed. Because the surgical trauma is limited, these operations result in a shorter hospital stay and less pain compared to conventional open surgery (41). Cosmetic outcome is excellent (Figure 3).

A similar muscle-split approach can be performed in an even more anterior position. This approach may be more difficult initially, because more organs are located between the abdominal muscles and the kidney, but the approach of the renal vessels is potentially easier. A concomitant advantage is that the intercostal nerves that innervate the oblique abdominal muscles are less likely to be injured and abdominal wall function may be superior.

A third option for minimally invasive open donor nephrectomy is a pararectal vertical skin-incision. This incision does not divide muscles but fascia only. This technique leads to superior postoperative results compared to conventional open approaches (57). The technique has only been compared to the classical open approach; there are no reports in which the technique is compared to laparoscopy or another type of mini incision donor nephrectomy (MIDN).

5.3.5. Evidence-based approach in the surgical management

Evidence has mounted that laparoscopic and retroperitoneoscopic approaches are superior to open surgery (58). Two European studies have been published; one from Great Britain and one from the Netherlands (42, 43). These prospective studies aimed to assess the superiority of either the laparoscopic or the minimally invasive open approach (MIDN) (Table 1). Kok et al. concluded that laparoscopic donor nephrectomy results in a better quality of life compared with mini-incision open donor nephrectomy with equal safety and graft function.

A comparative study between laparoscopic and traditional open donor nephrectomy by Oyen et al. from Norway randomized 122 live kidney donors (56). A relatively high complication rate in the laparoscopic group (including various re-operations) and minor differences with regard to postoperative pain, resulted in the cautious conclusion that the laparoscopic approach confers advantages in some donors only, but should not be applied to all donors. The authors suggested limiting laparoscopy to donors of normal weight or mildly overweight only, as complications mainly appeared in obese donors. Longer follow-up of the same Norwegian group confirmed a shorter recovery phase after laparoscopy (59). Various non-randomized studies have led to similar conclusions (60-70). Most of these studies were aimed at the safety and feasibility of the laparoscopic approach and presented laparoscopic donor nephrectomy as an alternative rather than as the preferred technique.

Only two randomized controlled trials comparing hand-assisted laparoscopic and conventional open techniques have been published (71, 72). Both studies compared left-sided hand-assisted laparoscopic donor nephrectomy with conventional open donor nephrectomy (Table 1). In the United States, Wolf et al. randomized 50 donors to either hand-assisted laparoscopic donor nephrectomy or conventional lumbotomy (72). Inclusion criteria included normal weight and interest in the laparoscopic approach. The main conclusion of the authors was that the hand-assisted approach resulted in shorter hospital stays and earlier recovery. Simforoosh et al. performed a comparable study in Iran (71). Donors with overweight (more than 28 kg/m2) and complex renal anatomy were excluded. The donors in this study were relatively young. Again, the hand-assisted laparoscopic approach appeared favorable. The unacceptably high complication rate in the open group (n=100), including 18 donors who sustained a pneumothorax, in this study was remarkable.

Currently, the literature does not provide enough evidence whether or not to use hand-assistance at some stage during laparoscopic donor nephrectomy. About half of the surgeons perform hand-assisted laparoscopic donor nephrectomy. In our aforementioned study we compared open surgery with total laparoscopic surgery, because at that time we did not see the possible benefits of hand-assistance (42). Other authors clearly had this experience (72). A total laparoscopic approach may be even less invasive, but hand-assisted donor nephrectomy may confer benefits such as shorter operation times (71, 73). A comparative study of hand-assisted and total laparoscopic donor nephrectomy is difficult to organize. To assess potential interesting differences in a superiority study, such as the rate of conversion and wound infections, hundreds of donors must be enrolled. Only non-inferiority studies are feasible. Comparative studies assessing the role of (hand-assisted) retroperitoneoscopic kidney donation alongside laparoscopic kidney donation are warranted.

5.4. Improvements in perioperative care

Two factors in live kidney donation may be influenced by improvements in perioperative care. These include postoperative pain and nausea and postoperative donor and recipient creatinine clearance. At our center we currently analyze the role of preoperative infusion of fluids to maintain adequate perfusion of the kidneys of the donor during laparoscopic donor nephrectomy.

For other surgical procedures, epidural anesthesia/analgesia has been reported to significantly reduce perioperative morbidity including ileus, acute renal failure (approximately 30%) and blood loss (approximately 30%), and not only improved analgesic efficacy but also reduced opioid demand and side-effects such as nausea, vomiting and sedation (74-77). The use of thoracic epidural analgesia (TEA) for laparoscopic procedures is becoming more common, especially with colon surgery, where TEA significantly improved early analgesia and had a significant, favorable impact on dietary tolerance and length of stay (77-79). To date, reports describing the effect of epidural analgesia during laparoscopic donor nephrectomy on postoperative pain and nausea have not been published to our knowledge.

Delayed graft function and slower initial graft function have been associated with a higher incidence of acute rejection and have been reported in the past to occur more frequently after laparoscopic donor nephrectomy (80-82). Most studies comparing laparoscopic and open donor nephrectomy observed higher serum creatinine values in recipients of laparoscopically procured kidneys in the first days to weeks following renal transplantation (38, 40, 61, 82-84). As mentioned earlier, studies that reported no differences did often not continuously assess renal function during the first weeks or did not adjust serum creatinine values for possible confounders at baseline (39, 71). Proposed mechanisms resulting in slower recovery of graft function after LDN included mechanical injury to the graft, longer operation time until nephrectomy, longer first warm ischemia time and increased abdominal pressure due to the pneumoperitoneum leading to decreased cardiac output and decreased renal blood flow (40, 85). The predictive value of these findings on graft survival remains unclear as the mean half life of a graft procured from a live donor is much longer than the time elapsed since the first laparoscopic donor nephrectomy by Ratner in 1995 (37).

Retrospective studies at our institution showed that higher recipient serum creatinine values remained present in spite of administration of a sufficient amount of intra-operative fluids (40, 83). Therefore, we hypothesized that not only intra-operative fluid management is important, but also prehydration. An adequate prehydration regimen may indeed improve donor and recipient creatinine clearance. In contrast to earlier findings, kidney function of the donor and recipient is comparable between open and laparoscopic donor nephrectomy after introduction of a fluid regimen with prehydration (86).

5.5. Improvements in follow-up

Fatigue and diminished quality of life may be present until one year after the donation (42, 87, 88). There is a subgroup of donors that does not return to preoperative values. Further studies to characterize these donors are warranted.

Regular follow-up may help donors who do not recover well and donors who have conflicts with their employers with regard to resumption of work. Incidentally we encounter disturbed relationships between donor and recipient. These are recognized early. Professional aid can then be offered if necessary. In our opinion, the transplant community and governmental organizations are obliged to provide help to struggling donors, because they have significantly benefited society.

Expansion of unrelated donation other than spousal donation and non-directed donation may increase the number of disappointed live donors, as the personal advantages for the donor are usually smaller with these types of donation. Further follow-up of these groups of donors in particular is required.

With regard to medical follow-up, donors may be monitored cautiously for hypertension and proteinuria as an expression of renal disease. Although individuals with one kidney do not appear to have an increased chance to develop renal insufficiency, they have a reduced functional reserve. Although most kidney diseases will affect both kidneys, early recognition of deteriorating kidney function may be beneficial in preventing end-stage renal disease and may also be considered a minimal service of society to our kidney donors (58, 89, 90). Follow up of the donors is also needed in order to gather more data regarding the long-term consequences of kidney donation. At our institution we schedule follow-up visits at the nephrology and surgery outpatient clinics at one, three and twelve months and annually thereafter.

6. CONCLUSION AND FUTURE PERSPECTIVES

Live kidney donor transplantation may develop as the most important live-saving procedure and the treatment that offers the best quality of life for patients with renal insufficiency. Further expansion of non-directed kidney donation and renal transplantation across blood group barriers will help those recipients with an incompatible blood group. An increase in pre-emptive transplantation may improve results of renal transplantation and reduce the costs of dialysis. Laparoscopic donor nephrectomy may be applied in the majority of donors and offers the best outcome to the donor with regard to quality of life. Future directions include addressing the position of the retroperitoneoscopic approach, long term outcomes of live kidney donors, in particular hypertensive, older and obese donors, and increasing the number of live kidney donors without compromising safety to the donor or the graft.

7. ACKNOWLEDGEMENTS

The authors equally contributed to this article.

8. REFERENCES

1. Davis CL, Delmonico FL. Living-donor kidney transplantation: a review of the current practices for the live donor. J Am Soc Nephrol 2005;16 (7): 2098-2110.
doi:10.1681/ASN.2004100824

2. Innocenti GR, Wadei HM, Prieto M, Dean PG, Ramos EJ, Textor S, Khamash H, Larson TS, Cosio F, Kosberg K, Fix L, Bauer C, Stegall MD. Preemptive living donor kidney transplantation: do the benefits extend to all recipients? Transplantation 2007;83 (2): 144-149.
doi:10.1097/01.tp.0000250555.46539.65

3. Guild WR, Harrison JH, Merrill JP, Murray J. Successful homotransplantation of the kidney in an identical twin. Trans Am Clin Climatol Assoc 1955;67: 167-173.

4. Kuss R, Teinturier J, Milliez P. (Some attempts at kidney transplantation in man.). Mem Acad Chir (Paris) 1951;77 (22-23-24): 755-764.

5. http://www.transplantatiestichting.nl

6. Kok NF, Weimar W, Alwayn IP, Ijzermans JN. The current practice of live donor nephrectomy in europe. Transplantation 2006;82 (7): 892-897.
doi:10.1097/01.tp.0000235511.19629.0d

7. Perico N, Cattaneo D, Sayegh MH, Remuzzi G. Delayed graft function in kidney transplantation. Lancet 2004;364 (9447): 1814-1827.
doi:10.1016/S0140-6736(04)17406-0

8. Humar A, Ramcharan T, Kandaswamy R, Gillingham K, Payne WD, Matas AJ. Risk factors for slow graft function after kidney transplants: a multivariate analysis. Clin Transplant 2002;16 (6): 425-429.
doi:10.1034/j.1399-0012.2002.02055.x

9. http://www.unos.com

10. Matas AJ, Payne WD, Sutherland DE, Humar A, Gruessner RW, Kandaswamy R, Dunn DL, Gillingham KJ, Najarian JS. 2,500 living donor kidney transplants: a single-center experience. Ann Surg 2001;234 (2): 149-164.
doi:10.1097/00000658-200108000-00004

11. Terasaki PI, Cecka JM, Gjertson DW, Takemoto S. High survival rates of kidney transplants from spousal and living unrelated donors. N Engl J Med 1995;333 (6): 333-336.
doi:10.1056/NEJM199508103330601

12. http://www.eurotransplant.nl

13. de Klerk M, Keizer KM, Claas FH, Witvliet M, Haase-Kromwijk BJ, Weimar W. The Dutch national living donor kidney exchange program. Am J Transplant 2005;5 (9): 2302-2305.
doi:10.1111/j.1600-6143.2005.01024.x

14. Morrissey PE, Dube C, Gohh R, Yango A, Gautam A, Monaco AP. Good samaritan kidney donation. Transplantation 2005;80 (10): 1369-1373.
doi:10.1097/01.tp.0000179153.36227.2d

15. de Klerk M, Witvliet MD, Haase-Kromwijk BJ, Claas FH, Weimar W. A highly efficient living donor kidney exchange program for both blood type and crossmatch incompatible donor-recipient combinations. Transplantation 2006;82 (12): 1616-1620.
doi:10.1097/01.tp.0000250906.66728.8d

16. Roth AE, Sonmez T, Unver MU, Delmonico FL, Saidman SL. Utilizing list exchange and nondirected donation through 'chain' paired kidney donations. Am J Transplant 2006;6 (11): 2694-2705.
doi:10.1111/j.1600-6143.2006.01515.x

17. Waterman AD, Schenk EA, Barrett AC, Waterman BM, Rodrigue JR, Woodle ES, Shenoy S, Jendrisak M, Schnitzler M. Incompatible kidney donor candidates' willingness to participate in donor-exchange and non-directed donation. Am J Transplant 2006;6 (7): 1631-1638.
doi:10.1111/j.1600-6143.2006.01350.x

18. Ishida H, Miyamoto N, Shirakawa H, Shimizu T, Tokumoto T, Ishikawa N, Shimmura H, Setoguchi K, Toki D, Iida S, Teraoka S, Takahashi K, Toma H, Yamaguchi Y, Tanabe K. Evaluation of Immunosuppressive Regimens in ABO-Incompatible Living Kidney Transplantation-Single Center Analysis. Am J Transplant 2007.

19. Norden G, Briggs D, Cockwell P, Lipkin G, Mjornstedt L, Molne J, Ready A, Rydberg L, Samuelsson O, Svalander CT, Breimer ME. ABO-incompatible live donor renal transplantation using blood group A/B carbohydrate antigen immunoadsorption and anti-CD20 antibody treatment. Xenotransplantation 2006;13 (2): 148-153.
doi:10.1111/j.1399-3089.2006.00280.x

20. Delmonico F. A Report of the Amsterdam Forum On the Care of the Live Kidney Donor: Data and Medical Guidelines. Transplantation 2005;79 (6 Suppl): S53-66.
doi:10.1097/01.TP.0000157524.61834.EC

21. Nguyen T, Vazquez M, Toto R. Living kidney donation and hypertension risk. Lancet 2007;369 (9556): 87-88.
doi:10.1016/S0140-6736(07)60046-4

22. Sever MS. Living unrelated-commercial-kidney transplantation: when there is no chance to survive. Pediatr Nephrol 2006;21 (10): 1352-1356.
doi:10.1007/s00467-006-0185-4

23. Choudhry S, Daar AS, Radcliffe Richards J, Guttmann RD, Hoffenberg R, Lock M, Sells RA, Tilney N. Unrelated living organ donation: ULTRA needs to go. J Med Ethics 2003;29 (3): 169-170.
doi:10.1136/jme.29.3.169

24. Levine DZ. Kidney vending: "Yes!" or "No!" Am J Kidney Dis 2000;35 (5): 1002-1018.
doi:10.1016/S0272-6386(00)70280-0

25. Carter JT, Freise CE, McTaggart RA, Mahanty HD, Kang SM, Chan SH, Feng S, Roberts JP, Posselt AM. Laparoscopic procurement of kidneys with multiple renal arteries is associated with increased ureteral complications in the recipient. Am J Transplant 2005;5 (6): 1312-1318.
doi:10.1111/j.1600-6143.2005.00859.x

26. Ames SA, Krol M, Nettar K, Goldman JP, Quinn TM, Herron DM, Pomp A, Bromberg JS. Pre-donation assessment of kidneys by magnetic resonance angiography and venography: accuracy and impact on outcomes. Am J Transplant 2005;5 (6): 1518-1528.
doi:10.1111/j.1600-6143.2005.00884.x

27. Hodgson DJ, Jan W, Rankin S, Koffman G, Khan MS. Magnetic resonance renal angiography and venography: an analysis of 111 consecutive scans before donor nephrectomy. BJU Int 2006;97 (3): 584-586.
doi:10.1111/j.1464-410X.2006.05966.x

28. El Fettouh HA, Herts BR, Nimeh T, Wirth SL, Caplin A, Sands M, Ramani AP, Kaouk J, Goldfarb DA, Gill IS. Prospective comparison of 3-dimensional volume rendered computerized tomography and conventional renal arteriography for surgical planning in patients undergoing laparoscopic donor nephrectomy. J Urol 2003;170 (1): 57-60.
doi:10.1097/01.ju.0000068039.79654.d3

29. el-Diasty TA, Shokeir AA, el-Ghar ME, Gad HM, Refaie AF, el-Din AB. Contrast enhanced spiral computerized tomography in live kidney donors: a single session for anatomical and functional assessment. J Urol 2004;171 (1): 31-34.
doi:10.1097/01.ju.0000099784.52825.8e

30. Feifer AH, Fong BC, Feldman L, Fried G, Stein LA, Metrakos P, Bergman S, Anidjar M. Preoperative evaluation of laparoscopic living renal donors with computerized tomography and its effect on donor morbidity and graft function. Can J Urol 2005;12 (3): 2713-2721.

31. Janoff DM, Davol P, Hazzard J, Lemmers MJ, Paduch DA, Barry JM. Computerized tomography with 3-dimensional reconstruction for the evaluation of renal size and arterial anatomy in the living kidney donor. J Urol 2004;171 (1): 27-30.
doi:10.1097/01.ju.0000100084.59864.8f

32. Johnson JE, Loveday EJ, Archer LJ, Lear P, Thornton MJ. Preoperative evaluation of live renal donors using multislice CT angiography. Clin Radiol 2005;60 (7): 771-777.
doi:10.1016/j.crad.2004.12.007

33. Sahani DV, Rastogi N, Greenfield AC, Kalva SP, Ko D, Saini S, Harris G, Mueller PR. Multi-detector row CT in evaluation of 94 living renal donors by readers with varied experience. Radiology 2005;235 (3): 905-910.
doi:10.1148/radiol.2353040496

34. Hussain SM, Kock MC, JN IJ, Pattynama PM, Hunink MG, Krestin GP. MR imaging: a "one-stop shop" modality for preoperative evaluation of potential living kidney donors. Radiographics 2003;23 (2): 505-520.
doi:10.1148/rg.232025063

35. Bjorkman H, Eklof H, Wadstrom J, Andersson LG, Nyman R, Magnusson A. Split renal function in patients with suspected renal artery stenosis: a comparison between gamma camera renography and two methods of measurement with computed tomography. Acta Radiol 2006;47 (1): 107-113.
doi:10.1080/02841850500406787

36. Kok NF, Alwayn IP, Schouten O, Tran KT, Weimar W, Ijzermans JN. Mini-incision open donor nephrectomy as an alternative to classic lumbotomy: evolution of the open approach. Transpl Int 2006;19 (6): 500-505.
doi:10.1111/j.1432-2277.2006.00324.x

37. Ratner LE, Ciseck LJ, Moore RG, Cigarroa FG, Kaufman HS, Kavoussi LR. Laparoscopic live donor nephrectomy. Transplantation 1995;60 (9): 1047-1049.

38. Nogueira JM, Cangro CB, Fink JC, Schweitzer E, Wiland A, Klassen DK, Gardner J, Flowers J, Jacobs S, Cho E, Philosophe B, Bartlett ST, Weir MR. A comparison of recipient renal outcomes with laparoscopic versus open live donor nephrectomy. Transplantation 1999;67 (5): 722-728.
doi:10.1097/00007890-199903150-00014

39. Hazebroek EJ, Gommers D, Schreve MA, van Gelder T, Roodnat JI, Weimar W, Bonjer HJ, JN IJ. Impact of intraoperative donor management on short-term renal function after laparoscopic donor nephrectomy. Ann Surg 2002;236 (1): 127-132.
doi:10.1097/00000658-200207000-00019

40. Kok NF, Alwayn IP, Lind MY, Tran KT, Weimar W, JN IJ. Donor nephrectomy: mini-incision muscle-splitting open approach versus laparoscopy. Transplantation 2006;81 (6): 881-887.
doi:10.1097/01.tp.0000203320.74256.fd

41. Derweesh IH, Goldfarb DA, Abreu SC, Goel M, Flechner SM, Modlin C, Zhou L, Streem SB, Novick AC, Gill IS. Laparoscopic live donor nephrectomy has equivalent early and late renal function outcomes compared with open donor nephrectomy. Urology 2005;65 (5): 862-866.
doi:10.1016/j.urology.2004.11.051

42. Kok NF, Lind MY, Hansson BM, Pilzecker D, Mertens zur Borg IR, Knipscheer BC, Hazebroek EJ, Dooper IM, Weimar W, Hop WC, Adang EM, van der Wilt GJ, Bonjer HJ, van der Vliet JA, JN IJ. Comparison of laparoscopic and mini incision open donor nephrectomy: single blind, randomised controlled clinical trial. Bmj 2006;333 (7561): 221.
doi:10.1136/bmj.38886.618947.7C

43. Lewis GR, Brook NR, Waller JR, Bains JC, Veitch PS, Nicholson ML. A comparison of traditional open, minimal-incision donor nephrectomy and laparoscopic donor nephrectomy. Transpl Int 2004;17 (10): 589-595.
doi:10.1111/j.1432-2277.2004.tb00391.x

44. Oyen O, Andersen M, Mathisen L, Kvarstein G, Edwin B, Line PD, Scholz T, Pfeffer PF. Laparoscopic versus open living-donor nephrectomy: experiences from a prospective, randomized, single-center study focusing on donor safety. Transplantation 2005;79 (9): 1236-1240.
doi:10.1097/01.TP.0000161669.49416.BA

45. Leventhal JR, Kocak B, Salvalaggio PR, Koffron AJ, Baker TB, Kaufman DB, Fryer JP, Abecassis MM, Stuart FP. Laparoscopic donor nephrectomy 1997 to 2003: lessons learned with 500 cases at a single institution. Surgery 2004;136 (4): 881-890.
doi:10.1016/j.surg.2004.06.025

46. Melcher ML, Carter JT, Posselt A, Duh QY, Stoller M, Freise CE, Kang SM. More than 500 consecutive laparoscopic donor nephrectomies without conversion or repeated surgery. Arch Surg 2005;140 (9): 835-839; discussion 839-840.
doi:10.1001/archsurg.140.9.835

47. Su LM, Ratner LE, Montgomery RA, Jarrett TW, Trock BJ, Sinkov V, Bluebond-Langner R, Kavoussi LR. Laparoscopic live donor nephrectomy: trends in donor and recipient morbidity following 381 consecutive cases. Ann Surg 2004;240 (2): 358-363.
doi:10.1097/01.sla.0000133351.98195.1c

48. Martin GL, Guise AI, Bernie JE, Bargman V, Goggins W, Sundaram CP. Laparoscopic donor nephrectomy: effects of learning curve on surgical outcomes. Transplant Proc 2007;39 (1): 27-29.
doi:10.1016/j.transproceed.2006.10.006

49. Maartense S, Idu M, Bemelman FJ, Balm R, Surachno S, Bemelman WA. Hand-assisted laparoscopic live donor nephrectomy. Br J Surg 2004;91 (3): 344-348.
doi:10.1002/bjs.4432

50. Bargman V, Sundaram CP, Bernie J, Goggins W. Randomized trial of laparoscopic donor nephrectomy with and without hand assistance. J Endourol 2006;20 (10): 717-722.
doi:10.1089/end.2006.20.717

51. Tanabe K, Miyamoto N, Ishida H, Tokumoto T, Shirakawa H, Yamamoto H, Kondo T, Okuda H, Shimmura H, Ishikawa N, Nozaki T, Toma H. Retroperitoneoscopic live donor nephrectomy (RPLDN): establishment and initial experience of RPLDN at a single center. Am J Transplant 2005;5 (4 Pt 1): 739-745.
doi:10.1111/j.1600-6143.2004.00702.x

52. Wadstrom J. Hand-assisted retroperitoneoscopic live donor nephrectomy: experience from the first 75 consecutive cases. Transplantation 2005;80 (8): 1060-1066.
doi:10.1097/01.tp.0000176477.81591.6f

53. Bachmann A, Wolff T, Ruszat R, Giannini O, Dickenmann M, Gurke L, Steiger J, Gasser TC, Stief CG, Sulser T. Retroperitoneoscopic donor nephrectomy: a retrospective, non-randomized comparison of early complications, donor and recipient outcome with the standard open approach. Eur Urol 2005;48 (1): 90-96; discussion 96.
doi:10.1016/j.eururo.2005.03.007

54. Gjertsen H, Sandberg AK, Wadstrom J, Tyden G, Ericzon BG. Introduction of hand-assisted retroperitoneoscopic living donor nephrectomy at Karolinska University Hospital Huddinge. Transplant Proc 2006;38 (8): 2644-2645.
doi:10.1016/j.transproceed.2006.07.042

55. Maartense S, Heintjes RJ, Idu M, Bemelman FJ, Bemelman WA. Renal artery clip dislodgement during hand-assisted laparoscopic living donor nephrectomy. Surg Endosc 2003;17 (11): 1851.
doi:10.1007/s00464-003-4230-0

56. Oyen O, Line PD, Pfeffer P, Edwin B, Jorgensen PF, Foss A, Lien B, Bentdal O, Husberg B, Brekke IB. Laparoscopic living donor nephrectomy: introduction of simple hand-assisted technique (without handport). Transplant Proc 2003;35 (2): 779-781.
doi:10.1016/S0041-1345(03)00040-X

57. Neipp M, Jackobs S, Becker T, zu Vilsendorf AM, Winny M, Lueck R, Klempnauer J, Nashan B. Living donor nephrectomy: flank incision versus anterior vertical mini-incision. Transplantation 2004;78 (9): 1356-1361.
doi:10.1097/01.TP.0000140975.96729.A7

58. Tooher RL, Rao MM, Scott DF, Wall DR, Francis DM, Bridgewater FH, Maddern GJ. A systematic review of laparoscopic live-donor nephrectomy. Transplantation 2004;78 (3): 404-414.
doi:10.1097/01.TP.0000128638.85491.76

59. Andersen MH, Mathisen L, Oyen O, Edwin B, Digernes R, Kvarstein G, Tonnessen TI, Wahl AK, Hanestad BR, Fosse E. Postoperative pain and convalescence in living kidney donors-laparoscopic versus open donor nephrectomy: a randomized study. Am J Transplant 2006;6 (6): 1438-1443.
doi:10.1111/j.1600-6143.2006.01301.x

60. Velidedeoglu E, Williams N, Brayman KL, Desai NM, Campos L, Palanjian M, Wocjik M, Bloom R, Grossman RA, Mange K, Barker CF, Naji A, Markmann JF. Comparison of open, laparoscopic, and hand-assisted approaches to live-donor nephrectomy. Transplantation 2002;74 (2): 169-172.
doi:10.1097/00007890-200207270-00005

61. Flowers JL, Jacobs S, Cho E, Morton A, Rosenberger WF, Evans D, Imbembo AL, Bartlett ST. Comparison of open and laparoscopic live donor nephrectomy. Ann Surg 1997;226 (4): 483-489; discussion 489-490.
doi:10.1097/00000658-199710000-00009

62. Lennerling A, Blohme I, Ostraat O, Lonroth H, Olausson M, Nyberg G. Laparoscopic or open surgery for living donor nephrectomy. Nephrol Dial Transplant 2001;16 (2): 383-386.
doi:10.1093/ndt/16.2.383

63. Hawasli A, Boutt A, Cousins G, Schervish E, Oh H. Laparoscopic versus conventional live donor nephrectomy: experience in a community transplant program. Am Surg 2001;67 (4): 342-345.

64. Kumar A, Dubey D, Gogoi S, Arvind NK. Laparoscopy-assisted live donor nephrectomy: a modified cost-effective approach for developing countries. J Endourol 2002;16 (3): 155-159.
doi:10.1089/089277902753716115

65. Wolf JS, Jr., Marcovich R, Merion RM, Konnak JW. Prospective, case matched comparison of hand assisted laparoscopic and open surgical live donor nephrectomy. J Urol 2000;163 (6): 1650-1653.
doi:10.1097/00005392-200006000-00005

66. Rawlins MC, Hefty TL, Brown SL, Biehl TR. Learning laparoscopic donor nephrectomy safely: a report on 100 cases. Arch Surg 2002;137 (5): 531-534; discussion 534-535.
doi:10.1001/archsurg.137.5.531

67. Leventhal JR, Deeik RK, Joehl RJ, Rege RV, Herman CH, Fryer JP, Kaufman D, Abecassis M, Stuart FP. Laparoscopic live donor nephrectomy--is it safe? Transplantation 2000;70 (4): 602-606.
doi:10.1097/00007890-200008270-00012

68. Stifelman MD, Hull D, Sosa RE, Su LM, Hyman M, Stubenbord W, Shichman S. Hand assisted laparoscopic donor nephrectomy: a comparison with the open approach. J Urol 2001;166 (2): 444-448.
doi:10.1016/S0022-5347(05)65960-5

69. Simforoosh N, Bassiri A, Ziaee SA, Tabibi A, Salim NS, Pourrezagholi F, Moghaddam SM, Maghsoodi R, Shafi H. Laparoscopic versus open live donor nephrectomy: the first randomized clinical trial. Transplant Proc 2003;35 (7): 2553-2554.
doi:10.1016/j.transproceed.2003.08.062

70. Buell JF, Hanaway MJ, Potter SR, Cronin DC, Yoshida A, Munda R, Alexander JW, Newell KA, Bruce DS, Woodle ES. Hand-assisted laparoscopic living-donor nephrectomy as an alternative to traditional laparoscopic living-donor nephrectomy. Am J Transplant 2002;2 (10): 983-988.
doi:10.1034/j.1600-6143.2002.21017.x

71. Wolf JS, Jr., Merion RM, Leichtman AB, Campbell DA, Jr., Magee JC, Punch JD, Turcotte JG, Konnak JW. Randomized controlled trial of hand-assisted laparoscopic versus open surgical live donor nephrectomy. Transplantation 2001;72 (2): 284-290.
doi:10.1097/00007890-200107270-00021

72. Simforoosh N, Basiri A, Tabibi A, Shakhssalim N, Hosseini Moghaddam SM. Comparison of laparoscopic and open donor nephrectomy: a randomized controlled trial. BJU Int 2005;95 (6): 851-855.
doi:10.1111/j.1464-410X.2005.05415.x

73. Kokkinos C, Nanidis T, Antcliffe D, Darzi AW, Tekkis P, Papalois V. Comparison of laparoscopic versus hand-assisted live donor nephrectomy. Transplantation 2007;83 (1): 41-47.
doi:10.1097/01.tp.0000248761.56724.9c

74. Friedman AL, Peters TG, Jones KW, Boulware LE, Ratner LE. Fatal and Nonfatal Hemorrhagic Complications of Living Kidney Donation. Ann Surg 2006;243 (1): 126-130.
doi:10.1097/01.sla.0000193841.43474.ec

75. Moraca RJ, Sheldon DG, Thirlby RC. The role of epidural anesthesia and analgesia in surgical practice. Ann Surg 2003;238 (5): 663-673.
doi:10.1097/01.sla.0000094300.36689.ad

76. Bonnet F, Marret E. Influence of anaesthetic and analgesic techniques on outcome after surgery. Br J Anaesth 2005;95 (1): 52-58.
doi:10.1093/bja/aei038

77. Dunet F, Pfister C, Deghmani M, Meunier Y, Demeilliers-Pfister G, Grise P. Clinical results of combined epidural and general anesthesia procedure in radical prostatectomy management. Can J Urol 2004;11 (2): 2200-2204.

78. Kozian A, Schilling, Th., Hachenberg, Th. Non-analgetic effects of thoraic epidural anaesthesia. Curr Opin Anesthesiol 2005;18: 29-34.
doi:10.1097/00001503-200502000-00006

79. Senagore AJ, Whalley D, Delaney CP, Mekhail N, Duepree HJ, Fazio VW. Epidural anesthesia-analgesia shortens length of stay after laparoscopic segmental colectomy for benign pathology. Surgery 2001;129 (6): 672-676.
doi:10.1067/msy.2001.114648

80. Senagore AJ, Delaney CP, Mekhail N, Dugan A, Fazio VW. Randomized clinical trial comparing epidural anaesthesia and patient-controlled analgesia after laparoscopic segmental colectomy. Br J Surg 2003;90 (10): 1195-1199.
doi:10.1002/bjs.4223

81. Brennan TV, Freise CE, Fuller TF, Bostrom A, Tomlanovich SJ, Feng S. Early graft function after living donor kidney transplantation predicts rejection but not outcomes. Am J Transplant 2004;4 (6): 971-979.
doi:10.1111/j.1600-6143.2004.00441.x

82. Troppmann C, Ormond DB, Perez RV. Laparoscopic (vs open) live donor nephrectomy: a UNOS database analysis of early graft function and survival. Am J Transplant 2003;3 (10): 1295-1301.
doi:10.1046/j.1600-6143.2003.00216.x

83. Ratner LE, Montgomery RA, Maley WR, Cohen C, Burdick J, Chavin KD, Kittur DS, Colombani P, Klein A, Kraus ES, Kavoussi LR. Laparoscopic live donor nephrectomy: the recipient. Transplantation 2000;69 (11): 2319-2323.
doi:10.1097/00007890-200006150-00016

84. Lind MY, Zur Borg IM, Hazebroek EJ, Hop WC, Alwayn IP, Weimar W, Ijzermans JN. The effect of laparoscopic and open donor nephrectomy on the long-term renal function in donor and recipient: a retrospective study. Transplantation 2005;80 (5): 700-703.
doi:10.1097/01.tp.0000172219.10178.0d

85. Goel MC, Modlin CS, Mottoo AM, Derweesh IH, Flechner SM, Streem S, Gill I, Goldfarb DA, Novick AC. Fate of donor kidney: laparoscopic versus open technique. J Urol 2004;172 (6 Pt 1): 2326-2330.
doi:10.1097/01.ju.0000144716.30222.12

86. London ET, Ho HS, Neuhaus AM, Wolfe BM, Rudich SM, Perez RV. Effect of intravascular volume expansion on renal function during prolonged CO2 pneumoperitoneum. Ann Surg 2000;231 (2): 195-201.
doi:10.1097/00000658-200002000-00007

87. Mertens zur Borg IR, Kok NF, Lambrou G, Jonsson D, Alwayn IP, Tran KT, Weimar W, Ijzermans JN, Gommers D. Beneficial effects of a new fluid regime on kidney function of donor and recipient during laparoscopic v open donor nephrectomy. J Endourol 2007;21 (12): 1509-1515.
doi:10.1089/end.2007.0026

88. Smith GC, Trauer T, Kerr PG, Chadban SJ. Prospective psychosocial monitoring of living kidney donors using the Short Form-36 health survey: results at 12 months. Transplantation 2004;78 (9): 1384-1389.
doi:10.1097/01.TP.0000140967.34029.F1

89. Kok NF, Alwayn IP, Tran KT, Hop WC, Weimar W, Ijzermans JN. Psychosocial and physical impairment after mini-incision open and laparoscopic donor nephrectomy: A prospective study. Transplantation 2006;82 (10): 1291-1297.
doi:10.1097/01.tp.0000239312.45050.05

90. Jordan J, Sann U, Janton A, Gossmann J, Kramer W, Kachel HG, Wilhelm A, Scheuermann E. Living kidney donors' long-term psychological status and health behavior after nephrectomy - a retrospective study. J Nephrol 2004;17 (5): 728-735.

91. Minz M, Udgiri N, Sharma A, Heer MK, Kashyap R, Nehra R, Sakhuja V. Prospective psychosocial evaluation of related kidney donors: Indian perspective. Transplant Proc 2005;37 (5): 2001-2003.
doi:10.1016/j.transproceed.2005.03.110

Key Words: Living Donors, Quality Of Life, Minimally Invasive, Cost-Effectiveness, Laparoscopic Donor Nephrectomy, Cross-Over, ABO incompatibility, Review

Send correspondence to: Jan Nicolaas IJzermans, Department of Surgery, Erasmus MC, PO BOX 2040, 3000 CA Rotterdam, The Netherlands, Phone number: 0031-10-7033733, Fax : 0031-10-7035615, E-mail:j.ijzermans@erasmusmc.nl