|
INTRAOPERATIVE
CELL SALVAGE DURING RADICAL PROSTATECTOMY: A SAFE TECHNIQUE FOR JEHOVAH’S
WITNESSES ALAN M. NIEDER, MICHAEL A. SIMON, SANDY S. KIM, MURUGESAN MANOHARAN, MARK S. SOLOWAY Department of Urology, University of Miami School of Medicine, Miami, Florida, USA ABSTRACT Radical retropubic prostatectomy (RRP) is an operation historically associated with the potential for significant blood loss. Patients who refuse a blood transfusion, such as Jehovah’s witnesses, may be only offered radiation therapy as potentially curative treatment for prostate cancer because of the potential for a transfusion. Intraoperative cell salvage (IOCS) is an effective blood management strategy for patients who are not willing to accept predonated autologous or allergenic blood. We present our management for Jehovah’s Witness patients with clinically localized prostate cancer, emphasizing our blood management approach. This is the first such report. Key
words: prostate cancer, prostatectomy, cell salvage, Jehovah’s
witness INTRODUCTION Radical
retropubic prostatectomy (RRP) is an operation, which may be associated
with significant blood loss. Variability in anatomy, difficulty in controlling
the dorsal venous complex, nerve sparing vs. non-nerve sparing, obesity,
and surgeon experience may all affect the estimated blood loss (EBL).
The mean EBL during RRP has been reported up to 1800 mL in previous series
(1). Even in contemporary series, the EBL ranges from 770 mL (2) to 1575
mL (3). Some patients may require a blood transfusion, either allogeneic
or autologous. Different means of managing blood loss include preoperative
donation of autologous blood (4), preoperative recombinant erythropoeitin
injection (5), intraoperative hemodilution (6), and intraoperative cell
salvage (IOCS) (7). IOCS is an attractive blood management strategy since
it is relatively inexpensive and prevents the risks associated with allogeneic
blood transfusion such as viral infection. For those patients who refuse
any blood transfusions on religious grounds, IOCS may by the only safe
method of blood management during RRP. CASE REPORTS Case 1 A
53-year-old gentleman was referred to our institution with clinical stage
T1c prostate cancer. The patient’s PSA was 4.5 ng/mL, and a prostate
biopsy revealed Gleason 6 prostate cancer in 4 of 10 cores. The prostate
was 30g and soft without nodules. The patient had previously been seen
by another urologist who refused to perform a RRP because the patient’s
avowed refusal of all blood products, secondary to his religious beliefs
as a Jehovah’s Witness. The patient was offered radiation therapy;
however, he preferred RRP. Case 2 A
45-year-old Jehovah’s Witness was referred to our institution with
clinical stage T1c prostate cancer (PSA 8.5, Gleason 6, small focus, 50g
soft prostate without nodules.). He refused any blood transfusion but
accepted the use of IOCS. The patient underwent a bilateral nerve-sparing
RRP under spinal anesthesia without complications. Case 3 A 68-year-old Jehovah’s Witness was referred to our institution with clinical stage T2b prostate cancer (PSA 10, Gleason 7 in multiple cores, 40 g prostate with bilateral induration). He refused any blood transfusion but accepted the use of IOCS. The patient underwent a bilateral nerve-sparing RRP under spinal anesthesia without complications. IOCS was available during the case; however, the EBL was 300 cc and he did not receive any cell-salvaged blood. His pathology revealed Gleason 7 prostate cancer, stage pT2b with negative margins. His PSA is undetectable and he is continent 3 months postoperatively. COMMENTS Oncologic
surgeons have been hesitant to embrace IOCS primarily because of a theoretical
risk of tumor dissemination. Ward et al. demonstrated that malignant prostatic
cells could be identified in cytological washings during RRP (9). However,
several studies have demonstrated the safety of IOCS during urological
oncology procedures (10,11). We do not believe that there is a significant,
if any, risk of tumor dissemination from IOCS. Davis et al. demonstrated
no difference in the risk of biochemical recurrence with the use of IOCS
in 408 patients undergoing RRP at our institution (8). Eighty-seven patients
who received cell-salvaged blood, 264 who received only an autologous
transfusion, and 57 who received no transfusions were compared. Biochemical
recurrence was detected in 67 patients (16%) and was not significantly
associated with the method of transfusion (chi-square, p = 0.784). In
a more updated analysis involving over 1,000 patients who underwent RRP
at the University of Miami School of Medicine, the 5-year PSA-recurrence
risk for those who did and did not receive cell-salvaged blood was 15%
and 18%, respectively (p = 0.76). In this large series, the risk of receiving
an allogeneic transfusion was 0.9%. CONCLUSION We present the first cases in the literature describing the use of IOCS during RRP for Jehovah’s Witnesses. IOCS enables these patients to safely undergo RRP without the need for blood transfusion. We do not believe that there is an increased risk of tumor dissemination by utilizing IOCS during RRP. We have IOCS available for RRP and other urologic oncology operations in which there is a potential for significant blood loss. REFERENCES
__________________________ _______________________ |