anesthesia for prostate biopsy

1
Anesthesia for Prostate Biopsy TO THE EDITOR: Kudos to Dr. Soloway 1 for clearly expressing the concept of maximal patient comfort during a procedure that has several givens—the rectal penetration is uncomfortable, the biopsies are painful, and the overall experience and potential outcome is frightening. I have found that in ad- dition to the prostate nerve block, the use of oral diazepam (10 mg) 1 hour before the procedure is useful in terms of easing anxiety and facilitating sphincteric relaxation and thus placement of the probe. What has also proven ex- tremely helpful is that on the day that the decision is made to pursue the prostate ultrasound and biopsy, the patient is walked down the hallway and introduced to the ultrasound technologist who will be assisting me who, in turn, shows the patient the ultrasound machine and biopsy room and reviews the entire process, in order to familiarize the pa- tient with the procedure and help assuage fears. It behooves us to treat all of our patients the way we would want our parents, siblings, children, spouses, and ourselves treated. REFERENCE 1. Soloway MS: Do unto others—why I would want anes- thesia for my prostate biopsy. Urology 62: 973–975, 2003. Andrew Siegel, M.D. Hackensack, New Jersey doi:10.1016/j.urology.2004.01.031 Prostate Cancer Cells: Detection and Isolation from Peripheral Blood and Bone Marrow TO THE EDITOR: In their article, Ellis and colleagues 1 speak vaguely of time spans in prostate cancer, as though the cell kinetics were not known. They refer to “late,” “more than 5 years after surgery,” and “long-term dormancy.” In fact, the ki- netics of prostate cancer is known with precision. Berges et al. told us that the doubling time of the primary was 475 days. This figure yielded, via the formula for compound interest, a 52-year history from the fatal chromosomal er- ror to death at 1000 cm 3 of total cancer. 2 We know also from the formula that at the time of radical prostatectomy, assuming an average cancer volume of 2.5 cm 3 and that metastases start at a diameter of 2 mm, 3 metastases have been occurring for 12 years. The mean time to death for T1c prostate cancer has been determined to be 17.5 years. 4 Excess mortality due to prostate cancer in men who have survived 10 years ceases at 20 to 23 years. 5 It is probably true that most of these cytokeratin-positive cells die in the marrow without establishing a “foothold.” The high apoptotic rate of some cancers has been known since the early 1970s. 6 However, it is surely equally true that not all die. Everybody has a story of how indolent the disease can be. 7 Surely these bone marrow results cry for acknowledgment that total prostatectomy, however prac- ticed, is a cytoreductive procedure, not cancer sterilizing. REFERENCES 1. Ellis WJ, Pfitzenmaier J, Colli J, et al: Detection and iso- lation of prostate cancer cells from peripheral blood and bone marrow. Urology 61: 277–281, 2003. 2. Berges RR, Vukanovic J, Epstein JI, et al: Implications of cell kinetic changes during the progression of human prostatic cancer. Clin Cancer Res 1:473– 480, 1995. 3. Li CY, Shan S, Cao Y, et al: Role of incipient angiogenesis in cancer metastasis. Cancer and Metastasis Rev 19: 7–11, 2000. 4. Horan AH, and McGehee M: Mean time to death of ap- parently clinically localized prostate cancer: implications for cut-off ages for PSA screening and ablative therapy. Br J Urol 39: 1063–1066, 2000. 5. Adolfsson J, Rutquist LE, and Steinbeck G: Prostate car- cinoma and long term survival. Cancer 80: 748–752, 1997. 6. Charbit A, Malaies EP, and Tubiana M: Relation between the pathological nature and growth rate of human tumors. Eur J Cancer 7: 307–315, 1971. 7. Grabstaid H, Chabon A, and McSherry C: Prostate can- cer: unusual metastases 20 years after 125 brachytherapy. J Urol 154: 203–204, 1995. Anthony H. Horan, M.D. Evanston, Wyoming doi:10.1016/j.urology.2003.03.001 Suprapubic Stab Cystostomy TO THE EDITOR: We read with great interest the article by Lawrentschuk et al. 1 They propose a safe combination of ultrasonography and flexible cystoscopy for suprapubic catheter insertion. In the article they state that the use of flexible cystoscopy for supra- pubic catheter insertion has not been previously discussed. Alagiri and Seidmon 2 described in 1998 a simple tech- nique based on the principle of the percutaneous endo- scopic gastrostomy procedure. They called the method percutaneous endoscopic cystostomy: the bladder dome and its relative position on the lower abdomen are localized using a flexible cystoscope, light source, and abdominal palpation. This reference was not credited in the article by Lawrentschuk et al. We routinely use ultrasonography with or without flex- ible cystoscopy in difficult cases of suprapubic tube inser- tion and we agree with Lawrentschuk and colleagues 1 that the combination of ultrasound and flexible cystoscopy is the safest technique for percutaneous cystostomy. LETTERS TO THE EDITOR © 2004 ELSEVIER INC. ALL RIGHTS RESERVED UROLOGY 64: 187–191, 2004 • 0090-4295/04/$30.00 187

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Page 1: Anesthesia for prostate biopsy

Anesthesia for Prostate Biopsy

TO THE EDITOR:

Kudos to Dr. Soloway1 for clearly expressing the conceptof maximal patient comfort during a procedure that hasseveral givens—the rectal penetration is uncomfortable,the biopsies are painful, and the overall experience andpotential outcome is frightening. I have found that in ad-dition to the prostate nerve block, the use of oral diazepam(10 mg) 1 hour before the procedure is useful in terms ofeasing anxiety and facilitating sphincteric relaxation andthus placement of the probe. What has also proven ex-tremely helpful is that on the day that the decision is madeto pursue the prostate ultrasound and biopsy, the patient iswalked down the hallway and introduced to the ultrasoundtechnologist who will be assisting me who, in turn, showsthe patient the ultrasound machine and biopsy room andreviews the entire process, in order to familiarize the pa-tient with the procedure and help assuage fears.

It behooves us to treat all of our patients the way wewould want our parents, siblings, children, spouses, andourselves treated.

REFERENCE1. Soloway MS: Do unto others—why I would want anes-

thesia for my prostate biopsy. Urology 62: 973–975, 2003.

Andrew Siegel, M.D.Hackensack, New Jersey

doi:10.1016/j.urology.2004.01.031

Prostate Cancer Cells: Detection andIsolation from Peripheral Blood andBone Marrow

TO THE EDITOR:

In their article, Ellis and colleagues1 speak vaguely oftime spans in prostate cancer, as though the cell kineticswere not known. They refer to “late,” “more than 5 yearsafter surgery,” and “long-term dormancy.” In fact, the ki-netics of prostate cancer is known with precision. Berges etal. told us that the doubling time of the primary was 475days. This figure yielded, via the formula for compoundinterest, a 52-year history from the fatal chromosomal er-ror to death at 1000 cm3 of total cancer.2 We know alsofrom the formula that at the time of radical prostatectomy,assuming an average cancer volume of 2.5 cm3 and thatmetastases start at a diameter of 2 mm,3 metastases havebeen occurring for 12 years. The mean time to death forT1c prostate cancer has been determined to be 17.5 years.4

Excess mortality due to prostate cancer in men who havesurvived 10 years ceases at 20 to 23 years.5

It is probably true that most of these cytokeratin-positivecells die in the marrow without establishing a “foothold.”The high apoptotic rate of some cancers has been knownsince the early 1970s.6 However, it is surely equally truethat not all die. Everybody has a story of how indolent thedisease can be.7 Surely these bone marrow results cry foracknowledgment that total prostatectomy, however prac-ticed, is a cytoreductive procedure, not cancer sterilizing.

REFERENCES1. Ellis WJ, Pfitzenmaier J, Colli J, et al: Detection and iso-

lation of prostate cancer cells from peripheral blood and bonemarrow. Urology 61: 277–281, 2003.

2. Berges RR, Vukanovic J, Epstein JI, et al: Implications ofcell kinetic changes during the progression of human prostaticcancer. Clin Cancer Res 1:473–480, 1995.

3. Li CY, Shan S, Cao Y, et al: Role of incipient angiogenesisin cancer metastasis. Cancer and Metastasis Rev 19: 7–11,2000.

4. Horan AH, and McGehee M: Mean time to death of ap-parently clinically localized prostate cancer: implications forcut-off ages for PSA screening and ablative therapy. Br J Urol39: 1063–1066, 2000.

5. Adolfsson J, Rutquist LE, and Steinbeck G: Prostate car-cinoma and long term survival. Cancer 80: 748–752, 1997.

6. Charbit A, Malaies EP, and Tubiana M: Relation betweenthe pathological nature and growth rate of human tumors. EurJ Cancer 7: 307–315, 1971.

7. Grabstaid H, Chabon A, and McSherry C: Prostate can-cer: unusual metastases 20 years after 125 brachytherapy.J Urol 154: 203–204, 1995.

Anthony H. Horan, M.D.Evanston, Wyoming

doi:10.1016/j.urology.2003.03.001

Suprapubic Stab Cystostomy

TO THE EDITOR:

We read with great interest the article by Lawrentschuk etal.1 They propose a safe combination of ultrasonography andflexible cystoscopy for suprapubic catheter insertion. In thearticle they state that the use of flexible cystoscopy for supra-pubic catheter insertion has not been previously discussed.

Alagiri and Seidmon2 described in 1998 a simple tech-nique based on the principle of the percutaneous endo-scopic gastrostomy procedure. They called the methodpercutaneous endoscopic cystostomy: the bladder domeand its relative position on the lower abdomen are localizedusing a flexible cystoscope, light source, and abdominalpalpation. This reference was not credited in the article byLawrentschuk et al.

We routinely use ultrasonography with or without flex-ible cystoscopy in difficult cases of suprapubic tube inser-tion and we agree with Lawrentschuk and colleagues1 thatthe combination of ultrasound and flexible cystoscopy isthe safest technique for percutaneous cystostomy.

LETTERS TO THE EDITOR

© 2004 ELSEVIER INC.ALL RIGHTS RESERVED UROLOGY 64: 187–191, 2004 • 0090-4295/04/$30.00 187