Skip to main content
Journal of the Royal Society of Medicine logoLink to Journal of the Royal Society of Medicine
. 1989 Dec;82(12):725–728. doi: 10.1177/014107688908201208

Metabolic effects of prostatectomy.

P A Hamilton Stewart 1, I M Barlow 1
PMCID: PMC1292414  PMID: 2614764

Abstract

Transurethral resection syndrome (TURS), complicating transurethral resection of the prostate (TURP) has been ascribed to hyponatraemia but reports have indicated that hyperammonaemia following metabolism of glycine can be the main cause. Prospective data has been collected on 96 prostatectomy patients (82 TURP and 14 retropubic). The retropubic group showed no significant postoperative change in the serum sodium or plasma ammonia. Of the TURP group, no TURS occurred although hyponatraemia was noted in 32 patients. The weight of prostate resected, the volume of glycine used, the time taken and the plasma ammonia levels were not significantly different in the normonatraemic or hyponatraemic groups. In severely hyponatraemic patients (13 out of 32 with a 10 mmol/l, or greater, decrease in serum sodium) there was a significant rise (P less than 0.05) in plasma ammonia, 1 or 4 h post TURP, which had decreased by 24 h. There was a highly significant increase in serum glycine level in the hyponatraemic compared with the normonatraemic group (P less than 0.001). There was no correlation between serum glycine and plasma ammonia levels in the normonatraemic or hyponatraemic group. There were nine patients with post TURP plasma ammonia levels greater than 100 mumol/l (mean 254) who experienced no mental confusion: six of these patients were hyponatraemic. The weight of prostate resected (mean 26 g), volume of glycine used (mean 181) and operation time (mean 39 min) were all relatively low. Subsequently, TURS has occurred in a patient, with severe hyponatraemia and hyperglycinaemia but no hyperammonaemia. This study shows that hyperammonaemia does not always correlate with hyponatraemia or hyperglycinaemia, and high plasma ammonia levels can occur in the absence of TURS.

Full text

PDF
725

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bartter F. C., Schwartz W. B. The syndrome of inappropriate secretion of antidiuretic hormone. Am J Med. 1967 May;42(5):790–806. doi: 10.1016/0002-9343(67)90096-4. [DOI] [PubMed] [Google Scholar]
  2. Decaux G., Waterlot Y., Genette F., Hallemans R., Demanet J. C. Inappropriate secretion of antidiuretic hormone treated with frusemide. Br Med J (Clin Res Ed) 1982 Jul 10;285(6335):89–90. doi: 10.1136/bmj.285.6335.89. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Drayna C. J., Titcomb C. P., Varma R. R., Soergel K. H. Hyperammonemic encephalopathy caused by infection in a neurogenic bladder. N Engl J Med. 1981 Mar 26;304(13):766–768. doi: 10.1056/NEJM198103263041307. [DOI] [PubMed] [Google Scholar]
  4. Glasgow J. F., Hicks E. M., Jenkins J. G., Keilty S. R., Black G. W., Fannin T. F. Reye's syndrome. Br J Hosp Med. 1985 Jul;34(1):42–45. [PubMed] [Google Scholar]
  5. Hoekstra P. T., Kahnoski R., McCamish M. A., Bergen W., Heetderks D. R. Transurethral prostatic resection syndrome--a new perspective: encephalopathy with associated hyperammonemia. J Urol. 1983 Oct;130(4):704–707. doi: 10.1016/s0022-5347(17)51414-7. [DOI] [PubMed] [Google Scholar]
  6. Kuntze J. R., Weinberg A. C., Ahlering T. E. Hyperammonemic coma due to Proteus infection. J Urol. 1985 Nov;134(5):972–973. doi: 10.1016/s0022-5347(17)47553-7. [DOI] [PubMed] [Google Scholar]
  7. Lockwood A. H., McDonald J. M., Reiman R. E., Gelbard A. S., Laughlin J. S., Duffy T. E., Plum F. The dynamics of ammonia metabolism in man. Effects of liver disease and hyperammonemia. J Clin Invest. 1979 Mar;63(3):449–460. doi: 10.1172/JCI109322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Rao P. N., Lister B., Livesey J. L., Barnard R. J. Are we using the right irrigation system? Br J Urol. 1983 Jun;55(3):287–293. doi: 10.1111/j.1464-410x.1983.tb03300.x. [DOI] [PubMed] [Google Scholar]
  9. Rhymer J. C., Bell T. J., Perry K. C., Ward J. P. Hyponatraemia following transurethral resection of the prostate. Br J Urol. 1985 Aug;57(4):450–452. doi: 10.1111/j.1464-410x.1985.tb06308.x. [DOI] [PubMed] [Google Scholar]
  10. Ryder K. W., Olson J. F., Kahnoski R. J., Karn R. C., Oei T. O. Hyperammonemia after transurethral resection of the prostate: a report of 2 cases. J Urol. 1984 Nov;132(5):995–997. doi: 10.1016/s0022-5347(17)49984-8. [DOI] [PubMed] [Google Scholar]
  11. Shepard R. L., Kraus S. E., Babayan R. K., Siroky M. B. The role of ammonia toxicity in the post transurethral prostatectomy syndrome. Br J Urol. 1987 Oct;60(4):349–351. doi: 10.1111/j.1464-410x.1987.tb04983.x. [DOI] [PubMed] [Google Scholar]
  12. Tannen R. L. Ammonia metabolism. Am J Physiol. 1978 Oct;235(4):F265–F277. doi: 10.1152/ajprenal.1978.235.4.F265. [DOI] [PubMed] [Google Scholar]
  13. Wada Y., Tada K., Takada G., Omura K., Yoshida T. Hyperglycinemia associated with hyperammonemia: in vitro glycine cleavage in liver. Pediatr Res. 1972 Jul;6(7):622–625. [PubMed] [Google Scholar]
  14. Watkins-Pitchford J. M., Payne S. R., Rennie C. D., Riddle P. R. Hyponatraemia during transurethral resection--its practical prevention. Br J Urol. 1984 Dec;56(6):676–678. doi: 10.1111/j.1464-410x.1984.tb06144.x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of the Royal Society of Medicine are provided here courtesy of Royal Society of Medicine Press

RESOURCES