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DOI: 10.1055/a-1684-9870
Harnblasentumoren als Langzeitfolge einer Querschnittlähmung – Bedeutung für die Praxis
Urinary Bladder Cancer as a Long-term Sequela of Spinal Cord Injury – Relevance to PracticeZusammenfassung
Das Harnblasenkarzinom ist, nach dem Lungenkrebs, bei Querschnittgelähmten die zweithäufigste zum Tode führende Tumorerkrankung. Die vorliegende Arbeit gibt einen umfassenden Überblick über die für den Urologen wichtigen Unterschiede im Vergleich zu Harnblasentumoren in der Allgemeinbevölkerung.
Querschnittgelähmte sind zum Zeitpunkt der Tumordiagnose im Durchschnitt 1 bis 2 Jahrzehnte jünger als Patienten ohne Querschnittlähmung. Der histopathologische Befund bei Erstdiagnose eines Harnblasenkarzinoms bei Menschen mit Querschnittlähmung ist wesentlich ungünstiger als bei Harnblasenkarzinomen in der Allgemeinbevölkerung. Muskelinvasive Tumoren und Tumoren mit geringer Differenzierung sind wesentlich häufiger und der Anteil an Plattenepithelkarzinomen ist deutlich erhöht. Die Häufigkeit nimmt nach über 10 Lähmungsjahren zu. Die Harnblasenkarzinom-Mortalität ist deutlich erhöht und steigt mit zunehmender Lähmungsdauer an.
Bei diagnostischen Eingriffen und insbesondere bei der radikalen Zystektomie sind klinisch wichtige Besonderheiten zu beachten. So können z. B. urodynamische Untersuchungen oder eine Zystoskopie eine Autonome Dysreflexie mit hypertensiven Krisen und der Gefahr einer lebensbedrohlichen Bradykardie triggern.
Bei einer radikalen Zystektomie sind intraoperativ u.a. die häufig auftretenden Verwachsungen und Verschwielungen der Harnblase zu beachten. Postoperativ treten u.a. häufig, bedingt durch die neurogene Störung des Darmes, schwere Paralysen und prolongierte Darmatonien auf. Die unmittelbar nach der Operation vorzunehmende Lagerung der Patienten zur Vermeidung von Dekubiti und zur Unterstützung der Atmung sowie das Querschnittgelähmten-spezifische Darmmanagement sind unbedingt zu beachten. Weitere Besonderheiten bei querschnittgelähmten Patienten mit Harnblasenkarzinom, die auch in der klinischen Praxis Beachtung finden sollten, sowie Überlegungen zum Screening nach Harnblasentumoren werden im Beitrag dargestellt.
Abstract
Urinary bladder cancer is the second most common tumour disease after lung cancer leading to death in people with a spinal cord injury. This paper provides a comprehensive overview of the differences relevant to urologists between urinary bladder tumours in this population compared with urinary bladder tumours in the general population.
People with a spinal cord injury are 1 to 2 decades younger on average at the time of tumour diagnosis than patients without a spinal cord injury. Histopathologic findings at the initial diagnosis of urinary bladder cancer in people with a spinal cord injury are much less favourable than for urinary bladder cancers in the general population. Muscle-invasive tumours and tumours with poor differentiation are much more common, and the proportion of squamous cell carcinomas is significantly higher. The incidence rises after more than 10 years of paralysis. Urinary bladder cancer mortality is significantly elevated and increases with the duration of paralysis. In diagnostic procedures and, in particular, in radical cystectomy, clinically important features have to be considered. For example, urodynamic examinations or cystoscopy may trigger autonomic dysreflexia with hypertensive crises and the risk of life-threatening bradycardia.
In the case of radical cystectomy, frequent adhesions and callosities of the urinary bladder, among other things, must be taken into account intraoperatively. Severe paralysis, prolonged intestinal atony and other conditions are frequently observed after the surgical procedure due to neurogenic bowel dysfunction. Correct positioning of the patient immediately after surgery to avoid decubitus and to support breathing, as well as bowel management specific to spinal cord injury, must be strictly observed.
Other special features of paraplegic patients with urinary bladder cancer that should also be considered in clinical practice, as well as considerations for screening for urinary bladder tumors, are presented in the article.
Schlüsselwörter
neurogene Harnblasenfunktionsstörung - urodynamische Untersuchung - Zystoskopie - radikale Zystektomie - ScreeningKeywords
urodynamic study - cystoscopy - radical cystectomy - screening - neurogenic lower urinary tract dysfunctionPublication History
Received: 24 August 2021
Accepted after revision: 27 October 2021
Article published online:
21 December 2021
© 2021. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
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Literatur
- 1 GBD 2016 Traumatic Brain Injury and Spinal Cord Injury Collaborators. Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol 2019; 18: 56-87
- 2 Savic G, DeVivo MJ, Frankel HL. et al. Causes of death after traumatic spinal cord injury – a 70-year British study. Spinal Cord 2017; 55: 891-897
- 3 National Spinal Cord Injury Statistical Center, University of Alabama at Birmingham, 2018 Annual Statistical Report – Complete Public Version. http://www.sci-info-pages.com/wp-content/media/NSCISC-2018-Annual-Report.pdf 13.08.2021
- 4 Robert Koch-Institut (Hrsg) und die Gesellschaft der epidemiologischen Krebsregister in Deutschland e.V. (Hrsg). Krebs in Deutschland für 2015/2016. 12. Ausgabe. Berlin, 2019 ISBN 978–3-89606–298–7.
- 5 Gui-Zhong L, Li-Bo M. Bladder cancer in individuals with spinal cord injuries: a meta-analysis. Spinal Cord 2017; 55: 341-345
- 6 Ismail S, Karsenty G, Chartier-Kastler E. et al. Prevalence, management, and prognosis of bladder cancer in patients with neurogenic bladder: a systematic review. Neurourol Urodyn 2018; 37: 1386-1395
- 7 Liu B, Welk B. Urological malignancies in neurogenic patients. Curr Opin Urol 2020; 30: 501-506
- 8 Böthig R, Tiburtius C, Schöps W. et al. Urinary bladder cancer as a late sequela of traumatic spinal cord injury. Mil Med Res 2021; 8: 29
- 9 Böthig R, Kowald B, Fiebag K. et al. Bladder management, severity of injury and period of latency: a descriptive study on 135 patients with spinal cord injury and bladder cancer. Spinal Cord 2021; 59: 971-977
- 10 Ferlay J, Colombet M, Soerjomataram I. et al. Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods. Int J Cancer 2019; 144: 1941-1953
- 11 Böthig R, Kurze I, Fiebag K. et al. Clinical characteristics of bladder cancer in patients with spinal cord injury: the experience from a single centre. Int Urol Nephrol 2017; 49: 983-994
- 12 Lee WY, Sun LM, Lin CL. et al. Risk of prostate and bladder cancers in patients with spinal cord injury: a population-based cohort study. Urol Oncol 2014; 32: 51.e1-7
- 13 Ho CH, Sung KC, Lim SW. et al. Chronic indwelling urinary catheter increase the risk of bladder cancer, even in patients without spinal cord injury. Medicine (Baltimore) 2015; 94: e1736
- 14 Nahm LS, Chen Y, DeVivo MJ. et al. Bladder cancer mortality after spinal cord injury over 4 decades. J Urol 2015; 193: 1923-1928
- 15 Dolin PJ, Darby SC, Beral V. Paraplegia and squamous cell carcinoma of the bladder in young women: findings from a case-control study. Br J Cancer 1994; 70: 167-168
- 16 Groah SL, Weitzenkamp DA, Lammertse DP. et al. Excess risk of bladder cancer in spinal cord injury: evidence for an association between indwelling catheter use and bladder cancer. Arch Phys Med Rehabil 2002; 83: 346-351
- 17 Stonehill WH, Dmochowski RR, Patterson AL. et al. Risk factors for bladder tumors in spinal cord injury patients. J Urol 1996; 155: 1248-1250
- 18 Welk B, McIntyre A, Teasell R. et al. Bladder cancer in individuals with spinal cord injuries. Spinal Cord 2013; 51: 516-521
- 19 Vereczkey ZA, Schmeidler J, Binard JE. et al. Bladder cancer risk in patients with spinal cord injury. J Spinal Cord Med 1998; 21: 230-239
- 20 Rove KO, Husmann DA, Wilcox DT. et al. Systematic review of bladder cancer outcomes in patients with spina bifida. J Pediatr Urol 2017; 13: 456.e1-e9
- 21 Kraywinkel K, Fiebig J, Schulz GB. Epidemiologie des Harnblasenkarzinoms in Deutschland. Onkologe 2018; 24: 6-13
- 22 Böthig R, Tiburtius C, Fiebag K. et al. Traumatic spinal cord injury confers bladder cancer risk to patients managed without permanent urinary catheterization: lessons from a comparison of clinical data with the national database. World J Urol 2020; 38: 2827-2834
- 23 Abol-Enein H, Kava BR, Carmack AJ. Nonurothelial cancer of the bladder. Urology 2007; 69: 93-104
- 24 Pannek J. Transitional cell carcinoma in patients with spinal cord injury: A high risk malignancy?. Urology 2002; 59: 240-244
- 25 Hollingsworth JM, Rogers MA, Krein SL. et al. Determining the noninfectious complications of indwelling urethral catheters: a systematic review and meta-analysis. Ann Intern Med 2021; 159: 401-410
- 26 Kalisvaart JF, Katsumi HK, Ronningen LD. et al. Bladder cancer in spinal cord injury patients. Spinal Cord 2010; 48: 257-261
- 27 Grabe M, Bartoletti R, Bjerklund Johansen TE. et al. EAU guidelines on urological infections. 2015. http://uroweb.org/wp-content/uploads/19-Urological-infections_LR2.pdf 13.08.2021
- 28 Paralyzed Veterans of America and Consortium for Spinal Cord Medicine. Bladder management for adults with spinal cord injury: a clinical practice guideline for health-care providers. 2006. . http://pva.org/research-resources/publications/clinical-practice-guidelines/ 13.08.2021
- 29 Biering-Sørensen F, DeVivo MJ, Charlifue S. et al. International Spinal Cord Injury Core Data Set (version 2.0) - including standardization of reporting. Spinal Cord 2017; 55: 759-764
- 30 Kirshblum SC, Burns SP, Biering-Sorensen F. et al. International standards for neurological classification of spinal cord injury (revised 2011). J Spinal Cord Med 2011; 34: 535-546
- 31 Rabadi MH, Aston C. Complications and urologic risks of neurogenic bladder in veterans with traumatic spinal cord injury. Spinal Cord 2015; 53: 200-203
- 32 Kantor AF, Hartge P, Hoover RN. et al. Urinary tract infection and risk of bladder cancer. Am J Epidemiol 1984; 119: 510-515
- 33 Esclarin De Ruz A, Garcia Leoni E, Herruzo Cabrera R. Epidemiology and risk factors for urinary tract infection in patients with spinal cord injury. J Urol 2000; 164: 1285-1289
- 34 Fouts DE, Pieper R, Szpakowski S. et al. Integrated next-generation sequencing of 16S rDNA and metaproteomics differentiate the healthy urine microbiome from asymptomatic bacteriuria in neuropathic bladder associated with spinal cord injury. J Transl Med 2012; 10: 174
- 35 Markowski MC, Boorjian SA, Burton JP. et al. The microbiome and genitourinary cancer: a collaborative review. Eur Urol 2019; 75: 637-646
- 36 Aragón IM, Herrera-Imbroda B, Queipo-Ortuño MI. et al. The urinary tract microbiome in health and disease. Eur Urol Focus 2018; 4: 128-138
- 37 Pottegård A, Kristensen KB, Friis S. et al. Urinary tract infections and risk of squamous cell carcinoma bladder cancer: a Danish nationwide case-control study. Int J Cancer 2020; 146: 1930-1936
- 38 Ord J, Lunn D, Reynard J. Bladder management and risk of bladder stone formation in spinal cord injured patients. J Urol 2003; 170: 1734-1737
- 39 Böthig R, Golka K, Tiburtius C. et al. Incidental bladder cancer at initial urological workup of spinal cord injury patients. Spinal Cord Ser Cases 2020; 6: 55
- 40 Manach Q, Cussenot O, Rouprêt M. et al. Analysis of bladder cancer subtypes in neurogenic bladder tumors. Can J Urol 2018; 25: 9161-9167
- 41 Haas U. Pflege von Menschen mit Querschnittlähmung. 2. Aufl. Bern: Hogrefe Verlag; 2021
- 42 Liu N, Zhou M, Biering-Sørensen F. et al. Iatrogenic urological triggers of autonomic dysreflexia: a systematic review. Spinal Cord 2015; 53: 500-509
- 43 Vírseda-Chamorro M, Salinas-Casado J, Gutiérrez-Martín P. et al. Risk factors to develop autonomic dysreflexia during urodynamic examinations in patients with spinal cord injury. Neurourol Urodyn 2017; 36: 171-175
- 44 Elliott SP. Screening for bladder cancer in individuals with spinal cord injury. J Urol 2015; 193: 1880-1881
- 45 Arbeitskreis Neuro-Urologie der DMGP. S2k-Leitlinie: Neuro-urologische Versorgung querschnittgelähmter Patienten (2021), AWMF-Register Nr: 179/001. http://www.awmf.org/uploads/tx_szleitlinien/179–001l_S2k_Neuro-urologische-Versorgung-querschnittgelaehmter-Patienten_2021-11.pdf 18.11.2021
- 46 Cameron AP, Rodriguez GM, Schomer KG. Systematic review of urological follow-up after spinal cord injury. J Urol 2012; 187: 391-397
- 47 Welk B. The argument against screening for bladder cancer in neuro-urological patients. World J Urol 2021;
- 48 Alimi Q, Hascoet J, Manunta A. et al. Reliability of urinary cytology and cystoscopy for the screening and diagnosis of bladder cancer in patients with neurogenic bladder: A systematic review. Neurourol Urodyn 2018; 37: 916-925
- 49 Böthig R, Schöps W, Zellner M. et al. Ursachenzusammenhang zwischen langjähriger Querschnittlähmung und malignen Harnblasentumoren. Vorschlag für eine Konvention. Trauma Berufskrankh 2019; 21: 61-73
- 50 Böthig R, Schöps W, Zellner M. et al. Harnblasenkarzinom als Spätfolge einer Querschnittlähmung. Entscheidungshilfe für eine Zusammenhangsbegutachtung. Urologe A 2020; 59: 700-709
- 51 Marrie RA, Maxwell C, Mahar A. et al. Cancer incidence and mortality rates in multiple sclerosis: A matched cohort study. Neurology 2021; 96: e501-e512
- 52 Böthig R, Schöps W, Kadhum T. et al. Reader response to: Marrie RA, Maxwell C, Mahar A et al. Cancer incidence and mortality rates in multiple sclerosis: A matched cohort study. Neurology 2021; 96: e501-e512
- 53 Marrie RA, Maxwell C, Groome P. Author response to: Marrie RA, Maxwell C, Mahar A et al. Cancer incidence and mortality rates in multiple sclerosis: A matched cohort study. Neurology 2021; 96: e501-e512
- 54 Böthig R, Domurath B, Kutzenberger J. et al. The real daily need for incontinence aids and appliances in patients with neurogenic bladder dysfunction in a community setting in Germany. J Multidiscip Healthc 2020; 13: 217-223