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Microhematuria: AUA/SUFU Guideline.
Barocas, Daniel A; Boorjian, Stephen A; Alvarez, Ronald D; Downs, Tracy M; Gross, Cary P; Hamilton, Blake D; Kobashi, Kathleen C; Lipman, Robert R; Lotan, Yair; Ng, Casey K; Nielsen, Matthew E; Peterson, Andrew C; Raman, Jay D; Smith-Bindman, Rebecca; Souter, Lesley H.
Afiliação
  • Barocas DA; Vanderbilt University Medical Center, Nashville, Tennessee.
  • Boorjian SA; Mayo Clinic.
  • Alvarez RD; Vanderbilt University Medical Center, Nashville, Tennessee.
  • Downs TM; University of Wisconsin.
  • Gross CP; Yale University.
  • Hamilton BD; University of Utah.
  • Kobashi KC; Virginia Mason.
  • Lipman RR; Bladder Cancer Advocacy Network.
  • Lotan Y; University of Texas, Southwestern.
  • Ng CK; Kaiser Permanente.
  • Nielsen ME; University of North Carolina, Chapel Hill, North Carolina.
  • Peterson AC; Duke University.
  • Raman JD; Penn State Health.
  • Smith-Bindman R; University of California, San Francisco, California.
J Urol ; 204(4): 778-786, 2020 10.
Article em En | MEDLINE | ID: mdl-32698717
ABSTRACT

PURPOSE:

Patients presenting with microhematuria represent a heterogeneous population with a broad spectrum of risk for genitourinary malignancy. Recognizing that patient-specific characteristics modify the risk of underlying malignant etiologies, this guideline sought to provide a personalized diagnostic testing strategy. MATERIALS AND

METHODS:

The systematic review incorporated evidence published from January 2010 through February 2019, with an updated literature search to include studies published up to December 2019. Evidence-based statements were developed by the expert Panel, with statement type linked to evidence strength, level of certainty, and the Panel's judgment regarding the balance between benefits and risks/burdens.

RESULTS:

Microhematuria should be defined as ≥ 3 red blood cells per high power field on microscopic evaluation of a single specimen. In patients diagnosed with gynecologic or non-malignant genitourinary sources of microhematuria, clinicians should repeat urinalysis following resolution of the gynecologic or non-malignant genitourinary cause. The Panel created a risk classification system for patients with microhematuria, stratified as low-, intermediate-, or high-risk for genitourinary malignancy. Risk groups were based on factors including age, sex, smoking and other urothelial cancer risk factors, degree and persistence of microhematuria, as well as prior gross hematuria. Diagnostic evaluation with cystoscopy and upper tract imaging was recommended according to patient risk and involving shared decision-making. Statements also inform follow-up after a negative microhematuria evaluation.

CONCLUSIONS:

Patients with microhematuria should be classified based on their risk of genitourinary malignancy and evaluated with a risk-based strategy. Future high-quality studies are required to improve the care of these patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hematúria Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: J Urol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hematúria Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: J Urol Ano de publicação: 2020 Tipo de documento: Article