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1 ble resistance and pain/blood during digital rectal examination.
2 ere was still no palpable disease on digital rectal examination.
3 and palpable stools in the rectum at digital rectal examination.
4 for prostate-specific antigen and a digital rectal examination.
5 were 85% for PSA testing and 86% for digital rectal examination.
6 esting and ranged from 41 to 46% for digital rectal examination.
7 d an annual measurement of PSA and a digital rectal examination.
8 ne screening or of stool obtained by digital rectal examination.
9 ite normal PSA levels and results of digital rectal examination.
10 udinal prostate-specific antigen and digital rectal examination.
11 periodic PSA testing (all cohorts), digital rectal examination (14 cohorts), and rebiopsy (14 cohort
12 for men with no cancer suspected on digital rectal examination, a PSA level of 4.0 to 5.0 ng/mL is a
13 years of age or older with a normal digital rectal examination and a prostate-specific antigen (PSA)
14 esponse to AD as assessed by monthly digital rectal examination and prostate-specific antigen (PSA).
15 ly detection of prostate cancer with digital rectal examination and prostate-specific antigen have co
16 eptable operating characteristics of digital rectal examination and prostate-specific antigen, a stag
19 ositive predictive value of combined digital rectal examination and PSA measurement has been defined,
20 set of assumptions is used, one-time digital rectal examination and PSA measurement may increase aver
21 ost-effectiveness model for one-time digital rectal examination and PSA measurement was constructed t
24 pecific antigen level or an abnormal digital rectal examination and was offered to all men at the tri
25 bnormal prostate-specific antigen or digital rectal examination) and 669 detected not for cause (with
26 state-specific antigen measurements, digital rectal examinations, and biopsies, with treatment at dis
30 n two steps, initially using PSA and digital rectal examination (DRE) alone and subsequently using th
31 tate needle biopsy due to suspicious digital rectal examination (DRE) findings and/or PSA levels (lim
32 ombined-modality therapy (CMT) using digital rectal examination (DRE) has been proposed as a means of
33 ence PSA doubling time, and positive digital rectal examination (DRE) of the prostatic fossa were all
34 dy included 118 patients with normal digital rectal examination (DRE) results but elevated prostate-s
35 ymptomatic, but 33 had heme-positive digital rectal examination (DRE) results or hematochezia at rout
37 igen (PSA) concentration, PSA slope, digital rectal examination, dysplastic glands or prostatitis on
38 were followed up with PSA assays and digital rectal examinations every 3 months for the first year, s
39 mission for lower gastrointestinal bleeding, rectal examination findings, heart rate, systolic blood
40 peated this interpretation with knowledge of rectal examination findings, sextant biopsy results, and
41 prostate-specific antigen levels and digital rectal examination findings, were correlated with biopsy
42 serum prostate-specific antigen and digital rectal examination, followed by transrectal ultrasound-g
44 re sensitive than sextant biopsy and digital rectal examination for sextant localization of cancer re
45 4.0 ng per milliliter or an abnormal digital rectal examination, had a final PSA determination, and u
47 ce/ethnicity, prior biopsy, PSA, and digital rectal examination) improved the stratification of cance
48 ore sensitive but less specific than digital rectal examination in the detection of local recurrence.
49 y and specificity of sextant biopsy, digital rectal examination, MR imaging, and MR spectroscopy were
51 ntigen (PSA) of 4.0 ng/mL or less, a digital rectal examination not suspicious for prostate cancer, a
52 igen level of 4 ng/mL or less, and a digital rectal examination not suspicious for prostate cancer.
54 e-specific-antigen (PSA) testing and digital rectal examination on the rate of death from prostate ca
55 opsy because of abnormal findings on digital rectal examination or elevated PSA (> or = 4 ng/ml) part
56 levels, usually in combination with digital rectal examination or transrectal prostatic ultrasonogra
57 preceding prostate-specific antigen/digital rectal examination prompt (yes/no) and noncases by biops
58 d the current clinical parameters of digital rectal examination, prostate-specific antigen, and Gleas
59 constipation criteria, stool diary, digital rectal examination, rectal diameter assessed from transa
60 tate biopsy on the basis of abnormal digital rectal examination results or elevated prostate-specific
61 igen (PSA) level, PSA density, race, digital rectal examination results, and biopsy results before MR
62 e-specific antigen (PSA) or abnormal digital rectal examination results, often with prior negative bi
63 to 0.78 for models without and with digital rectal examination results, respectively (P < .001 for b
64 nsrectal ultrasound (TRUS) findings, digital rectal examination results, serum PSA level, and excess
67 state specific antigen, and abnormal digital rectal examination, serum 25-OH D less than 30 ng/mL was
68 um prostate-specific antigen levels, digital rectal examination status, stage, grade, primary treatme
70 rostate-specific antigen testing and digital rectal examination (the latter available for >60% of res
71 n patients who have abnormalities on digital rectal examination, the risk for a large intracapsular t
74 ories are prostate specific antigen, digital rectal examination, transrectal biopsy and their repeate
75 elevated PSA levels and/or abnormal digital rectal examination underwent transrectal US-guided sexta
76 cted history, examination (including digital rectal examination), urinalysis and bladder diary as bei
82 :ERG (T2:ERG) RNA in the urine after digital rectal examination would improve specificity over measur
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