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1 conducted, which included a mammogram and a Papanicolaou test.
2 e excluded as they were likely not due for a Papanicolaou test.
3 the number of previous consecutive negative Papanicolaou tests.
4 mmography, 14.7% [95% CI, 13.7%-15.6%] had a Papanicolaou test, 23.3% [95% CI, 22.6%-24.0%] had a PSA
5 e breast imaging, 64 (16.9%) had undergone a Papanicolaou test, 274 (72.5%) rarely or never examined
6 .001), mammography (69.4% vs 75.1%; P<.001), Papanicolaou tests (69.2% vs 77.1%; P<.001), and psychia
7 as defined as screening every 3 years with a Papanicolaou test alone for women aged 21 to 29 years an
8 29 years and screening every 3 years with a Papanicolaou test alone or every 5 years with high-risk
12 of age and an average of 209,324 additional Papanicolaou tests and 11,502 colposcopic examinations i
13 gative test, an average of 69,665 additional Papanicolaou tests and 3861 colposcopic examinations wou
14 u tests, as well as the number of additional Papanicolaou tests and colposcopic examinations that wou
15 ds to increased rates of abnormal results of Papanicolaou tests and contributes to the increased rate
17 Medical record documentation of mammography, Papanicolaou testing, and colorectal cancer screening ac
18 tible health plan fully covered mammography, Papanicolaou tests, and fecal occult blood testing (FOBT
19 -based cytology and computerized analysis of Papanicolaou tests are examples of attempts at this appr
20 e of inhabitants who are up to date with the Papanicolaou test, are of Asian race, and have private i
21 ithin three years after one or more negative Papanicolaou tests, as well as the number of additional
22 to be percentage of women screened with the Papanicolaou test, Asian race, private insurance, and ce
23 creasing screening uptake of mammography and Papanicolaou testing, but their role in CRC screening is
24 uidelines suggest that the intervals between Papanicolaou tests can be extended to three years among
25 ion of HPV genotyping and cervical cytology (Papanicolaou testing) can identify the risk of precancer
26 mammography (95% CI, 0.06 to 0.19), 0.07 for Papanicolaou testing (CI, 0.01 to 0.12), and 0.13 for co
27 n between each primary outcome (mammography, Papanicolaou test, colonoscopy, influenza vaccine, and p
28 onusers, independent of sexual behavior, and Papanicolaou test diagnosis (AHR: 0.67 [95% CI: .49-.93]
29 the order in which they were performed (eg, Papanicolaou test followed by human papillomavirus [HPV]
30 a primary care clinician, had not received a Papanicolaou test for at least 3 years and 5 months, and
31 nt, and the positive predictive value of the Papanicolaou test for detecting vaginal cancer was 0 per
32 el, the estimated risk of cancer with annual Papanicolaou tests for three years was 2 in 100,000 amon
33 clinic, and were overdue for screening (ie, Papanicolaou test >=4 years ago or high-risk HPV test >=
34 Screening programs, such as colposcopy with Papanicolaou testing, have greatly improved mortality ra
35 g had a mammogram in the previous 2 years, a Papanicolaou test in the previous 3 years, and a fecal t
36 0.58 with usual care; the proportion who had Papanicolaou testing increased from 0.71 to 0.78 with th
37 squamous cells (ASC) depends on whether the Papanicolaou test is subcategorized as of undetermined s
38 have had three or more consecutive negative Papanicolaou tests is associated with an average excess
39 th plan enrollment duration, time since last Papanicolaou test, mammography, comorbidities, and color
41 eater with longer vs shorter time since last Papanicolaou test (no prior Papanicolaou test: RRs, 1.85
42 ation size, health-related variables (use of Papanicolaou test, obesity), income variables (median ho
46 reproductive health care services, including Papanicolaou tests or birth control, experienced in the
47 mammography (OR, 0.74 [95% CI, 0.71-0.77]), Papanicolaou test (OR, 0.84 [95% CI, 0.81-0.87]), influe
49 (mammography: OR, 0.32 [95% CI, 0.27-0.38]; Papanicolaou test: OR, 0.49 [95% CI, 0.44-0.54]; influen
50 : odds ratio [OR], 0.73 [95% CI, 0.67-0.80]; Papanicolaou test: OR, 0.78 [95% CI, 0.72-0.85]; influen
51 of cancer screening procedures (mammography, Papanicolaou test, prostate-specific antigen [PSA], and
53 ionally representative research has examined Papanicolaou testing rates from before the pandemic in 2
54 d cross-sectional study found that past-year Papanicolaou testing rates were lower in 2022 than 2019,
57 ual behavior, genital tract coinfection, and Papanicolaou test results were assessed at baseline and
58 time since last Papanicolaou test (no prior Papanicolaou test: RRs, 1.85-3.25; >=10 years: RR, 2.78;
59 creation of a diagnostic system to digitize Papanicolaou test samples and analyze them using a cloud
61 , 8.6%-9.1%) vs 22.0% (95% CI, 21.7%-22.5%); Papanicolaou test screening was received by 5.8% (95% CI
62 ilization showed a positive correlation with Papanicolaou test use (r = 0.75, P < .001), median house
65 vulvovaginal samples for HPV DNA testing and Papanicolaou testing were collected at gynecologic exami
69 squamous cells of undetermined significance Papanicolaou test with satisfactory results for all 4 HP
73 hs, a current primary care clinician, and no Papanicolaou test within the prior 3 years and 5 months
74 outine mammography (women aged 40-74 years), Papanicolaou test (women aged 21-65 years), colonoscopy