Conventional and liquid-based cervicovaginal cytology: A comparison study with clinical and histologic follow-up

2002 ◽  
Vol 27 (3) ◽  
pp. 185-188 ◽  
Author(s):  
John J. Baker
Keyword(s):  
2009 ◽  
Vol 45 (12) ◽  
pp. 2110-2115 ◽  
Author(s):  
Suzanne Polinder ◽  
Els M.L. Verschuur ◽  
Peter D. Siersema ◽  
Ernst J. Kuipers ◽  
Ewout W. Steyerberg

2020 ◽  
Vol 118 ◽  
pp. 105342
Author(s):  
Heidi Jacobsen ◽  
Tore Wentzel-Larsen ◽  
Hans Bugge Bergsund

1977 ◽  
Vol 7 (3) ◽  
pp. 147-155
Author(s):  
Ruth C. Resch ◽  
Roy K. Lilleskov ◽  
Helen M. Schur ◽  
Thelma Mihalov

2019 ◽  
Vol 43 (4) ◽  
pp. 201-209
Author(s):  
Yong Kwan Lim ◽  
Oh Joo Kweon ◽  
Jee-Hye Choi ◽  
Seungman Park ◽  
Keumsim Jung ◽  
...  

Abstract Background Recently, the QPLEX™ human papillomavirus (HPV) genotyping kit (QuantaMatrix, Seoul, Korea), a Microdisk™ technology-based multiplex system, was developed to detect 32 HPV genotypes. We evaluated the analytical performance of this kit by conducting a comparison study, precision evaluation and interference testing. Methods A total of 1594 cervical swab specimens were used to compare the QPLEX™ HPV genotyping kit with other commercially available kits (GeneFinder HPV Liquid Bead MicroArray Genotype polymerase chain reaction [PCR] kit, Infopia, Seoul, Korea; PANArray™ HPV Genotyping Chip, PANAGENE, Daejeon, Korea). For the determination of precision, we evaluated four types of precision profiles: repeatability, lot-to-lot variability, operator-to-operator variability and site-to-site variability. In addition, interference tests were performed with various interferents. Results The results of the QPLEX™ HPV genotyping kit showed almost perfect agreement with the other commercially available HPV genotyping assays. The combined precision was acceptable. In addition, there was no tested interferent that affected the results of the QPLEX™ HPV genotyping kit. Conclusions The QPLEX™ HPV genotyping kit showed acceptable analytical performance in our study. This assay could be a suitable option for HPV genotyping in routine and follow-up tests.


Author(s):  
Sandro M. Krieg ◽  
Nico Sollmann ◽  
Sebastian Ille ◽  
Lucia Albers ◽  
Bernhard Meyer

Abstract Lumbosacral instrumentation continues to be challenging due to complex biomechanical force distributions and poor sacral bone quality. Various techniques have therefore been established. The aim of this study was to investigate the outcome of patients treated with S2-alar-iliac (S2AI), S2-alar (S2A), and iliac (I) instrumentation as the most caudal level. Sixty patients underwent one of the 3 techniques between January 2012 and June 2017 (S2AI 18 patients, S2A 20 patients, I 22 patients). Mean age was 70.4 ± 8.5 years. Screw loosening (SL) and sacroiliac joint (SIJ) pain were evaluated during the course at 3-month and maximum follow-up (FU). All patients completed 3-month FU, the mean FU period was 2.5 ± 1.5 years (p = 0.38), and a median of 5 segments was operated on (p = 0.26), respectively. Bone mineral density (BMD), derived opportunistically from computed tomography (CT), did not significantly differ between the groups (p = 0.66), but cages were more frequently implanted in patients of the S2A group (p = 0.04). SL of sacral or iliac screws was more common in patients of the S2A and I groups compared with the S2AI group (S2AI 16.7%, S2A 55.0%, I 27.3% of patients; p = 0.03). SIJ pain was more often improved in the S2AI group not only after 3 months but also at maximum FU (S2AI 61.1%, S2A 25.0%, I 22.7% of patients showing improvement; p = 0.02). Even in shorter or mid-length lumbar or thoracolumbar constructs, S2AI might be considered superior to S2A and I instrumentation due to showing lower incidences of caudal SL and SIJ pain.


Ophthalmology ◽  
2011 ◽  
Vol 118 (3) ◽  
pp. 443-452 ◽  
Author(s):  
Donald L. Budenz ◽  
Keith Barton ◽  
William J. Feuer ◽  
Joyce Schiffman ◽  
Vital P. Costa ◽  
...  

2004 ◽  
Vol 19 (2) ◽  
pp. 254
Author(s):  
Vijay Rasquinha ◽  
Chitranjan Ranawat ◽  
Vipul Dua ◽  
Amar Ranawat ◽  
Jose Rodriguez

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