https://www.limswiki.org/index.php?title=Journal:Diagnostic_time_in_digital_pathology:_A_comparative_study_on_400_cases&feed=atom&action=historyJournal:Diagnostic time in digital pathology: A comparative study on 400 cases - Revision history2024-03-29T02:15:42ZRevision history for this page on the wikiMediaWiki 1.36.1https://www.limswiki.org/index.php?title=Journal:Diagnostic_time_in_digital_pathology:_A_comparative_study_on_400_cases&diff=24890&oldid=prevShawndouglas: Added rest of content.2016-04-02T20:01:39Z<p>Added rest of content.</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:01, 2 April 2016</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>A microscopic diagnosis was made on an Eclipse 80i light microscope (Nikon). Turnaround refers in this study to diagnostic (slide evaluation) and nondiagnostic time (dictation, sign off, access to clinical information, and previous history, etc.). A diagnostic time was measured from the point slides were made available to the point diagnosis was made or additional investigations were deemed necessary, recorded independently in minutes/session and compared. It did not include interruptions into the reporting sessions. An unstructured sessional log was recorded to identify factors contributing to improved diagnostic time. Broadband speeds were automatically recorded every 30 min into digital reporting sessions and analyzed.</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>A microscopic diagnosis was made on an Eclipse 80i light microscope (Nikon). Turnaround refers in this study to diagnostic (slide evaluation) and nondiagnostic time (dictation, sign off, access to clinical <ins style="font-weight: bold; text-decoration: none;">[[</ins>information<ins style="font-weight: bold; text-decoration: none;">]]</ins>, and previous history, etc.). A diagnostic time was measured from the point slides were made available to the point diagnosis was made or additional investigations were deemed necessary, recorded independently in minutes/session and compared. It did not include interruptions into the reporting sessions. An unstructured sessional log was recorded to identify factors contributing to improved diagnostic time. Broadband speeds were automatically recorded every 30 min into digital reporting sessions and analyzed.</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==Results==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==Results==</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==Discussion==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==Discussion==</div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Although numerous validation studies in digital pathology confirmed its value as a diagnostic tool, a longer time to diagnosis than traditional microscopy has been seen as the main obstacle to wider implementation of primary digital diagnostics. Early works showed up to 60% longer time to diagnosis in digital pathology comparing to traditional microscopy.<ref name="TreanorTheVirt07" /> Recent advances in digital working stations have shown slightly longer or similar digital diagnostic time to traditional microscopy in experimental studies on a limited number of cases or slides, involving though multiple pathologists. A high-resolution array of 28 computer screens allowed, after just a few minutes familiarization, tasks to be performed as quickly and confidently as a microscope.<ref name="TreanorVirt09" /></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Assessing the effect of display resolution, Randell ''et al.'' showed that time to diagnosis and time to first target were faster on the microscope than on the single and three-screen displays, viewing axillary lymph node slides.<ref name="RandellEffect15" /> Although there was no significant difference between the microscope and the three-screen display in time to first target, the time taken on the single-screen display was significantly higher than that on the microscope. The results suggested that a digital pathology workstation with an increased number of pixels may allow the quicker initial slide overview, however, in the case of a detailed slide search, increased resolution may not offer any additional benefits. Double 23” displays have been used in our study, one for LIMS and the other for image viewer, seen as a minimal requirement. In our validation of digital pathology, we have tested multiple displays available on the market, including ultra-high definition (4K), and purchased the ones mentioned above as the best value for money and benefits to digital diagnostics.<ref name="VodovnikDist15">{{cite journal |title=Distance reporting in digital pathology: A study on 950 cases |journal=Journal of Pathology Informatics |author=Vodovnik, A. |volume=6 |pages=18 |year=2015 |doi=10.4103/2153-3539.156168 |pmid=25969793 |pmc=PMC4421888}}</ref></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">In their further studies, Randell ''et al.'' achieved a similar time to diagnosis for the conventional and virtual microscope. Although the mean slide viewing time was also similar, participants spent a significantly greater proportion of the total task time viewing slides and revisited slides more often, or there was a significant difference in the mean magnification used between the two technologies, with participants working at a higher level of magnification on the virtual microscope.<ref name="RandellDiag14" /><ref name="RandellVirtual13" /> This may be related to the level of confidence and experience in digital reporting, and was not observed by the reporting pathologist in this study.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">More exact comparison of results was found to be limited due to differences with previous studies in design, image size, network speed, case number, case workload, and experience in digital reporting, all affecting digital diagnostic time [Table 6]. Similar to previous studies, multiple displays were seen as an advantage in our study as well. In contrast, our study was conducted in the routine diagnostic setting with a varied case workload and high case numbers. In addition to the wash-out period of 6 months, those are seen as strengths of this study. As adoption of primary digital reporting relays on individual preferences and learning curves for each pathologist, a number of participating pathologists has not been seen as an issue in this study.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">A shorter digital diagnostic time in our study has been achieved in the routine diagnostic setting with stable and adequate network speeds, full integration of digital scanner with LIMS and double displays as default parameters. As previously shown, an instant upload of digital images in the image viewer has been achieved at 20 Mbps.<ref name="VodovnikDist15" /> Average, median and variation of download and upload network speeds were both well above and accordingly regarded as stable. Correlations between digital and microscopic diagnosis were 99% for the reporting pathologist (unpublished data) and therefore not specifically addressed in this study. One percent of cases (six) showed a minor discordance (without clinical implications), with no cases showing a major discordance (with clinical implications) in that study, which was fully compliant to the College of American Pathologists recommendation.<ref name="PantanowitzValid13">{{cite journal |title=Validating whole slide imaging for diagnostic purposes in pathology: Guideline from the College of American Pathologists Pathology and Laboratory Quality Center |journal=Archives of Pathology and Laboratory Medicine |author=Pantanowitz, L.; Sinard, J.H.; Henricks, W.H. et al. |volume=137 |issue=12 |pages=1710-22 |doi=10.5858/arpa.2013-0093-CP |pmid=23634907}}</ref></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Improvements in digital diagnostic time also related to better ergonomics, larger viewing field, and absence of physical slide handling. Better ergonomics in the digital reporting setting, with less eye and wrist fatigue, has been recognized as an important advantage comparing to traditional microscopy, allowing longer uninterrupted diagnostic sessions to be carried out.<ref name="ThorstensonImp14" /><ref name="VodovnikDist15" /> Larger viewing field allowed completion of slide viewing in lesser number of fields, subject to magnifications used, for both small diagnostic biopsies, and large resections specimens. In the absence of physical slide handling, switching between slides and magnifications was nearly instant and superior to the traditional microscopy, as the focus was maintained throughout. The need for double checking of slides against request forms by pathologist has almost completely disappeared, as only digital slides belonging to the patient could be linked to the patient in LIMS. A number of specimens per sample could be still simultaneously checked by pathologist against digital slides as double displays were used, one for the LIMS and the other for viewing of digital slides.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Slide viewing patterns among pathologist with long experience in the digital review have been recently studied.<ref name="MolinSlide15">{{cite journal |title=Slide navigation patterns among pathologists with long experience of digital review |journal=Histopathology |author=Molin, J.; Fjeld, M.; Mello-Thoms, C.; Lundström, C. |volume=67 |issue=2 |pages=185-92 |doi=10.1111/his.12629 |pmid=25487230}}</ref> Combinations of directed and cover panning with dip-zooming were also experienced in this study as superior to traditional microscopy. That especially goes for chipping specimens from, for example, prostate, urinary bladder, or endometrium. The whole slide could be viewed at lower magnification in one field and dip-zoomed to the area of interest. The other advantage, comparing to traditional microscopy, is that images appear in the viewer fit to window at magnifications up to ×4, depending on the specimen size. That often allowed an instant diagnosis in the very first viewing field for smaller biopsies, shortening diagnostic time substantially.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">An average digital and microscopic diagnostic time in cytology was similar in this study. A majority of specimens were prepared using liquid-based cytology techniques with remaining traditional smears being done by pathologists. This way we were able to ascertain a high quality of slides with limited areas to scan and evaluate, contributing to the effective digital diagnostics and minimizing scanning issues. The routine use of a scanning magnification ×20 and a digital zoom to achieve ×40 caused no issues in this study.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Turnaround comprises of a diagnostic and nondiagnostic time. A shorter digital diagnostic time in this study amounted to additional 250 cases a year, for the reporting pathologist, as savings in the diagnostic time only. The nondiagnostic time has not been exactly measured due to logistical reason with the routine diagnostic setting and difficulties to repeat the same nondiagnostic variables during the secondary microscopic sessions. However, a consolidation of multiple tasks in digital reporting systems was seen as a contributory factor in shortening of the nondiagnostic time as well, especially in dictation, sign off and access to the previous history, as previously shown.<ref name="VodovnikDist15" /><ref name="RandellWork12">{{cite journal |title=Working at the microscope: Analysis of the activities involved in diagnostic pathology |journal=Histopathology |author=Randell R.; Ruddle, R.A.; Quirke, P. et al. |volume=60 |issue=3 |pages=504-10 |year=2012 |doi=10.1111/j.1365-2559.2011.04090.x |pmc=22176210}}</ref> Observations from this study suggest savings of at least 10% in the nondiagnostic time comparing to the traditional microscopy diagnostic setting amounting roughly to additional 350 cases a year. Extra savings in diagnostic and nondiagnostic time could be alternatively used for consultation, administration or teaching, depending on departmental needs or individual preferences of pathologists.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Four sessions with a shorter microscopic diagnostic time included more gastric, lung, and lymph node biopsies comparing to the rest of the sessions. Those required more extensive use of magnifications ×40 due to low bacterial or tumor loads and to ascertain nuclear features. Although all cases in this group were reported using a digital zoom to achieve magnifications ×40, it took a longer time to make a confident diagnosis due to digital zoom's focusing imperfections. As a result of this study, we are considering to routinely scan all minute diagnostic biopsies with queries of malignancy at ×40 instead.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Conclusions==</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Digital reporting systems allow today multiple advances in working settings comparing to the traditional microscopy. It is up to individual pathologists to discover their own ways to take the advantage of this new working environment to the benefit of the patient and hospital budget.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">A shorter diagnostic time in digital pathology comparing with traditional microscopy can be achieved in the routine diagnostic setting with adequate and stable network speeds, fully integrated LIMS and double displays as default parameters, in addition to better ergonomics, larger viewing field, and absence of physical slide handling, with effects on the both diagnostic and nondiagnostic time. Further advancements in working stations and gained experience in digital reporting are expected to improve the diagnostic time and widen applications of digital pathology.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Acknowledgements==</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">This study was supported by Digital Pathology Project at our institution, sponsored by the Health Authority-West (Helse vest), project number 795421. The author is grateful to the departmental laboratory staff for their support and encouragement, as well as members of the project group and the regional IT Department (HVIKT) for their valuable contributions to the success of our digital pathology project.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Financial support and sponsorship==</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Health Authority West grant 795421.</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Conflicts of interest==</ins></div></td></tr>
<tr><td colspan="2"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">There are no conflicts of interest.</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==References==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==References==</div></td></tr>
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</table>Shawndouglashttps://www.limswiki.org/index.php?title=Journal:Diagnostic_time_in_digital_pathology:_A_comparative_study_on_400_cases&diff=24889&oldid=prevShawndouglas: Created stub. Saving and adding more.2016-04-02T19:40:43Z<p>Created stub. Saving and adding more.</p>
<p><b>New page</b></p><div>{{Infobox journal article<br />
|name = <br />
|image = <br />
|alt = <!-- Alternative text for images --><br />
|caption = <br />
|title_full = Diagnostic time in digital pathology: A comparative study on 400 cases<br />
|journal = ''Journal of Pathology Informatics''<br />
|authors = Vodovnik, Aleksandar<br />
|affiliations = Forde Central Hospital<br />
|contact = Email: N/A<br />
|editors = <br />
|pub_year = 2016<br />
|vol_iss = '''7'''<br />
|pages = 4<br />
|doi = [http://doi.org/10.4103/2153-3539.175377 10.4103/2153-3539.175377]<br />
|issn = 2153-3539<br />
|license = [http://creativecommons.org/licenses/by-nc-sa/3.0/ Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported]<br />
|website = [http://www.jpathinformatics.org/article.asp?issn=2153-3539;year=2016;volume=7;issue=1;spage=4;epage=4;aulast=Vodovnik http://www.jpathinformatics.org]<br />
|download = [http://www.jpathinformatics.org/temp/JPatholInform714-5222773_143027.pdf http://www.jpathinformatics.org/temp/JPatholInform714-5222773_143027.pdf] (PDF)<br />
}}<br />
==Abstract==<br />
'''Background:''' Numerous validation studies in digital pathology confirmed its value as a diagnostic tool. However, a longer time to diagnosis than traditional microscopy has been seen as a significant barrier to the routine use of digital pathology. As a part of our validation study, we compared a digital and microscopic diagnostic time in the routine diagnostic setting. <br />
<br />
'''Materials and methods:''' One senior staff pathologist reported 400 consecutive cases in histology, nongynecological, and fine needle aspiration cytology (20 sessions, 20 cases/session), over 4 weeks. Complex, difficult, and rare cases were excluded from the study to reduce the bias. A primary diagnosis was digital, followed by traditional microscopy, six months later, with only request forms available for both. Microscopic slides were scanned at ×20, digital images accessed through the fully integrated [[laboratory information management system]] (LIMS) and viewed in the image viewer on double 23” displays. A median broadband speed was 299 Mbps. A diagnostic time was measured from the point slides were made available to the point diagnosis was made or additional investigations were deemed necessary, recorded independently in minutes/session and compared. <br />
<br />
'''Results:''' A digital diagnostic time was 1841 and microscopic 1956 min; digital being shorter than microscopic in 13 sessions. Four sessions with shorter microscopic diagnostic time included more cases requiring extensive use of magnifications over ×20. Diagnostic time was similar in three sessions. <br />
<br />
'''Conclusions:''' A diagnostic time in digital pathology can be shorter than traditional microscopy in the routine diagnostic setting, with adequate and stable network speeds, fully integrated LIMS and double displays as default parameters. This also related to better ergonomics, larger viewing field, and absence of physical slide handling, with effects on both diagnostic and nondiagnostic time. Differences with previous studies included a design, image size, number of cases, specimen type, network speed, and participant's level of confidence and experience in digital reporting. Further advancements in working stations and gained experience in digital reporting are expected to improve diagnostic time and widen routine applications of digital pathology.<br />
<br />
'''Keywords:''' Diagnostic time, digital pathology, turnaround<br />
<br />
==Introduction==<br />
Numerous validation studies in digital pathology confirmed its value as a diagnostic tool.<ref name="StathonikosGoing13">{{cite journal |title=Going fully digital: Perspective of a Dutch academic pathology lab |journal=Journal of Pathology Informatics |author=Stathonikos, N.; Veta, M.; Huisman, A.; van Diest, P.J. |volume=4 |page=15 |year=2013 |doi=10.4103/2153-3539.114206 |pmid=23858390 |pmc=PMC3709427}}</ref><ref name="ThorstensonImp14">{{cite journal |title=Implementation of large-scale routine diagnostics using whole slide imaging in Sweden: Digital pathology experiences 2006-2013 |journal=Journal of Pathology Informatics |author=Thorstenson, S.; Molin, J.; Lundström, C. |volume=5 |page=14 |year=2014 |doi=10.4103/2153-3539.129452 |pmid=24843825 |pmc=PMC4023034}}</ref><ref name="BauerValid14">{{cite journal |title=Validating whole-slide imaging for consultation diagnoses in surgical pathology |journal=Archives of Pathology and Laboratory Medicine |author=Bauer, T.W.; Slaw, R.J. |volume=138 |issue=11 |page=1459-65 |year=2014 |doi=10.5858/arpa.2013-0541-OA |pmid=24840034}}</ref> Main advantages for wider implementation of digital pathology, in comparison to traditional microscopy, include better ergonomics, immediate access to slides, and distance reporting. However, a longer time to diagnosis than traditional microscopy has been seen as a significant barrier to the routine use of digital pathology, especially in early studies.<ref name="TreanorTheVirt07">{{cite journal |title=The virtual slide and conventional microscope — A direct comparison of their diagnostic efficiency |journal=The Journal of Pathology |author=Treanor, D.; Quirke, P. |volume=213 |page=7a |year=2007}}</ref> Advances in working stations led to the narrowing or equaling of the diagnostic time gap and further improvements of the digital diagnostic experience, in experimental studies on a limited number of cases.<ref name="TreanorVirt09">{{cite journal |title=Virtual reality Powerwall versus conventional microscope for viewing pathology slides: An experimental comparison |journal=Histopathology |author=Treanor, D.; Jordan-Owers, N.; Hodrien, J. et al. |volume=55 |issue=3 |pages=294-300 |doi=10.1111/j.1365-2559.2009.03389.x |pmid=19723144}}</ref><ref name="RandellEffect15">{{cite journal |title=Effect of display resolution on time to diagnosis with virtual pathology slides in a systematic search task |journal=Journal of Digital Imaging |author=Randell, R.; Ambepitiya, T.; Mello-Thoms, C. et al. |volume=28 |issue=1 |pages=68–76 |doi=10.1007/s10278-014-9726-8 |pmid=25128321 |pmc=PMC4305057}}</ref><ref name="RandellDiag14">{{cite journal |title=Diagnosis of major cancer resection specimens with virtual slides: Impact of a novel digital pathology workstation |journal=Human Pathology |author=Randell, R.; Ruddle, R.A., Thomas, R.G. et al. |volume=45 |issue=10 |pages=2101–6 |doi=10.1016/j.humpath.2014.06.017 |pmid=25128229}}</ref><ref name="RandellVirtual13">{{cite journal |title=Virtual reality microscope versus conventional microscope regarding time to diagnosis: An experimental study |journal=Histopathology |author=Randell, R.; Ruddle, R.A., Mello-Thoms, C. et al. |volume=62 |issue=2 |pages=351-8 |doi=10.1111/j.1365-2559.2012.04323.x |pmid=22882289}}</ref> As a part of our validation study, we compared digital and microscopic diagnostic time in the routine diagnostic setting. Technical issues were seen as potential obstacles and shortened turnaround, through the faster digital diagnostic time, desired benefits.<br />
<br />
==Materials and methods==<br />
One senior staff pathologist reported 400 consecutive cases (1396 slides) in histology, nongynecological and fine needle aspiration cytology, by means of digital pathology and traditional microscopy (20 sessions and 20 cases/session), over four weeks [Figure 1]. <br />
<br />
[[File:Fig1 Vodovnik JofPathInformatics2016 7.jpg|600px]]<br />
{{clear}}<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| border="0" cellpadding="5" cellspacing="0" width="600px"<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"| <blockquote>'''Figure 1.''' Case workload reported in this study</blockquote><br />
|- <br />
|}<br />
|}<br />
<br />
Complex, difficult, and rare cases were excluded from the study to reduce the bias, as pathologists often remember those cases for a long time. This group nevertheless included one complex, one difficult, and two rare cases. A primary diagnosis was digital, used for clinical management, followed by traditional microscopy, six months later. Only request forms were available for both primary and secondary diagnosis. Microscopic slides were prepared by standard techniques and routinely stained hematoxylin-eosin. In addition, upper gastrointestinal diagnostic biopsies were stained Alcian blue/periodic acid-Schiff and liver core biopsies Masson trichrome/iron/reticulin, respectively. Cytological slides were routinely stained either Romanowsky or Romanowsky/Papanicolaou and were not prescreened. Microscopic slides were scanned at ×20 using Scan Scope AT Turbo digital scanner (Leica). Digital images were accessed through the fully integrated laboratory information management system (LIMS) SymPathy (Tieto) and viewed in ImageScope (Leica) on a desktop PC with double displays [Table 1] using a broadband connection [Table 2]. <br />
<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| class="wikitable" border="1" cellpadding="5" cellspacing="0" width="500"<br />
|-<br />
| style="padding-left:10px; padding-right:10px;" colspan="2"| '''Table 1.''' Technical specification for equipment used in digital reporting<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|'''Make and model'''<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Dell OptiPlex 7010<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|'''Operative system'''<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Windows 7 Enterprise 64 bit<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|'''Processor'''<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|i3-3240M 3.40 GHz<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|'''Display size and resolution'''<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Double 23", 1920x1200<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|'''Read-only memory'''<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|500 GB<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|'''Random access memory'''<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|8 GB<br />
|- <br />
|}<br />
|}<br />
<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| class="wikitable" border="1" cellpadding="5" cellspacing="0" width="500"<br />
|-<br />
| style="padding-left:10px; padding-right:10px;" colspan="4"| '''Table 2.''' Broadband speed (Mbps) - variation, median and average<br />
|-<br />
! <br />
! Variation<br />
! Median<br />
! Average<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Download speed<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|150–400<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|299<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|250<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Upload speed<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|35–150<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|55<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|50<br />
|- <br />
|}<br />
|}<br />
<br />
A microscopic diagnosis was made on an Eclipse 80i light microscope (Nikon). Turnaround refers in this study to diagnostic (slide evaluation) and nondiagnostic time (dictation, sign off, access to clinical information, and previous history, etc.). A diagnostic time was measured from the point slides were made available to the point diagnosis was made or additional investigations were deemed necessary, recorded independently in minutes/session and compared. It did not include interruptions into the reporting sessions. An unstructured sessional log was recorded to identify factors contributing to improved diagnostic time. Broadband speeds were automatically recorded every 30 min into digital reporting sessions and analyzed.<br />
<br />
==Results==<br />
A total digital diagnostic time was shorter than microscopic, 1841 versus 1956 min, respectively. Distributions of digital and microscopic diagnostic time per session are shown in [Table 3] and [Figure 2]. <br />
<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| class="wikitable" border="1" cellpadding="5" cellspacing="0" width="500"<br />
|-<br />
| style="padding-left:10px; padding-right:10px;" colspan="4"| '''Table 3.''' Diagnostic time per session (min) - variation, median and average<br />
|-<br />
! <br />
! Variation<br />
! Median<br />
! Average<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Digital<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|79–106<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|93<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|92.05<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Microscopic<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|84–109<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|99.5<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|97.8<br />
|- <br />
|}<br />
|}<br />
<br />
[[File:Fig2 Vodovnik JofPathInformatics2016 7.jpg|600px]]<br />
{{clear}}<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| border="0" cellpadding="5" cellspacing="0" width="600px"<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"| <blockquote>'''Figure 2.''' Distribution of diagnostic time</blockquote><br />
|- <br />
|}<br />
|}<br />
<br />
A digital diagnostic time was shorter than microscopic in 13 sessions. Four sessions with shorter microscopic diagnostic time included more cases requiring extensive use of magnifications over ×20 [Table 4]. <br />
<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| class="wikitable" border="1" cellpadding="5" cellspacing="0" width="500"<br />
|-<br />
| style="padding-left:10px; padding-right:10px;" colspan="2"| '''Table 4.''' Main reasons for more extensive use of magnification over ×20<br />
|-<br />
! Reason<br />
! Diagnostic problem<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Low bacterial load<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Presence of ''Helicobacter pylori''<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Low tumour load<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Presence of nonsmall cell cancer<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Nuclear features<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Lymphoma versus carcinoma<br />
|- <br />
|}<br />
|}<br />
<br />
The diagnostic time was similar in three sessions. Data analysis from the unstructured sessional log identified factors contributing most to the shorter digital diagnostic time [Table 5]. Differences with previous studies are listed in [Table 6].<br />
<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| class="wikitable" border="1" cellpadding="5" cellspacing="0" width="500"<br />
|-<br />
| style="padding-left:10px; padding-right:10px;" colspan="2"| '''Table 5.''' Factors contributing to shortened digital diagnostic time<br />
|-<br />
! Factors<br />
! Benefits<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Ergonomics<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Less tiring reporting sessions<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Larger viewing field<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Lesser number of viewing fields<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Absence of physical slide handling<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Faster switching between slides/magnifications; reduced checking slides against requisitions<br />
|- <br />
|}<br />
|}<br />
<br />
{| <br />
| STYLE="vertical-align:top;"|<br />
{| class="wikitable" border="1" cellpadding="5" cellspacing="0" width="500"<br />
|-<br />
| style="padding-left:10px; padding-right:10px;" colspan="3"| '''Table 6.''' Differences with previous studies in digital reporting<br />
|-<br />
! Variables<br />
! Previous studies<br />
! Present study<br />
|-<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Design<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Experimental<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Routine<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Network speed<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Variable<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Stable<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Image size<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Scan at x20 and x40<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Scan at x20<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Number of cases<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Low<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|High<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Specimen type<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Organ-specific<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Mixed<br />
|- <br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Experience<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Variable<br />
| style="background-color:white; padding-left:10px; padding-right:10px;"|Long<br />
|- <br />
|}<br />
|}<br />
<br />
==Discussion==<br />
<br />
==References==<br />
{{Reflist|colwidth=30em}}<br />
<br />
==Notes==<br />
This presentation is faithful to the original, with only a few minor changes to presentation. In some cases important information was missing from the references, and that information was added. Numbers 0 through 9 were changed from numerals to words when appropriate.<br />
<br />
<!--Place all category tags here--><br />
[[Category:LIMSwiki journal articles (added in 2016)]]<br />
[[Category:LIMSwiki journal articles (all)]]<br />
[[Category:LIMSwiki journal articles on pathology informatics]]</div>Shawndouglas