Daniel Perez

Dr. Daniel Perez

Department of General, Visceral and Thoracic Surgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2018 in European Journal of Surgical Oncology
Verified
Journal Article
Closed access
Daniel PerezDaniel Perez
Daniel Perez
NMNathaniel Melling
Nathaniel Melling
Matthias BieblMatthias Biebl
Matthias Biebl
MRMatthias Reeh
Matthias Reeh
JGJulia-Kristin Graß
Julia-Kristin Graß
FAFelix Aigner
Felix Aigner

27 September 2018 in Journal of Robotic Surgery
Verified
Journal Article
Closed access
PDF file
NMNathaniel Melling
Nathaniel Melling
JBJustin Barr
Justin Barr
RSRobin Schmitz
Robin Schmitz
APAdam Polonski
Adam Polonski
JMJameel Miro
Jameel Miro
Daniel PerezDaniel Perez
Daniel Perez

21 October 2021 in American Journal of Surgical Pathology
Verified
Journal Article
Open access
RURia Uhlig
Ria Uhlig
HCHendrina Contreras
Hendrina Contreras
SWSören Weidemann
Sören Weidemann
NGNatalia Gorbokon
Natalia Gorbokon
AMAnne Menz
Anne Menz
TCTill Sebastian Clauditz
Till Sebastian Clauditz
Carboxypeptidase A1 (CPA1) is a zinc metalloprotease that is produced in pancreatic acinar cells and plays a role in cleaving C-terminal branched-chain and aromatic amino acids from dietary proteins. This study assessed the utility of immunohistochemical CPA1 staining for diagnosing pancreatic acinar cell carcinoma (ACC). A total of 12,274 tumor samples from 132 different tumor types and subtypes as well as 8 samples each of 76 different normal tissue types were interpretable by immunohistochemistry in a tissue microarray format. CPA1 was strongly expressed in acinar cells of all normal pancreas samples but not in any other normal tissues. CPA1 immunostaining was detected in 100% of 11 pancreatic ACCs and 1 mixed acinar endocrine carcinoma, but absent in 449 pancreatic ductal adenocarcinomas, 75 adenocarcinomas of the ampulla Vateri, and 11,739 other evaluable cancers from 128 different tumor entities. A weak to moderate diffuse staining of epithelial and stromal cells of cancer tissues immediately adjacent to non-neoplastic pancreatic acinar cells often occurred and was considered to be caused by the diffusion of the highly abundant CPA1 from normal acinar cells that may have suffered some autolytic cell damage. In conclusion, our data show that CPA1 is a highly sensitive and largely specific marker for normal and neoplastic pancreatic acinar cells. CPA1 immunohistochemistry greatly facilitates the otherwise often difficult diagnosis of pancreatic ACC.

1 April 2019 in European Journal of Surgical Oncology
Verified
Journal Article
Closed access
JGJulia-Kristin Graß
Julia-Kristin Graß
Daniel PerezDaniel Perez
Daniel Perez
JIJakob R. Izbicki
Jakob R. Izbicki
MRMatthias Reeh
Matthias Reeh

15 June 2023 in Cancers
Verified
Journal Article
Open access
PDF file
KLKatharina Lucia Lucas
Katharina Lucia Lucas
NMNathaniel Melling
Nathaniel Melling
AGAnastasios D. Giannou
Anastasios D. Giannou
MRMatthias Reeh
Matthias Reeh
OMOliver Mann
Oliver Mann
JGJulia-Kristin Graß
Julia-Kristin Graß
An optimized lymph node yield leads to better survival in colon cancer, but extended lymphadenectomy is not associated with survival benefits. Lymphatic mapping shows several colon cancers feature aberrant drainage pathways inducing local recurrence when not resected. Currently, different protocols exist for lymphatic mapping procedures. This meta-analysis assessed which protocol has the best capacity to detect tumor-draining and possibly metastatic lymph nodes. A systematic review was conducted according to PRISMA guidelines, including prospective trials with in vivo tracer application. The risk of bias was evaluated using the QUADAS-2 tool. Traced lymph nodes, total resected lymph nodes, and aberrant drainage detection rate were analyzed. Fifty-eight studies met the inclusion criteria, of which 42 searched for aberrant drainage. While a preoperative tracer injection significantly increased the traced lymph node rates compared to intraoperative tracing (30.1% (15.4, 47.3) vs. 14.1% (11.9, 16.5), p = 0.03), no effect was shown for the tracer used (p = 0.740) or the application sites comparing submucosal and subserosal injection (22.9% (14.1, 33.1) vs. 14.3% (12.1, 16.8), p = 0.07). Preoperative tracer injection resulted in a significantly higher rate of detected aberrant lymph nodes compared to intraoperative injection (26.3% [95% CI 11.5, 44.0] vs. 2.5% [95% CI 0.8, 4.7], p < 0.001). Analyzing 112 individual patient datasets from eight studies revealed a significant impact on aberrant drainage detection for injection timing, favoring preoperative over intraoperative injection (OR 0.050 [95% CI 0.010–0.176], p < 0.001) while indocyanine green presented itself as the superior tracer (OR 0.127 [95% CI 0.018–0.528], p = 0.012). Optimized lymphatic mapping techniques result in significantly higher detection of aberrant lymphatic drainage patterns and thus enable a personalized approach to reducing local recurrence.

9 November 2021 in Surgical Endoscopy
Verified
Journal Article
Open access
PDF file
MSMona Wanda Schmidt
Mona Wanda Schmidt
CHCaelan M. Haney
Caelan M. Haney
KKKarl-Friedrich Kowalewski
Karl-Friedrich Kowalewski
VBVasile Bintintan
Vasile Bintintan
Mohammed Abu HilalMohammed Abu Hilal
Mohammed Abu Hilal
FNFelix Nickel
Felix Nickel
Introduction: The aim of this study was to develop a reliable objective structured assessment of technical skills (OSATS) score for linear-stapled, hand-sewn closure of enterotomy intestinal anastomoses (A-OSATS). Materials and methods: The Delphi methodology was used to create a traditional and weighted A-OSATS score highlighting the more important steps for patient outcomes according to an international expert consensus. Minimally invasive novices, intermediates, and experts were asked to perform a minimally invasive linear-stapled intestinal anastomosis with hand-sewn closure of the enterotomy in a live animal model either laparoscopically or robot-assisted. Video recordings were scored by two blinded raters assessing intrarater and interrater reliability and discriminative abilities between novices (n = 8), intermediates (n = 24), and experts (n = 8). Results: The Delphi process included 18 international experts and was successfully completed after 4 rounds. A total of 4 relevant main steps as well as 15 substeps were identified and a definition of each substep was provided. A maximum of 75 points could be reached in the unweighted A-OSATS score and 170 points in the weighted A-OSATS score respectively. A total of 41 anastomoses were evaluated. Excellent intrarater (r = 0.807–0.988, p < 0.001) and interrater (intraclass correlation coefficient = 0.923–0.924, p < 0.001) reliability was demonstrated. Both versions of the A-OSATS correlated well with the general OSATS and discriminated between novices, intermediates, and experts defined by their OSATS global rating scale. Conclusion: With the weighted and unweighted A-OSATS score, we propose a new reliable standard to assess the creation of minimally invasive linear-stapled, hand-sewn anastomoses based on an international expert consensus. Validity evidence in live animal models is provided in this study. Future research should focus on assessing whether the weighted A-OSATS exceeds the predictive capabilities of patient outcomes of the unweighted A-OSATS and provide further validity evidence on using the score on different anastomotic techniques in humans.