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@ARTICLE{Oertel:281641,
      author       = {Oertel, Frederike Cosima and Cabrera Debuc, Delia and
                      Calabresi, Peter A and Chen, Mei and Cordano, Christian and
                      Dietrich, Michael and Feltgen, Nicolas and Gramlich, Oliver
                      and Green, Ari J and Groh, Janos and Huang, Su-Chun and
                      Knier, Benjamin and Korn, Thomas and Leocani, Letizia and
                      Loewenstein, Anat and van Oterendorp, Christian and Peto,
                      Tunde and Schippling, Sven and Schmetterer, Leopold and
                      Schmitz-Valckenberg, Steffen and Seeliger, Mathias W and
                      Shindler, Kenneth S and Schuman, Joel S and Sindi, Mustafa
                      and Tufail, Adnan and Wang, Jui-Kai and Wolf, Sebastian and
                      You, Yuyi and Zinkernagel, Martin and Lagrèze, Wolf and
                      Albrecht, Philipp},
      collaboration = {consortium, IMSVISUAL},
      title        = {{APOSTEL}-{R} {R}ecommendations for {R}eporting {R}etinal
                      {O}ptical {C}oherence {T}omography {S}tudies in {R}odents.},
      journal      = {Neurology: Neuroimmunology $\&$ Neuroinflammation ;
                      official journal of the American Academy of Neurology},
      volume       = {12},
      number       = {6},
      issn         = {2332-7812},
      address      = {Philadelphia, Pa.},
      publisher    = {Wolters Kluwer},
      reportid     = {DZNE-2025-01159},
      pages        = {e200489},
      year         = {2025},
      abstract     = {Retinal optical coherence tomography (OCT) in rodent models
                      has been used to longitudinally image retinal changes, to
                      define end points for more costly or time-consuming
                      experiments, and to better understand the pathophysiology
                      underlying OCT findings in human diseases. No
                      standardization of rodent OCT reporting currently exists.
                      Here, we aim to establish consensus recommendation for
                      reporting results from retinal OCT studies in
                      rodents.Initial recommendations were developed based on the
                      APOSTEL criteria for quantitative OCT reporting in humans by
                      a core team. Using a modified Delphi process, an expert
                      panel of rodent OCT researchers (N = 31) and the wider
                      scientific community discussed, refined, and voted on these
                      initial recommendations. The list of recommendations was
                      then revised and approved by the expert panel.The final
                      7-point checklist includes reporting recommendations
                      regarding the study protocol, OCT device, acquisition
                      settings and modifications, scanning protocol, funduscopic
                      imaging, postacquisition data selection and image data
                      analyses, and qualitative and quantitative results. With a
                      median agreement score of 3 or 4 out of 4, the scientific
                      community agreed with these recommendations. After
                      revisions, the expert panel accepted the final
                      recommendations.The Advised Protocol for OCT Study
                      Terminology and Elements for reporting OCT studies in
                      rodents (APOSTEL-R) originates from an expert consensus.
                      They will provide guidance throughout the experimental
                      process and will contribute to the standardization and
                      quality improvement of preclinical OCT studies.},
      keywords     = {Tomography, Optical Coherence: standards / Tomography,
                      Optical Coherence: methods / Animals / Retina: diagnostic
                      imaging / Rodentia / Rats / Consensus},
      cin          = {AG Simons},
      ddc          = {610},
      cid          = {I:(DE-2719)1110008},
      pnm          = {351 - Brain Function (POF4-351)},
      pid          = {G:(DE-HGF)POF4-351},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:41061181},
      doi          = {10.1212/NXI.0000000000200489},
      url          = {https://pub.dzne.de/record/281641},
}