TY - JOUR
T1 - Applicability and accuracy of pretest probability calculations implemented in the NICE clinical guideline for decision making about imaging in patients with chest pain of recent onset
AU - Roehle, Robert
AU - Wieske, Viktoria
AU - Schuetz, Georg M.
AU - Gueret, Pascal
AU - Andreini, Daniele
AU - Meijboom, Willem Bob
AU - Pontone, Gianluca
AU - Garcia, Mario
AU - Alkadhi, Hatem
AU - Honoris, Lily
AU - Hausleiter, Jörg
AU - Bettencourt, Nuno
AU - Zimmermann, Elke
AU - Leschka, Sebastian
AU - Gerber, Bernhard
AU - Rochitte, Carlos
AU - Schoepf, U. Joseph
AU - Shabestari, Abbas Arjmand
AU - Nørgaard, Bjarne
AU - Sato, Akira
AU - Knuuti, Juhani
AU - Meijs, Matthijs F.L.
AU - Brodoefel, Harald
AU - Jenkins, Shona M.M.
AU - Øvrehus, Kristian Altern
AU - Diederichsen, Axel Cosmus Pyndt
AU - Hamdan, Ashraf
AU - Halvorsen, Bjørn Arild
AU - Mendoza Rodriguez, Vladimir
AU - Wan, Yung Liang
AU - Rixe, Johannes
AU - Sheikh, Mehraj
AU - Langer, Christoph
AU - Ghostine, Said
AU - Martuscelli, Eugenio
AU - Niinuma, Hiroyuki
AU - Scholte, Arthur
AU - Nikolaou, Konstantin
AU - Ulimoen, Geir
AU - Zhang, Zhaoqi
AU - Mickley, Hans
AU - Nieman, Koen
AU - Kaufmann, Philipp A.
AU - Buechel, Ronny Ralf
AU - Herzog, Bernhard A.
AU - Clouse, Melvin
AU - Halon, David A.
AU - Leipsic, Jonathan
AU - Bush, David
AU - Jakamy, Reda
AU - Sun, Kai
AU - Yang, Lin
AU - Johnson, Thorsten
AU - Laissy, Jean Pierre
AU - Marcus, Roy
AU - Muraglia, Simone
AU - Tardif, Jean Claude
AU - Chow, Benjamin
AU - Paul, Narinder
AU - Maintz, David
AU - Hoe, John
AU - de Roos, Albert
AU - Haase, Robert
AU - Laule, Michael
AU - Schlattmann, Peter
AU - Dewey, Marc
N1 - Funding Information:
JH reports grants from Siemens Medical Solutions, outside the submitted work. UJS reports grants from Bayer, grants from Bracco, grants from GE, grants from Medrad, grants from Siemens Healthcare, outside the submitted work. JK reports personal fees from Lantheus Inc, grants from Orion Pharma, outside the submitted work. KN reports non-financial support from Siemens Medical Solutions, grants from GE Healthcare, other from Toshiba Medical Systems, non-financial support from Abbott Vascular, grants from Bayer healthcare, outside the submitted work. PK, RRB, and BH report that the University Hospital Zurich holds a research contract with GE Healthcare. JL reports personal fees from GE Healthcare, personal fees from Heartflow, outside the submitted work. BC reports research grants from GE healthcare and educational support from TeraRecon, outside the submitted work. NP reports grants from Toshiba Medical System, outside the submitted work. JH reports grants and personal fees from Toshiba Medical Systems, during the conduct of the study. RH reports grants from Toshiba, outside the submitted work. PS reports grants from Ministry of Education and Research (BMBF) for meta-analyses as part of the joint programme "clinical trials" of the BMBF and the German Science Foundation (DFG), during the conduct of the study; grants from German Science Foundation (DFG), grants from European Union, outside the submitted work. MD has received grant support from the Heisenberg Program of the DFG for a professorship (DE 1361/14-1), the FP7 Program of the European Commission for the randomized multicentre DISCHARGE trial (603266-2, HEALTH-2012.2.4.-2), the European Regional Development Fund (20072013 2/05, 20072013 2/48), the German Heart Foundation/German Foundation of Heart Research (F/23/08, F/27/10), the Joint Program from the German Research Foundation (DFG) and the German Federal Ministry of Education and Research (BMBF) for meta-analyses (01KG1013, 01KG1110, 01KG1110)
Funding Information:
Funding The authors of this manuscript state that the CoMe-CCT project received funding from the joint program of the German Research Foundation (DFG) and the German Federal Ministry of Education and Research (BMBF) for meta-analyses.
Publisher Copyright:
© 2018, European Society of Radiology.
PY - 2018/9/1
Y1 - 2018/9/1
N2 - Objectives: To analyse the implementation, applicability and accuracy of the pretest probability calculation provided by NICE clinical guideline 95 for decision making about imaging in patients with chest pain of recent onset. Methods: The definitions for pretest probability calculation in the original Duke clinical score and the NICE guideline were compared. We also calculated the agreement and disagreement in pretest probability and the resulting imaging and management groups based on individual patient data from the Collaborative Meta-Analysis of Cardiac CT (CoMe-CCT). Results: 4,673 individual patient data from the CoMe-CCT Consortium were analysed. Major differences in definitions in the Duke clinical score and NICE guideline were found for the predictors age and number of risk factors. Pretest probability calculation using guideline criteria was only possible for 30.8 % (1,439/4,673) of patients despite availability of all required data due to ambiguity in guideline definitions for risk factors and age groups. Agreement regarding patient management groups was found in only 70 % (366/523) of patients in whom pretest probability calculation was possible according to both models. Conclusions: Our results suggest that pretest probability calculation for clinical decision making about cardiac imaging as implemented in the NICE clinical guideline for patients has relevant limitations. Key Points: • Duke clinical score is not implemented correctly in NICE guideline 95. • Pretest probability assessment in NICE guideline 95 is impossible for most patients. • Improved clinical decision making requires accurate pretest probability calculation. • These refinements are essential for appropriate use of cardiac CT.
AB - Objectives: To analyse the implementation, applicability and accuracy of the pretest probability calculation provided by NICE clinical guideline 95 for decision making about imaging in patients with chest pain of recent onset. Methods: The definitions for pretest probability calculation in the original Duke clinical score and the NICE guideline were compared. We also calculated the agreement and disagreement in pretest probability and the resulting imaging and management groups based on individual patient data from the Collaborative Meta-Analysis of Cardiac CT (CoMe-CCT). Results: 4,673 individual patient data from the CoMe-CCT Consortium were analysed. Major differences in definitions in the Duke clinical score and NICE guideline were found for the predictors age and number of risk factors. Pretest probability calculation using guideline criteria was only possible for 30.8 % (1,439/4,673) of patients despite availability of all required data due to ambiguity in guideline definitions for risk factors and age groups. Agreement regarding patient management groups was found in only 70 % (366/523) of patients in whom pretest probability calculation was possible according to both models. Conclusions: Our results suggest that pretest probability calculation for clinical decision making about cardiac imaging as implemented in the NICE clinical guideline for patients has relevant limitations. Key Points: • Duke clinical score is not implemented correctly in NICE guideline 95. • Pretest probability assessment in NICE guideline 95 is impossible for most patients. • Improved clinical decision making requires accurate pretest probability calculation. • These refinements are essential for appropriate use of cardiac CT.
KW - Coronary artery disease
KW - Duke clinical score
KW - Multidetector computed tomography
KW - NICE clinical guideline
KW - Pretest probability
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U2 - 10.1007/s00330-018-5322-5
DO - 10.1007/s00330-018-5322-5
M3 - Article
C2 - 29556770
AN - SCOPUS:85044175665
SN - 0938-7994
VL - 28
SP - 4006
EP - 4017
JO - European Radiology
JF - European Radiology
IS - 9
ER -