Franz M. Kainberger

Prof. Dr. Franz M. Kainberger


Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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1 September 2012 in Bone
Verified
Journal Article
Closed access
AVAlexander Valentinitsch
Alexander Valentinitsch
JPJanina M Patsch
Janina M Patsch
JDJulia Deutschmann
Julia Deutschmann
CSClaudia Schueller-Weidekamm
Claudia Schueller-Weidekamm
Heinrich ReschHeinrich Resch
Heinrich Resch
GLGeorg Langs
Georg Langs

29 May 2009 in Trials
Verified
Journal Article
Open access
PDF file
UTUrsula Thiem
Ursula Thiem
Georg HeinzeGeorg Heinze
Georg Heinze
RSRudolf Segel
Rudolf Segel
TPThomas Perkmann
Thomas Perkmann
FKFranz M. Kainberger
Franz M. Kainberger
KBKyra Borchhardt
Kyra Borchhardt
Background: Vitamin D does not only regulate calcium homeostasis but also plays an important role as an immune modulator. It influences the immune system through the induction of immune shifts and regulatory cells resulting in immunologic tolerance. As such, vitamin D is thought to exert beneficial effects within the transplant setting, especially in kidney transplant recipients, considering the high prevalence of vitamin D deficiency in kidney transplant recipients.Methods/Design: The VITA-D study, a randomized, placebo-controlled, double-blind study with two parallel groups including a total of 200 kidney transplant recipients, is designed to investigate the immunomodulatory and renoprotective effects of cholecalciferol (vitamin D3) within the transplant setting. Kidney transplant recipients found to have vitamin D deficiency defined as 25-hydroxyvitamin D3< 50 nmol per liter will be randomly assigned to receive either oral cholecalciferol therapy or placebo and will be followed for one year. Cholecalciferol will be administered at a dose of 6800 International Units daily over a time period of one year.The objective is to evaluate the influence of vitamin D3substitution in vitamin D deficient kidney transplant recipients on the post-transplant outcome. As a primary endpoint glomerular filtration rate calculated with the MDRD formula (modification of diet in renal disease) one year after kidney transplantation will be evaluated. Incidence of acute rejection episodes, and the number and severity of infections (analyzed by means of C-reactive protein) within the first year after transplantation will be monitored as well. As a secondary endpoint the influence of vitamin D3on bone mineral density within the first year post-transplant will be assessed. Three DXA analyses will be performed, one within the first four weeks post-transplant, one five months and one twelve months after kidney transplantation.Trial Registration: ClinicalTrials.gov NCT00752401

2 July 2018 in Obesity Surgery
Verified
Journal Article
Open access
PDF file
MLMaria Luger
Maria Luger
RKRenate Kruschitz
Renate Kruschitz
EWEva Winzer
Eva Winzer
KSKarin Schindler
Karin Schindler
Igor GrabovacIgor Grabovac
Igor Grabovac
BLBernhard Ludvik
Bernhard Ludvik
Little is known about changes in bone mineral density (BMD) following weight loss after one-anastomosis gastric bypass (OAGB) and the role of serum vitamin D and its supplementation on bone metabolism. We evaluated BMD after OAGB as a function of vitamin D supplementation with respect to a minimum threshold of 25-hydroxy-vitamin-D [25(OH)D] concentration, which could prevent or decelerate an eventual bone loss.

26 September 2016 in Wiener klinische Wochenschrift
Verified
Journal Article
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FKFranz M. Kainberger
Franz M. Kainberger

14 March 2024 in Journal of Imaging Informatics in Medicine
Verified
Journal Article
Open access
PDF file
MBMartin Bittner-Frank
Martin Bittner-Frank
ASAndreas Strassl
Andreas Strassl
EUEwald Unger
Ewald Unger
Lena HirtlerLena Hirtler
Lena Hirtler
BEBarbara Eckhart
Barbara Eckhart
EBEmir Benca
Emir Benca
The introduction of three-dimensional (3D) printed anatomical models has garnered interest in pre-operative planning, especially in orthopedic and trauma surgery. Identifying potential error sources and quantifying their effect on the model dimensional accuracy are crucial for the applicability and reliability of such models. In this study, twenty radii were extracted from anatomic forearm specimens and subjected to osteotomy to simulate a defined fracture of the distal radius (Colles’ fracture). Various factors, including two different computed tomography (CT) technologies (energy-integrating detector (EID) and photon-counting detector (PCD)), four different CT scanners, two scan protocols (i.e., routine and high dosage), two different scan orientations, as well as two segmentation algorithms were considered to determine their effect on 3D model accuracy. Ground truth was established using 3D reconstructions of surface scans of the physical specimens. Results indicated that all investigated variables significantly impacted the 3D model accuracy (p < 0.001). However, the mean absolute deviation fell within the range of 0.03 ± 0.20 to 0.32 ± 0.23 mm, well below the 0.5 mm threshold necessary for pre-operative planning. Intra- and inter-operator variability demonstrated fair to excellent agreement for 3D model accuracy, with an intra-class correlation (ICC) of 0.43 to 0.92. This systematic investigation displayed dimensional deviations in the magnitude of sub-voxel imaging resolution for all variables. Major pitfalls included missed or overestimated bone regions during the segmentation process, necessitating additional manual editing of 3D models. In conclusion, this study demonstrates that 3D bone fracture models can be obtained with clinical routine scanners and scan protocols, utilizing a simple global segmentation threshold, thereby providing an accurate and reliable tool for pre-operative planning.