Olav Kjær Monsson

Dr. Olav Kjær Monsson

orcid

Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

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

Representative Publications

View All Publications
17 May 2025 in Diagnostics
Verified
Journal Article
Open access
PDF file
OMOlav Kjær Monsson
Olav Kjær Monsson
MNMarc Oestergaard Nielsen
Marc Oestergaard Nielsen
KKKümler Kümler
Kümler Kümler
CHChristian Haarmark
Christian Haarmark
BZBo Zerahn
Bo Zerahn
Background: Left ventricular ejection fraction remains the primary focus in cardiac monitoring for oncology patients undergoing potentially cardiotoxic chemotherapy, while right ventricular function is seldom examined. This study evaluates how established risk factors for left ventricular dysfunction affect right ventricular function. Methods: This retrospective cohort study included 1770 patients undergoing cadmium–zinc–telluride equilibrium radionuclide angiocardiography before chemotherapy. Patients were categorized based on risk factors for left ventricular dysfunction—diabetes (DM), atrial fibrillation (AF), coronary heart disease (CHD), and previous oncological therapy—and compared to controls using independent t-tests. Results: Patients with previous oncological therapy exhibited a significantly lower right ventricular end-diastolic volume (RVEDV) (mean difference: −4.4 mL/m2, 95% CI: −6.1 to −2.7, p < 0.001), lower right ventricular end-systolic volume (RVESV) (−2.3 mL/m2, 95% CI: −3.4 to −1.2, p < 0.001), and lower right ventricular stroke volume (RVSV) (−2.1 mL/m2, 95% CI: −3 to −1.2, p < 0.001). In patients with CHD, there was a higher right ventricular ejection fraction (RVEF) (3.0 mL/m2, 95% CI: 0.8 to 5.2, p < 0.01), whereas patients with DM had lower RVEDV (−5.1 mL/m2, 95% CI: −9.2 to −1, p < 0.05) and RVESV (−3.0 mL/m2, 95% CI: −5.5 to −0.4, p < 0.05). No ventricular variables differed from the control group among patients with AF. Conclusions: Risk factors known to affect the left ventricle also impacted the right ventricle, with the exception of AF.

14 May 2026 in Seizure: European Journal of Epilepsy
Verified
Journal Article
Open access
MNMadina Nazhaeva
Madina Nazhaeva
CDCharlotte Damien
Charlotte Damien
LKLeena Kämppi
Leena Kämppi
LRLars Egil Roberg
Lars Egil Roberg
OMOlav Kjær Monsson
Olav Kjær Monsson
CBChristoph P. Beier
Christoph P. Beier
To validate the complication burden index (CBI), a score quantifying 13 types of complications during status epilepticus (SE) treatment and evaluate its impact and that of its components on 6-month mortality. This retrospective multicenter cohort study included adult patients with non-anoxic SE treated at Odense University Hospital (Denmark) between 2008 and 2017 and at Erasme Hospital (Belgium) between 2014 and 2017. The association of CBI and its components -obtained from clinical records- with functional outcome, in-hospital, and 6-month mortality was assessed using uni- and multivariable analyses. Long-term survival depending on CBI was compared using the log-rank test. The combined cohort comprised 537 patients (n = 261 from Denmark and n = 276 from Belgium), with a median CBI of 3 in both cohorts (range: 0-10) with similar, though not identical, patterns observed in both. CBI was associated with treatment response in the emergency room, SE duration, comorbidities, and etiology, but not with age. CBI independently predicted in-hospital mortality in multivariate analyses in both cohorts. In contrast, in patients discharged alive from hospital, CBI was only weakly linked to 6 month-mortality. In multivariable analyses adjusted for age, duration and etiology, cardiovascular, respiratory and renal complications were the only components independently associated with in-hospital mortality. Cardiovascular, coagulative, infectious and renal complications independently predicted all-cause mortality at six months. CBI proves to be a valid tool for quantifying complication burden during SE. CBI and especially cardiovascular, respiratory, and renal complications are associated with in-hospital mortality. CBI was not an independent predictor of mortality after 6 months in patients discharged alive highlighting the temporal nature of complication-related mortality.