Fajko F. Bajrović
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Fajko F. Bajrović has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Daša Stupica
Department of Infectious Diseases, University Medical Centre Ljubljana, Ljubljana, Slovenia
3 shared publications - Franc Strle
Department of Infectious Diseases, University Medical Centre Ljubljana, Japljeva 2, 1525 Ljubljana, Slovenia
2 shared publications - Janja Pretnar Oblak
Department of Vascular Neurology and Intensive Neurological Therapy, University Medical Centre Ljubljana , Ljubljana
2 shared publications - Katja Pavšič
Department of Vascular Neurology and Intensive Therapy, University Medical Centre Ljubljana, Slovenia; Faculty of Medicine, University of Ljubljana, Slovenia
2 shared publications - Leja Dolenc Grošelj
Institute of Clinical Neurophysiology, University Medical Centre Ljubljana, Ljubljana, Slovenia
2 shared publications - Maša Velušček
Department of Infectious Diseases, University Medical Center Ljubljana, Japljeva 2, Ljubljana 1525, Slovenia
2 shared publications
Latest Publications
- 13 October 2025
- Published by Springer Nature in Neuroradiology
- Vol. 67 (12) , 3543-3553
Computed tomography–derived Ktrans and serum S100B in quantitative evaluation of blood–brain barrier permeability in traumatic brain injury
Purpose Traumatic brain injury (TBI) often leads to blood-brain barrier (BBB) disruption, contributing to secondary brain damage. Perfusion computed tomography (PCT) may assess BBB permeability through the transfer constant (Ktrans), while serum S100 calcium-binding protein B (S100B) serves as a biomarker of BBB integrity. However, the relationship between PCT derived Ktrans and serum S100B concentrations in TBI has not been fully explored. Methods This observational study included 26 adult patients with moderate or severe TBI. PCT was performed 12–24 h after admission to measure Ktrans values in the pericontusional edema region. Serum S100B levels were measured at regular intervals during the first 36 h. Correlations between Ktrans and S100B were analyzed using Spearman’s rank correlation, and the predictive capacity of mean Ktrans for serum S100B rise was evaluated using receiver operating characteristic (ROC) analysis. Results A significant positive correlation was found between both initial and peak serum S100B concentrations and mean Ktrans (rs = 0.52, p = 0.018 and rs = 0.47, p = 0.029, respectively) and maximum Ktrans values (rs = 0.47, p = 0.029 and rs = 0.56, p = 0.011, respectively). ROC analysis showed that mean Ktrans values predicted serum S100B rise with AUC of 0,74 (CI 95%: 0.55, 0.91). Conclusions Our findings demonstrated a significant correlation between pericontusional Ktrans values and serum S100B concentrations, with mean Ktrans values showing potential as an early predictor for serum S100B rise. These findings suggest that combining PCT and serum biomarkers could improve assessment of BBB integrity and aid in the management of TBI.
- 13 October 2025
- Published by Springer Nature in Neuroradiology
- Vol. 67 (12) , 3543-3553
Computed tomography–derived Ktrans and serum S100B in quantitative evaluation of blood–brain barrier permeability in traumatic brain injury
Purpose Traumatic brain injury (TBI) often leads to blood-brain barrier (BBB) disruption, contributing to secondary brain damage. Perfusion computed tomography (PCT) may assess BBB permeability through the transfer constant (Ktrans), while serum S100 calcium-binding protein B (S100B) serves as a biomarker of BBB integrity. However, the relationship between PCT derived Ktrans and serum S100B concentrations in TBI has not been fully explored. Methods This observational study included 26 adult patients with moderate or severe TBI. PCT was performed 12–24 h after admission to measure Ktrans values in the pericontusional edema region. Serum S100B levels were measured at regular intervals during the first 36 h. Correlations between Ktrans and S100B were analyzed using Spearman’s rank correlation, and the predictive capacity of mean Ktrans for serum S100B rise was evaluated using receiver operating characteristic (ROC) analysis. Results A significant positive correlation was found between both initial and peak serum S100B concentrations and mean Ktrans (rs = 0.52, p = 0.018 and rs = 0.47, p = 0.029, respectively) and maximum Ktrans values (rs = 0.47, p = 0.029 and rs = 0.56, p = 0.011, respectively). ROC analysis showed that mean Ktrans values predicted serum S100B rise with AUC of 0,74 (CI 95%: 0.55, 0.91). Conclusions Our findings demonstrated a significant correlation between pericontusional Ktrans values and serum S100B concentrations, with mean Ktrans values showing potential as an early predictor for serum S100B rise. These findings suggest that combining PCT and serum biomarkers could improve assessment of BBB integrity and aid in the management of TBI.
- 1 March 2021
- Published by Elsevier in Respiratory Physiology & Neurobiology
- Vol. 285, 103592
Breathing patterns in relation to sleep stages in acute unilateral lateral medullary infarction: An exploratory study
- 1 March 2021
- Published by Elsevier in Respiratory Physiology & Neurobiology
- Vol. 285, 103592
Breathing patterns in relation to sleep stages in acute unilateral lateral medullary infarction: An exploratory study
- 16 February 2020
- Published by Springer Nature in Sleep and Breathing
- Vol. 24 (4) , 1557-1563
Prospective study of sleep-disordered breathing in 28 patients with acute unilateral lateral medullary infarction
Objective Acute unilateral lateral medullary infarction (ULMI) is complicated by respiratory failure in 2–6% of patients. However, studies investigating milder respiratory disorders not leading to overt respiratory failure, i.e., sleep-disordered breathing (SDB) and its outcome, are lacking. The aim of our study was to identify and prospectively follow SDB in acute ULMI. Methods We prospectively followed 28 patients with MRI-confirmed acute ULMI. Polysomnography (PSG) was performed 1–3 times in the acute phase (at 1–4, 5–10, and 14–21 days after onset of symptoms) and after 3–6 months. PSG recordings in the acute phase were analyzed and compared to the follow-up. Results Apnea-hypopnea index (AHI) ≥ 5/h, AHI ≥ 15/h, and AHI ≥ 30/h in the acute phase were observed in 22 (79%), 19 (68%), and 10 (36%) patients, respectively. CSA, OSA, mixed CSA/OSA, or multiple interchanging SDB types were observed in the acute phase in 12 (43%), 2 (7%), 2 (7%), and 6 (21%) patients, respectively. Peak AHI varied in individual patients (median at 7 (3–14) days after onset). At follow-up, AHI and central AHI tended to decrease (p = 0.007, p = 0.003, respectively), obstructive AHI did not change (p = 0.396). Sleep architecture partially improved with significantly higher percentage of N2 and lower percentage of wakefulness after sleep onset (p = 0.007, p = 0.012, respectively). Conclusions Our data show that SDB, particularly CSA, is common in the acute phase of ULMI and that the frequency of central events decreases in the subacute phase. Further studies are needed to clarify the clinical significance and possible treatment options of SDB in these patients.
- 16 February 2020
- Published by Springer Nature in Sleep and Breathing
- Vol. 24 (4) , 1557-1563
Prospective study of sleep-disordered breathing in 28 patients with acute unilateral lateral medullary infarction
Objective Acute unilateral lateral medullary infarction (ULMI) is complicated by respiratory failure in 2–6% of patients. However, studies investigating milder respiratory disorders not leading to overt respiratory failure, i.e., sleep-disordered breathing (SDB) and its outcome, are lacking. The aim of our study was to identify and prospectively follow SDB in acute ULMI. Methods We prospectively followed 28 patients with MRI-confirmed acute ULMI. Polysomnography (PSG) was performed 1–3 times in the acute phase (at 1–4, 5–10, and 14–21 days after onset of symptoms) and after 3–6 months. PSG recordings in the acute phase were analyzed and compared to the follow-up. Results Apnea-hypopnea index (AHI) ≥ 5/h, AHI ≥ 15/h, and AHI ≥ 30/h in the acute phase were observed in 22 (79%), 19 (68%), and 10 (36%) patients, respectively. CSA, OSA, mixed CSA/OSA, or multiple interchanging SDB types were observed in the acute phase in 12 (43%), 2 (7%), 2 (7%), and 6 (21%) patients, respectively. Peak AHI varied in individual patients (median at 7 (3–14) days after onset). At follow-up, AHI and central AHI tended to decrease (p = 0.007, p = 0.003, respectively), obstructive AHI did not change (p = 0.396). Sleep architecture partially improved with significantly higher percentage of N2 and lower percentage of wakefulness after sleep onset (p = 0.007, p = 0.012, respectively). Conclusions Our data show that SDB, particularly CSA, is common in the acute phase of ULMI and that the frequency of central events decreases in the subacute phase. Further studies are needed to clarify the clinical significance and possible treatment options of SDB in these patients.
- Open Access
- 20 October 2019
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 8 (10) , 1740
Antibiotic Use and Long-Term Outcome in Patients with Tick-Borne Encephalitis and Co-Infection with Borrelia Burgdorferi Sensu Lato in Central Europe. A Retrospective Cohort Study
In this retrospective cohort study of patients with tick-borne encephalitis (TBE), the clinical outcome in relation to co-infection with B. burgdorferi sensu lato (s.l.) and, specifically, the effect of antibiotic treatment on clinical outcome in patients with TBE who were seropositive for borreliae but who did not fulfil clinical or microbiologic criteria for proven co-infection, were assessed at a single university medical center in Slovenia, a country where TBE and Lyme borreliosis are endemic with high incidence. Among 684 patients enrolled during a seven-year period from 2007 through 2013, 382 (55.8%) had TBE alone, 62 (9.1%) had proven co-infection with borreliae and 240 (35.1%) had possible co-infection. The severity of acute illness was similar in all the groups. The odds for incomplete recovery decreased during a 12-month follow-up but were higher in women, older patients, and in those with more severe acute illness. Incomplete recovery was not associated with either proven (odds ratio (OR) 1.21, 95% confidence interval (CI) 0.49–2.95; p = 0.670) or possible co-infection (OR 0.95, 95% CI 0.55–1.65; p = 0.853). Among patients with possible co-infection, older patients were more likely to be prescribed antibiotics, but the odds for incomplete recovery were similar in those who received antibiotics and those who did not (OR 0.82, 95% CI 0.36–1.87; p = 0.630), suggesting that routine antibiotic treatment in patients with TBE and possible co-infection may not be warranted.
- 20 October 2019
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 8 (10) , 1740
Open AccessAntibiotic Use and Long-Term Outcome in Patients with Tick-Borne Encephalitis and Co-Infection with Borrelia Burgdorferi Sensu Lato in Central Europe. A Retrospective Cohort Study
In this retrospective cohort study of patients with tick-borne encephalitis (TBE), the clinical outcome in relation to co-infection with B. burgdorferi sensu lato (s.l.) and, specifically, the effect of antibiotic treatment on clinical outcome in patients with TBE who were seropositive for borreliae but who did not fulfil clinical or microbiologic criteria for proven co-infection, were assessed at a single university medical center in Slovenia, a country where TBE and Lyme borreliosis are endemic with high incidence. Among 684 patients enrolled during a seven-year period from 2007 through 2013, 382 (55.8%) had TBE alone, 62 (9.1%) had proven co-infection with borreliae and 240 (35.1%) had possible co-infection. The severity of acute illness was similar in all the groups. The odds for incomplete recovery decreased during a 12-month follow-up but were higher in women, older patients, and in those with more severe acute illness. Incomplete recovery was not associated with either proven (odds ratio (OR) 1.21, 95% confidence interval (CI) 0.49–2.95; p = 0.670) or possible co-infection (OR 0.95, 95% CI 0.55–1.65; p = 0.853). Among patients with possible co-infection, older patients were more likely to be prescribed antibiotics, but the odds for incomplete recovery were similar in those who received antibiotics and those who did not (OR 0.82, 95% CI 0.36–1.87; p = 0.630), suggesting that routine antibiotic treatment in patients with TBE and possible co-infection may not be warranted.
- Open Access
- 3 August 2018
- Published by Springer Nature in BMC Infectious Diseases
- Vol. 18 (1) , 365
Doxycycline-induced photosensitivity in patients treated for erythema migrans
Doxycycline is one of the recommended antibiotics for treating erythema migrans (EM). Since EM predominantly occurs during summer, the potential of doxycycline to induce photosensitivity is of concern. In studies on the efficacy of doxycycline for treating relatively small numbers of patients with EM, the reported frequency of photosensitivity has varied from none to 15%. The aim of this study was to elucidate the frequency and clinical symptoms of doxycycline-induced photosensitivity in a large cohort of patients with EM treated in a single medical centre. Prospectively collected data on adverse events were analysed in adult patients with EM treated with doxycycline 100 mg twice daily for 10–15 days. Photosensitivity reactions ranging from itching and burning sensations to transient mild erythema of sun-exposed skin were documented in 16/858 (1.9, 95% CI 1.1–3.0%) patients and appeared from June to October with highest frequency in July. These adverse events were more frequent in patients treated for 14 or 15 days (16/750 [2.1%]; 95% CI 1.2–3.4%) than in those treated for 10 days (0/108 [0%]; 95% CI 0.0–3.4%); however, the difference was not significant (P = 0.24). Women were more often affected than men (13/475 [2.7%], 95% CI 1.5–4.6% versus 3/383 [0.8%], 95% CI 0.2–2.3%; P = 0.04). Of the 16 patients who developed photosensitivity, 13 did not adhere to the recommendation to avoid sun exposure. None of the patients had any long-term sequelae of photosensitivity. Photosensitivity reactions in adult patients with EM treated with doxycycline 100 mg twice daily for 10–15 days occurred rarely, were not severe, and had no long-term sequelae. Registered at http://clinicaltrials.gov , Identifiers NCT00910715, May 28th 2009, NCT01163994, July 13th 2010 and NCT03584919, June 19th 2018 retrospectively registered.
- 3 August 2018
- Published by Springer Nature in BMC Infectious Diseases
- Vol. 18 (1) , 365
Open AccessDoxycycline-induced photosensitivity in patients treated for erythema migrans
Doxycycline is one of the recommended antibiotics for treating erythema migrans (EM). Since EM predominantly occurs during summer, the potential of doxycycline to induce photosensitivity is of concern. In studies on the efficacy of doxycycline for treating relatively small numbers of patients with EM, the reported frequency of photosensitivity has varied from none to 15%. The aim of this study was to elucidate the frequency and clinical symptoms of doxycycline-induced photosensitivity in a large cohort of patients with EM treated in a single medical centre. Prospectively collected data on adverse events were analysed in adult patients with EM treated with doxycycline 100 mg twice daily for 10–15 days. Photosensitivity reactions ranging from itching and burning sensations to transient mild erythema of sun-exposed skin were documented in 16/858 (1.9, 95% CI 1.1–3.0%) patients and appeared from June to October with highest frequency in July. These adverse events were more frequent in patients treated for 14 or 15 days (16/750 [2.1%]; 95% CI 1.2–3.4%) than in those treated for 10 days (0/108 [0%]; 95% CI 0.0–3.4%); however, the difference was not significant (P = 0.24). Women were more often affected than men (13/475 [2.7%], 95% CI 1.5–4.6% versus 3/383 [0.8%], 95% CI 0.2–2.3%; P = 0.04). Of the 16 patients who developed photosensitivity, 13 did not adhere to the recommendation to avoid sun exposure. None of the patients had any long-term sequelae of photosensitivity. Photosensitivity reactions in adult patients with EM treated with doxycycline 100 mg twice daily for 10–15 days occurred rarely, were not severe, and had no long-term sequelae. Registered at http://clinicaltrials.gov , Identifiers NCT00910715, May 28th 2009, NCT01163994, July 13th 2010 and NCT03584919, June 19th 2018 retrospectively registered.
- Open Access
- 18 November 2014
- Published by Springer Nature in BMC Infectious Diseases
- Vol. 14 (1) , 1-3
Tick borne encephalitis without cerebrospinal fluid pleocytosis
Tick borne encephalitis is the most frequent vector-transmitted infectious disease of the central nervous system in Europe and Asia. The disease caused by European subtype of tick borne encephalitis virus has typically a biphasic clinical course with the second phase presenting as meningitis, meningoencephalitis, or meningoencephalomyelitis. Cerebrospinal fluid pleocytosis is considered a condition sine qua non for the diagnosis of neurologic involvement in tick borne encephalitis, which in routine clinical practice is confirmed by demonstration of serum IgM and IgG antibodies to tick borne encephalitis virus. Here we present a patient from Slovenia, an area highly endemic for tick borne encephalitis, with encephalitis but without cerebrospinal fluid pleocytosis in whom tick borne encephalitis virus infection of the central nervous system was demonstrated. Cerebrospinal fluid pleocytosis is not mandatory in encephalitis caused by tick borne encephalitis virus. In daily clinical practice, in patients with neurologic symptoms/signs compatible with tick borne encephalitis and the risk of exposure to ticks in a tick borne encephalitis endemic region, the search for central nervous system infection with tick borne encephalitis virus is warranted despite the lack of cerebrospinal fluid pleocytosis.
- 18 November 2014
- Published by Springer Nature in BMC Infectious Diseases
- Vol. 14 (1) , 1-3
Open AccessTick borne encephalitis without cerebrospinal fluid pleocytosis
Tick borne encephalitis is the most frequent vector-transmitted infectious disease of the central nervous system in Europe and Asia. The disease caused by European subtype of tick borne encephalitis virus has typically a biphasic clinical course with the second phase presenting as meningitis, meningoencephalitis, or meningoencephalomyelitis. Cerebrospinal fluid pleocytosis is considered a condition sine qua non for the diagnosis of neurologic involvement in tick borne encephalitis, which in routine clinical practice is confirmed by demonstration of serum IgM and IgG antibodies to tick borne encephalitis virus. Here we present a patient from Slovenia, an area highly endemic for tick borne encephalitis, with encephalitis but without cerebrospinal fluid pleocytosis in whom tick borne encephalitis virus infection of the central nervous system was demonstrated. Cerebrospinal fluid pleocytosis is not mandatory in encephalitis caused by tick borne encephalitis virus. In daily clinical practice, in patients with neurologic symptoms/signs compatible with tick borne encephalitis and the risk of exposure to ticks in a tick borne encephalitis endemic region, the search for central nervous system infection with tick borne encephalitis virus is warranted despite the lack of cerebrospinal fluid pleocytosis.