Vasil Dimitrov

Prof. Vasil Dimitrov

University Hospital Aleksandrovska, Sofia, Bulgaria
orcid

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 March 2010 in Journal of Allergy and Clinical Immunology
Verified
Journal Article
Closed access
MSMaria Staevska
Maria Staevska
TPTodor Popov
Todor Popov
TKTanya Kralimarkova
Tanya Kralimarkova
CLCvetelina Lazarova
Cvetelina Lazarova
SKSteliana Kraeva
Steliana Kraeva
MCMartin K. Church
Martin K. Church

23 December 2008 in Allergy
Verified
Journal Article
Closed access
PDF file
CBC. Bachert
C. Bachert
PKP. Kuna
P. Kuna
FSF. Sanquer
F. Sanquer
PIP. Ivan
P. Ivan
VDVasil Dimitrov
Vasil Dimitrov
TGThe Bilastine International Working Group
The Bilastine International Working Group

28 January 2014 in British Journal of Dermatology
Verified
Journal Article
Open access
PDF file
MSM. Staevska
M. Staevska
MGM. Gugutkova
M. Gugutkova
CLC. Lazarova
C. Lazarova
TKT. Kralimarkova
T. Kralimarkova
VDVasil Dimitrov
Vasil Dimitrov
TPTodor Popov
Todor Popov
Background Many physicians believe that the most effective way to treat chronic urticaria is to take a nonsedating second‐generation H1‐antihistamine in the morning and a sedating first‐generation H1‐antihistamine, usually hydroxyzine, at night to enhance sleep. But is this belief well founded? Objectives To test this belief by comparing the effectiveness and prevalence of unwanted sedative effects when treating patients with chronic spontaneous urticaria (CSU) with levocetirizine 15 mg daily plus hydroxyzine 50 mg at night (levocetirizine plus hydroxyzine) vs. levocetirizine 20 mg daily (levocetirizine monotherapy). Methods In this randomized, double‐blind, cross‐over study, 24 patients with difficult‐to‐treat CSU took levocetirizine plus hydroxyzine or levocetirizine monotherapy for periods of 5 days each. At the end of each treatment period, assessments were made of quality of life (Chronic Urticaria Quality of Life Questionnaire, CU‐Q2oL), severity of urticaria symptoms (Urticaria Activity Score, UAS), sleep disturbance during the night and daytime somnolence. Results Both treatments significantly decreased UAS, night‐time sleep disturbances and CU‐Q2oL scores (P < 0·001) without significant differences between the two. Compared with baseline, daytime somnolence was significantly reduced by levocetirizine monotherapy (P = 0·006) but not by levocetirizine plus hydroxyzine (P = 0·218). Direct comparison of the two treatment modalities in terms of daytime somnolence favoured levocetirizine monotherapy (P = 0·026). Conclusions The widespread belief that sleep is aided by the addition of a sedating first‐generation H1‐antihistamine, usually hydroxyzine, at night is not supported. These results are in line with the urticaria guidelines, which state that first‐line treatment for urticaria should be new‐generation, nonsedating H1‐antihistamines only.

1 May 2004 in Current Allergy and Asthma Reports
Verified
Journal Article
Closed access
PDF file
MSMaria T. Staevska
Maria T. Staevska
MMMariana A. Mandajieva
Mariana A. Mandajieva
VDVasil Dimitrov
Vasil Dimitrov

1 January 2012 in Breathe
Verified
Journal Article
Open access
PDF file
TPTodor Popov
Todor Popov
TKT.Z. Kralimarkova
T.Z. Kralimarkova
VDVasil Dimitrov
Vasil Dimitrov
Educational aims: To review the link between inflammation and increased vascularity and blood flow of the airways, and exhaled breath temperature. To position exhaled breath temperature (EBT) as a physiological characteristic differing from core temperature measured at other body sites. To review the existing experience about measuring EBT in different disease states of the respiratory system. To emphasise the influence of airway remodeling/destruction in modulating EBT. Summary: Evaluation of the exhaled breath temperature (EBT) has been suggested as a new method to detect and monitor pathological processes in the respiratory system. The putative mechanism of this approach is based upon changes in the blood flow in the conducting airways that are characteristic of different disease states, which influence the temperature of the exhaled gases. The first attempts to prove this concept were made in conjunction with measurement of exhaled nitric oxide fraction (FeNO) about a decade ago. They made use of an open-circuit, single-breath method in a closed indoor environment, and demonstrated associations between EBT on the one hand, and bronchial blood flow,FeNOand sputum cellular content on the other.These findings have been further extended to practical applicability with the introduction of multiple-breath, portable hand-held devices. Measurement of EBT using these is less dependent on the ambient environment and easier to perform. Studies have been conducted to explore the relationship between EBT and different physiological characteristics, and to assess possible confounding influences in the process of measurement. The value of the method has been explored in the diagnosis and monitoring of asthma, chronic obstructive pulmonary disease and other respiratory diseases. While initially, emphasis focused on airway inflammation as the primary process to be captured by this method, it was subsequently realised that destructive and other remodelling processes reducing the integral contact surface of the conducting airways and/or damaging their vasculature would also affect the end result by shifting EBT downwards. As obstructive airway disease is, in most cases, a combination of airway inflammation and remodelling/destruction, EBT should be viewed as an individual characteristic indicating fluctuating changes in the balance of these processes. Hence, an important potential application of the method is in monitoring airway diseases.EBT measurement has emerged as an attractive noninvasive new approach in respiratory and, possibly, other diseases. Systematic research will determine its place in clinical practice.

1 June 2006 in Inflammation Research
Verified
Journal Article
Closed access
PDF file
TPTodor Popov
Todor Popov
DDD. Dumitrascu
D. Dumitrascu
ABA. Bachvarova
A. Bachvarova
CBC. Bocsan
C. Bocsan
VDVasil Dimitrov
Vasil Dimitrov
MCM. K. Church
M. K. Church