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Dive into the research topics where Birger Hesse is active.

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Featured researches published by Birger Hesse.


European Journal of Nuclear Medicine and Molecular Imaging | 2005

EANM/ESC procedural guidelines for myocardial perfusion imaging in nuclear cardiology

Birger Hesse; Kristina Tägil; Alberto Cuocolo; C Anagnostopoulos; Manuel Bardiès; Jeroen J. Bax; Frank M. Bengel; Ellinor Busemann Sokole; G Davies; Maurizio Dondi; Lars Edenbrandt; P Franken; Andreas Kjær; Juhani Knuuti; Michael Lassmann; Michael Ljungberg; Claudio Marcassa; Py Marie; F. McKiddie; Michael K. O'Connor; E Prvulovich; Richard Underwood; B. L. F. van Eck-Smit

The European procedural guidelines for radionuclide imaging of myocardial perfusion and viability are presented in 13 sections covering patient information, radiopharmaceuticals, injected activities and dosimetry, stress tests, imaging protocols and acquisition, quality control and reconstruction methods, gated studies and attenuation-scatter compensation, data analysis, reports and image display, and positron emission tomography. If the specific recommendations given could not be based on evidence from original, scientific studies, we tried to express this state-of-art. The guidelines are designed to assist in the practice of performing, interpreting and reporting myocardial perfusion SPET. The guidelines do not discuss clinical indications, benefits or drawbacks of radionuclide myocardial imaging compared to non-nuclear techniques, nor do they cover cost benefit or cost effectiveness.


Circulation | 2008

Trimetazidine, a Metabolic Modulator, Has Cardiac and Extracardiac Benefits in Idiopathic Dilated Cardiomyopathy

Helena Tuunanen; Erik Engblom; Alexandru Naum; Kjell Någren; Mika Scheinin; Birger Hesse; K.E. Juhani Airaksinen; Pirjo Nuutila; Heikki Ukkonen; Lionel H. Opie; Juhani Knuuti

Background— The anti-ischemic agent trimetazidine improves ejection fraction in heart failure that is hypothetically linked to inhibitory effects on cardiac free fatty acid (FFA) oxidation. However, FFA oxidation remains unmeasured in humans. We investigated the effects of trimetazidine on cardiac perfusion, efficiency of work, and FFA oxidation in idiopathic dilated cardiomyopathy. Methods and Results— Nineteen nondiabetic patients with idiopathic dilated cardiomyopathy on standard medication were randomized to single-blind trimetazidine (n=12) or placebo (n=7) for 3 months. Myocardial perfusion, FFA, and total oxidative metabolism were measured using positron emission tomography with [15O]H2O, [11C]acetate, and [11C]palmitate. Cardiac function was assessed echocardiographically; insulin sensitivity was assessed by the homeostasis model assessment index. Trimetazidine increased ejection fraction from 30.9±8.5% to 34.8±12% (P=0.027 versus placebo). Myocardial FFA uptake was unchanged, and &bgr;-oxidation rate constant decreased only 10%. Myocardial perfusion, oxidative metabolism, and work efficiency remained unchanged. Trimetazidine decreased insulin resistance (glucose: 5.9±0.7 versus 5.5±0.6 mmol/L, P=0.047; insulin: 10±6.9 versus 7.6±3.6 mU/L, P=0.031; homeostasis model assessment index: 2.75±2.28 versus 1.89±1.06, P=0.027). The degree of &bgr;-blockade and trimetazidine interacted positively on ejection fraction. Plasma high-density lipoprotein concentrations increased 11% (P<0.001). Conclusions— In idiopathic dilated cardiomyopathy with heart failure, trimetazidine increased cardiac function and had both cardiac and extracardiac metabolic effects. Cardiac FFA oxidation modestly decreased and myocardial oxidative rate was unchanged, implying increased oxidation of glucose. Trimetazidine improved whole-body insulin sensitivity and glucose control in these insulin-resistant idiopathic dilated cardiomyopathy patients, thus hypothetically countering the myocardial damage of insulin resistance. Additionally, the trimetazidine-induced increase in ejection fraction was associated with greater &bgr;1-adrenoceptor occupancy, suggesting a synergistic mechanism.


Circulation | 2006

Free Fatty Acid Depletion Acutely Decreases Cardiac Work and Efficiency in Cardiomyopathic Heart Failure

Helena Tuunanen; Erik Engblom; Alexandru Naum; Kjell Någren; Birger Hesse; K.E. Juhani Airaksinen; Pirjo Nuutila; Heikki Ukkonen; Lionel H. Opie; Juhani Knuuti

Background— Metabolic modulators that enhance myocardial glucose metabolism by inhibiting free fatty acid (FFA) metabolism may improve cardiac function in heart failure patients. We studied the effect of acute FFA withdrawal on cardiac function in patients with heart failure caused by idiopathic dilated cardiomyopathy (IDCM). Methods and Results— Eighteen fasting nondiabetic patients with IDCM (14 men, 4 women, aged 58.8±8.0 years, ejection fraction 33±8.8%) and 8 matched healthy controls underwent examination of myocardial perfusion and oxidative and FFA metabolism, before and after acute reduction of serum FFA concentrations by acipimox, an inhibitor of lipolysis. Metabolism was monitored by positron emission tomography and [15O]H2O, [11C]acetate, and [11C]palmitate. Left ventricular function and myocardial work were echocardiographically measured, and efficiency of forward work was calculated. Acipimox decreased myocardial FFA uptake by >80% in both groups. Rate–pressure product and myocardial perfusion remained unchanged, whereas stroke volume decreased similarly in both groups. In the healthy controls, reduced cardiac work was accompanied by decreased oxidative metabolism (from 0.071±0.019 to 0.055±0.016 min−1, P<0.01). In IDCM patients, cardiac work fell, whereas oxidative metabolism remained unchanged and efficiency fell (from 35.4±12.6 to 31.6±13.3 mm Hg · L · g−1, P<0.05). Conclusions— Acutely decreased serum FFA depresses cardiac work. In healthy hearts, this is accompanied by parallel decrease in oxidative metabolism, and myocardial efficiency is preserved. In failing hearts, FFA depletion did not downregulate oxidative metabolism, and myocardial efficiency deteriorated. Thus, failing hearts are unexpectedly more dependent than healthy hearts on FFA availability. We propose that both glucose and fatty acid oxidation are required for optimal function of the failing heart.


The Journal of Physiology | 2008

Effects of passive heating on central blood volume and ventricular dimensions in humans

Craig G. Crandall; Thad E. Wilson; Jens Marving; Thomas W. Vogelsang; Andreas Kjær; Birger Hesse; Niels H. Secher

Mixed findings regarding the effects of whole‐body heat stress on central blood volume have been reported. This study evaluated the hypothesis that heat stress reduces central blood volume and alters blood volume distribution. Ten healthy experimental and seven healthy time control (i.e. non‐heat stressed) subjects participated in this protocol. Changes in regional blood volume during heat stress and time control were estimated using technetium‐99m labelled autologous red blood cells and gamma camera imaging. Whole‐body heating increased internal temperature (> 1.0°C), cutaneous vascular conductance (approximately fivefold), and heart rate (52 ± 2 to 93 ± 4 beats min−1), while reducing central venous pressure (5.5 ± 07 to 0.2 ± 0.6 mmHg) accompanied by minor decreases in mean arterial pressure (all P < 0.05). The heat stress reduced the blood volume of the heart (18 ± 2%), heart plus central vasculature (17 ± 2%), thorax (14 ± 2%), inferior vena cava (23 ± 2%) and liver (23 ± 2%) (all P≤ 0.005 relative to time control subjects). Radionuclide multiple‐gated acquisition assessment revealed that heat stress did not significantly change left ventricular end‐diastolic volume, while ventricular end‐systolic volume was reduced by 24 ± 6% of pre‐heat stress levels (P < 0.001 relative to time control subjects). Thus, heat stress increased left ventricular ejection fraction from 60 ± 1% to 68 ± 2% (P= 0.02). We conclude that heat stress shifts blood volume from thoracic and splanchnic regions presumably to aid in heat dissipation, while simultaneously increasing heart rate and ejection fraction.


European Journal of Nuclear Medicine and Molecular Imaging | 2011

Hybrid cardiac imaging: SPECT/CT and PET/CT. A joint position statement by the European Association of Nuclear Medicine (EANM), the European Society of Cardiac Radiology (ESCR) and the European Council of Nuclear Cardiology (ECNC)

Albert Flotats; Juhani Knuuti; Matthias Gutberlet; Claudio Marcassa; Frank M. Bengel; Philippe A. Kaufmann; Michael R. Rees; Birger Hesse

Improvements in software and hardware have enabled the integration of dual imaging modalities into hybrid systems, which allow combined acquisition of the different data sets. Integration of positron emission tomography (PET) and computed tomography (CT) scanners into PET/CT systems has shown improvement in the management of patients with cancer over stand-alone acquired CT and PET images. Hybrid cardiac imaging either with single photon emission computed tomography (SPECT) or PET combined with CT depicts cardiac and vascular anatomical abnormalities and their physiologic consequences in a single setting and appears to offer superior information compared with either stand-alone or side-by-side interpretation of the data sets in patients with known or suspected coronary artery disease (CAD). Hybrid systems are also advantageous for the patient because of the single short dual data acquisition. However, hybrid cardiac imaging has also generated controversy with regard to which patients should undergo such integrated examination for clinical effectiveness and minimization of costs and radiation dose, and if software-based fusion of images obtained separately would be a useful alternative. The European Association of Nuclear Medicine (EANM), the European Society of Cardiac Radiology (ESCR) and the European Council of Nuclear Cardiology (ECNC) in this paper want to present a position statement of the institutions on the current roles of SPECT/CT and PET/CT hybrid cardiac imaging in patients with known or suspected CAD.


European Journal of Nuclear Medicine and Molecular Imaging | 2008

EANM/ESC guidelines for radionuclide imaging of cardiac function

Birger Hesse; T. B. Lindhardt; Wanda Acampa; Constantinos D. Anagnostopoulos; J. Ballinger; Jeroen J. Bax; Lars Edenbrandt; Albert Flotats; Guido Germano; T. Gmeiner Stopar; P Franken; A. Kelion; Andreas Kjær; D. Le Guludec; Michael Ljungberg; A. F. Maenhout; Claudio Marcassa; Jens Marving; F. McKiddie; Wolfgang M. Schaefer; L. Stegger; Richard Underwood

Radionuclide imaging of cardiac function represents a number of well-validated techniques for accurate determination of right (RV) and left ventricular (LV) ejection fraction (EF) and LV volumes. These first European guidelines give recommendations for how and when to use first-pass and equilibrium radionuclide ventriculography, gated myocardial perfusion scintigraphy, gated PET, and studies with non-imaging devices for the evaluation of cardiac function. The items covered are presented in 11 sections: clinical indications, radiopharmaceuticals and dosimetry, study acquisition, RV EF, LV EF, LV volumes, LV regional function, LV diastolic function, reports and image display and reference values from the literature of RVEF, LVEF and LV volumes. If specific recommendations given cannot be based on evidence from original, scientific studies, referral is given to “prevailing or general consensus”. The guidelines are designed to assist in the practice of referral to, performance, interpretation and reporting of nuclear cardiology studies for the evaluation of cardiac performance.


European Journal of Nuclear Medicine and Molecular Imaging | 2009

EANM-EORTC general recommendations for sentinel node diagnostics in melanoma

Annette Hougaard Chakera; Birger Hesse; Zeynep Burak; James R. Ballinger; Allan Britten; Corrado Caracò; Alistair J. Cochran; Martin G. Cook; Krzysztof T. Drzewiecki; Richard Essner; Einat Even-Sapir; Alexander M.M. Eggermont; tanja Gmeiner Stopar; Christian Ingvar; Martin C. Mihm; Stanley W. McCarthy; Nicola Mozzillo; Omgo E. Nieweg; Richard A. Scolyer; Hans Starz; John F. Thompson; Gianluca Trifirò; Giuseppe Viale; Sergi Vidal-Sicart; Roger F. Uren; Wendy Waddington; Arturo Chiti; Alain Spatz; Alessandro Testori

The accurate diagnosis of a sentinel node in melanoma includes a sequence of procedures from different medical specialities (nuclear medicine, surgery, oncology, and pathology). The items covered are presented in 11 sections and a reference list: (1) definition of a sentinel node, (2) clinical indications, (3) radiopharmaceuticals and activity injected, (4) dosimetry, (5) injection technique, (6) image acquisition and interpretation, (7) report and display, (8) use of dye, (9) gamma probe detection, (10) surgical techniques in sentinel node biopsy, and (11) pathological evaluation of melanoma-draining sentinel lymph nodes. If specific recommendations given cannot be based on evidence from original, scientific studies, referral is given to “general consensus” and similar expressions. The recommendations are designed to assist in the practice of referral to, performance, interpretation and reporting of all steps of the sentinel node procedure in the hope of setting state-of-the-art standards for good-quality evaluation of possible spread to the lymphatic system in intermediate-to-high risk melanoma without clinical signs of dissemination.


European Journal of Heart Failure | 2004

Natriuretic peptides in the monitoring of anthracycline induced reduction in left ventricular ejection fraction

Gedske Daugaard; Ulrik Lassen; Peter Bie; Erling Bjerregaard Pedersen; Kaare Jensen; Ulrik Abildgaard; Birger Hesse; Andreas Kjær

The use of anthracyclines in treatment of cancer is limited by cardiotoxicity of these compounds and may lead to heart failure. Therefore monitoring of cardiac function is necessary during therapy.


European Heart Journal | 2008

Clinical value, cost-effectiveness, and safety of myocardial perfusion scintigraphy: a position statement

Claudio Marcassa; Jeroen J. Bax; Frank M. Bengel; Birger Hesse; Claus Leth Petersen; Eliana Reyes; Richard Underwood

Mortality rates due to coronary artery disease (CAD) have declined in recent years as result of improved prevention, diagnosis, and management. Nonetheless, CAD remains the leading cause of death worldwide with most casualties expected to occur in developing nations. Myocardial perfusion scintigraphy (MPS) provides a highly cost-effective tool for the early detection of obstructive CAD in symptomatic individuals and contributes substantially to stratification of patients according to their risk of cardiac death or nonfatal myocardial infarction. MPS also provides valuable information that assists clinical decision-making with regard to medical treatment and intervention. A large body of evidence supports the current applications of MPS, which has become integral to several guidelines for clinical practice.


Circulation | 2005

NOGA-Guided Analysis of Regional Myocardial Perfusion Abnormalities Treated With Intramyocardial Injections of Plasmid Encoding Vascular Endothelial Growth Factor A-165 in Patients With Chronic Myocardial Ischemia Subanalysis of the EUROINJECT-ONE Multicenter Double-Blind Randomized Study

Mariann Gyöngyösi; Aliasghar Khorsand; Sholeh Zamini; Wolfgang Sperker; Christoph Strehblow; Jens Kastrup; Eric Jorgensen; Birger Hesse; Kristina Tägil; Hans Erik Bøtker; Witold Rużyłło; Anna Teresińska; Dariusz Dudek; Alicja Hubalewska; Andreas Rück; Søren Steen Nielsen; Senta Graf; Gerald Mundigler; Jacek Novak; Heinz Sochor; Gerald Maurer; Dietmar Glogar; Christer Sylvén

Background—The aim of this substudy of the EUROINJECT-ONE double-blind randomized trial was to analyze changes in myocardial perfusion in NOGA-defined regions with intramyocardial injections of plasmid encoding plasmid human (ph)VEGF-A165 using an elaborated transformation algorithm. Methods and Results—After randomization, 80 no-option patients received either active, phVEGF-A165 (n=40), or placebo plasmid (n=40) percutaneously via NOGA-Myostar injections. The injected area (region of interest, ROI) was delineated as a best polygon by connecting of the injection points marked on NOGA polar maps. The ROI was projected onto the baseline and follow-up rest and stress polar maps of the 99m-Tc-sestamibi/tetrofosmin single-photon emission computed tomography scintigraphy calculating the extent and severity (expressed as the mean normalized tracer uptake) of the ROI automatically. The extents of the ROI were similar in the VEGF and placebo groups (19.4±4.2% versus 21.5±5.4% of entire myocardium). No differences were found between VEGF and placebo groups at baseline with regard to the perfusion defect severity (rest: 69±11.7% versus 68.7±13.3%; stress: 63±13.3% versus 62.6±13.6%; and reversibility: 6.0±7.7% versus 6.7±9.0%). At follow-up, a trend toward improvement in perfusion defect severity at stress was observed in VEGF group as compared with placebo (68.5±11.9% versus 62.5±13.5%, P=0.072) without reaching normal values. The reversibility of the ROI decreased significantly at follow-up in VEGF group as compared with the placebo group (1.2±9.0% versus 7.1±9.0%, P=0.016). Twenty-one patients in VEGF and 8 patients in placebo group (P<0.01) exhibited an improvement in tracer uptake during stress, defined as a ≥5% increase in the normalized tracer uptake of the ROI. Conclusions—Projection of the NOGA-guided injection area onto the single-photon emission computed tomography polar maps permits quantitative evaluation of myocardial perfusion in regions treated with angiogenic substances. Injections of phVEGF A165 plasmid improve, but do not normalize, the stress-induced perfusion abnormalities.

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Andreas Kjær

University of Copenhagen

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Jens D. Hove

University of Copenhagen

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Jens Kastrup

University of Copenhagen

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Søren Holm

University of Manchester

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Ingolf Nielsen

University of Copenhagen

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Juhani Knuuti

Turku University Hospital

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