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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004788naa a2200445 4500
001oai:DiVA.org:liu-116549
003SwePub
008150327s2015 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:227533964
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1165492 URI
024a https://doi.org/10.1093/ehjcvp/pvu0212 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:2275339642 URI
040 a (SwePub)liud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Karlsson, Jan-Eriku Linköpings universitet,Avdelningen för kardiovaskulär medicin,Hälsouniversitetet,Department of Internal Medicine, County Council of Jönköping, Ryhov County Hospital, Jönköping, Sweden4 aut0 (Swepub:liu)janka97
2451 0a Mangafodipir as a cardioprotective adjunct to reperfusion therapy: a feasibility study in patients with ST-segment elevation myocardial infarction
264 c 2015-01-01
264 1b European Society of Cardiology,c 2015
338 a print2 rdacarrier
520 a Aims The aim of the present study was to examine the feasibility of applying the catalytic antioxidant mangafodipir [MnDPDP, manganese (Mn) dipyridoxyl diphosphate] as a cardioprotective adjunct to primary percutaneous coronary intervention (pPCI) in patients with ST-segment elevation (STE) myocardial infarction (STEMI). Both MnDPDP and a metabolite (Mn dipyridoxyl ethyldiamine) possess properties as mitochondrial superoxide dismutase mimetics and iron chelators, and combat oxidative stress in various tissues and conditions.Methods and resultsThe study tested MnDPDP (n ¼ 10) vs. saline placebo (n ¼ 10), given as a brief intravenous (i.v.) infusion prior to balloon inflation during pPCI in patients with STEMI. Mangafodipir waswell tolerated and did not affect heart rate or blood pressure. Despite longer ischaemic time (205 vs. 144 min, P ¼ 0.019) in theMnDPDPgroup, plasma biomarker releaseswere identical for the two groups. With placebo vs.MnDPDP, mean STE resolutions were 69.8 vs. 81.9% (P ¼ 0.224) at 6 h and 73.1 vs. 84.3% (P ¼ 0.077) at 48 h. Cardiac magnetic resonance revealed mean infarct sizes of 32.5 vs. 26.2% (P ¼ 0.406) andmeanleft ventricular (LV) ejection fractions of 41.8 vs. 47.7% (P ¼ 0.617) with placebovs.MnDPDP.More LVthrombi were detected in placebo hearts (5 of 8) than MnDPDP-treated hearts (1 of 10; P ¼ 0.011).Conclusions Mangafodipir is a safe drug for use as an adjunct to reperfusion therapy. A tendency to benefit of MnDPDP needs confirmation in a larger population. The study revealed important information for the design of a Phase II trial. 
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Kardiologi0 (SwePub)302062 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cardiac and Cardiovascular Systems0 (SwePub)302062 hsv//eng
653 a Cardiac reperfusion injury; Primary PCI; STEMI; Oxidative stress; Mitochondrial superoxide dismutase
700a El-Saadi, Walidu Department of Internal Medicine, County Council of Jönköping, Ryhov County Hospital, Jönköping, Sweden4 aut
700a Ali, Mustafau Department of Internal Medicine, County Council of Jönköping, Ryhov County Hospital, Jönköping, Sweden; Department of Radiology, County Council of Jönköping, Jönköping, Sweden4 aut
700a Puskar, Werneru Department of Radiology, County Council of Jönköping, Jönköping, Sweden4 aut
700a Skogvard, Patriku Department of Internal Medicine, County Council of Jönköping, Ryhov County Hospital, Jönköping, Sweden4 aut
700a Engvall, Jan Eu Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kardiovaskulär medicin,Hälsouniversitetet,Fysiologiska kliniken US4 aut0 (Swepub:liu)janen74
700a Andersson, Rolfu Linköpings universitet,Avdelningen för läkemedelsforskning,Hälsouniversitetet4 aut0 (Swepub:liu)rolan40
700a Maret, Evau Karolinska Institutet4 aut
700a Jynge, Peru Linköpings universitet,Avdelningen för läkemedelsforskning,Hälsouniversitetet,PledPharma AB, Stockholm, Sweden4 aut0 (Swepub:liu)perjy52
710a Linköpings universitetb Avdelningen för kardiovaskulär medicin4 org
773t European Heart Journal - Cardiovascular Pharmacotherapyd : European Society of Cardiologyg 1:1, s. 39-45q 1:1<39-45x 2055-6837x 2055-6845
856u https://academic.oup.com/ehjcvp/article-pdf/1/1/39/8066482/pvu021.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-116549
8564 8u https://doi.org/10.1093/ehjcvp/pvu021
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:227533964

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