2018
Hypersensitivity to material and environmental burden as a possible cause of late complications of cardiac implantable electronic devices
MAŇOUSEK, Jan, Irena ANDRŠOVÁ, Vera STEJSKAL, Jitka VLAŠÍNOVÁ, Milan SEPŠI et. al.Základní údaje
Originální název
Hypersensitivity to material and environmental burden as a possible cause of late complications of cardiac implantable electronic devices
Autoři
MAŇOUSEK, Jan (203 Česká republika), Irena ANDRŠOVÁ (203 Česká republika), Vera STEJSKAL (752 Švédsko, domácí), Jitka VLAŠÍNOVÁ (203 Česká republika), Milan SEPŠI (203 Česká republika, garant, domácí), Jan KUTA (203 Česká republika, domácí), Jana KLÁNOVÁ (203 Česká republika, domácí), Michal MAZÍK (703 Slovensko), Jiří JARKOVSKÝ (203 Česká republika, domácí), Lenka ŠNAJDROVÁ (203 Česká republika, domácí), Klára BENEŠOVÁ (203 Česká republika, domácí), Tomáš NOVOTNÝ (203 Česká republika), Andrea ZADÁKOVÁ (203 Česká republika) a Jindřich ŠPINAR (203 Česká republika)
Vydání
EP Europace, Oxford, Oxford University Press, 2018, 1099-5129
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 5.047
Kód RIV
RIV/00216224:14110/18:00104323
Organizační jednotka
Lékařská fakulta
UT WoS
000444551400003
Klíčová slova anglicky
Pacemaker; Implantable cardioverter-defibrillator; Late complication; Metal pollutants; Delayed-type hypersensitivity; Lymphocyte transformation test
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 26. 3. 2019 10:48, Soňa Böhmová
Anotace
V originále
Aims To evaluate whether patients with late complications of pacemakers or implantable cardioverter-defibrillators have hypersensitivity reactions to some of the materials used in generators or in electrodes, or to environmental metal burden. Methods and results The cohort consisted of 20 men and 4 women (mean age: 62.3 +/- 17.2 years) who had a history of late complications of implanted devices. The control group involved 25 men and 8 women (mean age: 64.6 +/- 14.0 years) who had comparable devices, but no history of late complications. Lymphocyte transformation test was used to evaluate hypersensitivity to eight metal pollutants (antimony, manganese, mercury, molybdenum, nickel, platinum, tin, and titanium) selected by results of questionnaires on environmental burden, and by material analysis of generators and electrode surfaces. Exposures to metal pollutants were approximately the same in patients and in controls. Titanium alloy used in generators contained at least 99.32% of titanium and trace levels of other metals; higher levels of tin and platinum were detected in electrode surfaces. Hypersensitivity reactions to mercury and tin were significantly more frequent in patients than in controls (patients and controls: mercury: 68.2 and 31.1%, respectively; P = 0.022; tin: 25.0 and 3.2%, respectively; P = 0.035). In contrast, hypersensitivity to manganese was significantly more frequent in controls than in patients (patients and controls: 13.6 and 50.0%, respectively; P = 0.008). Conclusion Our findings suggest a possible relation between hypersensitivity to metals used in implantable devices or to environmental metal burden and the occurrence of their late complications.
Návaznosti
ED2.1.00/19.0382, projekt VaV |
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LM2015051, projekt VaV |
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