Matches in SemOpenAlex for { <https://semopenalex.org/work/W2723291288> ?p ?o ?g. }
Showing items 1 to 76 of
76
with 100 items per page.
- W2723291288 abstract "Background Duchenne Muscular Dystrophy (DMD) is an X-linked disorder, the most common muscular dystrophy in children. It presents in early childhood and become fatal in the 2nd decade, mostly because of respiratory involvement and approximate 10% of cases because of cardiac failure. Cardiac changes become present after first decade. It leads to dilated cardiomiopathy, congestive cardiac failure, arrhythmias and finally cardiac death. Main ECG changes are sinus tachycardia, short PR interval, right ventricular hypertrophy, prolonged QTc, ST depression and rarely may be associated with WPW syndrome. Aim Study the ECG findings in DMD patients. Methods We analysed a total of 22 male patients admitted in‘Dr. Victor Gomoiu’ Children’s Clinical Hospital in paediatric cardiology department. The diagnostic of DMD was established using clinical and biochemical criteria and confirmed by genetic test. All patients were under corticotherapy. Patients underwent 12 lead ECG, 24 hour ECG holter, in order to detect ECG changes. It was noted the HR, R waves, R/S ratio, PR interval. Q waves, QT interval, ST segment, T waves. The parameters were measured manually and compared with standard age matched normal values. Results The characteristic of the study were: the mean age was 11 years; the mean weight of patients was 38.3 kg, 32% of them were wheelchair bounded. Tall R waves with R/S ratio more than 1 were present in 54% of all patients, RR` patter was found in 32%, QTc at higher limit was found of 40%. Conclusions Electrocardiographical changes are common in DMD patients, revealing early cardiac involvement. In order to delay cardiac changes, further studies (such as strain and cardiac RM) need to be done in order to sustain cardiac function in normal limits as long as possible." @default.
- W2723291288 created "2017-06-30" @default.
- W2723291288 creator A5009130278 @default.
- W2723291288 creator A5016844726 @default.
- W2723291288 creator A5040516945 @default.
- W2723291288 creator A5043556422 @default.
- W2723291288 creator A5043655989 @default.
- W2723291288 creator A5061304163 @default.
- W2723291288 creator A5070216591 @default.
- W2723291288 creator A5082625938 @default.
- W2723291288 date "2017-06-01" @default.
- W2723291288 modified "2023-10-18" @default.
- W2723291288 title "P315 Electrocardiographic changes in duchenne muscular dystrophy" @default.
- W2723291288 doi "https://doi.org/10.1136/archdischild-2017-313273.403" @default.
- W2723291288 hasPublicationYear "2017" @default.
- W2723291288 type Work @default.
- W2723291288 sameAs 2723291288 @default.
- W2723291288 citedByCount "0" @default.
- W2723291288 crossrefType "proceedings-article" @default.
- W2723291288 hasAuthorship W2723291288A5009130278 @default.
- W2723291288 hasAuthorship W2723291288A5016844726 @default.
- W2723291288 hasAuthorship W2723291288A5040516945 @default.
- W2723291288 hasAuthorship W2723291288A5043556422 @default.
- W2723291288 hasAuthorship W2723291288A5043655989 @default.
- W2723291288 hasAuthorship W2723291288A5061304163 @default.
- W2723291288 hasAuthorship W2723291288A5070216591 @default.
- W2723291288 hasAuthorship W2723291288A5082625938 @default.
- W2723291288 hasConcept C118441451 @default.
- W2723291288 hasConcept C126322002 @default.
- W2723291288 hasConcept C164705383 @default.
- W2723291288 hasConcept C192244848 @default.
- W2723291288 hasConcept C2778198053 @default.
- W2723291288 hasConcept C2778943923 @default.
- W2723291288 hasConcept C2779030066 @default.
- W2723291288 hasConcept C2779703243 @default.
- W2723291288 hasConcept C2780040984 @default.
- W2723291288 hasConcept C2780144208 @default.
- W2723291288 hasConcept C71924100 @default.
- W2723291288 hasConceptScore W2723291288C118441451 @default.
- W2723291288 hasConceptScore W2723291288C126322002 @default.
- W2723291288 hasConceptScore W2723291288C164705383 @default.
- W2723291288 hasConceptScore W2723291288C192244848 @default.
- W2723291288 hasConceptScore W2723291288C2778198053 @default.
- W2723291288 hasConceptScore W2723291288C2778943923 @default.
- W2723291288 hasConceptScore W2723291288C2779030066 @default.
- W2723291288 hasConceptScore W2723291288C2779703243 @default.
- W2723291288 hasConceptScore W2723291288C2780040984 @default.
- W2723291288 hasConceptScore W2723291288C2780144208 @default.
- W2723291288 hasConceptScore W2723291288C71924100 @default.
- W2723291288 hasLocation W27232912881 @default.
- W2723291288 hasOpenAccess W2723291288 @default.
- W2723291288 hasPrimaryLocation W27232912881 @default.
- W2723291288 hasRelatedWork W1493087742 @default.
- W2723291288 hasRelatedWork W1505699942 @default.
- W2723291288 hasRelatedWork W1843508656 @default.
- W2723291288 hasRelatedWork W1955161220 @default.
- W2723291288 hasRelatedWork W1965058790 @default.
- W2723291288 hasRelatedWork W2009285920 @default.
- W2723291288 hasRelatedWork W2050519130 @default.
- W2723291288 hasRelatedWork W2063476468 @default.
- W2723291288 hasRelatedWork W2106264345 @default.
- W2723291288 hasRelatedWork W2131152930 @default.
- W2723291288 hasRelatedWork W2157038355 @default.
- W2723291288 hasRelatedWork W2349411665 @default.
- W2723291288 hasRelatedWork W2408387634 @default.
- W2723291288 hasRelatedWork W2417337313 @default.
- W2723291288 hasRelatedWork W2460742285 @default.
- W2723291288 hasRelatedWork W2673319876 @default.
- W2723291288 hasRelatedWork W2921763549 @default.
- W2723291288 hasRelatedWork W3165311247 @default.
- W2723291288 hasRelatedWork W3181720865 @default.
- W2723291288 hasRelatedWork W3206700517 @default.
- W2723291288 isParatext "false" @default.
- W2723291288 isRetracted "false" @default.
- W2723291288 magId "2723291288" @default.
- W2723291288 workType "article" @default.