Kalp damar kliniğimizdeki 14 yıllık konjenital kalp hastalığı deneyimlerimiz
Yükleniyor...
Tarih
2014
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Dicle Üniversitesi Tıp Fakültesi
Erişim Hakkı
Attribution-NonCommercial 3.0 United States
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
Özet
Amaç: Kliniğimizde konjenital kalp hastalığı tanısı ile tedavi edilen hastaların tanı ve tedavi sonuçlarını tartışmayı amaçladık. Yöntemler: Dicle Üniversitesi Kalp Damar Cerrahisi Anabilim Dalında, 2000-2014 tarihleri arasında konjenital kalp hastalığı tanıları ile tedavi edilen 78 hastaya ait kayıtlar retrospektif olarak incelendi. Hastalar 16 yaş ve altı (Grup I) ve 16 yaş üstü (Grup II) olmak üzere gruplandırıldı. Her iki grubun demografik özellikleri, sıklık sırasına göre görülen patalojileri ve tedavi sonuçları karşılaştırıldı.
Bulgular: Grup I’de 35 hasta, grup II’de 43 hasta vardı. Grup I’deki olguların 17’si (%49) erkek, 18’i (%51) kadın, yaş ortalaması 6,2 idi. Grup I’deki hastaların 17’si atrial septal defekt (ASD) mevcuttu. Bu ASD’ lerin birine pulmoner darlık (PD), birine kleft mitrale, birine patent duktus arteriozus (PDA), birine de total pulmoner venöz dönüş anomalisi (TPVDA) eşlik ediyordu. Grup I’deki diğer hastaların 11’i de PDA 7’si ventriküler septal defekt (VSD) , 1’i fallot tetralojisi (TOF), idi. Grup II’deki olguların 9’u (%21) erkek, 34’ü (%79) kadın, yaş ortalaması 22,5 idi. Grup II’deki hastaların ise 36’inde ASD mevcuttu.Bu ASD’lerin
2’sinde PD, birinde kleft mitrale, birinde de PDA eşlik ediyordu. Grup II’deki diğer hastaların 3’ünde VSD, 2’sinde TOF, 2’sinde de PDA saptandı. Postoperatif erken dönemde 1 hasta kaybedildi. Sonuç: Birinci grupta en sık görülen patoloji ASD, ikinci grupta ise PDA idi. Birinci grupta çeşitli kompleks anomaliler görülürken ikinci grupta daha çok izole ASD gibi basit patolojiler tespit edildi.
Objective: We aimed to discuss the treatment results of the patients with congenital cardiovascular diseases who were operated in our clinic Methods: Between 2000-2014, there were 78 patients with diagnosis of congenital heart disease, who were treated at Dicle University Cardiovascular Surgery Department, were retrospectively analyzed. Patients were separated into two groups as under the age of 16 (Group I) and older than 16 years (Group II). The demographic characteristics of both groups, frequency of observed pathology and treatment outcomes were compared. Results: There were 35 patients at group I, 43 patients at group II. 17 (49%) cases were male, 18 (51%) cases were female and the mean age was 6.18 at group I. Seventeen patients had atrial septal defect (ASD) in Group I. One pulmonary stenosis (PS), 1 cleft mitrale, 1 patent ductus arteriosus (PDA), and 1 total anomalous of pulmonary venous return (TAPVR) anomaly was accompanied to these ASD pathologies. Eleven patient had PDA, 7 had ventricular septal defect (VSD), 1 had Tetralogy of Fallot (TOF) in other patients group I. Nine of cases were male (21%) , 34 of cases (79%) were female, mean age was 22.47 at group II. Thirty six ASD was detected in Group II. Two of ASD were accompanied with pulmonary stenosis, one with cleft mitrale and 2 with PDA. Three VSD, 2 tetralogy of fallot (TOF), 2 PDA were detected in other patients in group II. One patient died at early postoperative period. Conclusion: In the group of children age, 48.5% of patients were male. The group of over 16 age , %79 of patient were male. At the group of children age, the common pathology was ASD however PDA is the common pathology at second group. While more complex anomalies were detected in the first group,at the second group rather non complex isolated anomalies as ASD were detected
Objective: We aimed to discuss the treatment results of the patients with congenital cardiovascular diseases who were operated in our clinic Methods: Between 2000-2014, there were 78 patients with diagnosis of congenital heart disease, who were treated at Dicle University Cardiovascular Surgery Department, were retrospectively analyzed. Patients were separated into two groups as under the age of 16 (Group I) and older than 16 years (Group II). The demographic characteristics of both groups, frequency of observed pathology and treatment outcomes were compared. Results: There were 35 patients at group I, 43 patients at group II. 17 (49%) cases were male, 18 (51%) cases were female and the mean age was 6.18 at group I. Seventeen patients had atrial septal defect (ASD) in Group I. One pulmonary stenosis (PS), 1 cleft mitrale, 1 patent ductus arteriosus (PDA), and 1 total anomalous of pulmonary venous return (TAPVR) anomaly was accompanied to these ASD pathologies. Eleven patient had PDA, 7 had ventricular septal defect (VSD), 1 had Tetralogy of Fallot (TOF) in other patients group I. Nine of cases were male (21%) , 34 of cases (79%) were female, mean age was 22.47 at group II. Thirty six ASD was detected in Group II. Two of ASD were accompanied with pulmonary stenosis, one with cleft mitrale and 2 with PDA. Three VSD, 2 tetralogy of fallot (TOF), 2 PDA were detected in other patients in group II. One patient died at early postoperative period. Conclusion: In the group of children age, 48.5% of patients were male. The group of over 16 age , %79 of patient were male. At the group of children age, the common pathology was ASD however PDA is the common pathology at second group. While more complex anomalies were detected in the first group,at the second group rather non complex isolated anomalies as ASD were detected
Açıklama
Anahtar Kelimeler
Konjenital kalp hastalığı, Cerrahi, Klinik sonuçlar, Congenital heart disease, Surgery, Clinic outcomes
Kaynak
Dicle Tıp Dergisi
WoS Q Değeri
Scopus Q Değeri
Cilt
41
Sayı
3
Künye
Tezcan, O., Güçlü, O., Yazıcı, S., Benli, E.D., Demirtaş, S., Yavuz, C. ve diğerleri. (2014). Kalp damar kliniğimizdeki 14 yıllık konjenital kalp hastalığı deneyimlerimiz. Dicle Tıp Dergisi, 41(3), 479-482.
