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Makale detayı · 2024 · article

Baseline Characteristics and Clinical Insights from the ARTEMIS Registry: A Comprehensive Study of Peripartum Cardiomyopathy in Türkiye

ISSN1016-5169
YÖKSİS OpenAlex Açık erişim · diamond TR Index
Yıl2024
Atıf2OpenAlex
Atıf4Semantic Scholar · 1 etkili
Yüzdelik%71,9
FWCI0,581,00 = dünya ortalaması
Scopus (SJR)Q4
WoS (JCR)Q4

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıTurk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology
  • Katalog eşleşmesi (ISSN)Turk Kardiyoloji Dernegi Arsivi
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

OBJECTIVE: Peripartum Cardiomyopathy (PPCM) is a life-threatening, rare disorder that occurs during the late stages of pregnancy or the early postpartum period. The ARTEMIS (A RegisTry of pEripartuM cardIomyopathy in Turkish patientS) aims to investigate the clinical characteristics and outcomes of PPCM in Türkiye, providing insights into its management within this specific population. METHODS: The ARTEMIS registry retrospectively enrolled patients diagnosed with PPCM within the last five years at 44 cardiology centers across Türkiye. Eligible participants were women over 18 years old, diagnosed with PPCM and without other known cardiac pathology. Data collected included demographic information, clinical presentation, diagnostic modalities, treatment regimens, and outcomes. RESULTS: The study included 293 patients, predominantly between 25 and 35 years old. The majority presented with symptoms such as dyspnea and palpitations, diagnosed postpartum via echocardiography. A low use of advanced diagnostic imaging was noted, relying primarily on echocardiography for evaluation. Common treatments included beta blockers (97.8%), angiotensin-converting enzyme (ACE) inhibitors (71.3%), and in severe cases, bromocriptine (6.9%). The study highlighted a mortality rate of 5.1%, with surviving patients often requiring continued management for heart failure. Diagnostic challenges and variations in treatment responses were noted, reflecting the complexity of PPCM diagnosis and care. CONCLUSION: The ARTEMIS registry provides valuable insights into the management of PPCM in Türkiye, highlighting the need for targeted educational programs for healthcare providers and patients. It also underscores the importance of national registries in understanding and improving outcomes for rare diseases like PPCM.

Konular

Atıflar

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  1. 2025 Very Rare Cause of Cardiomyopathy in a Child: Peripartum CardiomyopathyAtıf 0 · OpenAlex

Yazarlar

20
  1. LATİFE MERAL KAYIKÇIOĞLU 1
  2. MURAT BİTEKER 2
  3. FERİT ONUR MUTLUER 3
  4. TUNCAY GÜZEL 4
  5. EMRE YILMAZ 5
  6. EMRE DEMİR 6
  7. SANEM NALBANTGİL 7
  8. FARUK ERTAŞ 8
  9. DİLEK ÇİÇEK YILMAZ 9
  10. AHMET TEMİZHAN 10
  11. LÜTFÜ AŞKIN 11
  12. LALE DİNÇ ASARCIKLI 12
  13. MURAT AKÇAY 13
  14. RECEP DEMİRBAĞ 14
  15. SEDAT KÖROĞLU KAHRAMANMARAŞ SÜTÇÜ İMAM ÜNİVERSİTESİ 15
  16. ENDER ÖRNEK 16
  17. AHMET ÇELİK 17
  18. MEHMET ATA AKIL 18
  19. BAYRAM ARSLAN 19
  20. SADBERK LALE TOKGÖZOĞLU 20