Diagnosis dan Tatalaksana Sindrom Brugada

Penulis

  • Herick Alvenus Willim Fakultas Kedokteran Universitas Tanjungpura, Pontianak, Kalimantan Barat, Indonesia
  • Infan Ketaren SMF Kardiologi dan Kedokteran Vaskular, Rumah Sakit Umum Daerah dr. Soedarso, Pontianak, Kalimantan Barat, Indonesia

DOI:

https://doi.org/10.55175/cdk.v46i5.467

Kata Kunci:

Fibrilasi ventrikel, henti jantung mendadak, sindrom brugada

Abstrak

Sindrom Brugada (SB) adalah abnormalitas listrik jantung bawaan yang langka. SB merupakan salah satu penyebab utama kematian mendadak pada usia muda tanpa penyakit jantung organik. SB dapat bersifat asimptomatik ataupun simptomatik. Beberapa pasien dapat mengalami sinkop, bahkan aritmia yang mengancam nyawa seperti fibrilasi ventrikel. EKG menjadi kunci utama diagnosis SB. Diperlukan stratifikasi risiko dan strategi lanjutan untuk mencegah henti jantung mendadak.

Brugada syndrome (BS) is a rare inherited abnormality of heart electrical activity. BS is one of the leading causes of sudden cardiac death among youth without underlying organic heart disease. BS can be asymptomatic or symptomatic. Some patients may experience syncope, even lifethreatening arrhythmia such as ventricular fibrillation. ECG test is the main key of diagnosis. Risk stratification and further strategies are needed to prevent sudden cardiac death.

Unduhan

Data unduhan belum tersedia.

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Diterbitkan

2019-05-01

Cara Mengutip

Willim, H. A., & Ketaren, I. (2019). Diagnosis dan Tatalaksana Sindrom Brugada. Cermin Dunia Kedokteran, 46(5), 353–357. https://doi.org/10.55175/cdk.v46i5.467

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