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Kanserli Çocuklarda Artan Kümülatif Antrasiklin Dozunda Kalp Hızı Değişkenliğinin Değerlendirilmesi: Prospektif Bir Çalışma

Yıl 2021, Cilt: 15 Sayı: 3, 216 - 221, 25.05.2021
https://doi.org/10.12956/tchd.826263

Öz

Amaç: Kemoterapi protokollerinin temel ilacı olan antrasiklinler en sık kardiyotoksisite yan etkisine sahiptir. Antrasiklin ile tedavi edilen kanserli çocuklarda kalp hızı değişkenliğini 24 saatlik Holter elektrokardiyografi (EKG) ile prospektif olarak değerlendirmeyi amaçladık.

Gereç ve Yöntemler: Antrasiklin ile tedavi edilen kanserli hastalarda hiç tedavi almadan, 120mg/m2 ve ≥240 mg/m2 kümülatif antrasiklin dozunda 24 saatlik Holter EKG monitörizasyonu yapıldı. Kalp atış hızı değişkenliğinin (HRV) zaman alanı ve frekans alanı ölçümleri elde edildi. Hastalar üç gruba ayrıldı: hiç tedavi almadan Grup 1 (n = 54), Grup 2 :≥120 mg/m2 (n = 54), Grup 3: ≥240 mg/m2 (n = 54) seklinde ayrıldı.

Bulgular: Ortanca yaş 48 aydı (aralık 9-192 ay). 38 (% 70.4) hasta akut lösemi, iki hasta T lenfoblastik lenfoma (% 3.8) ve 14 hasta (% 25.8) diğer çocukluk çağı kanserleridir. Bununla birlikte, tüm kalp hızı değişkenleri, nSDNN indeksi, rMSSD, pNN50 gibi zaman parametreleri ve LF, HF ve Toplam güç gibi frekans parametreleri gibi her artan kümülatif antrasiklin dozu ile azalma görüldüğü belirlendi. LF/HF oranı da Grup 3’te istatistiksel olarak anlamlı şekilde artış gösterdiği saptandı. Kalp hızı parametrelerine göre, ortalama kalp hızı, ortalama minimum kalp hızı ve ortalama RR, kümülatif doz artıkça istatistiksel olarak anlamlı şekilde uzadığı belirlendi.

Sonuç: Kalp hızı değişkenleri, kardiyak otonomik nöral disfonksiyonu ve erken miyokardiyal hasarın gösterilmesi için invazif olmayan bir tekniktir. 24 saatlik Holter EKG’si, her artan 120 mg/m2 antrasiklin kümilatif dozu ile antrasiklin tedavisi sırasında erken kardiyak dysautonomia etkisini saptamak için kullanılabilir.

Destekleyen Kurum

yok

Proje Numarası

yok

Kaynakça

  • 1.Lipshultz SE, Alvarez JA, Scully RE. Anthracycline associated cardiotoxicity in survivors of childhood cancer. Heart. 2008;94:525–33.
  • 2.Van Dalen EC, van der Pal HJ, Kok WE, Caron HN,Kremer LC. Clinical heart failure in a cohort of children treated with anthracyclines: a long-term follow up study. Eur J Cancer. 2006;42:3191–8.
  • 3.Sorensen K, Levitt G, Bull C, Chessells J, Sullivan I. Anthracycline dose in childhood acute lymphoblasticleukemia: issues of early survival versus latecardiotoxicity. J Clin Oncol. 1997;15:61–8.
  • 4.Lipshultz SE, Colan SD, Gelber RD, et al. Late cardiac effects of doxorubicin therapy for acute lymphoblastic leukemia in childhood. N Engl J Med. 1991;324:808–15.
  • 5.Swain SM, Whaley FS, Ewer MS. Congestive heart failure in patients treated with doxorubicin: a retrospective analysis of three trials. Cancer. 2003;97:2869–79.
  • 6.Zimetbaum PJ, Josephson ME. The evolving role of ambulatory arrhythmia monitoring in general clinical practice. Ann Intern Med. 1999;130:848.
  • 7.Joshi AK, Kowey PR, Prystowsky EN, et al. First experience with a Mobile Cardiac Outpatient Telemetry (MCOT) system for the diagnosis and management of cardiac arrhythmia. Am J Cardiol. 2005;95:878.
  • 8.Mulrooney DA, Yeazel MW, Kawashima T, et al. Cardiac outcomes in a cohort of adult survivors of childhood and adolescent cancer: retrospective analysis of the Childhood Cancer Survivor Study cohort. BMJ. 2009;339:b4606.
  • 9.Karacan M, Ceviz N, Olgun H. Heart rate variability in children with acute rheumatic fever. Cardiol Young. 2012;22:285-92.
  • 10.Task Force of The European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Heart rate variability-standards of measurement, physiological interpretation, and clinical use. Eur Heart J. 1996;17:354–81.
  • 11.Stachowiak P, Milchert-Leszczyńska M, Falco M, et al. Heart rate variability during and after chemotherapy with anthracycline in patients with breast cancer. Kardiol Pol. 2018;76:914-6.
  • 12.Makikallio TH, Huikuri HV, MakikalliobA et al. Prediction of sudden cardiac death by fractal analysis of heart rate variability in elderly subjects. J Am Coll Cardiol. 2001;37:1395–402.
  • 13.Kim K, Chae J, Lee S. The role of heart rate variability in advanced non-small-cell lung cancer patients. J Palliat Care. 2015;31:103–8.
  • 14.Zamorano J, Lancellotti P, Muñoz D, et al. Stanowisko ESC dotyczące toksycznego wpływuleczenia onkologicznego na układ sercowo-naczyniowy w 2016 roku, opracowane pod auspicjami Komisji ESC do spraw Wytycznych Postępowania [Position Paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for Practice Guidelines]. Kardiol Pol. 2016;74:1193–233.
  • 15.Asensio-López MC, Soler F, Sánchez-Más J, et al. Early oxidative damage induced by doxorubicin: Source of production, protection by GKT137831 and effect on Ca(2+) transporters in HL-1 cardiomyocytes. Arch Biochem Biophys. 2016;594:26–36.
  • 16.Poręba M, Poręba R, Gać P, et al. Heart rate variability and heart rate turbulence in patients with hematologic malignancies subjected to high-dose chemotherapy in the course of hematopoietic stem cell transplantation. Ann Noninvasive Electrocardiol. 2014;19:157–65.

Assessment of Heart Rate Variability in Children with Cancer after Elevated Cumulative Anthracycline Dose: A Prospective Study

Yıl 2021, Cilt: 15 Sayı: 3, 216 - 221, 25.05.2021
https://doi.org/10.12956/tchd.826263

Öz

Objective: Anthracyclines which are the main drug of chemotherapy protocols had cardiotoxicity as the most frequent and well-known side effect. We aimed to evaluate prospectively the heart rate variability with 24-hour Holter electrocardiography (ECG) in children with cancer who treated with anthracycline drugs.


Material and Methods:
The 24-hour Holter ECG monitoring was performed at the baseline, at time of 120 mg/m2 and ≥240 mg/m2 of cumulative anthracycline dose in patients with cancer who treated with anthracycline. The time-domain and frequency-domain measurements of heart rate variability (HRV) were obtained. The patients were classified into three groups as Group1:at baseline (n=54), Group 2:≥120mg/m2 (n=54), Group 3:≥240mg/m2 (n=54).

Results: The median age was 48 months (range 9-192 months). All types of cancer were 38 patients (70.4%) of acute leukemia, two patients (3.8%) of T lymphoblastic lymphoma, and 14patients (25.8%) of other childhood cancer who treated with anthracycline. However, all heart rate variability parameters were decreased after each increased cumulative anthracycline dose, especially time-domain parameters such as nSDNN index, rMSSD, pNN50, frequency parameters such as LF, HF, and Total power were significantly altered among Group1 and Group 3. LF/HF ratio was also statistically significantly increased in Group 3. According the heart rate parameters, the mean average heart rate, mean minimum heart rate and mean RR were statistically significantly prolonged from Group1 to Group 3.

Conclusion: Heart rate variability parameters are a noninvasive technique to demonstrate cardiac autonomic neural dysfunction and early myocardial injury. The 24-hour Holter ECG may be used for detecting early cardiac dysautonomia effect during anthracycline treatment with each elevated 120mg/m2 anthracycline of cumulative dose.

Proje Numarası

yok

Kaynakça

  • 1.Lipshultz SE, Alvarez JA, Scully RE. Anthracycline associated cardiotoxicity in survivors of childhood cancer. Heart. 2008;94:525–33.
  • 2.Van Dalen EC, van der Pal HJ, Kok WE, Caron HN,Kremer LC. Clinical heart failure in a cohort of children treated with anthracyclines: a long-term follow up study. Eur J Cancer. 2006;42:3191–8.
  • 3.Sorensen K, Levitt G, Bull C, Chessells J, Sullivan I. Anthracycline dose in childhood acute lymphoblasticleukemia: issues of early survival versus latecardiotoxicity. J Clin Oncol. 1997;15:61–8.
  • 4.Lipshultz SE, Colan SD, Gelber RD, et al. Late cardiac effects of doxorubicin therapy for acute lymphoblastic leukemia in childhood. N Engl J Med. 1991;324:808–15.
  • 5.Swain SM, Whaley FS, Ewer MS. Congestive heart failure in patients treated with doxorubicin: a retrospective analysis of three trials. Cancer. 2003;97:2869–79.
  • 6.Zimetbaum PJ, Josephson ME. The evolving role of ambulatory arrhythmia monitoring in general clinical practice. Ann Intern Med. 1999;130:848.
  • 7.Joshi AK, Kowey PR, Prystowsky EN, et al. First experience with a Mobile Cardiac Outpatient Telemetry (MCOT) system for the diagnosis and management of cardiac arrhythmia. Am J Cardiol. 2005;95:878.
  • 8.Mulrooney DA, Yeazel MW, Kawashima T, et al. Cardiac outcomes in a cohort of adult survivors of childhood and adolescent cancer: retrospective analysis of the Childhood Cancer Survivor Study cohort. BMJ. 2009;339:b4606.
  • 9.Karacan M, Ceviz N, Olgun H. Heart rate variability in children with acute rheumatic fever. Cardiol Young. 2012;22:285-92.
  • 10.Task Force of The European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Heart rate variability-standards of measurement, physiological interpretation, and clinical use. Eur Heart J. 1996;17:354–81.
  • 11.Stachowiak P, Milchert-Leszczyńska M, Falco M, et al. Heart rate variability during and after chemotherapy with anthracycline in patients with breast cancer. Kardiol Pol. 2018;76:914-6.
  • 12.Makikallio TH, Huikuri HV, MakikalliobA et al. Prediction of sudden cardiac death by fractal analysis of heart rate variability in elderly subjects. J Am Coll Cardiol. 2001;37:1395–402.
  • 13.Kim K, Chae J, Lee S. The role of heart rate variability in advanced non-small-cell lung cancer patients. J Palliat Care. 2015;31:103–8.
  • 14.Zamorano J, Lancellotti P, Muñoz D, et al. Stanowisko ESC dotyczące toksycznego wpływuleczenia onkologicznego na układ sercowo-naczyniowy w 2016 roku, opracowane pod auspicjami Komisji ESC do spraw Wytycznych Postępowania [Position Paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for Practice Guidelines]. Kardiol Pol. 2016;74:1193–233.
  • 15.Asensio-López MC, Soler F, Sánchez-Más J, et al. Early oxidative damage induced by doxorubicin: Source of production, protection by GKT137831 and effect on Ca(2+) transporters in HL-1 cardiomyocytes. Arch Biochem Biophys. 2016;594:26–36.
  • 16.Poręba M, Poręba R, Gać P, et al. Heart rate variability and heart rate turbulence in patients with hematologic malignancies subjected to high-dose chemotherapy in the course of hematopoietic stem cell transplantation. Ann Noninvasive Electrocardiol. 2014;19:157–65.
Toplam 16 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Klinik Tıp Bilimleri
Bölüm ORIGINAL ARTICLES
Yazarlar

Sultan Aydin Köker 0000-0002-8801-7776

Bengü Demirağ 0000-0003-4399-0844

Timur Meşe 0000-0002-4433-3929

Murat Yılmazer 0000-0003-0819-5829

Yesim Oymak 0000-0002-6908-8309

Rahmi Özdemir 0000-0002-2775-166X

Tuba Hilkay Karapınar 0000-0002-4714-332X

Dilek İnce 0000-0002-7914-7886

Raziye Vergin 0000-0002-8594-9762

Proje Numarası yok
Yayımlanma Tarihi 25 Mayıs 2021
Gönderilme Tarihi 15 Kasım 2020
Yayımlandığı Sayı Yıl 2021 Cilt: 15 Sayı: 3

Kaynak Göster

Vancouver Aydin Köker S, Demirağ B, Meşe T, Yılmazer M, Oymak Y, Özdemir R, Karapınar TH, İnce D, Vergin R. Assessment of Heart Rate Variability in Children with Cancer after Elevated Cumulative Anthracycline Dose: A Prospective Study. Türkiye Çocuk Hast Derg. 2021;15(3):216-21.

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