EHA Library - The official digital education library of European Hematology Association (EHA)

WHICH IS THE ETIOLOGY OF BREATH HOLDING SPELL? CARDIAC CONTRACTION OR IRON DEFICIENCY ANEMIA
Author(s): ,
Saadet Akarsu
Affiliations:
University of Firat,Faculty of Medicine, Pediatric Haematology,Elazig,Turkey
Taner Kasar
Affiliations:
University of Ordu,Faculty of Medicine, Pediatric Cardiology,Ordu,Turkey
(Abstract release date: 05/17/18) EHA Library. Akarsu S. 06/14/18; 216769; PB2072
Prof. Dr. Saadet Akarsu
Prof. Dr. Saadet Akarsu
Contributions
Abstract

Abstract: PB2072

Type: Publication Only

Background
Breath-holding spell (BHS) is a prevalent, nonepileptic, recurrent, potentially frightening early childhood disease with varying clinical manifestations. In addition to underlying genetic predisposition, dysregulation of central nervous system (CNS) is responsible for BHS. Autonomic dysfunction which leads to cardiac arrest, and cerebral anoxia, and increased vagal tonus play roles in its pathogenesis. It may accompany iron deficiency anemia (IDA). In cases with BHS, increase in corrected QT (QTc), and QTc dispersion (QTcd) which are electrocardiographic (ECG) reflection of regional differences in myocardial repolarization have been demonstrated.

Aims
In our study, we determined whether BHS develops as a result of dysrhytmia secondary to abnormal ventricular depolarization inherent to the disease, or as an outcome of IDA.

 

 

Methods

Study groups were formulated prospectively.  BHS-IDA group consisted of cyanotic children aged between 9 and 60 months. The cases were evaluated in 3 groups as follows: Group 1 (Group BHS-IDA, n: 12), Group 2 (Group IDA without BHS, n: 34), Group 3 (Healthy control group, n: 26). ECGs were evaluated by the same pediatric cardiologist at one session. The difference between the longest, and the shortest QTc intervals was accepted as QTcd. Cases in all three groups were compared as for QTc, and QTcd values. Statistically analysis was performed using Student’s t, and  Mann-Whitney U tests, and p<0.05 was accepted as the level of statistical significance.

Results

QTc intervals were 412.5±19.1 ms in Groups 1, 394.4±27.1 ms in Group 2, and 395.8±20.2 ms in Group 3. QTcd intervals in children diagnosed as BHS-IDA 12.0±6.5 ms, IDA 16.4±10.5 ms, and healthy control group 27.6±9.0 ms were as indicated  (p>0.05).

Conclusion
IDA may affect cardiac, and nervous system which play an important role in changing autonomic nervous system balance. It induces hypoxia which leads to dysrhytmia. However in cases with BHS, ventricular repolarization which develops as a result of autonomic dysregulation, and increased vagal stimulation may differ.

Session topic: 30. Iron metabolism, deficiency and overload

Keyword(s): Iron deficiency anemia

Abstract: PB2072

Type: Publication Only

Background
Breath-holding spell (BHS) is a prevalent, nonepileptic, recurrent, potentially frightening early childhood disease with varying clinical manifestations. In addition to underlying genetic predisposition, dysregulation of central nervous system (CNS) is responsible for BHS. Autonomic dysfunction which leads to cardiac arrest, and cerebral anoxia, and increased vagal tonus play roles in its pathogenesis. It may accompany iron deficiency anemia (IDA). In cases with BHS, increase in corrected QT (QTc), and QTc dispersion (QTcd) which are electrocardiographic (ECG) reflection of regional differences in myocardial repolarization have been demonstrated.

Aims
In our study, we determined whether BHS develops as a result of dysrhytmia secondary to abnormal ventricular depolarization inherent to the disease, or as an outcome of IDA.

 

 

Methods

Study groups were formulated prospectively.  BHS-IDA group consisted of cyanotic children aged between 9 and 60 months. The cases were evaluated in 3 groups as follows: Group 1 (Group BHS-IDA, n: 12), Group 2 (Group IDA without BHS, n: 34), Group 3 (Healthy control group, n: 26). ECGs were evaluated by the same pediatric cardiologist at one session. The difference between the longest, and the shortest QTc intervals was accepted as QTcd. Cases in all three groups were compared as for QTc, and QTcd values. Statistically analysis was performed using Student’s t, and  Mann-Whitney U tests, and p<0.05 was accepted as the level of statistical significance.

Results

QTc intervals were 412.5±19.1 ms in Groups 1, 394.4±27.1 ms in Group 2, and 395.8±20.2 ms in Group 3. QTcd intervals in children diagnosed as BHS-IDA 12.0±6.5 ms, IDA 16.4±10.5 ms, and healthy control group 27.6±9.0 ms were as indicated  (p>0.05).

Conclusion
IDA may affect cardiac, and nervous system which play an important role in changing autonomic nervous system balance. It induces hypoxia which leads to dysrhytmia. However in cases with BHS, ventricular repolarization which develops as a result of autonomic dysregulation, and increased vagal stimulation may differ.

Session topic: 30. Iron metabolism, deficiency and overload

Keyword(s): Iron deficiency anemia

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies