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Choroidal thickness changes in children with chronic heart failure due to dilated cardiomyopathy
Klaudia Rakusiewicz1, Krystyna Kanigowska2, Wojciech Hautz2
1Department of Ophthalmology, Children's Memorial Health Institute, Warsaw, Poland. k.rakusiewicz@ipczd.pl.
Insights
Children with chronic heart failure (CHF) due to dilated cardiomyopathy (DCM) exhibit thinner choroidal thickness (CTh) compared to healthy peers. This finding suggests CTh may aid in monitoring pediatric DCM progression.
Area of Science:
- Ophthalmology
- Cardiology
- Pediatrics
Background:
- Chronic heart failure (CHF) in children, often secondary to dilated cardiomyopathy (DCM), presents complex physiological challenges.
- Choroidal thickness (CTh) is a key indicator of ocular health and vascular status.
- Understanding ocular changes in pediatric CHF is crucial for comprehensive patient management.
Purpose of the Study:
- To evaluate choroidal thickness (CTh) in children with CHF secondary to DCM using spectral domain optical coherence tomography (SD-OCT).
- To compare CTh measurements in children with CHF due to DCM against those of age- and sex-matched healthy children.
Main Methods:
- Prospective enrollment of 30 children with CHF due to DCM and 30 healthy controls.
- Transthoracic echocardiography to assess left ventricular ejection fraction (LVEF) and NT-proBNP levels.
- SD-OCT imaging to measure subfoveal choroidal thickness (SFCTh) and CTh at multiple locations.
Main Results:
- Children with CHF due to DCM demonstrated statistically significantly lower CTh at all measured locations compared to controls.
- Mean CTh differences ranged from 38.13 to 65.69 μm across different measurement points.
- No significant correlation was found between CTh and age, gender, biometry, refractive error, LVEF, or NT-proBNP levels.
Conclusions:
- Pediatric patients with CHF secondary to DCM exhibit reduced choroidal thickness.
- CTh is a potentially valuable parameter for monitoring the clinical course of DCM in children.
- Further research can explore the implications of these findings for early detection and management strategies.
Purpose:
To evaluate choroidal thickness (CTh) in children with chronic heart failure (CHF) secondary to dilated cardiomyopathy (DCM) using spectral domain optical coherence tomography (SD-OCT) and to compare their values to those of healthy children.
Methods:
Sixty eyes of thirty children (mean age 9.9 ± 3.57 years) with chronic heart failure (left ventricular ejection fraction, LVEF ≤ 55%) due to DCM lasting for over 6 months were prospectively enrolled. The control group consisted of 30 age- (mean age 10.16 ± 3.42 years) and sex-matched healthy children. All participants underwent transthoracic echocardiography with LVEF measured using the Simpson method and had the blood serum level of N-terminal-pro-brain natriuretic peptide marker (NT-proBNP) determined. All children underwent SD-OCT and had subfoveal choroidal thickness (SFCTh) and CTh measured at 1500 µm (μm) nasally, temporally, superiorly and inferiorly from the fovea in both eyes by two investigators.
Results:
CTh at all locations was statistically significantly lower in children with DCM compared to the control group. Mean CTh in the group with CHF compared to the control group were (304.03 vs. 369.72 μm, p < 0.05) at the subfoveal location, (245.87 vs. 284 μm, p < 0.05) 1500 μm nasally from the fovea, (291.5 vs. 355.95 μm, p < 0.05) 1500 μm temporally from the fovea, (303.98 vs. 357.58 μm, p < 0.05) 1500 μm superiorly from the fovea and (290.92 vs. 344.96 μm, p < 0.05) 1500 μm inferiorly from the fovea. The average difference CTh between the study groups ranged from 38.13 to 65.69 μm at individual locations. In both groups, CTh was the thickest at subfoveal location (304.03 vs. 369.72 μm, p < 0.05) and the thinnest was 1500 μm nasally from the fovea (262.37 vs. 336.87 μm, p < 0.05). There was no correlation between CTh and age, gender, biometry and refractive error. No correlation was found between CTh and LVEF and NT-proBNP.
Conclusion:
Patients with CHF due to DCM had a thinner CTh at all measured locations. The results of our research indicate that CHF affects CTh and this parameter may be very helpful in monitoring the clinical course of the disease in children with DCM.
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