Bubshait Khlood, Dizon Olivia, Krueger Charlene
Fundamental of Nursing Department, Imam Abdulrahman Bin Faisal University, Dammam 1980, Saudi Arabia.
University of Florida, Gainesville, FL 32610-0197, USA.
Int J Pediatr. 2024 Jan 27;2024:6671906. doi: 10.1155/2024/6671906. eCollection 2024.
Respiratory difficulties are a common concern in preterm infants, and they can lead to long-term health problems. Few studies have investigated the use of spectral analysis as a biomarker to quantify respiration patterns in preterm infants.
To evaluate the feasibility of using spectral analysis of heart rate variability as a biomarker for the quantification of respiratory patterns in very-low-birth-weight preterm infants compared to direct observation.
In a comparative, small-scale feasibility study, 18 preterm infants born during their 27 to 28 gestational week (weighing <1500 grams) participated by convenience. Respiratory patterns (regular or irregular; shallow or deep) were directly observed on the 28 week during playback of speech recording. Heart rate variability was simultaneously measured using spectral analysis of heart periods, from which the mean values influenced by respiratory sinus arrhythmia (frequencies of 0.30-1.0 Hz) were compared to each observed respiratory pattern. The magnitudes of respiratory sinus arrhythmia and the area under the curve were determined.
The magnitude of respiratory sinus arrhythmia (frequencies of 0.30-1.0 Hz) in infants observed to be displaying irregular shallow respiration was greater than that in infants with regular deep respiration. Further, there was a shift from lower frequencies (frequency peak = 0.30 Hz) to higher frequencies (peak = 0.70 Hz).
In contrast with direct observation, spectral analysis allowed for the quantification of respiratory patterns in a vulnerable population of preterm infants of interest to the nursing scientific and practice community. Future directions include applying this biomarker to evaluate both developmental and pathological trends in the respiratory patterns of preterm infants.
呼吸困难是早产儿常见的问题,可能导致长期健康问题。很少有研究调查使用频谱分析作为生物标志物来量化早产儿的呼吸模式。
与直接观察相比,评估使用心率变异性频谱分析作为生物标志物来量化极低出生体重早产儿呼吸模式的可行性。
在一项比较性的小规模可行性研究中,18名孕27至28周出生(体重<1500克)的早产儿方便抽样参与。在播放语音记录的第28周直接观察呼吸模式(规律或不规律;浅或深)。同时使用心动周期频谱分析测量心率变异性,将受呼吸性窦性心律不齐影响的平均值(频率为0.30 - 1.0Hz)与每种观察到的呼吸模式进行比较。确定呼吸性窦性心律不齐的幅度和曲线下面积。
观察到表现为不规则浅呼吸的婴儿的呼吸性窦性心律不齐幅度(频率为0.30 - 1.0Hz)大于规律深呼吸的婴儿。此外,存在从较低频率(频率峰值 = 0.30Hz)到较高频率(峰值 = 0.70Hz)的转变。
与直接观察相比,频谱分析能够量化护理科研和实践领域关注的脆弱早产儿群体的呼吸模式。未来的方向包括应用这种生物标志物来评估早产儿呼吸模式的发育和病理趋势。