新生儿重症监护室收治的不同胎龄新生儿腋温和直肠温度的比较评估:一项横断面研究。

IF 2 3区 医学 Q2 PEDIATRICS BMC Pediatrics Pub Date : 2024-11-12 DOI:10.1186/s12887-024-05224-w
Shaimaa Halabi, Rana Almuqati, Amenah Al Essa, Manal Althubaiti, Musab Alshareef, Abdulaziz Homedi, Ahmed Alwatban, Mohanned Alrahili, Saif Alsaif, Kamal Ali
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引用次数: 0

摘要

目的:保持体温正常对新生儿的存活至关重要,尤其是对容易出现体温不稳定的早产儿。本研究评估了新生儿重症监护室(NICU)收治的胎龄范围为 23-28、29-32、33-36 和 ≥ 37 周的新生儿的腋窝和直肠温度之间的相关性和变异性,旨在为改进新生儿热管理策略提供参考:这项横断面研究于 2023 年 10 月至 2024 年 4 月在利雅得阿卜杜勒阿齐兹国王医疗城进行,共涉及 160 名婴儿。使用数字温度计测量入院体温。数据分析包括连续变量的方差分析/Kruskal-Wallis、分类数据的卡方检验、评估一致性的布兰德-阿尔特曼法以及评估体温相关性的皮尔逊相关系数:平均腋温从孕 23-28 周组的 36.4 ℃升至 29-32 周组的 36.5 ℃,33-36 周组和≥37 周组升至 36.7 ℃,(p = 0.033)。直肠温度从 23-28 周组的 36.5 °C升高到 29-32 周组的 36.6 °C,在 33-36 周组和≥ 37 周组都达到了 36.8 °C(p = 0.006)。在 33-36 周组和≥37 周组中,不同测量方法之间存在显著差异(p 结论:腋窝和直肠温度均高于体温:直肠温度和腋窝温度在不同年龄组均有差异,但总体上有很大的相关性。在 33-36 周组和≥37 周组,两种方法之间存在显著差异。年龄较小的早产儿表现出更大的变异性,而年龄较大的婴儿则表现出更大的一致性。
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Comparative evaluation of axillary and rectal temperatures across different gestational ages in newborns admitted to the neonatal intensive care unit: a cross-sectional study.

Objective: Maintaining normothermia is crucial for neonatal survival, especially in preterm infants prone to temperature instability. This study evaluates the correlation and variability between axillary and rectal temperatures at Neonatal Intensive Care (NICU) admission across gestational age ranges of 23-28, 29-32, 33-36, and ≥ 37 weeks, aiming to inform improved neonatal thermal management strategies.

Methods: This cross-sectional study was conducted at King Abdulaziz Medical City, Riyadh, from October 2023 to April 2024, involving 160 infants. Admission temperatures were measured using digital thermometers. Data analysis included ANOVA/Kruskal-Wallis for continuous variables, Chi-square tests for categorical data, Bland-Altman method for agreement assessment, and Pearson correlation coefficients to evaluate temperature correlations.

Results: Mean axillary temperature increased from 36.4 °C in the 23-28 weeks gestational group, to 36.5 °C in the 29-32 weeks group, and to 36.7 °C in the 33-36 weeks and ≥ 37 weeks groups, (p = 0.033). Rectal temperature increased from 36.5 °C in the 23-28 weeks group, to 36.6 °C in the 29-32 weeks group, and reached 36.8 °C in both the 33-36 weeks and ≥ 37 weeks groups (p = 0.006). Notable differences between measurement methods were observed in the 33-36 and ≥ 37 weeks groups (p < 0.001), with less pronounced differences in the 23-28 and 29-32 weeks groups. While temperature differences between rectal and axillary measurements remained consistent across all groups at 0.1 °C (p = 0.779), neonatal outcomes varied significantly across gestational age groups, with younger infants exhibiting lower survival rates (p < 0.001), higher incidences of hypoglycemia (p < 0.001) and sepsis (p < 0.001), and extended durations of ventilation (p < 0.001) and hospital stay (p < 0.001). Strong correlations between rectal and axillary temperature were found across all age ranges (Pearson coefficients: 0.953 for 23-28 weeks, 0.762 for 29-32 weeks, 0.910 for 33-36 weeks, and 0.761 for ≥ 37 weeks; all p < 0.001). Bland-Altman analysis indicated higher variability in agreement for younger preterm groups, showing limits of agreement ranging from - 0.5 to 0.65 °C for 23-28 weeks and - 0.5 to 0.69 °C for 29-32 weeks, improving in older groups with - 0.2 to 0.4 °C for 33-36 weeks and similarly narrow ranges for ≥ 37 weeks.

Conclusion: Both rectal and axillary temperatures showed variation across different age groups, exhibiting a substantial overall correlation. Notable differences between the two methods were observed in the 33-36 weeks and ≥ 37 weeks groups. Younger preterm infants demonstrated greater variability, with enhanced agreement observed in older infants.

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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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