Joshi A, Gerhardt T, Shandloff P, Bancalari E
Pediatrics. 1987 Jul;80(1):79-84.
Anemia may increase the risk of tissue hypoxia in preterm infants. This could lead to respiratory center depression and an increased risk for apnea. Heart rate and breathing pattern were recorded in 30 preterm infants (gestational age 30.0 +/- 2.3 weeks, postnatal age 46.6 +/- 20.8 days, and weight 1,438 +/- 266 g) before and after a transfusion of 10 mL/kg of packed RBCs. All infants were stable clinically, breathing room air, and free of prolonged apneic episodes. After transfusion, hematocrit levels increased from 27.0% +/- 2.5% to 35.8% +/- 4.7%. Heart rate decreased from 157.2 +/- 13.6 beats per minute to 148.4 +/- 13.9 beats per minute. There was no change in respiratory rate or BP. The duration of periodic breathing decreased significantly, as did the duration of the longest periodic breathing episode (P less than .01). The number of respiratory pauses lasting 5 to 10 seconds and the number of pauses lasting 11 to 20 seconds also decreased significantly (P less than .05). The total duration of respiratory pauses, excluding pauses during periodic breathing, were significantly lower after transfusion (P less than .05), as was the number of episodes of bradycardia. These results indicate that preterm infants have a more irregular breathing pattern while anemic than after correction of the anemia. The irregular breathing pattern is probably caused by mild hypoxic respiratory center depression.
贫血可能会增加早产儿组织缺氧的风险。这可能导致呼吸中枢抑制以及呼吸暂停风险增加。在给30名早产儿(胎龄30.0±2.3周,出生后年龄46.6±20.8天,体重1438±266克)输注10毫升/千克浓缩红细胞前后记录心率和呼吸模式。所有婴儿临床情况稳定,呼吸室内空气,且无长时间呼吸暂停发作。输血后,血细胞比容水平从27.0%±2.5%升至35.8%±4.7%。心率从每分钟157.2±13.6次降至148.4±13.9次。呼吸频率或血压无变化。周期性呼吸持续时间显著缩短,最长周期性呼吸发作的持续时间也显著缩短(P<0.01)。持续5至10秒的呼吸暂停次数和持续11至20秒的呼吸暂停次数也显著减少(P<0.05)。输血后,不包括周期性呼吸期间的呼吸暂停总持续时间显著降低(P<0.05),心动过缓发作次数也显著降低。这些结果表明,早产儿贫血时呼吸模式比贫血纠正后更不规则。这种不规则呼吸模式可能是由轻度缺氧性呼吸中枢抑制引起的。