Martin A
Service de Gynécologie-Obstétrique, Hôpital Saint-Jacques, CHRU de Besançon, Besançon Cedex, France.
J Gynecol Obstet Biol Reprod (Paris). 2008 Feb;37 Suppl 1:S34-45. doi: 10.1016/j.jgyn.2007.11.009. Epub 2008 Jan 8.
Continuous fetal heart rate monitoring is widely used during labor even in low risk pregnancies. Consensus is necessary to define and interpret accurately the different FHR patterns. The normal FHR tracing include baseline rate between 110-160 beats per minute (bpm), moderate variability (6-25 bpm), presence of accelerations and no decelerations. Uterine activity is monitored simultaneously: contractions frequency, duration, amplitude and relaxation time must be also normal. Abnormal baseline heart rate during 10 minutes or more is termed tachycardia above 160 bpm (except for FIGO above 150) and bradycardia below 110 bpm. Variability is minimal below 6 bpm and absent when non visible. Decelerations are classified as early, variable, late, and prolonged. Early and late decelerations have an onset gradual decrease of FHR, in contrast variable decelerations have an abrupt onset. Early deceleration is coincident in timing with uterine contraction. Variable deceleration is variable in onset, duration and timing, and may be described as typical or non reassuring. Late deceleration is associated with uterine contraction; the onset, nadir, and recovery occur after onset, peak and end of the contraction. Prolonged deceleration is lasting more than two but less 10 minutes, with almost onset abrupt and no repetition. Electronic fetal monitoring is a method to detect risk of fetal asphyxia; analysis and interpretation of FHR patterns are difficult with a high false positive rate, increasing operative deliveries. The patterns who are predictive of severe fetal acidosis include recurrent late or variable or prolonged decelerations or bradycardia, with absent FHR variability, and sudden severe bradycardia. The other FHR patterns are not conclusive and defined as non reassuring; obstetrical risk factors must be considered and other method (like scalp sampling for pH) utilised to evaluate fetal state.
即使在低风险妊娠的分娩过程中,持续胎儿心率监测也被广泛应用。对于准确界定和解读不同的胎儿心率模式,达成共识很有必要。正常的胎儿心率描记包括每分钟110 - 160次(bpm)的基线率、中等变异度(6 - 25 bpm)、存在加速且无减速。同时监测子宫活动:宫缩频率、持续时间、幅度和松弛时间也必须正常。10分钟或更长时间的异常基线心率,高于160 bpm(国际妇产科联合会规定高于150 bpm除外)称为心动过速,低于110 bpm称为心动过缓。变异度低于6 bpm时极小,不可见时则消失。减速分为早期、变异型、晚期和延长型。早期和晚期减速的胎儿心率呈逐渐下降,相比之下,变异型减速起病突然。早期减速与子宫收缩在时间上一致。变异型减速的起始、持续时间和时间点各不相同,可描述为典型或非令人安心型。晚期减速与子宫收缩相关;其起始、最低点和恢复发生在宫缩的起始、峰值和结束之后。延长型减速持续超过2分钟但少于10分钟,几乎起病突然且无重复。电子胎儿监护是检测胎儿窒息风险的一种方法;胎儿心率模式的分析和解读难度较大,假阳性率高,导致手术分娩增加。预测严重胎儿酸中毒的模式包括反复出现的晚期或变异型或延长型减速或心动过缓、胎儿心率变异度消失以及突然出现的严重心动过缓。其他胎儿心率模式尚无定论,被定义为非令人安心型;必须考虑产科危险因素,并采用其他方法(如头皮pH值采样)来评估胎儿状况。