临床儿科杂志
臨床兒科雜誌
림상인과잡지
2014年
10期
951-955
,共5页
易兰芬%红霞%曹晓晓%张京杨%邱梅%李思%王文娟
易蘭芬%紅霞%曹曉曉%張京楊%邱梅%李思%王文娟
역란분%홍하%조효효%장경양%구매%리사%왕문연
心前区不适%心率变异性%自主神经功能%儿童
心前區不適%心率變異性%自主神經功能%兒童
심전구불괄%심솔변이성%자주신경공능%인동
precardial distress%heat rate variability%autonomic nerve function%child
目的:探讨心率减速力(DC)、心率加速力(AC)及心率变异性(HRV)在不明原因心前区不适患儿中的变化。方法56例不明原因心前区不适患儿(患儿组)和63例健康儿童(对照组),年龄6~17岁,行24 h动态心电图检查,并对其DC及HRV各项指标进行对比及相关性分析。结果患儿组的DC值小于对照组,AC值大于对照组,心率(HR)大于对照组,差异有统计学意义(P均<0.05);患儿与对照组间HRV指标的差异无统计学意义(P>0.05)。患儿组中,DC与HRV多项指标呈显著正相关(r=0.27~0.40,P均<0.05),与HR呈显著负相关(r=–0.46,P=0.000);而AC与HRV多项指标呈显著负相关(r=–0.57~–0.34,P均<0.05),与HR呈显著正相关(r=0.61,P=0.000)。<12岁男性患儿HR大于同龄男性对照儿童、相邻RR间期差值的均方根(RMSSD)小于后者;≥12岁男性患儿DC小于、AC大于同龄男性对照儿童;≥12岁女性患儿DC小于同龄女性对照儿童,差异均有统计学意义(P<0.05)。结论不明原因心前区不适患儿的迷走神经张力降低,DC明显低于正常组,且与HRV多项指标有密切相关性。患儿组DC、HRV性别差异不明显。≥12岁患儿组DC明显低于同龄对照组,提示青春期儿童易发生自主神经功能紊乱。
目的:探討心率減速力(DC)、心率加速力(AC)及心率變異性(HRV)在不明原因心前區不適患兒中的變化。方法56例不明原因心前區不適患兒(患兒組)和63例健康兒童(對照組),年齡6~17歲,行24 h動態心電圖檢查,併對其DC及HRV各項指標進行對比及相關性分析。結果患兒組的DC值小于對照組,AC值大于對照組,心率(HR)大于對照組,差異有統計學意義(P均<0.05);患兒與對照組間HRV指標的差異無統計學意義(P>0.05)。患兒組中,DC與HRV多項指標呈顯著正相關(r=0.27~0.40,P均<0.05),與HR呈顯著負相關(r=–0.46,P=0.000);而AC與HRV多項指標呈顯著負相關(r=–0.57~–0.34,P均<0.05),與HR呈顯著正相關(r=0.61,P=0.000)。<12歲男性患兒HR大于同齡男性對照兒童、相鄰RR間期差值的均方根(RMSSD)小于後者;≥12歲男性患兒DC小于、AC大于同齡男性對照兒童;≥12歲女性患兒DC小于同齡女性對照兒童,差異均有統計學意義(P<0.05)。結論不明原因心前區不適患兒的迷走神經張力降低,DC明顯低于正常組,且與HRV多項指標有密切相關性。患兒組DC、HRV性彆差異不明顯。≥12歲患兒組DC明顯低于同齡對照組,提示青春期兒童易髮生自主神經功能紊亂。
목적:탐토심솔감속력(DC)、심솔가속력(AC)급심솔변이성(HRV)재불명원인심전구불괄환인중적변화。방법56례불명원인심전구불괄환인(환인조)화63례건강인동(대조조),년령6~17세,행24 h동태심전도검사,병대기DC급HRV각항지표진행대비급상관성분석。결과환인조적DC치소우대조조,AC치대우대조조,심솔(HR)대우대조조,차이유통계학의의(P균<0.05);환인여대조조간HRV지표적차이무통계학의의(P>0.05)。환인조중,DC여HRV다항지표정현저정상관(r=0.27~0.40,P균<0.05),여HR정현저부상관(r=–0.46,P=0.000);이AC여HRV다항지표정현저부상관(r=–0.57~–0.34,P균<0.05),여HR정현저정상관(r=0.61,P=0.000)。<12세남성환인HR대우동령남성대조인동、상린RR간기차치적균방근(RMSSD)소우후자;≥12세남성환인DC소우、AC대우동령남성대조인동;≥12세녀성환인DC소우동령녀성대조인동,차이균유통계학의의(P<0.05)。결론불명원인심전구불괄환인적미주신경장력강저,DC명현저우정상조,차여HRV다항지표유밀절상관성。환인조DC、HRV성별차이불명현。≥12세환인조DC명현저우동령대조조,제시청춘기인동역발생자주신경공능문란。
Objectives To explore the clinical application of deceleration capacity of rate (DC), acceleration capacity of rate (AC) and heart rate variability (HRV) in children with precardial distress of unknown origin. Methods A total of 56 children with precardial distress of unknown origin and 63 healthy children aged 6 to 17 years were examined by 24 h dynamic elec-trocardiogram, and the indexes of DC and HRV were compared between these two groups. Results DC value of children with precardial distress is less than that of the control group (P<0.05), AC value is greater than that of the control group (P<0.05), and heat rate (HR) is greater than that of the control group (P<0.05). No statistical differences were observed in the indexes of HRV between the two groups. The indexes of DC show a signiifcant positive correlation with HRV in children with precardial distress(r=0.27~0.40, P<0.05), while appear a negative relation with HR (r=-0.46, P=0.000). In contrast, the indexes of AC show a signiifcant negative correlation with HRV (r=-0.57~-0.34, P<0.05), and appears a positive relation with HR(r=0.61, P=0.000). HR value is higher in male children less than 12 years old with precardial distress than that of age-matched males in control group, and RMSSD is lower than the latter. DC value of male children more than 12 years with precardial distress is lower than that of age-matched males in control group, while AC value is higher than that of the latter;DC value is signiifcant lower in fe-male children more than 12 yeares with precardial distress than that of age-matched females in the control group (P<0.05). Con-clusions The activity of vagus nerve in children with precardial distress of unknown origin is decreased. DC value is signiifcantly lower than that of control group, and shows correlation with indexes of HRV. There is no signiifcant difference in DC and HRV value between male and female children with precardial distress. DC value is lower in children aged 12 or older with precardial distress than that of age-matched children in the control group, which indicates adolescents are vulnerable to autonomic nerve functional disorder.