中华儿科杂志
中華兒科雜誌
중화인과잡지
Chinese Journal of Pediatrics
2009年
2期
140-145
,共6页
林振浪%余波%梁志强%陈鲜威%刘江勤%陈尚勤%张姿英%张弩
林振浪%餘波%樑誌彊%陳鮮威%劉江勤%陳尚勤%張姿英%張弩
림진랑%여파%량지강%진선위%류강근%진상근%장자영%장노
婴儿,新生%脑室%颅内出血%脑积水%硬膜下积液
嬰兒,新生%腦室%顱內齣血%腦積水%硬膜下積液
영인,신생%뇌실%로내출혈%뇌적수%경막하적액
Infant,newborn%Cerebral ventricles%Intracranial hemorrhages%Hydrocephalus%Subdural effusion
目的 脑室内出血后脑积水是新生儿严重的并发症,存活后往往伴有严重的神经系统后遗症,目前对脑室内出血后脑积水处理仍然相当棘手,没有统一的方案.用储液囊埋植引流治疗新侣生儿脑室出血后脑积水,就其疗效和安全性作一初步评价.方法 对2003年1月至2005年12月期间,相继入住我院的15例新生儿脑窜内出血Ⅲ度以上合并脑积水,且1周内脑室进行性扩大,头围每天增大>2 mm伴有颅内压增高症状患儿,进行储液囊埋植引流治疗.储液囊埋植后根据临床和头颅超声或头颅CT检查结果,决定脑脊液引流次数,间歇引流时间和引流量,并观察脑脊液中细胞数、蛋白质和葡萄糖浓度的变化及术中和术后的并发症.若储液囊引流无效,改行脑室-腹腔分流术.出院后临床随访1.5~3年.结果 15例患儿中早产儿11例,孕龄(31.5±0.5)周;足月儿4例,其中3例为维生素K缺乏性颅内出血.脑室出血Ⅲ级13例,Ⅳ级2例.脑室出血平均诊断日龄:早产儿(9±1)d,足月儿(22±7)d.埋植Ommaya囊时日龄:早产儿(18±1)d,足月儿(31±7)d.平均每例患儿脑脊液引流次数(21.5±4.6)次,每次引流量为(10.2±1.3)ml/kg.15例经储液囊脑脊液引流后30 d脑脊液中细胞计数和葡萄糖分别为(14±6)×106个/L、(2.2±0.2)mmol/L;引流后39 d蛋白质为(0.48±0.10)g/L.13例经储液囊脑脊液引流后在1~4周内头围增长速度每周<1 cm,病情改善,其中12例至12~18个月时脑室恢复正常大小,1例在36个月时仍有轻度扩大.2例储液囊脑脊液引流无效,其中1例转行脑室.腹腔分流术后好转,1例放弃治疗出院后3个月死亡.术中和术后病情稳定,1例术后16 d储液囊出现渗漏,并发颅内感染(感染发生率为1/15),加用抗菌素治疗痊愈.14例术后1.5~3年时间随访:11例生长发育正常;2例早产儿发生两下肢痉挛性脑瘫,其中1例合并弱视;1例足月儿有癫癎发作.结论 采用储液囊脑室埋植引流治疗新生儿重型脑室出血合并脑积水,初步显示疗效满意和比较安全,为进一步明确其疗效需前瞻性临床多中心随机对照试验.
目的 腦室內齣血後腦積水是新生兒嚴重的併髮癥,存活後往往伴有嚴重的神經繫統後遺癥,目前對腦室內齣血後腦積水處理仍然相噹棘手,沒有統一的方案.用儲液囊埋植引流治療新侶生兒腦室齣血後腦積水,就其療效和安全性作一初步評價.方法 對2003年1月至2005年12月期間,相繼入住我院的15例新生兒腦竄內齣血Ⅲ度以上閤併腦積水,且1週內腦室進行性擴大,頭圍每天增大>2 mm伴有顱內壓增高癥狀患兒,進行儲液囊埋植引流治療.儲液囊埋植後根據臨床和頭顱超聲或頭顱CT檢查結果,決定腦脊液引流次數,間歇引流時間和引流量,併觀察腦脊液中細胞數、蛋白質和葡萄糖濃度的變化及術中和術後的併髮癥.若儲液囊引流無效,改行腦室-腹腔分流術.齣院後臨床隨訪1.5~3年.結果 15例患兒中早產兒11例,孕齡(31.5±0.5)週;足月兒4例,其中3例為維生素K缺乏性顱內齣血.腦室齣血Ⅲ級13例,Ⅳ級2例.腦室齣血平均診斷日齡:早產兒(9±1)d,足月兒(22±7)d.埋植Ommaya囊時日齡:早產兒(18±1)d,足月兒(31±7)d.平均每例患兒腦脊液引流次數(21.5±4.6)次,每次引流量為(10.2±1.3)ml/kg.15例經儲液囊腦脊液引流後30 d腦脊液中細胞計數和葡萄糖分彆為(14±6)×106箇/L、(2.2±0.2)mmol/L;引流後39 d蛋白質為(0.48±0.10)g/L.13例經儲液囊腦脊液引流後在1~4週內頭圍增長速度每週<1 cm,病情改善,其中12例至12~18箇月時腦室恢複正常大小,1例在36箇月時仍有輕度擴大.2例儲液囊腦脊液引流無效,其中1例轉行腦室.腹腔分流術後好轉,1例放棄治療齣院後3箇月死亡.術中和術後病情穩定,1例術後16 d儲液囊齣現滲漏,併髮顱內感染(感染髮生率為1/15),加用抗菌素治療痊愈.14例術後1.5~3年時間隨訪:11例生長髮育正常;2例早產兒髮生兩下肢痙攣性腦癱,其中1例閤併弱視;1例足月兒有癲癎髮作.結論 採用儲液囊腦室埋植引流治療新生兒重型腦室齣血閤併腦積水,初步顯示療效滿意和比較安全,為進一步明確其療效需前瞻性臨床多中心隨機對照試驗.
목적 뇌실내출혈후뇌적수시신생인엄중적병발증,존활후왕왕반유엄중적신경계통후유증,목전대뇌실내출혈후뇌적수처리잉연상당극수,몰유통일적방안.용저액낭매식인류치료신려생인뇌실출혈후뇌적수,취기료효화안전성작일초보평개.방법 대2003년1월지2005년12월기간,상계입주아원적15례신생인뇌찬내출혈Ⅲ도이상합병뇌적수,차1주내뇌실진행성확대,두위매천증대>2 mm반유로내압증고증상환인,진행저액낭매식인류치료.저액낭매식후근거림상화두로초성혹두로CT검사결과,결정뇌척액인류차수,간헐인류시간화인류량,병관찰뇌척액중세포수、단백질화포도당농도적변화급술중화술후적병발증.약저액낭인류무효,개행뇌실-복강분류술.출원후림상수방1.5~3년.결과 15례환인중조산인11례,잉령(31.5±0.5)주;족월인4례,기중3례위유생소K결핍성로내출혈.뇌실출혈Ⅲ급13례,Ⅳ급2례.뇌실출혈평균진단일령:조산인(9±1)d,족월인(22±7)d.매식Ommaya낭시일령:조산인(18±1)d,족월인(31±7)d.평균매례환인뇌척액인류차수(21.5±4.6)차,매차인류량위(10.2±1.3)ml/kg.15례경저액낭뇌척액인류후30 d뇌척액중세포계수화포도당분별위(14±6)×106개/L、(2.2±0.2)mmol/L;인류후39 d단백질위(0.48±0.10)g/L.13례경저액낭뇌척액인류후재1~4주내두위증장속도매주<1 cm,병정개선,기중12례지12~18개월시뇌실회복정상대소,1례재36개월시잉유경도확대.2례저액낭뇌척액인류무효,기중1례전행뇌실.복강분류술후호전,1례방기치료출원후3개월사망.술중화술후병정은정,1례술후16 d저액낭출현삼루,병발로내감염(감염발생솔위1/15),가용항균소치료전유.14례술후1.5~3년시간수방:11례생장발육정상;2례조산인발생량하지경련성뇌탄,기중1례합병약시;1례족월인유전간발작.결론 채용저액낭뇌실매식인류치료신생인중형뇌실출혈합병뇌적수,초보현시료효만의화비교안전,위진일보명학기료효수전첨성림상다중심수궤대조시험.
Objective Intra-ventrieular hemorrhage (IVH) is one of the most serious complications of preterm infants. Significant numbers of the surviving infants with severe IVH go on to develop post-hemorrhagic hydrocephalus (PHH). The management of PHH remains a very challenging problem for both neonatologists and pediatric neurosurgeons. This study aimed to evaluate the efficacy and safety of the use of Ommaya reservoirs and serial cerebrospinal fluid (CSF) drainage in the management of a series of neonates with PHH. Method Between January 1, 2003 and December 30, 2005, 15 consecutive newborn infants with IVH grades Ⅲ to Ⅳ, complicated with progressive ventricular dilatation, underwent placement of an Ommaya reservoir. CSF was intermittently aspirated percutaneonsly from the reservoir. The amount and frequency of CSF aspiration were based on the clinical presentation and the follow-up results of serial cranial ultrasonograms or CT scans. The changes of CSF cell counts and chemistries were also followed. Patients whose progressive ventricular dilatation persisted despite serial CSF aspiration through Ommaya reservoir eventually had ventriculo-peritoneal shunts (V-P shunt) placed. All the patients were followed up in the outpatient clinic after discharge from the hospital and the neurodevelopmental outcomes were evaluated through 18-36 months of age. Result A total of 15 infants were included in this series. Of them, 11 were preterm infants who were at gestational ages of 29 to 34 weeks and 4 infants were full-term. All of the 4 full term infants presented with progressive ventrieular dilatation after suffering from the intra-cranial hemorrhage (3 infants were due to vitamin K deficiency and 1 was due to birth trauma). Thirteen infants had grade ⅢIVH, and 2 had grade Ⅳ IVH based on initial cranial ultrasonographic and CT scans. The mean age when IVH was diagnosed was (9±1) days in preterm infants and (22±7) days in full-term infants; the mean age when Ommaya reservoir was placed was (18±11) days in preterm infants and (31±7) days in full-term infants. All the infants tolerated the surgical procedure welL The Ommaya reservoir was tapped for an average of (21.5±4.6) times per patient. The mean CSF volume per tap was (10.2±1.3) mL/kg. The values of CSF protein, glucose and cell counts slowly reached normal levels at approximately 3-5 weeks after the placement of the reservoir. The velocity of head circumference increase per week was less than 1 cm in 13 patients in 1-4 weeks after the placement of the reservoir and the size of ventricles decreased gradually. By 12-18 months, 12 infants had normal size ventricles, and 1 patient still had mild ventricular dilation at 36 months. Two infants developed progressive hydrocephalus after serial CSF aspiration through Ommaya reservoir. One infant had a V-P shunt placed at 2 months of age and another infant died at 3 months of age at home after parents refused further therapy. Complications consisted of reservoir leaking and CSF infection at 16th day of placement in one patient after repeated tapping. By the end of 18-36 months of follow-up, 11 of 14 infants were considered normal, two patients had mild impairment in neuredevelopmental outcome (both had spastic bilateral lower limbs paresis, and one of whom also had ambliopia) and the other had seizure disorder. Conclusion The results from this series indicate that the placement of an Ommaya reservoir is relatively safe in newborn infants and is useful in the initial management of neonates with PHH and may be beneficial in improving their neurodevelopmental outcomes. A multicenter randomized trial may be needed to further validate the results of this report.