中华传染病杂志
中華傳染病雜誌
중화전염병잡지
CHINESE JOURNAL OF INFECTIOUS DISEASES
2013年
3期
155-159
,共5页
林苏%张彦亮%邵凌云%黄玉仙%张文宏%翁心华
林囌%張彥亮%邵凌雲%黃玉仙%張文宏%翁心華
림소%장언량%소릉운%황옥선%장문굉%옹심화
脑膜炎,隐球菌性%颅神经损伤%两性霉素B%三唑类%预后
腦膜炎,隱毬菌性%顱神經損傷%兩性黴素B%三唑類%預後
뇌막염,은구균성%로신경손상%량성매소B%삼서류%예후
Meningitis,cryptococcal%Cranial nerve injuries%Amphotericin B%Triazoles%Prognosis
目的 了解非AIDS相关隐球菌性脑膜炎患者并发颅神经损伤的危险因素及预后因素.方法 回顾性分析复旦大学附属华山医院2000年1月至2010年12月住院治疗的隐球菌性脑膜炎145例,总结临床特征、抗真菌治疗和恢复情况.采用多因素分析法对相关危险因素和预后因素进行研究.连续变量采用f检验,离散变量采用x2检验或Fisher确切概率检验.结果 145例患者中52例出现颅神经损伤,发生率为35.9%,其中视神经、动眼神经、听神经、外展神经、嗅神经和面神经受累分别为25、22、12、6、4、3例,分别占所有颅神经损伤患者的48.1%、42.3%、23.1%、11.5%、7.7%和5.8%.确诊时间是发生颅神经损伤的最强危险因素(OR=1.056,95% CI为1.002~1.111),诊断时间每延长1周,颅神经损伤发生率就增加5.6%.颅内压高及脑脊液有核细胞数降低也是发生颅神经损伤的独立预测因素(均P<0.05).发生颅神经损伤后有73.3%患者可以完全恢复,恢复中位时间为3个月(0.5~24.0个月).受累神经数量(OR=0.230,95%CI为0.066~0.800,P=0.021)和两性霉素B联合三唑类药物治疗(AmB+ 5-FC+三唑类药物)(OR=10.317,95%CI为2.086~51.025,P=0.004)是神经损伤恢复的独立预测因素.结论 颅神经损伤在隐球菌性脑膜炎中很常见,其发生率与确诊时间延长、颅内压增高及脑脊液有核细胞数降低有关,而受累神经数量和联合治疗是神经恢复的独立预测因素.早期诊断和积极有效抗真菌治疗对防治颅神经损伤至关重要.
目的 瞭解非AIDS相關隱毬菌性腦膜炎患者併髮顱神經損傷的危險因素及預後因素.方法 迴顧性分析複旦大學附屬華山醫院2000年1月至2010年12月住院治療的隱毬菌性腦膜炎145例,總結臨床特徵、抗真菌治療和恢複情況.採用多因素分析法對相關危險因素和預後因素進行研究.連續變量採用f檢驗,離散變量採用x2檢驗或Fisher確切概率檢驗.結果 145例患者中52例齣現顱神經損傷,髮生率為35.9%,其中視神經、動眼神經、聽神經、外展神經、嗅神經和麵神經受纍分彆為25、22、12、6、4、3例,分彆佔所有顱神經損傷患者的48.1%、42.3%、23.1%、11.5%、7.7%和5.8%.確診時間是髮生顱神經損傷的最彊危險因素(OR=1.056,95% CI為1.002~1.111),診斷時間每延長1週,顱神經損傷髮生率就增加5.6%.顱內壓高及腦脊液有覈細胞數降低也是髮生顱神經損傷的獨立預測因素(均P<0.05).髮生顱神經損傷後有73.3%患者可以完全恢複,恢複中位時間為3箇月(0.5~24.0箇月).受纍神經數量(OR=0.230,95%CI為0.066~0.800,P=0.021)和兩性黴素B聯閤三唑類藥物治療(AmB+ 5-FC+三唑類藥物)(OR=10.317,95%CI為2.086~51.025,P=0.004)是神經損傷恢複的獨立預測因素.結論 顱神經損傷在隱毬菌性腦膜炎中很常見,其髮生率與確診時間延長、顱內壓增高及腦脊液有覈細胞數降低有關,而受纍神經數量和聯閤治療是神經恢複的獨立預測因素.早期診斷和積極有效抗真菌治療對防治顱神經損傷至關重要.
목적 료해비AIDS상관은구균성뇌막염환자병발로신경손상적위험인소급예후인소.방법 회고성분석복단대학부속화산의원2000년1월지2010년12월주원치료적은구균성뇌막염145례,총결림상특정、항진균치료화회복정황.채용다인소분석법대상관위험인소화예후인소진행연구.련속변량채용f검험,리산변량채용x2검험혹Fisher학절개솔검험.결과 145례환자중52례출현로신경손상,발생솔위35.9%,기중시신경、동안신경、은신경、외전신경、후신경화면신경수루분별위25、22、12、6、4、3례,분별점소유로신경손상환자적48.1%、42.3%、23.1%、11.5%、7.7%화5.8%.학진시간시발생로신경손상적최강위험인소(OR=1.056,95% CI위1.002~1.111),진단시간매연장1주,로신경손상발생솔취증가5.6%.로내압고급뇌척액유핵세포수강저야시발생로신경손상적독립예측인소(균P<0.05).발생로신경손상후유73.3%환자가이완전회복,회복중위시간위3개월(0.5~24.0개월).수루신경수량(OR=0.230,95%CI위0.066~0.800,P=0.021)화량성매소B연합삼서류약물치료(AmB+ 5-FC+삼서류약물)(OR=10.317,95%CI위2.086~51.025,P=0.004)시신경손상회복적독립예측인소.결론 로신경손상재은구균성뇌막염중흔상견,기발생솔여학진시간연장、로내압증고급뇌척액유핵세포수강저유관,이수루신경수량화연합치료시신경회복적독립예측인소.조기진단화적겁유효항진균치료대방치로신경손상지관중요.
Objective To understand the predictors and prognostic significance of cranial nerve impairment in non-acquired immune deficiency syndrome (AIDS) patients with cryptococcal meningitis.Methods A total of 145 non-AIDS patients with cryptococcal meningitis admitted to Huashan Hospital,Fudan University from Jan 2000 to Dec 2010 were reviewed retrospectively.Clinical characteristics,initial antifungal therapies and outcome of these patients were analyzed.Continuous variables were analyzed using t test and categorical variables were compared by x2 test or Fisher's exact test.Multivariate analysis was performed by binary Logistic regressions.Results Out of 145 patients,52 (35.9%) patients had cranial nerve impairment at enrollment.Optic (25/52,48.1%) and oculomotor (22/52,42.3%) nerves were the most commonly involved,followed by auditory (12/52,23.1%),abducens (6/52,11.5%),olfactory (4/52,7.7%) and facial (3/52,5.8%) nerves.The best predictive factor of cranial nerve injury was duration of diagnosis (OR =1.056,95% CI:1.002-1.111).The risk of cranial injury would increase by 5.6% with one-week delay of diagnosis.Intracranial hypertension and low cerebrospinal fluid cell count were also the independent predictive factors (both P<0.05).In the follow-up period,73.3% patients who had cranial nerve injuries were fully recovered,with a median time of 3 (0.5-24.0) months.The independent predictors of recovery were numbers of nerve involved (OR =0.230,95 % CI:0.066-0.800,P=0.021) and amphotericin B (AmB) plus 5-fluorocytosine,triazole antifungal agent therapy (OR=10.317,95%CI:2.086-51.025,P=0.004).Conclusions Cranial nerve impairment occurs in one-third of non-AIDS patients with cryptococcal meningitis.Delay in diagnosis,intracranial hypertension and low cerebrospinal fluid cell count are independent predictive factors.Less cranial nerve involvement and AmB plus triazole therapy predict recovery.