Treatment of cryptococcal meningitis associated with the acquired immunodeficiency syndrome

被引:519
作者
vanderHorst, CM
Saag, MS
Cloud, GA
Hamill, RJ
Graybill, JR
Sobel, JD
Johnson, PC
Tuazon, CU
Kerkering, T
Moskovitz, BL
Powderly, WG
Dismukes, WE
Riser, L
Thomas, C
Lacke, C
White, AC
Patterson, S
Davis, D
Flanigan, C
Harden, T
Phillips, D
Ullom, I
Vasquez, J
McMullen, S
Flowers, D
Bosha, M
Britton, M
Fisher, JF
Newman, C
Willis, B
Henderson, H
Johnson, E
Dungo, L
Pierce, M
Morgan, M
Stern, J
Petrosky, N
Bamberger, D
Farnan, R
Feinberg, J
Apuzzo, L
Royal, W
Thompson, S
Barrett, K
Kauffman, C
Gutsch, H
McKinsey, D
Lee, B
Hyslop, N
Greenspan, D
机构
[1] UNIV ALABAMA, SCH MED, DEPT MED, DIV INFECT DIS, BIRMINGHAM, AL USA
[2] UNIV ALABAMA, SCH MED, CTR COMPREHENS CANC, BIOSTAT UNIT, BIRMINGHAM, AL USA
[3] VET AFFAIRS MED CTR, INFECT DIS SECT, HOUSTON, TX 77030 USA
[4] BAYLOR COLL MED, HOUSTON, TX 77030 USA
[5] UNIV TEXAS, HLTH SCI CTR, SAN ANTONIO, TX USA
[6] WAYNE STATE UNIV, DIV INFECT DIS, DETROIT, MI USA
[7] UNIV TEXAS, HOUSTON MED CTR, DEPT MED, HOUSTON, TX USA
[8] GEORGE WASHINGTON UNIV, DEPT MED, WASHINGTON, DC USA
[9] VIRGINIA COMMONWEALTH UNIV MED COLL VIRGINIA, DIV INFECT DIS, RICHMOND, VA USA
[10] JANSSEN RES FDN, TITUSVILLE, NJ USA
[11] WASHINGTON UNIV, SCH MED, DIV INFECT DIS, ST LOUIS, MO 63130 USA
[12] DETROIT MED CTR, DETROIT, MI USA
[13] GEORGE WASHINGTON UNIV, MED CTR, WASHINGTON, DC 20052 USA
[14] UNIV MISSISSIPPI, MED CTR, UNIVERSITY, MS 38677 USA
[15] ST MICHAELS HOSP, NEWARK, NJ 07102 USA
[16] VANDERBILT UNIV, NASHVILLE, TN 37203 USA
[17] PENN HOSP, PHILADELPHIA, PA 19107 USA
[18] UNIV MISSOURI, KANSAS CITY, MO 64110 USA
[19] JOHNS HOPKINS UNIV, BALTIMORE, MD 21218 USA
[20] EMORY UNIV, ATLANTA, GA 30322 USA
[21] UNIV MICHIGAN, ANN ARBOR, MI 48109 USA
[22] INFECT DIS ASSOCIATES KANSAS CITY, KANSAS CITY, MO USA
[23] TULANE UNIV, NEW ORLEANS, LA 70118 USA
[24] PERMANENTE MED GRP INC, SACRAMENTO, CA USA
[25] ALTON OCHSNER MED FDN & OCHSNER CLIN, NEW ORLEANS, LA 70121 USA
[26] FRONTIER SCI & TECHNOL RES FDN INC, CTR DATA, AMHERST, NY 14226 USA
[27] SOCIAL & SCI SYST, OPERAT OFF, BETHESDA, MD 20814 USA
[28] UNIV CALIF SAN FRANCISCO, SAN FRANCISCO, CA 94143 USA
[29] BETH ISRAEL MED CTR, NEW YORK, NY 10003 USA
[30] YALE UNIV, NEW HAVEN, CT 06520 USA
[31] UNIV SO CALIF, LOS ANGELES, CA 90089 USA
[32] INDIANA UNIV, BLOOMINGTON, IN 47405 USA
[33] OHIO STATE UNIV, COLUMBUS, OH 43210 USA
[34] UNIV PENN, PHILADELPHIA, PA 19104 USA
[35] UNIV CINCINNATI, CINCINNATI, OH 45221 USA
[36] UNIV ROCHESTER, ROCHESTER, NY 14627 USA
[37] HARVARD UNIV, CAMBRIDGE, MA 02138 USA
[38] HARLEM HOSP MED CTR, NEW YORK, NY 10037 USA
[39] UNIV MASSACHUSETTS, AMHERST, MA 01003 USA
[40] ALBERT EINSTEIN COLL MED, NEW YORK, NY USA
[41] UNIV TEXAS, GALVESTON, TX USA
[42] CORNELL UNIV, ITHACA, NY 14853 USA
[43] ST LUKES ROOSEVELT HOSP, NEW YORK, NY USA
关键词
D O I
10.1056/NEJM199707033370103
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Treatment with low-dose amphotericin B (0.4 mg per kilogram of body weight per day) or oral azole therapy in patients with the acquired immunodeficiency syndrome (AIDS) and cryptococcal meningitis has been associated with high mortality and low rates of cerebrospinal fluid sterilization. Methods In a double-blind multicenter trial we randomly assigned patients with a first episode of AIDS-associated cryptococcal meningitis to treatment with higher-dose amphotericin B (0.7 mg per kilogram per day) with or without flucytosine (100 mg per kilogram per day) for two weeks (step one), followed by eight weeks of treatment with itraconazole (400 mg per day) or fluconazole (400 mg per day) (step two). Treatment was considered successful if cerebrospinal fluid cultures were negative at 2 and 10 weeks or if the patient was clinically stable at 2 weeks and asymptomatic at 10 weeks. Results At two weeks, the cerebrospinal fluid cultures were negative in 60 percent of the 202 patients receiving amphotericin B plus flucytosine and in 51 percent of the 179 receiving amphotericin B alone (P=0.06). Elevated intracranial pressure was associated with death in 13 of 14 patients during step one. The clinical outcome did not differ significantly between the two groups. Seventy-two percent of the 151 fluconazole recipients and 60 percent of the 155 itraconazole recipients had negative cultures at 10 weeks (95 percent confidence interval for the difference in percentages, -100 to 21). The proportion of patients who had clinical responses was similar with fluconazole (68 percent) and itraconazole (70 per cent). Overall mortality was 5.5 percent in the first two weeks and 3.9 percent in the next eight weeks, with no significant difference between the groups. In a multivariate analysis, the addition of flucytosine during the initial two weeks and treatment with fluconazole for the next eight weeks were independently associated with cerebrospinal fluid sterilization. Conclusions For the initial treatment of AIDS-associated cryptococcal meningitis, the use of higher-dose amphotericin B plus flucytosine is associated with an increased rate of cerebrospinal fluid sterilization and decreased mortality at two weeks, as compared with regimens used in previous studies. Although consolidation therapy with fluconazole is associated with a higher rate of cerebrospinal fluid sterilization, itraconazole may be a suitable alternative for patients unable to take fluconazole. (C) 1997, Massachusetts Medical Society.
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页码:15 / 21
页数:7
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