Management of community-acquired pneumonia in the era of pneumococcal resistance -: A report from the Drug-Resistant Streptococcus pneumoniae Therapeutic Working Group

被引:455
作者
Heffelfinger, JD
Dowell, SF
Jorgensen, JH
Klugman, KP
Mabry, LR
Musher, DM
Plouffe, JF
Rakowsky, A
Schuchat, A
Whitney, CG
机构
[1] Ctr Dis Control & Prevent, Resp Dis Branch, Atlanta, GA USA
[2] Natl Comm Clin Lab Stand, Wayne, PA USA
[3] S African Inst Med Res, Johannesburg, South Africa
[4] Amer Acad Family Physicians, Leahwood, MO USA
[5] Coll Amer Pathologists, Northfield, IL USA
[6] Ohio State Univ, Med Ctr, Infect Dis Sect, Columbus, OH 43210 USA
[7] US FDA, Rockville, MD 20857 USA
关键词
D O I
10.1001/archinte.160.10.1399
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective: To provide recommendations for the management of community-acquired pneumonia and the surveillance of drug-resistant Streptococcus pneumoniae (DRSP). Methods: We addressed the following questions: (1) Should pneumococcal resistance to beta-lactam antimicrobial agents influence pneumonia treatment? (2) What are suitable empirical antimicrobial regimens for outpatient treatment of community-acquired pneumonia in the DRSP era! (3) What are suitable empirical antimicrobial regimens for treatment of hospitalized patients with community-acquired pneumonia in the DRSP era! and (4) How should clinical laboratories report antibiotic susceptibility patterns for S pneumoniae, and what drugs should be included in surveillance if community-acquired pneumonia is the syndrome of interest? Experts in the management of pneumonia and the DRSP Therapeutic Working Group, which includes clinicians, academicians, and public health practitioners, met at the Centers for Disease Control and Prevention in March 1998 to discuss the management of pneumonia in the era of DRSP. Published and unpublished data were summarized from the scientific literature and experience of participants. After group presentations and review of background materials, subgroup, chairs prepared draft responses, which were discussed as a group. Conclusions: When implicated in cases of pneumonia, S pneumoniac should be considered susceptible if penicillin minimum inhibitory concentration (MIC) is no greater than 1 mu g/mL, of intermediate susceptibility if MIC is 2 mu g/ Int, and resistant if MIC is no less than 4 mu g/mL. For outpatient treatment of community-acquired pneumonia, suitable empirical oral antimicrobial agents include a macrolide leg, erythromycin, clarithromycin, azithromycin), doxycycline (or tetracycline) for children aged 8 years or older, or an oral beta-lactam with good activity against pneumococci (eg, cefuroxime axetil, amoxicillin, or a combination of amoxicillin and clavulanate potassium). Suitable empirical antimicrobial regimens for inpatient pneumonia include an intravenous beta-lactam, such as cefuroxime, ceftriaxone sodium, cefotaxime sodium, or a combination of ampicillin sodium and sulbactam sodium plus a macrolide. New fluoroquinolones with improved activity against 5 pneumoniae can also be used to treat adults with community-acquired pneumonia. To limit the emergence of fluoroquinolone-resistant strains, the neu fluoroquinolones should he limited to adults (1) for whom one of the above regimens has already failed, (2) who are allergic to alternative agents, or (3) who have a documented infection with highly drug-resistant pneumococci (eg, penicillin MIC greater than or equal to 4 mu g/mL). Vancomycin hydrochloride is not routinely indicated for the treatment of community-acquired pneumonia or pneumonia caused by DRSP.
引用
收藏
页码:1399 / 1408
页数:10
相关论文
共 80 条
[1]
Once-daily sparfloxacin versus high-dosage amoxicillin in the treatment of community-acquired, suspected pneumococcal pneumonia in adults [J].
Aubier, M ;
Verster, R ;
Regamey, C ;
Geslin, P ;
Vercken, JB .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (06) :1312-1320
[2]
Sparfloxacin for the treatment of community-acquired pneumonia: A pooled data analysis of two studies [J].
Aubier, M ;
Lode, H ;
GialdroniGrassi, G ;
Huchon, G ;
Hosie, J ;
Legakis, N ;
Regamey, C ;
Segev, S ;
Vester, R ;
Wijnands, WJ ;
Tolstuchow, N .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 :73-82
[3]
PNEUMOCOCCAL BACTEREMIA WITH ESPECIAL REFERENCE TO BACTEREMIC PNEUMOCOCCAL PNEUMONIA [J].
AUSTRIAN, R ;
GOLD, J .
ANNALS OF INTERNAL MEDICINE, 1964, 60 (05) :759-+
[4]
Community-acquired pneumonia in adults: Guidelines for management [J].
Bartlett, JG ;
Breiman, RF ;
Mandell, LA ;
File, TM .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) :811-838
[5]
ETIOLOGY OF COMMUNITY-ACQUIRED PNEUMONIA IN OUT-PATIENTS [J].
BERNTSSON, E ;
LAGERGARD, T ;
STRANNEGARD, O ;
TROLLFORS, B .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1986, 5 (04) :446-447
[6]
EMERGENCE OF DRUG-RESISTANT PNEUMOCOCCAL INFECTIONS IN THE UNITED-STATES [J].
BREIMAN, RF ;
BUTLER, JC ;
TENOVER, FC ;
ELLIOTT, JA ;
FACKLAM, RR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (23) :1831-1835
[7]
Penicillin dosing for pneumococcal pneumonia [J].
Bryan, CS ;
Talwani, R ;
Stinson, S .
CHEST, 1997, 112 (06) :1657-1664
[8]
Breakthrough bacteremia and meningitis during treatment with cephalosporins parenterally for pneumococcal pneumonia [J].
Buckingham, SC ;
Brown, SP ;
San Joaquin, VH .
JOURNAL OF PEDIATRICS, 1998, 132 (01) :174-176
[9]
Bactericidal activities of cefprozil, penicillin, cefaclor, cefixime, and loracarbef against penicillin-susceptible and -resistant Streptococcus pneumoniae in an in vitro pharmacodynamic infection model [J].
Cappelletty, DM ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (05) :1148-1152
[10]
FAILURE OF CEFOTAXIME IN THE TREATMENT OF MENINGITIS DUE TO RELATIVELY RESISTANT STREPTOCOCCUS-PNEUMONIAE [J].
CATALAN, MJ ;
FERNANDEZ, JM ;
VAZQUEZ, A ;
DESEIJAS, EV ;
SUAREZ, A ;
DEQUIROS, JCLB .
CLINICAL INFECTIOUS DISEASES, 1994, 18 (05) :766-769