Clinical features and outcomes of persons with cystic fibrosis and nocardia isolation: a systematic review

被引:0
|
作者
Terlizzi, Vito [1 ]
Ballerini, Tommaso [2 ]
Castaldo, Alice [2 ,3 ,4 ]
Dolce, Daniela [1 ]
Campana, Silvia [1 ]
Taccetti, Giovanni [1 ]
Chiappini, Elena [5 ,6 ]
机构
[1] IRCCS, Meyer Childrens Hosp, Cyst Fibrosis Reg Reference Ctr, Dept Paediat Med, Florence, Italy
[2] Univ Florence, Meyer Childrens Univ Hosp IRCCS, Dept Hlth Sci, Pediat resident, Florence, Italy
[3] AORN Santobono Pausilipon, SC Pneumol, Naples, Italy
[4] UTSIR, AORN Santobono Pausilipon, Naples, Italy
[5] Meyer Childrens Hosp IRCCS, Infect Dis Unit, Florence, Italy
[6] Univ Florence, Meyer Childrens Hosp IRCCS, Dept Hlth Sci, Viale Pieraccini 24, I-50139 Florence, Italy
来源
BMC PULMONARY MEDICINE | 2024年 / 24卷 / 01期
关键词
FEV1; Lung transplantation; Therapy; Eradication; Children;
D O I
10.1186/s12890-024-03217-0
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
BackgroundRecurrent respiratory infections are a leading cause of morbidity and mortality in persons with Cystic Fibrosis (pwCF). Recently, the emergence of Nocardia species as a potential pathogen in CF has raised questions about its role and management, as its clinical significance and the optimal patient management remain unclear in current clinical practice. This review explores the clinical implications of Nocardia species in patients with Cystic Fibrosis (pwCF) through a comprehensive literature review. Key objectives include assessing its impact on lung function, identifying colonization risk factors, and evaluating an appropriate treatment.MethodsThe literature review, conducted until June 30, 2023, from databases like MEDLINE, PubMed, Embase, and Cochrane, included 16 articles involving 89 pwCF with Nocardia species isolation according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guideline recommendations. Articles reporting Nocardia prevalence and symptoms based on original data in adult and paediatric pwCF were included. All the retrieved studies were observational ones, thus, they were categorized by study type as case report and case series.ResultsOverall 89 pwCF and Nocardia species isolation were included: 42 children and 47 adults. Where reported, we found these main following bacterial species: Nocardia asteroides (35%, 23/64), Nocardia farcinica (21%, 14/64), Nocardia tranvalensis (13%, 8/64) and Nocardia cyriacigeorgica (11%, 7/64). A co-infection was reported in 85% of patients (61/72). Of patients whose lung function was reported before and after Nocardia isolation, 23% (16/68) showed a decline in FEV1. Above all, 82 patients were treated at least once after isolation of Nocardia strain. In 93% (77/82) of cases, treatment was started immediately upon isolation. Antibiotic treatment was performed per os or intravenously depending on the clinical condition of the individual patient. Nocardia eradication was attempted in only 32 cases out of 82, and 78% (25/32) of these patients were successfully eradicated after one or more courses of antibiotics. Death was reported in 3 patients, 2 of which were children.ConclusionIn general the isolation of the bacteria does not necessarily imply therapy, but patients need to be monitored closely to assess the possible occurrence of active infection. The treatment seems to be indicated in patients showing lung involvement with the possible appearance of pneumonia, pleural effusion, fever, cough, or a decrease in FEV1, as in the case that we described, or in patients undergoing pulmonary transplantation. center dot A strength of this study is that it provides an updated systematic review on the management of Nocardia's isolation in patients with Cystic Fibrosis. By synthesising findings across all included studies we propose a therapeutic management algorithm.center dot This systematic review protocol follows the Joanna Briggs Institute, mixed-method systematic review protocol.center dot Limitations of the study is the paucity of randomised controlled trials and the heterogeneity among available publications.center dot There is potential for heterogeneity of published data, which may limit the conclusions that can be drawn from this study.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Incidence, prevalence, clinical features, and outcomes of COVID-19 in persons with cystic fibrosis: a systematic review protocol
    Antony, Sherly
    Vargese, Saritha Susan
    Idikula, Mercy John
    Cherian, Carol Sara
    Mathew, Elsheba
    Green, Heidi
    Fernandez, Ritin
    [J]. JBI EVIDENCE SYNTHESIS, 2022, 20 (11) : 2721 - 2726
  • [2] Isolation of Nocardia species patients with cystic fibrosis
    Barrio, M. Isabel
    Martinez, M. Carmen
    Prados, Concepcion
    Giron, Rosa A.
    Maiz, Luis
    Martinez, M. Teresa
    [J]. ARCHIVOS DE BRONCONEUMOLOGIA, 2008, 44 (02): : 109 - 112
  • [3] Dietary Macronutrient Distribution and Nutrition Outcomes in Persons with Cystic Fibrosis: An Evidence Analysis Center Systematic Review
    McDonald, Catherine M.
    Bowser, Ellen K.
    Farnham, Kristen
    Alvarez, Jessica A.
    Padula, Laura
    Rozga, Mary
    [J]. JOURNAL OF THE ACADEMY OF NUTRITION AND DIETETICS, 2021, 121 (08) : 1574 - U96
  • [4] Isolation of infectious cystic fibrosis patients: Results of a systematic review
    Vonberg, RP
    Gastmeier, P
    [J]. INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2005, 26 (04): : 401 - 409
  • [5] Isolation of infectious cystic fibrosis patients - Results of a systematic review
    Vonberg, RP
    Gastmeier, P
    [J]. INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 294 : 189 - 189
  • [6] Cystic fibrosis, body composition, and health outcomes: a systematic review
    Calella, Patrizia
    Valerio, Giuliana
    Brodlie, Malcolm
    Donini, Lorenzo Maria
    Siervo, Mario
    [J]. NUTRITION, 2018, 55-56 : 131 - 139
  • [7] Antimicrobial susceptibility testing (AST) and associated clinical outcomes in individuals with cystic fibrosis: A systematic review
    Somayaji, Ranjani
    Parkins, Michael D.
    Shah, Anand
    Martiniano, Stacey L.
    Tunney, Michael M.
    Kahle, Jennifer S.
    Waters, Valerie J.
    Elborn, J. Stuart
    Bell, Scott C.
    Flume, Patrick A.
    VanDevanter, Donald R.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2019, 18 (02) : 236 - 243
  • [8] Clinical features, treatment and outcomes in patients with tracheal adenoid cystic carcinoma: a systematic literature review
    Ran, Juntao
    Qu, Guofeng
    Chen, Xiaohua
    Zhao, Da
    [J]. RADIATION ONCOLOGY, 2021, 16 (01)
  • [9] Clinical features, treatment and outcomes in patients with tracheal adenoid cystic carcinoma: a systematic literature review
    Juntao Ran
    Guofeng Qu
    Xiaohua Chen
    Da Zhao
    [J]. Radiation Oncology, 16
  • [10] Isolation measures for prevention of infection with respiratory pathogens in cystic fibrosis: a systematic review?
    Hoiby, N.
    Johansen, H. Krogh
    [J]. JOURNAL OF HOSPITAL INFECTION, 2007, 65 (04) : 374 - 375