Literature DB >> 7522353

Effect of antibiotic treatment on inflammatory markers and lung function in cystic fibrosis patients with Pseudomonas cepacia.

D Peckham1, S Crouch, H Humphreys, B Lobo, A Tse, A J Knox.   

Abstract

BACKGROUND: The acquisition of Pseudomonas cepacia in patients with cystic fibrosis is associated with increasing deterioration in lung function and more frequent hospital admissions. Pseudomonas cepacia is usually resistant to several antibiotics in vitro, but the response of patients colonised with the organism has not been extensively studied in vivo.
METHODS: A three month prospective study was performed to investigate the response of 14 Ps cepacia positive patients and 10 Ps cepacia negative patients to a two week course of intravenous antibiotics. All those who were Ps cepacia negative and six of the 14 Ps cepacia positive patients had Ps aeruginosa in their sputum which was sensitive to the prescribed therapy. The inflammatory markers C-reactive protein, white blood cell count, serum lactoferrin, neutrophil elastase/alpha 1-antitrypsin complex, and tumour necrosis factor alpha were measured at the start and end of each antibiotic course.
RESULTS: The median (range) % improvement in baseline FEV1 and FVC following treatment in the group as a whole was 15.2% (-23.5% to 156.3%) and 23.9% (-36.8% to 232.7%) respectively. There was no statistical difference in improvement in lung function, body weight, or inflammatory markers between individuals who were Ps cepacia positive and those who were Ps cepacia negative.
CONCLUSIONS: Patients who are Ps cepacia positive appear to respond as well to intravenous antibiotics as those who are Ps cepacia negative, despite having lower lung function and a bacterium in their sputum which is resistant in vitro to the antibiotics used.

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Year:  1994        PMID: 7522353      PMCID: PMC475128          DOI: 10.1136/thx.49.8.803

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  23 in total

1.  Reduction of sputum Pseudomonas aeruginosa density by antibiotics improves lung function in cystic fibrosis more than do bronchodilators and chest physiotherapy alone.

Authors:  W E Regelmann; G R Elliott; W J Warwick; C C Clawson
Journal:  Am Rev Respir Dis       Date:  1990-04

2.  In vitro activity of multiple antimicrobial combinations against Pseudomonas cepacia isolates.

Authors:  A Kumar; R Wofford-McQueen; R C Gordon
Journal:  Chemotherapy       Date:  1989       Impact factor: 2.544

Review 3.  Neutrophil granule constituents and their release in health and disease.

Authors:  L A Boxer; J E Smolen
Journal:  Hematol Oncol Clin North Am       Date:  1988-03       Impact factor: 3.722

4.  Pseudomonas cepacia: a new pathogen in patients with cystic fibrosis referred to a large centre in the United Kingdom.

Authors:  E J Simmonds; S P Conway; A T Ghoneim; H Ross; J M Littlewood
Journal:  Arch Dis Child       Date:  1990-08       Impact factor: 3.791

5.  Plasma tumour necrosis factor alpha in cystic fibrosis.

Authors:  D Norman; J S Elborn; S M Cordon; R J Rayner; M S Wiseman; E J Hiller; D J Shale
Journal:  Thorax       Date:  1991-02       Impact factor: 9.139

6.  Synergy of new C-3 substituted cephalosporins and tobramycin against Pseudomonas aeruginosa and Pseudomonas cepacia.

Authors:  N X Chin; H C Neu
Journal:  Diagn Microbiol Infect Dis       Date:  1989 Jul-Aug       Impact factor: 2.803

7.  Ciprofloxacin, imipenem and rifampicin: in-vitro synergy of two and three drug combinations against Pseudomonas cepacia.

Authors:  A Kumar; R Wofford-McQueen; R C Gordon
Journal:  J Antimicrob Chemother       Date:  1989-06       Impact factor: 5.790

Review 8.  Microbiology of airway disease in patients with cystic fibrosis.

Authors:  P H Gilligan
Journal:  Clin Microbiol Rev       Date:  1991-01       Impact factor: 26.132

9.  A mouse model of chronic pulmonary infection with Pseudomonas aeruginosa and Pseudomonas cepacia.

Authors:  J R Starke; M S Edwards; C Langston; C J Baker
Journal:  Pediatr Res       Date:  1987-12       Impact factor: 3.756

10.  Effect of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients.

Authors:  L O Lewin; P J Byard; P B Davis
Journal:  J Clin Epidemiol       Date:  1990       Impact factor: 6.437

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  3 in total

Review 1.  Should patients with cystic fibrosis infected with Burkholderia cepacia undergo lung transplantation?

Authors:  A K Webb; J Egan
Journal:  Thorax       Date:  1997-08       Impact factor: 9.139

2.  Clinical utility of C-reactive protein to predict treatment response during cystic fibrosis pulmonary exacerbations.

Authors:  Ashutosh Sharma; Gordon Kirkpatrick; Virginia Chen; Kate Skolnik; Zsuzsanna Hollander; Pearce Wilcox; Bradley S Quon
Journal:  PLoS One       Date:  2017-02-08       Impact factor: 3.240

3.  Role of C-reactive protein as a biomarker for prediction of the severity of pulmonary exacerbations in patients with cystic fibrosis.

Authors:  Rosa Maria Girón-Moreno; José L Justicia; Sara Yamamoto; Claudia Valenzuela; Carolina Cisneros; Rosa Mar Gómez-Punter; Gilda Fernandes-Vasconcelos; Julio Ancochea
Journal:  BMC Pulm Med       Date:  2014-09-23       Impact factor: 3.317

  3 in total

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