Skip to main content
Erschienen in: Lung 5/2011

01.10.2011

Improved Outcomes of Patients with End-stage Cystic Fibrosis Requiring Invasive Mechanical Ventilation for Acute Respiratory Failure

verfasst von: Don Hayes Jr., Heidi M. Mansour

Erschienen in: Lung | Ausgabe 5/2011

Einloggen, um Zugang zu erhalten

Abstract

Study Objectives

The aim of this study was to determine the effects of an antibiotic strategy with intravenous (IV) continuous infusion of a β-lactam (CIBL) antibiotic and high-dose extended-interval (HDEI) tobramycin upon outcomes in patients with cystic fibrosis (CF) requiring invasive mechanical ventilation (IMV) for acute respiratory failure.

Design

The study was a retrospective review from June 1, 2006, to December 1, 2010, of patients at a university hospital with an adult CF center.

Results

The study population included adult CF patients requiring IMV. A total of 15 hospitalizations with IMV episodes were reviewed, involving 10 adult (31.4 ± 11.1 years) CF patients with end-stage lung disease (FEV1 = 23.6 ± 7.8% predicted) and malnutrition (body mass index = 20.5 ± 3.1). Each patient survived to discharge and to follow-up 6 months later without the need for lung transplantation during the study period.

Conclusions

A novel antibiotic strategy with a CIBL antibiotic and HDEI tobramycin improved survival in a small cohort of critically ill CF patients with end-stage lung disease and malnutrition requiring IMV.
Literatur
1.
Zurück zum Zitat Boat TF, Cheng PW (1989) Epithelial cell dysfunction in cystic fibrosis: implications for airways disease. Acta Paediatr Scand Suppl 363:25–29; discussion 29–30PubMed Boat TF, Cheng PW (1989) Epithelial cell dysfunction in cystic fibrosis: implications for airways disease. Acta Paediatr Scand Suppl 363:25–29; discussion 29–30PubMed
2.
Zurück zum Zitat Matsui H, Randell SH, Peretti SW, Davis CW, Boucher RC (1998) Coordinated clearance of periciliary liquid and mucus from airway surfaces. J Clin Invest 102(6):1125–1131PubMedCrossRef Matsui H, Randell SH, Peretti SW, Davis CW, Boucher RC (1998) Coordinated clearance of periciliary liquid and mucus from airway surfaces. J Clin Invest 102(6):1125–1131PubMedCrossRef
3.
Zurück zum Zitat Puchelle E, Bajolet O, Abély M (2002) Airway mucus in cystic fibrosis. Paediatr Respir Rev 3:115–119PubMedCrossRef Puchelle E, Bajolet O, Abély M (2002) Airway mucus in cystic fibrosis. Paediatr Respir Rev 3:115–119PubMedCrossRef
4.
Zurück zum Zitat Ulrich M, Worlitzsch D, Viglio S et al (2010) Alveolar inflammation in cystic fibrosis. J Cyst Fibros 9:217–227PubMedCrossRef Ulrich M, Worlitzsch D, Viglio S et al (2010) Alveolar inflammation in cystic fibrosis. J Cyst Fibros 9:217–227PubMedCrossRef
5.
Zurück zum Zitat Davis PB (1999) Clinical pathophysiology and manifestations of lung disease. In: Yankaskas JR, Knowles MR (eds) Cystic fibrosis in adults, 1st edn. Lippincott-Raven, Philadelphia, pp 45–67 Davis PB (1999) Clinical pathophysiology and manifestations of lung disease. In: Yankaskas JR, Knowles MR (eds) Cystic fibrosis in adults, 1st edn. Lippincott-Raven, Philadelphia, pp 45–67
6.
Zurück zum Zitat Davis PB, di Sant’Agnese PA (1974) Assisted ventilation for patients with cystic fibrosis. JAMA 239:1851–1854CrossRef Davis PB, di Sant’Agnese PA (1974) Assisted ventilation for patients with cystic fibrosis. JAMA 239:1851–1854CrossRef
7.
Zurück zum Zitat Lloyd-Still JD, Khaw KT, Shwachman H (1974) Severe respiratory disease in infants with cystic fibrosis. Pediatrics 53:678–682PubMed Lloyd-Still JD, Khaw KT, Shwachman H (1974) Severe respiratory disease in infants with cystic fibrosis. Pediatrics 53:678–682PubMed
8.
Zurück zum Zitat Garland JS, Chan YM, Kelly KJ, Rice TB (1989) Outcome of infants with cystic fibrosis requiring mechanical ventilation for respiratory failure. Chest 96:136–138PubMedCrossRef Garland JS, Chan YM, Kelly KJ, Rice TB (1989) Outcome of infants with cystic fibrosis requiring mechanical ventilation for respiratory failure. Chest 96:136–138PubMedCrossRef
9.
Zurück zum Zitat Sood N, Paradowski LJ, Yankaskas JR (2001) Outcomes of intensive care unit care in adults with cystic fibrosis. Am J Respir Crit Care Med 163:335–338PubMed Sood N, Paradowski LJ, Yankaskas JR (2001) Outcomes of intensive care unit care in adults with cystic fibrosis. Am J Respir Crit Care Med 163:335–338PubMed
10.
Zurück zum Zitat Berlinski A, Fan LL, Kozinetz CA, Oermann CM (2002) Invasive mechanical ventilation for acute respiratory failure in children with cystic fibrosis: outcome analysis and case-control study. Pediatr Pulmonol 34:297–303PubMedCrossRef Berlinski A, Fan LL, Kozinetz CA, Oermann CM (2002) Invasive mechanical ventilation for acute respiratory failure in children with cystic fibrosis: outcome analysis and case-control study. Pediatr Pulmonol 34:297–303PubMedCrossRef
11.
Zurück zum Zitat Vedam H, Moriarty C, Torzillo PJ, McWilliam D, Bye PT (2004) Improved outcomes of patients with cystic fibrosis admitted to the intensive care unit. J Cyst Fibros 3:8–14PubMedCrossRef Vedam H, Moriarty C, Torzillo PJ, McWilliam D, Bye PT (2004) Improved outcomes of patients with cystic fibrosis admitted to the intensive care unit. J Cyst Fibros 3:8–14PubMedCrossRef
12.
Zurück zum Zitat Slieker MG, van Gestel JP, Heijerman HG et al (2006) Outcome of assisted ventilation for acute respiratory failure in cystic fibrosis. Intensive Care Med 32:754–758PubMedCrossRef Slieker MG, van Gestel JP, Heijerman HG et al (2006) Outcome of assisted ventilation for acute respiratory failure in cystic fibrosis. Intensive Care Med 32:754–758PubMedCrossRef
13.
Zurück zum Zitat Rosenstein BJ, Cutting GR (1998) The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr 132:589–595PubMedCrossRef Rosenstein BJ, Cutting GR (1998) The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr 132:589–595PubMedCrossRef
14.
Zurück zum Zitat Padoan R, Cambisano W, Costantini D et al (1987) Ceftazidime monotherapy vs. combined therapy in Pseudomonas pulmonary infections in cystic fibrosis. Pediatr Infect Dis J 6:648–653PubMedCrossRef Padoan R, Cambisano W, Costantini D et al (1987) Ceftazidime monotherapy vs. combined therapy in Pseudomonas pulmonary infections in cystic fibrosis. Pediatr Infect Dis J 6:648–653PubMedCrossRef
15.
Zurück zum Zitat Leeder JS, Spino M, Isles AF, Tesoro AM, Gold R, MacLeod SM (1984) Ceftazidime disposition in acute and stable cystic fibrosis. Clin Pharmacol Ther 36:355–362PubMedCrossRef Leeder JS, Spino M, Isles AF, Tesoro AM, Gold R, MacLeod SM (1984) Ceftazidime disposition in acute and stable cystic fibrosis. Clin Pharmacol Ther 36:355–362PubMedCrossRef
16.
Zurück zum Zitat Rappaz I, Decosterd LA, Bille J, Pilet M, Bélaz N, Roulet M (2000) Continuous infusion of ceftazidime with a portable pump is as effective as thrice-a-day bolus in cystic fibrosis children. Eur J Pediatr 159:919–925PubMedCrossRef Rappaz I, Decosterd LA, Bille J, Pilet M, Bélaz N, Roulet M (2000) Continuous infusion of ceftazidime with a portable pump is as effective as thrice-a-day bolus in cystic fibrosis children. Eur J Pediatr 159:919–925PubMedCrossRef
17.
Zurück zum Zitat Roosendaal R, Bakker-Woudenberg IA, Van den Berghe Van-Raffe M, Vink-van den Berg JC, Michel BM (1989) Impact of the dosage schedule on the efficacy of ceftazidime, gentamicin and ciprofloxacin in Klebsiella pneumoniae pneumonia and septicemia in leukopenic rats. Eur J Clin Microbiol Infect Dis 8:878–887PubMedCrossRef Roosendaal R, Bakker-Woudenberg IA, Van den Berghe Van-Raffe M, Vink-van den Berg JC, Michel BM (1989) Impact of the dosage schedule on the efficacy of ceftazidime, gentamicin and ciprofloxacin in Klebsiella pneumoniae pneumonia and septicemia in leukopenic rats. Eur J Clin Microbiol Infect Dis 8:878–887PubMedCrossRef
18.
Zurück zum Zitat Craig WA, Ebert SC (1992) Continuous infusion of beta-lactam antibiotics. Antimicrob Agents Chemother 36:2577–2583PubMed Craig WA, Ebert SC (1992) Continuous infusion of beta-lactam antibiotics. Antimicrob Agents Chemother 36:2577–2583PubMed
19.
Zurück zum Zitat Daenen S, Erjavec Z, Uges DR, De Vries-Hospers HG, De Jonge P, Halie MR (1995) Continuous infusion of ceftazidime in febrile neutropenic patients with acute myeloid leukemia. Eur J Clin Microbiol Infect Dis 14:188–192PubMedCrossRef Daenen S, Erjavec Z, Uges DR, De Vries-Hospers HG, De Jonge P, Halie MR (1995) Continuous infusion of ceftazidime in febrile neutropenic patients with acute myeloid leukemia. Eur J Clin Microbiol Infect Dis 14:188–192PubMedCrossRef
20.
Zurück zum Zitat Nicolau DP, Nightingale CH, Banevicius MA, Fu Q, Quintiliani R (1996) Serum bactericidal activity of ceftazidime: continuous infusion versus intermittent injections. Antimicrob Agents Chemother 40:61–64PubMed Nicolau DP, Nightingale CH, Banevicius MA, Fu Q, Quintiliani R (1996) Serum bactericidal activity of ceftazidime: continuous infusion versus intermittent injections. Antimicrob Agents Chemother 40:61–64PubMed
21.
Zurück zum Zitat Vogelman B, Craig WA (1986) Kinetics of antimicrobial activity. J Pediatr 108(5 Pt 2):835–840PubMed Vogelman B, Craig WA (1986) Kinetics of antimicrobial activity. J Pediatr 108(5 Pt 2):835–840PubMed
22.
Zurück zum Zitat Vondracek TG (1995) Beta-lactam antibiotics: is continuous infusion the preferred method of administration? Ann Pharmacother 29:415–424PubMed Vondracek TG (1995) Beta-lactam antibiotics: is continuous infusion the preferred method of administration? Ann Pharmacother 29:415–424PubMed
23.
Zurück zum Zitat Rafati MR, Rouini MR, Mojtahedzadeh M et al (2006) Clinical efficacy of continuous infusion of piperacillin compared with intermittent dosing in septic critically ill patients. Int J Antimicrob Agents 28:122–127PubMedCrossRef Rafati MR, Rouini MR, Mojtahedzadeh M et al (2006) Clinical efficacy of continuous infusion of piperacillin compared with intermittent dosing in septic critically ill patients. Int J Antimicrob Agents 28:122–127PubMedCrossRef
24.
Zurück zum Zitat Lau WK, Mercer D, Itani KM et al (2006) Randomized, open-label, comparative study of piperacillin-tazobactam administered by continuous infusion versus intermittent infusion for treatment of hospitalized patients with complicated intra-abdominal infection. Antimicrob Agents Chemother 50:3556–3561PubMedCrossRef Lau WK, Mercer D, Itani KM et al (2006) Randomized, open-label, comparative study of piperacillin-tazobactam administered by continuous infusion versus intermittent infusion for treatment of hospitalized patients with complicated intra-abdominal infection. Antimicrob Agents Chemother 50:3556–3561PubMedCrossRef
25.
Zurück zum Zitat Roberts JA, Paratz J, Paratz E, Krueger WA, Lipman J (2007) Continuous infusion of beta-lactam antibiotics in severe infections: a review of its role. Int J Antimicrob Agents 30:11–18PubMedCrossRef Roberts JA, Paratz J, Paratz E, Krueger WA, Lipman J (2007) Continuous infusion of beta-lactam antibiotics in severe infections: a review of its role. Int J Antimicrob Agents 30:11–18PubMedCrossRef
26.
Zurück zum Zitat Roberts JA, Webb S, Paterson D, Ho KM, Lipman J (2009) A systematic review on clinical benefits of continuous administration of beta-lactam antibiotics. Crit Care Med 37:2071–2078PubMedCrossRef Roberts JA, Webb S, Paterson D, Ho KM, Lipman J (2009) A systematic review on clinical benefits of continuous administration of beta-lactam antibiotics. Crit Care Med 37:2071–2078PubMedCrossRef
27.
Zurück zum Zitat Riethmueller J, Junge S, Schroeter TW et al (2009) Continuous vs thrice-daily ceftazidime for elective intravenous antipseudomonal therapy in cystic fibrosis. Infection 37:418–423PubMedCrossRef Riethmueller J, Junge S, Schroeter TW et al (2009) Continuous vs thrice-daily ceftazidime for elective intravenous antipseudomonal therapy in cystic fibrosis. Infection 37:418–423PubMedCrossRef
28.
Zurück zum Zitat Hubert D, Le Roux E, Lavrut T et al (2009) Continuous versus intermittent infusions of ceftazidime for treating exacerbation of cystic fibrosis. Antimicrob Agents Chemother 53:3650–3656PubMedCrossRef Hubert D, Le Roux E, Lavrut T et al (2009) Continuous versus intermittent infusions of ceftazidime for treating exacerbation of cystic fibrosis. Antimicrob Agents Chemother 53:3650–3656PubMedCrossRef
29.
Zurück zum Zitat Paradisi F, Corti G (1995) Once-daily dosing regimen for aminoglycoside plus betalactam combination therapy of serious lower respiratory tract infections. J Chemother 7:338–343PubMed Paradisi F, Corti G (1995) Once-daily dosing regimen for aminoglycoside plus betalactam combination therapy of serious lower respiratory tract infections. J Chemother 7:338–343PubMed
30.
Zurück zum Zitat Powell SH, Thompson WL, Luthe MA et al (1983) Once-daily vs. continuous aminoglycoside dosing: efficacy and toxicity in animal and clinical studies of gentamicin, netilmicin, and tobramycin. J Infect Dis 147:918–932PubMedCrossRef Powell SH, Thompson WL, Luthe MA et al (1983) Once-daily vs. continuous aminoglycoside dosing: efficacy and toxicity in animal and clinical studies of gentamicin, netilmicin, and tobramycin. J Infect Dis 147:918–932PubMedCrossRef
31.
Zurück zum Zitat Bates RD, Nahata MC, Jones JW et al (1997) Pharmacokinetics and safety of tobramycin after once-daily administration in patients with cystic fibrosis. Chest 112:1208–1213PubMedCrossRef Bates RD, Nahata MC, Jones JW et al (1997) Pharmacokinetics and safety of tobramycin after once-daily administration in patients with cystic fibrosis. Chest 112:1208–1213PubMedCrossRef
32.
Zurück zum Zitat Bragonier R, Brown NM (1998) The pharmacokinetics and toxicity of once-daily tobramycin therapy in children with cystic fibrosis. J Antimicrob Chemother 42:103–106PubMedCrossRef Bragonier R, Brown NM (1998) The pharmacokinetics and toxicity of once-daily tobramycin therapy in children with cystic fibrosis. J Antimicrob Chemother 42:103–106PubMedCrossRef
33.
Zurück zum Zitat Vic P, Ategbo S, Turck D et al (1998) Efficacy, tolerance, and pharmacokinetics of once daily tobramycin for pseudomonas exacerbations in cystic fibrosis. Arch Dis Child 78:536–539PubMedCrossRef Vic P, Ategbo S, Turck D et al (1998) Efficacy, tolerance, and pharmacokinetics of once daily tobramycin for pseudomonas exacerbations in cystic fibrosis. Arch Dis Child 78:536–539PubMedCrossRef
34.
Zurück zum Zitat Aminimanizani A, Beringer PM, Kang J, Tsang L, Jelliffe RW, Shapiro BJ (2002) Distribution and elimination of tobramycin administered in single or multiple daily doses in adult patients with cystic fibrosis. J Antimicrob Chemother 50:553–559PubMedCrossRef Aminimanizani A, Beringer PM, Kang J, Tsang L, Jelliffe RW, Shapiro BJ (2002) Distribution and elimination of tobramycin administered in single or multiple daily doses in adult patients with cystic fibrosis. J Antimicrob Chemother 50:553–559PubMedCrossRef
35.
Zurück zum Zitat Smyth A, Tan KH, Hyman-Taylor P et al (2005) Once versus three-times daily regimens of tobramycin treatment for pulmonary exacerbations of cystic fibrosis–the TOPIC study: a randomised controlled trial. Lancet 365:573–578PubMed Smyth A, Tan KH, Hyman-Taylor P et al (2005) Once versus three-times daily regimens of tobramycin treatment for pulmonary exacerbations of cystic fibrosis–the TOPIC study: a randomised controlled trial. Lancet 365:573–578PubMed
36.
Zurück zum Zitat Riethmueller J, Ballmann M, Schroeter TW et al (2009) Tobramycin once- vs thrice-daily for elective intravenous antipseudomonal therapy in pediatric cystic fibrosis patients. Infection 37:424–431PubMedCrossRef Riethmueller J, Ballmann M, Schroeter TW et al (2009) Tobramycin once- vs thrice-daily for elective intravenous antipseudomonal therapy in pediatric cystic fibrosis patients. Infection 37:424–431PubMedCrossRef
37.
Zurück zum Zitat Burkhardt O, Lehmann C, Madabushi R, Kumar V, Derendorf H, Welte T (2006) Once-daily tobramycin in cystic fibrosis: better for clinical outcome than thrice-daily tobramycin but more resistance development? J Antimicrob Chemother 58:822–829PubMedCrossRef Burkhardt O, Lehmann C, Madabushi R, Kumar V, Derendorf H, Welte T (2006) Once-daily tobramycin in cystic fibrosis: better for clinical outcome than thrice-daily tobramycin but more resistance development? J Antimicrob Chemother 58:822–829PubMedCrossRef
38.
Zurück zum Zitat Soulsby N, Bell S, Greville H, Doecke C (2009) Intravenous aminoglycoside usage and monitoring of patients with cystic fibrosis in Australia. What’s new? Intern Med J 39:527–531PubMedCrossRef Soulsby N, Bell S, Greville H, Doecke C (2009) Intravenous aminoglycoside usage and monitoring of patients with cystic fibrosis in Australia. What’s new? Intern Med J 39:527–531PubMedCrossRef
39.
Zurück zum Zitat Prescott WA Jr, Nagel JL (2010) Extended-interval once-daily dosing of aminoglycosides in adult and pediatric patients with cystic fibrosis. Pharmacotherapy 30:95–108PubMedCrossRef Prescott WA Jr, Nagel JL (2010) Extended-interval once-daily dosing of aminoglycosides in adult and pediatric patients with cystic fibrosis. Pharmacotherapy 30:95–108PubMedCrossRef
40.
Zurück zum Zitat Contopoulos-Ioannidis DG, Giotis ND, Baliatsa DV, Ioannidis JP (2004) Extended-interval aminoglycoside administration for children: a meta-analysis. Pediatrics 114:e111–e118PubMedCrossRef Contopoulos-Ioannidis DG, Giotis ND, Baliatsa DV, Ioannidis JP (2004) Extended-interval aminoglycoside administration for children: a meta-analysis. Pediatrics 114:e111–e118PubMedCrossRef
41.
Zurück zum Zitat Smyth AR, Bhatt J (2010) Once-daily versus multiple-daily dosing with intravenous aminoglycosides for cystic fibrosis. Cochrane Database Syst Rev (1):CD002009 Smyth AR, Bhatt J (2010) Once-daily versus multiple-daily dosing with intravenous aminoglycosides for cystic fibrosis. Cochrane Database Syst Rev (1):CD002009
42.
Zurück zum Zitat Flume PA, Mogayzel PJ Jr, Robinson KA et al (2009) Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations. Am J Respir Crit Care Med 180:802–808PubMedCrossRef Flume PA, Mogayzel PJ Jr, Robinson KA et al (2009) Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations. Am J Respir Crit Care Med 180:802–808PubMedCrossRef
Metadaten
Titel
Improved Outcomes of Patients with End-stage Cystic Fibrosis Requiring Invasive Mechanical Ventilation for Acute Respiratory Failure
verfasst von
Don Hayes Jr.
Heidi M. Mansour
Publikationsdatum
01.10.2011
Verlag
Springer-Verlag
Erschienen in
Lung / Ausgabe 5/2011
Print ISSN: 0341-2040
Elektronische ISSN: 1432-1750
DOI
https://doi.org/10.1007/s00408-011-9311-6

Weitere Artikel der Ausgabe 5/2011

Lung 5/2011 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Therapiestart mit Blutdrucksenkern erhöht Frakturrisiko

25.04.2024 Hypertonie Nachrichten

Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.