Transcript NPPV
Nichtinvasive Beatmung bei COPD Wolfram Windisch Lungenklinik Merheim • Diaphragmale Abflachung • Verkürzung der Insp.-Zeit • Vordehnung der M.-Fasern • Atemwegsobstruktion • Systemmanifestation • Dynamische Überblähung • Intrinsic PEEP • Inflammation • Steroide • Thorakale Vordehnung • VIDD • Erhöter ventilatorsicher Bedarf • Co-Morbiditäten • Herzinsuffizienz • Oxygenierungsstörung • Pulmonale Hypertonie • Anämie • Diabetes mellitus • Herzinsuffizienz Jolley CJ and Moxham J. Eur Respir Rev 2009; 18:112,1-14 Evans TW. Intensive Care Med 2001; 27:166-178 NPPV: Conclusions NPPV should be the first line intervention in addition to usual medical care to manage respiratory failure secondary to an acute exacerbation of chronic obstructive pulmonary disease in all suitable patients. NPPV should be tried early in the course of respiratory failure and before severe acidosis, to reduce mortality, avoid endotracheal intubation, and decrease treatment failure. NPPV = noninvasive positive pressure ventilation first line pH: 7.20–7,35 Improves outcome Lightowler JV. et al. BMJ 2003; 326:185-189 • NIV verhindert Intubation (NNT = 5) • NIV reduziert die Mortalität (NNT = 8) NNT = number needed to treat Lightowler JV. et al. BMJ 2003; 326:185-189 80% 70% 35% Chu CM. et al. Thorax 2004; 59:1020-1025 5 cmH2O 15/5 cmH2O Cheung APS. et al. Int J Tuberc Lung Dis 2010; 14:642–649 6-min-Gehstrecke nach 3 Monaten 20/5 cmH2O N = 13 N = 13 Funk GC. et al. Respir Med 20011; 105:427-434 Wijkstra PJ. et al. Chest 2003; 124:337-343 2 years follow-up 1 year follow-up NPPV + LTOT vs. LTOT alone IPAP (cmH2O) Casanaova 12 EPAP ΔPaCO2 Survival (cmH2O) (mmHg) 4 NPPV: +0.4 LTOT: -0.9 No benefit NPPV: -1.0 LTOT: +0.5 No benefit et al. Clini 14 2 et al. Casanova C. et al. Chest 2000; 118:1582-1590 (1 year) (2 years) Clini E. et al. Eur Respir J 2002; 20:529-538 McEvoy RD. et al. Thorax 2009; 64:561-566 mean adherence to NIV: 4.5 ± 3.2 hours McEvoy RD. et al. Thorax 2009; 64:561-566 McEvoy RD. et al. Thorax 2009; 64:561-566 Wolfram Windisch Windisch W. Breathe 2011; 8:114-123 If the targeted physiological parameter (PaCO2) remains unaffected by the specific treatment modality (long-term NPPV)… If artificial ventilation does not improve alveolar ventilation … How can we expect an improved outcome? BGA (mmHg) mmHg 100 90 80 70 60 BGA (mmHg) PaCO2 PaO2 100 90 80 NPPV (assPCV) 70 60 50 - mean IPAP 30 ±4 mbar - mean bf ±2 /min 23 50 40 40 30 301 2 3 5 1 2 Days Zeit (Tage) 9 3 5 Zeit (Tage) 9 Windisch W. et al. Respir Med 2002; 96:572-579 N = 34 NPPV (assPCV): IPAP 28 ±6 mbar; bf 21 ±3 /min 2-year survival: 86% Windisch W. et al. Chest 2005; 128:657-662 N = 141 NPPV (assPCV) - mean IPAP 20 ±4 mbar - mean bf ±4 /min 20 BMI <20 kg/m2 = 21% Budweiser S. et al. Respir Care 2006; 51:126-132 Severe Respiratory Insufficiency Questionnaire SRI Social Functioning SF Respiratory Complaints RC • • • • • • • • • • • German English French Spanish Dutch Swedish Norwegian Polish Greek Hebrew Japanese ATS homepage: SRI Physical Functioning PF Summary Scale SS Attendant Symptoms and Sleep AS http://www.atsqol.org/sections/instruments/pt/pages/sri.html Well-Being WB Anxieties AX Social Relationships SR Windisch W. et al. J Clin Epidemiol 2003; 56:752-759 Windisch W. et al. Intensive Care Med 2003; 29:615-621 Windisch W. et al. J Clin Epidemiol 2008; 61:848-853 N = 137 • COPD • Restrictive thoracic diseases • ObesityHypoventilations-Syndrome • Neuromuscular disorders • Miscellaneous Windisch W. Eur Respir J 2008; 32:1328-1336 SRI-Summary Scale (SRI-SS) 65 IPAP/EPAP (mbar) P < 0.001 restrictive thoracic 20/3 19/4 P < 0.001 neuromuscular 25/1 P < 0.001 COPD 55 kulär Changes in SRI-SS independent from the underlying disease MANOVA; F=0,62; P=0,65. 45 T0 T1 T0 COPD T12 T1 RTD T12 NMD Windisch W. Eur Respir J 2008; 32:1328-1336 N = 73 5-year survival: 58% Windisch W. et al. Int J Med Sci 2009; 6:72-76 IPAP [cmH20] EPAP [cmH20] Breathing frequ. Oxygen [L* min-1] [min-1] Insp. volume Low-intensity 14.6 ± 0.8 4.0 ± 0 8.0 ± 0 2.2 ± 0.8 (pneumotachygraph) Mean treatment effect: 325 High-intensity 28.6 ± 1.9 4.5 ± 0.7 17.5 ± 2.1 2.2 ± 0.8 : mL 95%CI [159 , 492 mL]; P=0.002 Exp. volume (pneumotachygraph) Mean treatment effect: 96 : mL 95%CI [23 , 169 mL]; P=0.015 Leak volume (pneumotachygraph) : Mean treatment effect: 226 95%CI [28 , 425 mL]; P=0.030 mL Dreher M. et al. Thorax 2010, 65:303-308 high: 29 cmH2O; controlled ventilation low: 15 cmH2O; assisted ventilation Primary outcome:Nocturnal PaCO2 Mean treatment effect: -9.2 mmHg 95%CI [-13.7 , -4.6 mmHg]; P<0.001 No period effect: P=0.96 No carry over effect: P=0.87 Compliance (daily use): Mean treatment effect: 3.6 hours 95%CI [0.6 , 6.7 hours]; P=0.024 Lowintensity Dyspnea (BDS) QoL (SRI-SS) FEV1 (L) Highintensity + + + Dreher M. et al. Thorax 2010, 65:303-308 Mean IPAP: high: 29 cmH2O; low:14 cmH2O Dreher M. et al. Chest 2011, 140:939-945 P < 0.001 85 50 80 PaO2 (mmHg) 75 P<0.001 70 65 6 209 Borg Dyspnea Scale Walking distance P<0.001 P<0.05 4 252 53 60 55 50 45 mean before after mean PaCO2 [mmHg] P < 0.001 110 [m] 100 50 PaO2 (mmHg) 90 80 n.s. 70 51 60 50 mean before after mean Dreher M. et al. Eur Respir J 2007; 29:930-936 Rehab Rehab + NPPV [20/6 cmH20; 18 breaths/min] Rehab + NPPV baseline 3 months Rehab alone baseline 3 months Duiverman ML. et al. Thorax 2008; 63:1052-1057 Windisch W. et al. Pneumologie 2010, 64:207-240 Windisch W. et al. Pneumologie 2010, 64:207-240