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1.
Scand J Surg ; 101(3): 166-9, 2012.
Article in English | MEDLINE | ID: mdl-22968239

ABSTRACT

BACKGROUND: Giant pulmonary bullae (GPB) are rare and there is little information on incidence, long-term prognosis, and outcome of treatment. OBJECTIVES: To assess the incidence of GPB in the Icelandic population and to evaluate the outcome of surgical treatment. METHODS: Twelve consecutive patients (11 males; mean age 60 ± 15.7 years) underwent resection for GPB in Iceland between 1992 and 2009. All were heavy smokers and had bullae occupying > 30% of the involved lung. There were 8 bilateral and 3 unilateral bullectomies and one lobectomy. Pulmonary function tests were performed preoperatively, and at one month and 5.4 years postoperatively. Age-standardized incidence rate (ASR) was calculated, complications and operative mortality were registered, and overall survival was estimated. Mean follow-up time was 8.2 years. RESULTS: The ASR for GPB was 0.40 and 0.03 per 100,000 per year for men and women, respectively. There was no operative mortality, but prolonged air leakage (75%) and pneumonia (17%) were the most common postoperative complications. One month postoperatively, mean FEV1 increased from 1.0 ± 0.48 L (33% predicted) to 1.75 ± 0.75 L (57.5% predicted) (p < 0.01), but FVC remained unchanged. RV decreased from 3.9 ± 0.8 L (177% predicted) to 3.0 ± 1.0 L (128% predicted) (p < 0.05), but TLC and DLCO did not change after operation. At long-term follow-up the FEV1 and FVC had declined to near-baseline values. Five-year and 10-year survival were 100% and 60%, respectively. CONCLUSIONS: The ASR of GPB in Iceland was 0.21 per 100,000 per year. In this small series, bullectomy was found to be a safe procedure that significantly improved pulmonary function. The functional improvement then declined over time. Prolonged air leakage was a common postoperative complication that prolonged hospital stay.


Subject(s)
Blister/epidemiology , Blister/surgery , Lung Diseases/epidemiology , Lung Diseases/surgery , Pneumonectomy , Adult , Aged , Blister/etiology , Blister/mortality , Female , Follow-Up Studies , Humans , Iceland/epidemiology , Incidence , Kaplan-Meier Estimate , Lung Diseases/etiology , Lung Diseases/mortality , Male , Middle Aged , Postoperative Complications/epidemiology , Pulmonary Emphysema/complications , Registries , Respiratory Function Tests , Retrospective Studies , Smoking/adverse effects , Survival Rate , Treatment Outcome
2.
Eur Respir J ; 17(4): 674-80, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11401063

ABSTRACT

The effect of high altitude (HA) on exercise-induced diaphragm fatigue in normal subjects was examined. Eight normal subjects completed an incremental exercise test at sea level (SL) and at 3,325 m. Before (baseline), during, and after exercise (recovery), maximal transdiaphragm pressure (Pdi,sniff), breathing pattern, and diaphragmatic effort (PTPdi) were measured. Arterialized blood lactate was measured at baseline and during recovery. At maximal exercise (WRmax) Pdi,sniff fell to 72% and 61% of baseline at SL and HA respectively, recovering to baseline in 60 min at SL, and >60 min at HA. At the 5th min of recovery, circulating lactate was six-fold and seven-fold baseline at SL and HA, respectively. The time course of circulating lactate recovery was as for Pdi,sniff. At WRmax PTPdi was 80.74+/-9.87 kPa.s(-1) at SL and 64.13+/-8.21 kPa.s(-1) at HA. HA WRmax compared to isowork rate, SL data showed a lower Pdi,sniff (8.90+/-0.68 versus 11.24+/-0.59 kPa) and higher minute ventilation (117+/-11 versus 91+/-13 L.min(-1)), PTPdi being equal. To conclude, in normal subjects hypoxia-related effects, and not an increase in diaphragm work, hastens exercise-induced diaphragm fatigue and delays its recovery at high altitude compared to sea level.


Subject(s)
Altitude , Diaphragm/physiology , Exercise , Hypoxia/physiopathology , Muscle Fatigue/physiology , Adult , Humans , Lactic Acid/blood , Male , Workload
3.
Am J Respir Crit Care Med ; 161(4 Pt 1): 1115-23, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10764299

ABSTRACT

To investigate the pathophysiologic mechanisms of ventilator dependence, we took physiologic measurements in 28 patients with COPD and 11 postcardiac surgery (PCS) patients receiving long-term mechanical ventilation during a spontaneous breathing trial, and in 20 stable, spontaneously breathing patients matched for age and disease. After 40 +/- 14 min of spontaneous breathing, 20 of 28 patients with COPD and all 11 PCS patients were judged ventilator-dependent (VD). We found that in the 31 VD patients tidal volume was low (VT: 0.36 +/- 0.12 and 0.31 +/- 0.08 L for COPD and PCS, respectively), neuromuscular drive was high (P(0.1): 5.6 +/- 1. 6 and 3.9 +/- 1.9 cm H(2)O), inspiratory muscle strength was reduced (Pdi(max): 42 +/- 12 and 28 +/- 15 cm H(2)O), and lung mechanics were abnormal, particularly PEEPi (5.9 +/- 3.0 cm H(2)O) and lung resistance (22.2 +/- 9.2 cm H(2)O/L/s) in COPD. The load/capacity balance was altered (Pdi/Pdi(max) and Ppl/Ppl(max) > 0.4) and the effective inspiratory impedance was high (P(0.1)/VT/TI >/= 10 cm H(2)O/L/s). Failure to wean occurred in patients with f/VT > 105 breaths/min/L and 56% of patients with COPD with f/VT < 80 breaths/min/L. Those who failed despite a low f/VT ( < 80 breaths/min/L) either showed ineffective inspiratory efforts, which artificially lowered f/ VT (n = 8), or did not increase breathing frequency (n = 5), but P(0.1) and P(0.1)/VT/TI were as high as in other VD patients. In the 31 VD patients, Pa(CO(2)) increased during the weaning trial (+12.3 +/- 8.0 mm Hg). We conclude that in the presence of a high drive to breathe, the imbalance between increased work load and reduced inspiratory muscle strength causes respiratory distress and CO(2) retention. Noninvasive measurements (breathing pattern, P(0.1), P(0.1)/ VT/TI) may give better insight into weaning failure useful in clinical decision-making, particularly in patients with COPD not showing rapid shallow breathing (56% in this study).


Subject(s)
Respiration, Artificial , Ventilator Weaning , Aged , Cardiac Surgical Procedures , Case-Control Studies , Female , Humans , Lung Diseases, Obstructive/therapy , Male , Postoperative Care , Respiratory Mechanics/physiology , Respiratory Muscles/physiopathology , Time Factors , Work of Breathing/physiology
4.
Am J Respir Crit Care Med ; 159(5 Pt 1): 1510-7, 1999 May.
Article in English | MEDLINE | ID: mdl-10228119

ABSTRACT

To investigate the physiologic effects of proportional assist ventilation (PAV) in difficult-to-wean, mechanically ventilated patients with advanced COPD, we measured in eight ICU patients the breathing pattern, neuromuscular drive (P0.1), lung mechanics, and inspiratory muscle effort (PTPdi and PTPpl) during both spontaneous breathing (SB) and ventilatory support with PAV, CPAP, and CPAP + PAV (in random sequence). PAV (volume assist [VA] and flow assist [FA]) was set as follows: dynamic lung elastance and inspiratory pulmonary resistance were measured during SB; then VA and FA were set to counterbalance the elastic and resistive loads exceeding the normal values, respectively, the inspiratory muscles bearing a normal elastic and resistive workload. CPAP was set close to dynamic intrinsic PEEP (8.3 +/- 3.4 cm H2O). We found significant reductions in P0.1 and PTPdi during both CPAP (-45 and -37%, respectively) and PAV (-50 and -48%, respectively). However, only the combination of PAV and CPAP brought P0.1 (1.69 +/- 0.97 cm H2O) and PTPdi (100 +/- 68 cm H2O. s) within normal values, and ameliorated the breathing pattern compared with SB (tidal volume: 0.69 +/- 0.33 versus 0.33 +/- 0.14 L; breathing frequency, 14.6 +/- 4.6 versus 21.0 +/- 6.5 breaths/min, respectively), without generating ineffective inspiratory efforts. We conclude that in difficult-to-wean COPD patients, (1) PAV improves ventilation and reduces both P0.1 and inspiratory muscle effort; (2) the combination of PAV and CPAP can unload the inspiratory muscles to values close to those found in normal subjects.


Subject(s)
Lung Diseases, Obstructive/therapy , Positive-Pressure Respiration , Respiration, Artificial/methods , Ventilator Weaning , Aged , Female , Humans , Lung Diseases, Obstructive/physiopathology , Male , Respiration , Respiratory Function Tests , Respiratory Muscles/physiopathology
6.
Am J Respir Crit Care Med ; 157(4 Pt 1): 1044-50, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9563717

ABSTRACT

Intrinsic positive end-expiratory pressure (PEEPi) is routinely determined under static conditions by occluding the airway at end-expiration (PEEPi,st). This procedure may be difficult in patients with chronic obstructive pulmonary disease (COPD) during spontaneous breathing, as both expiratory muscle activity and increased respiratory frequency often occur. To overcome these problems, we tested the hypothesis that the difference between maximum airway opening (MIP) and maximum esophageal (Ppl max) pressures, obtained with a Mueller maneuver from the end-expiratory lung volume (EELV), can accurately measure PEEPi,st. Using this method, we found that, in eight ventilator-dependent tracheostomized COPD patients (age 71+/-7 yr), PEEPi,st averaged 13.0+/-2.9 cm H2O. That measurement was validated by comparison with a reference static PEEPi (PEEPi,st-Ref) taken at the same EELV adopted by patients during spontaneous breathing, and measured on the passive quasi-static pressure-volume (P/V) curve of the respiratory system, obtained during mechanical ventilation. PEEPi,st-Ref averaged 13.1+/-3.0 cm H2O, i.e., a value essentially equal to PEEPi,st measured by means of our technique. We conclude that PEEPi,st can be accurately assessed in spontaneous breathing COPD patients by the difference between MIP and Ppl max during the Mueller maneuver.


Subject(s)
Lung Diseases, Obstructive/physiopathology , Positive-Pressure Respiration, Intrinsic/complications , Respiration , Aged , Aged, 80 and over , Esophagus/physiopathology , Female , Humans , Lung Diseases, Obstructive/complications , Lung Volume Measurements , Male , Middle Aged , Positive-Pressure Respiration, Intrinsic/diagnosis , Pressure , Respiration, Artificial , Respiratory Function Tests/methods , Respiratory Mechanics , Tracheostomy
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