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a Chest Department, b Department of Anaesthesia, c Llandough Hospital & Community NHS Trust, Penarth, South
Glamorgan CF62 2XX, UK
Correspondence to: Dr A P Smith.
Received 12 December 1996; Returned to authors 26 February 1997; Revised version received 27 January 1998; Accepted for publication 2 February 1998
BACKGROUND
There is increasing interest in the use
of non-invasive nocturnal intermittent positive pressure ventilation
(NIPPV) in the management of patients with chronic hypercapnoeic (type
II) respiratory failure. Although this treatment enables patients
requiring mechanical ventilatory support to be treated more readily at
home, few studies have been done to demonstrate its long term benefits
in chronic obstructive pulmonary disease (COPD) and the application of
NIPPV in these circumstances remains controversial.
METHODS
Eleven patients in severe stable chronic
type II respiratory failure due to COPD who were unresponsive to
conventional treatments experienced symptomatic hypercapnia when
receiving sufficient supplementary oxygen to result in an arterial
oxygen saturation (SaO2) of >90%. They were
assessed for treatment with NIPPV, and its effects were observed for
over two years using arterial blood gas tensions, spirometric
parameters and body mass index (BMI), survival, hospital admissions,
use of general practitioner resources, and patient satisfaction.
RESULTS
Hospital admissions and GP consultations
were halved after one year compared with the year before NIPPV and
there was a sustained improvement in arterial blood gas tensions at 12 and 24 months when breathing air, despite progressive deterioration in
ventilatory function. BMI did not change during the period of
observation. The median survival was 920 days, with no patient dying
within the first 500 days.
CONCLUSIONS
Domiciliary NIPPV results in
improvements in arterial blood gas tensions which are sustained after
two years of treatment and reduces both hospital admissions and general
practitioner visits by patients with severe COPD in hypercapnoeic
respiratory failure. It is well tolerated and, although there was no
control group, survival appears to be prolonged when these results are compared with those of the NOTT and MRC (LTOT) trials.
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