Search PubMed⌕ Search

PubMed · 7599496

Oxygen therapy.

Abstract

It is essential that nurses understand the potentially harmful effects of oxygen therapy. This article reviews the biochemical role of oxygen, particularly its vital physiological function, and discusses clinical situations in which oxygen is used as therapy. It also outlines how patients receiving oxygen may be effectively monitored in order to optimise treatment.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

S Ashurst. Oxygen therapy.. https://doi.org/10.12968/bjon.1995.4.9.508

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Accuracy of a point-of-care blood gas analyzer in gastric tonometry measurements of intramucosal pH (pHi) and P(CO2) gap.

PURPOSE: We assessed the accuracy of a point-of-care blood gas analyzer in providing data from saline samples obtained by gastrointestinal tonometry (Tonometrics Catheter; Tonometrics Division, Instrumentarium, Helsinki, Finland) for the calculation of intramucosal pH (pHi) and the P(CO)(2) gap (intramucosal P(CO)(2) - Pa(CO)(2)). METHODS: We compared the point-of-care analyzer (Opti; AVL Medical Instruments, Schaffhausen, Switzerland; "Opt") with a conventional analyzer (Compact 2 AVL Medical Instruments, Schaffhausen; "Elect") in a clinical study (Elect being taking as the standard). In an in vitro study, P(CO)(2) data of tonometer saline (Pr(CO)(2)) from Opt and Elect were compared with P(CO)(2) data from a continuous air tonometer (Tonocap Tonometrics Division, Instrumentarium) for a bottle containing a mixed P(CO)(2) gas. Data were evaluated by the Bland-Altman method. RESULTS: In the clinical study, the bias (B) and precision (P) were: B = 0.223 and P = 0.056 for pHi, B = -14.0 and P = 2.43 (mmHg) for Pr(CO)(2), and B = -16.7 and P = 2.6 (mmHg) for the P(CO)(2) gap ( n = 27). In the in vitro study, the bias between the two values (Pr(CO)(2) and bottle P(CO)(2)) was -1.98 mmHg and precision was 1.23 mmHg for Elect, but for Opt, these values were -22.09 mmHg and 3.15 mmHg, respectively ( n = 18). CONCLUSION: Opt is not suitable for measuring pHi and the P(CO)(2) gap because it does not provide an accurate P(CO)(2) for tonometry saline.

Blood Gas Analysis↗

Diastolic left ventricular function in preterm infants with a patent ductus arteriosus: a serial Doppler echocardiography study.

In very low birth weight neonates, a left-to-right shunt via persistent ductus arteriosus (PDA) may interact with diastolic left ventricular function, but specific changes of Doppler parameters have yet to be reported. In a serial transmitral Doppler study, we investigated the impact of a PDA on diastolic function parameters. Twenty-two patients with and without PDA were examined on day 3.8+/-1 and day 14+/-2 after birth. By the first examination, 13 out of 22 patients had a PDA; by the second examination, the number was still 8 out of 22. Peak early and atrial flow velocities (44.8+/-15 and 50.1+/-13 cm/s, respectively) were higher (p<0.05) for neonates with PDA compared to those with closed duct (30.9+/-6 and 34.2 cm/s, respectively). Isovolumic relaxation time (IVRT) was shorter in neonates with PDA (45+/-7 ms, N=21) compared to those with a closed duct (55.3+/-5 ms, N=23) (p<0.01). IVRT correlated inversely with cardiac index (R=-0.79, p<0.01). All observed changes reversed to the normal range after closure of the PDA. When premature infants with a PDA experience a preload challenge, early and atrial peak velocities increase and IVRT shortens significantly. This coincidence of elevated transvalvular pressure differences and decreased IVRT in neonates with immature diastolic function can best be explained as a result of left atrial pressure elevation. Consequently, pulmonary venous pressure must be elevated, with its inherent effect on pulmonary capillary physiology. Thus, the monitoring of left ventricular diastolic function adds significant information to the care of preterm infants with a PDA.

Blood Gas Analysis↗