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PaO2 and Lung Function After Orthopedic Surgery

Oxygen Partial Pressure and Lung Function After Orthopedic Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05227573
Enrollment
60
Registered
2022-02-07
Start date
2022-02-09
Completion date
2024-05-01
Last updated
2023-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthopedic Disorder, Postoperative Complications

Brief summary

Hypoxia and reduced oxygen partial pressure is commonly occurring after abdominal surgery. This study aims to investigate whether similar changes also occur after orthopedic surgery in the form of upper limb surgery. Inclusion: 60 patients undergoing orthopedic surgery in the form o knee-, hip-, shoulder- or elbow surgery. Exclusion: Dementia or cognitive impairment that makes it impossible to participate in studies. Arterial blood gas and lung function are undertaken before surgery, the day after surgery and at follow-up.

Detailed description

Postoperative hypoxia complicates 30% - 50% of abdominal surgeries. People at particular risk for postoperative pulmonary complications including severe hypoxia are those who undergo abdominal surgery, emergency surgery or have a respiratory failure due to chronic lung disease including obstructive sleep apnea. The cause of postoperative restrictive lung function and hypoxia is unknown. Previous studies report that PaO2 decreases by an average of 2 kPa after abdominal surgery, while PaCO2 is unchanged and vital capacity decreases by 35%. The effect of orthopedic surgery on oxygen and carbon dioxide partial pressure and lung function has previously not been investigated. This study aims to investigate possible changes in oxygen partial pressure and vital capacity after orthopedic surgery. Design: Prospective cohort study Inclusion: 60 patients undergoing orthopedic surgery in the form o knee-, hip-, shoulder- or elbow surgery.. Exclusion: Dementia or cognitive impairment that makes it impossible to participate in studies. Method: Blood gas measurements and Lung function (Vital capacity and FEV1) The day before surgery, the day after surgery and at follow-up. Power analysis: There is a need to investigate 34 patients if the mean (SD) difference is 1 (2) kPa. Due to drop-outs the investigators calculate a need to include 60 patients. Primary outcome measures: • PaO2 from atrial blood gas Secondary outcomes * Vital capacity * PaCO2 from atrial blood gas * Forced expiratory volume in one second (FEV1) Other variables examined: age, sex, height, weight, type of surgery, type of anesthesia, smoking status, length of surgery and previous diseases

Interventions

PROCEDUREOrthopedic surgery

Knee-, hip-, shoulder- and elbow surgery

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients undergoing shoulder or elbow surgery -

Exclusion criteria

Dementia or cognitive impairment that makes it impossible to participate in studies. Not willing to participate \-

Design outcomes

Primary

MeasureTime frameDescription
Oxygen partial pressure1 dayChange in oxygen partial pressure after surgery

Secondary

MeasureTime frameDescription
Vital capacity1 dayChange in vital capacity after surgery
Oxygen partial pressure1 monthChange in oxygen partial pressure after surgery
Carbon dioxide partial pressure1 dayChange in carbon dioxide partial pressure after surgery
Forced expiratory volume in one second1 dayChange in Forced expiratory volume in one second after surgery

Countries

Sweden

Contacts

Primary ContactKarl A Franklin, Prof
karl.franklin@umu.se+46 706884745

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026