Hemi-diaphragmatic Paresis and Erector Spinae Plane Block

Antalya Training and Research Hospital

Status: Completed

Conditions: Anesthesia, Regional; Shoulder

Treatments: Other: ESP block

Study type: Observational

Funder types: Other

Identifiers

NCT05096377

8/12

Details and patient eligibility

About

To assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane (ESP) block

Full description

The aim of the study is to assess the effect of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane block.

Enrollment: 20 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 18 - 85 years
• American Society of Anesthesiology (ASA) I-III
• elective shoulder surgery

Exclusion criteria

• patient's refusal
• under 18 years of age or over 65 years of age
• ASA IV and above
• known allergy to local anaesthetic drugs
• the block cannot be applied due to bleeding disorders or localized skin infection at the injection site
• history of neurological and/or neuromucular disease
• history of severe bronchopulmonary disease
• a moderate to severe decrease in preoperative pulmonary function, or abnormality in preoperative chest radiography data (pleural effusion, pneumothorax, or hemidiaphragm elevation)

Trial design

20 participants in 1 patient group

ESP block group

Description:

Diaphragmatic excursion was measured using M-mode ultrasound during normal breathing, deep breathing and with the sniff manoeuvre.

Treatment:

Other: ESP block