cardiac postoperative pain
Conditions
Interventions
Experimental group:"Internet +" pharmaceutical care platform (pain management APP)
Sponsors
Fujian Medical University Union Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Patients or their family members can read Chinese and use smart phones; 2.Patients aged 18 to 65 years; 3.Patients who will undergo their first cardiac surgery with median sternotomy and who will be released from mechanical ventilation within 48 hours; 4.Patients must understand the study process and evaluation, agree to participate in the study, and sign the informed consent form; 5.Patients who can complete pain assessment.
Exclusion criteria
Exclusion criteria: 1.Patients with hearing impairment, visual impairment or intellectual impairment; 2.Cardiac surgery patients undergoing emergency median sternotomy; 3.Hepatic insufficiency (ALT>=2.5xULN, AST>=2.5xULN, TBIL>=1.5xULN), renal insufficiency (Cr>=2.5xULN); 4.Patients with postoperative cardiac arrest, subsequent cardiac surgery or other serious complications are not suitable for this study; 5.Opioids, non-steroidal anti-inflammatory drugs and other pain drugs allergy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score;Quality of life;Incidence of pain;Opioid consumption; | — |
Countries
China
Contacts
Public ContactLiu Maobai
Fujian Medical University Union Hospital
Outcome results
None listed