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The study has completed the collection of all target cases as planned, reaching the anticipated sample size. Data collection has ended, and the study has now entered the data cleaning and analysis phase.
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Objective To investigate the safety and effectiveness of interference electrical stimulation in the prevention of silent aspiration after heart valve surgery in elderly patients. Silent aspiration was diagnosed when either pepsin level >200 ng/ml or α-amylase level >1685 U/L was detected in airway secretions.
In this study, a randomized controlled trial was conducted in elderly patients undergoing heart valve surgery at Fujian Medical University Union Hospital. Patients were selected according to the inclusion and exclusion criteria and randomly allocated to either the experimental group (routine nursing + interference electrical stimulation) or the control group (routine nursing + blank stimulation). Silent aspiration was diagnosed when either pepsin level >200 ng/ml or α-amylase level >1685 U/L was detected in airway secretions. Airway secretions were collected upon ICU admission after surgery, every 12 hours thereafter (depending on endotracheal tube indwelling time), before extubation, 24 hours after extubation, and on day 6 after surgery. The incidence of silent aspiration, swallowing function, clinical pulmonary infection score, mechanical ventilation duration, ICU length of stay, total hospital stay, and adverse events were compared between the two groups.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Usual care and interference with electrical stimulation | Experimental | In order to reduce the incidence of silent aspiration, interference electrical stimulation was performed in elderly patients after valve operation. Interference electrical stimulation can stimulate the afferent nerve deeper in the pharynx and larynx, enhance the ability of airway protection, and increase the frequency of swallowing, reduce the occurrence of silent aspiration. This measure is non-invasive and safe, and the side effect is only itchy skin caused by an allergic electrode. |
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| Usual care and blank stimulation | Placebo Comparator | In the experimental group, interference electrical stimulation was given on the basis of conventional care, but no current was provided. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| The intervention was delivered using the Gentle Stim Electrical Stimulation Therapy Device (Model: JC-2071) | Device | Prior to the intervention, the patient's skin was inspected for symptoms such as redness, swelling, or ulceration, and cleansed with an alcohol swab. The leads of the Gentle Stim electrical stimulation therapy device were checked to ensure they were safe and unobstructed. After resetting all settings to zero, the device was switched on. Electrode pads were attached, with two pairs of electrodes placed on the upper and lower lateral aspects of the thyroid cartilage, spaced 4 cm apart, and properly secured. The stimulation intensity was adjusted: one pair of electrodes was set to an output of 2050 Hz, and the other pair to 2000 Hz. The current was set between 2 and 2.5 mA. |
| Measure | Description | Time Frame |
|---|---|---|
| α-Amylase Level in Airway Secretions | α-Amylase level in airway secretions was measured as a biomarker for silent aspiration. A level >1685 U/L was considered positive for silent aspiration. | Upon admission to ICU after surgery, every 12 hours thereafter (depending on endotracheal catheter indwelling time), before extubation, 24 hours after extubation, 6 days after surgery. |
| Pepsin Level in Airway Secretions | Pepsin level in airway secretions was measured as a biomarker for silent aspiration. A level >200 ng/ml was considered positive for silent aspiration. | Upon admission to ICU after surgery, every 12 hours thereafter (depending on endotracheal catheter indwelling time), before extubation, 24 hours after extubation, 6 days after surgery. |
| Measure | Description | Time Frame |
|---|---|---|
| Mechanical Ventilation Duration | Total duration of postoperative mechanical ventilation, measured in hours, from the time of ICU admission after surgery (initiation of mechanical ventilation) to the time of successful extubation. | During the ICU stay, assessed at the time of extubation. |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fujian Medical University Union Hospital | Fuzhou | Fujian | 350000 | China |
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| Usual Care Group | Other | A sham intervention was performed using the Gentle Stim electrical stimulation therapy device. The device was applied identically to the experimental group but without delivering any electrical current. The wearing duration was consistent with that of the experimental group. |
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