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Effect of Incentive Spirometer and Pursed Lip Breathing After Whipple Procedure.

Not Applicable
Recruiting
Conditions
Hospital Stay
Interventions
Other: Incentive Spirometer
Other: Pursed Lip Breathing
Registration Number
NCT06460584
Lead Sponsor
Riphah International University
Brief Summary

Whipple procedure is one of the most complex surgeries among hepatobiliary surgeries. It has named as Pancreaticoduodenectomy. It can cause many PPCs. Lung volumes are reduced due to atelectasis and pneumonia. Incentive spirometer (IS) is used to prevent PPCs. Due to general anesthesia, atelectasis is among most frequent PPCs. Pursed Lip Breathing (PLB) supports the patient to control the breath. The shriveling lips provide resistance to the air flowing out of the lungs. Airway collapse can be prevented by prolonged exhalation. Dyspnea occurs during 6MWT when patient performs walk in corridor. The aim of this study is to check the effect of Incentive Spirometer and Pursed Lip Breathing to improve dyspnea, oxygen saturation and hospital stay after Whipple procedure. This research of RCT will check the effect of IS and PLB by taking sample size of 60 post-operative patients through convenient sampling technique by allocating them randomly in group A and group B. Group A will receive PLB and group B will receive IS with baseline treatment chest percussions up to the duration of every day till discharge (reading will be collected on every 4rth day), dyspnea will be assessed through 6MWT and measured by Modified MRC dyspnea scale. The data will be analyzed through SPSS 26.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age (45 to 70)
  • Type of Abdominal Surgery (Whipple Procedure) (11)
  • Gender (Male and Female)
  • Patients who has no history of pulmonary disease
  • Smokers and nonsmokers
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Exclusion Criteria
  • COPD (COPD patient with postoperative whipple procedure)
  • Heart patient (patients who had history of heart disease along with whipple procedure)
  • Uncontrolled Hypertension (patients who has have history of uncontrolled hypertension in postoperative whipple procedure)
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Incentive SpirometerIncentive SpirometerThe intervention will be given every day till the patient discharged from hospital. Patient will perform 5 sets, in each set, 10 times will be included and hold for 3 seconds but not more than 5 seconds. Reading will be taken on every 4rth POD and comparison will be done with 1st POD reading and so on.
Pursed Lip BreathingPursed Lip BreathingFor the use of PLB exercise, the intervention will be given every day till the patient discharged from hospital. Patient will perform 5 sets. In each set, 10 times will be included
Primary Outcome Measures
NameTimeMethod
Pulse Oximeterbaseline and fourth week

Pulse oximetry is a simple and non-invasive method used to examine oxygen saturation (SpO2) in various parts of body. Convenient use, speed and high accuracy in detection of hypoxia and continuous monitoring of patients are other features of pulse oximetry

Modified MRC Dyspnea Scalebaseline and fourth week

Medical Research Council (MRC) dyspnea scale the first clinical scale for the determination of dyspnea, is a 5-point scale based on the sensation of breathing difficulty experienced by the patient during daily life activities Patients, reading the 10 scale, are invited to recognize their own level of respiratory fatigue or, as is more often the case, the MRC can be directly administered

6-MWTbaseline and fourth week

For the performance ability in many cardiopulmonary diseases, the most commonly used assessment tool is six minute walk test (6MWT). It has been widely used in research to evaluate the exercise capacity of various patient population (15). The test is standardized and reproducible self-paced exercise test. Patient is being asked to walk in a long hallway corridor for 6 minute between two cones on a flat surface. Ask the patient to keep walking. If the patient feels dyspnea, he or she may sit for a while. In healthy subjects with no history of pulmonary disease, the 6-min walk distance ranges from 400 to 700 m

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sheikh Zayed Hospital,

🇵🇰

Lahore, Punjab, Pakistan

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