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Effectiveness of Reanimator Muller in Patients With Chest Tube

U

University of Campinas, Brazil

Status and phase

Unknown
Phase 3
Phase 2

Conditions

Mechanical Ventilation Complication

Treatments

Device: Reanimator group
Device: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT02472041
20300313.9.0000.5404

Details and patient eligibility

About

This study evaluates the comparison of two of re-expansion pulmonary physiotherapy in patients with chest tube. The study group received intermittent positive pressure intervention and the control group received incentive spirometry intervention associated with manual operation.

Full description

All the re-expansion methods increase lung volume increasing gradient of transpulmonary pressure (PL) representing the difference alveolar pressure and pleural pressure. Spontaneous deep breath increases the PL by reducing pleural pressure (active breathing exercises, breathing supporters and manual operation).

Muller resuscitator consists of a pneumatic valve feature designed to operate with medical oxygen. It is used intermittently or continuously for pulmonary re-expansion, with lower load imposed work, and increase the efficiency of gas exchange by improving volumes, lung capacity and breathing pattern, and reverse atelectasis.

However, studies show the paucity of data in the literature regarding the Muller Resuscitator in different forms and respiratory rehabilitation protocols. In addition, studies show lack of standardization of methods and resources used in respiratory therapy in patients with chest tube.

Enrollment

32 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with old more 18 years untill 65 years
  • Patients undergoing thoracic drainage
  • That does not include in any exclusion criteria

Exclusion criteria

  • Contraindications breathing equipment use positive pressure

    • Patient intolerance
    • Phobia
    • Hemodynamic instability
    • Use of vasopressiva therapy
    • Shock (systolic pressure <90 mmHg)
    • Face trauma
    • Nausea or vomiting
    • Acute myocardial infarction
    • Lobectomy
    • Lung cancer
    • Gastrointestinal surgery
    • Pleural fistula.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

32 participants in 2 patient groups

Reanimator Group
Experimental group
Description:
Reanimator of Muller Group (intermittent positive pressure): Patients allocated to this group received intermittent positive pressure breathing (resuscitator Muller, Engemed, Brazil), adjusting the positive pressure around 1.5 kgf / cm2, which corresponds to 15 20 cm / H2O, positive pressure was applied through a face mask (Respironics®), which was connected in a circuit extending along the Muller Resuscitator equipment applied continuously for four series 10 of the patient breaths active and with an interval of two minutes between them in Fowler 45 position
Treatment:
Device: Reanimator group
Control Group
Experimental group
Description:
Control Group: In position Fowler 45, patients assigned to this group was administered as treatment lung expansion exercises using the incentive inspiratory flow (Respiron, NCS, Mexico) and concomitantly blocking contralateral to the drain maneuvers were performed, compression / decompression associated with the incentive spirometry (Respiron) consisting of 4 sets of 10 active patient breaths with an interval of two minutes between sets. Since the load of the respiratory stimulator will be zero throughout treatment (Table 1). Guidelines to the active, progressive and early mobilization.
Treatment:
Device: Control

Trial contacts and locations

2

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Central trial contact

Ana Paula R Dos Anjos, mestranda; Luiz C Martins, Doutor

Data sourced from clinicaltrials.gov

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