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Myofunctional treatment of sleep disordered breathing in children

Brasili Luca, Susy Martella, Ottavio Vitelli, Carlotta Bianchini, Silvia Miano, Alessandro Ferretti, Marco Del Pozzo, Maria Pia Villa
European Respiratory Journal 2013 42: P4670; DOI:
Brasili Luca
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Susy Martella
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Ottavio Vitelli
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Carlotta Bianchini
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Silvia Miano
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Alessandro Ferretti
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Marco Del Pozzo
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Maria Pia Villa
1Nesmos, Pediatric Unit, Sant'Andrea Hospital, La Sapienza University, Rome, Italy
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Abstract

Introduction: Notwithstanding adenotonsillar hypertrophy is the main causative factor of pediatric obstructive sleep apnea (OSA), a residual OSA after adenotonsillectomy (AT) is often reported and we hypothesise that oropharyngeal hypotonia is implicated in the pathogenesis of OSA and oropharingeal exercises (myofunctional therapy) may improve stomatognathics functions and reduce neuromuscular impairment.

Aim: To evaluate efficacy of myofunctional treatment in children with residual OSA.

Methods: Polysomnographic recordings have been performed before the surgical therapy (T0) and 6 months after AT (T1). Thereafter, patients with a residual OSA (apnea hypopnea index, AHI>1) have been randomized in a group treated with myofunctional therapy (group 1) and a control group (group 2). A morphofunctional evaluation with Glatzel and Rosenthal tests were performed before (T1) and after 3 months of exercises (T2). All subjects were reevalueted at T2.

The improvement of OSA was defined by ΔAHI: (AHI at T1-AHI at T2)/AHI at T1*100.

Result

Group 1 was composed by 12 subjects (males 10; mean age 5.37 ± 1.71) and Group 2 was composed by 9 subjects (males 8; mean age 4.25 ± 0.39). The AHI was 16.31 ± 9.51 in T0 ad 3.46 ± 2.32 in T1 (p<0.0001).

The ΔAHI was significantly higher (p<0.05) in group 1 (52.64% ± 29.39%) respectively group 2 (1.01% ± 56.35%).

Myofunctional evaluation demonstrated: reduction of oral breathing (12/12 vs 3/12, p<0.0001), positive Glatzel test (9/12 vs 3/12, p<0.05), positive Rosenthal test (9/12 vs 3/12, p<0.05) and increase lip competence (1/12 vs 10/12, p<0.0001),.

Conclusion

Myofunctional therapy could be an efficacious treatment in pediatric OSA in addition to AT.

  • Children
  • Sleep disorders
  • Treatments
  • © 2013 ERS
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Myofunctional treatment of sleep disordered breathing in children
Brasili Luca, Susy Martella, Ottavio Vitelli, Carlotta Bianchini, Silvia Miano, Alessandro Ferretti, Marco Del Pozzo, Maria Pia Villa
European Respiratory Journal Sep 2013, 42 (Suppl 57) P4670;

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Myofunctional treatment of sleep disordered breathing in children
Brasili Luca, Susy Martella, Ottavio Vitelli, Carlotta Bianchini, Silvia Miano, Alessandro Ferretti, Marco Del Pozzo, Maria Pia Villa
European Respiratory Journal Sep 2013, 42 (Suppl 57) P4670;
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