Marco Gitto

Dr. Marco Gitto

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 March 2025 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
MGMarco Gitto
Marco Gitto
NMNoemi Motta*
Noemi Motta*
MAMirko Aldè
Mirko Aldè
Diego ZanettiDiego Zanetti
Diego Zanetti
FBFederica Di Berardino
Federica Di Berardino
Background: Auditory Processing Disorder (APD) manifests as impaired auditory information processing despite normal peripheral hearing. Current clinical protocols lack standardization, hampering evidence-based intervention development. Objective: This review analyzes APD research developments from 2011 to 2025, examining diagnostic criteria, assessment protocols, and treatment effectiveness. Methods: Medline, Embase, Scopus, and Cochrane Library databases were analyzed (January 2011–January 2025), following PRISMA guidelines. Two reviewers independently screened 413 articles, with 156 meeting inclusion criteria. Analysis included chi-square tests for intervention distribution and t-tests for diagnostic comparisons (α = 0.05). Results: Among 156 studies analyzed, medical interventions were markedly underrepresented (n = 4) compared to rehabilitative approaches (n = 52; χ2 = 50.28, p < 0.001). The Random Gap Detection Test and Dichotic Digits Difference Test were most frequently used (12.86% and 10.48% of studies, respectively). Cognitive skill enhancement dominated intervention strategies (52.8%), followed by computer-based rehabilitation (26.4%). Publication frequency showed consistent annual growth, peaking at 57 studies in 2024. Sample sizes were comparable between APD and CAPD studies (mean difference = 4.2 cases, t = 0.416, p = 0.679). Environmental modifications appeared in 15.1% of interventions, while speech therapy was reported in only 3.8% of studies. Conclusions: The substantial imbalance between medical and rehabilitative interventions necessitates standardized diagnostic protocols and enhanced multidisciplinary collaboration. Implementation of a hierarchical processing framework is recommended for assessment and treatment. Future research should prioritize large-scale controlled trials and unified diagnostic criteria development.

4 September 2024 in European Archives of Oto-Rhino-Laryngology
Verified
Journal Article
Open access
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FMFrancesco Mozzanica
Francesco Mozzanica
NPNicole Pizzorni
Nicole Pizzorni
MGMarco Gitto
Marco Gitto
CDClaudia Dosi
Claudia Dosi
AMAnna Mandelli
Anna Mandelli
ASAntonio Schindler
Antonio Schindler
Purpose: Although dysphagia is a common symptom among patients with Spinal Muscular Atrophy Type 1 (SMA1), scant data exist on the application of Fiberoptic Endoscopic Evaluation of Swallowing (FEES) in this population. The aim was to analyze FEES feasibility, swallow safety and efficacy, dysphagia phenotype, and agreement with VideoFluoroscopic Swallow Study (VFSS) in children with symptomatic, medication-treated SMA1 and oral feeding. Methods: 10 children with SMA1 underwent FEES. Six patients had also a VFSS. Two clinicians independently rated FEES and VFSS videos. Swallowing safety was assessed using the Penetration-Aspiration scale (PAS). Dysphagia phenotypes were defined according to the classification defined by Warnecke et al. Swallowing efficacy was evaluated with the Yale Pharyngeal Residue Severity Rating Scale (YPRSRS) in FEES, whereas pharyngeal residue was rated as present or absent in VFSS. Results: FEES was performed in all children without complications. Four children tolerated bolus trials during FEES, in 4 children swallowing characteristics were inferred based on post-swallow residues, while 2 children refused to eat and only saliva management was assessed. The dysphagia phenotype of predominance of residue in the piriform sinuses was documented in 7/8 children. The PAS score was < 3 in 3 children and > 5 in one child. Swallowing efficacy was impaired in 8/8 children. VFSS showed complete agreement with FEES. Conclusions: FEES is a feasible examination in children with SMA1. Swallowing safety and efficacy are impaired in nearly all patients with strong agreement between FEES and VFSS. Dysphagia is characterized by the predominance of residue in the piriform sinus.

16 April 2025 in Current Oncology
Verified
Journal Article
Open access
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MGMarco Gitto
Marco Gitto
FMFrancesco Mozzanica
Francesco Mozzanica
VPVincenzo Porpiglia
Vincenzo Porpiglia
LMLuca Morelli
Luca Morelli
ANAurora Ninfa
Aurora Ninfa
ASAntonio Schindler
Antonio Schindler
Late radiation-associated dysphagia (late-RAD) remains a challenge in head and neck cancer (HNC) survivorship, despite advancements in treatment methods. Although Fiberoptic Endoscopic Evaluation of Swallowing (FEES) stands as the preferred diagnostic approach for oropharyngeal dysphagia assessment in the HNC population, current studies lack a FEES-derived swallowing parameter characterization and phenotypic classification within this specific cohort. This study sought to employ FEES-based assessment to characterize swallowing safety and efficacy profiles, identify distinct phenotypes in HNC patients suffering from late-RAD, and examine potential correlations between safety and efficacy parameters. A retrospective analysis included twenty-four post-radiotherapy HNC patients evaluated using standardized FEES protocols across three bolus consistencies (liquid, semisolid, and solid). Swallowing safety was quantified using the Penetration–Aspiration Scale (PAS), while efficacy was measured via the Yale Pharyngeal Residue Severity Rating Scale (YPRSRS). Additionally, six distinct dysphagia phenotypes were characterized within the cohort. Propulsion deficit was the predominant phenotype (92%), followed by delayed pharyngeal phase (37.5%) and protective deficit (25%), with 46% of patients exhibiting multiple phenotypes. Unsafe swallowing occurred most frequently with liquid consistency (62.5%), while residue was most prevalent with semisolid (82.6% valleculae, 52.2% pyriform sinuses) and solid consistencies (92.3% valleculae, 53.8% pyriform sinuses). Significant correlations were found between penetration–aspiration and pharyngeal residue scores across consistencies (p < 0.05). FEES examination revealed distinct phenotypes in late radiation-associated dysphagia, with a predominance of propulsion deficit and significant interdependence between safety and efficacy parameters.

22 March 2025 in Reports
Verified
Journal Article
Open access
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MGMarco Gitto
Marco Gitto
ACAnna Colombo
Anna Colombo
ACAlessandro Campari
Alessandro Campari
EBEleonora Bonaventura
Eleonora Bonaventura
SRsara rocca
sara rocca
Background and Clinical Significance: Cricopharyngeal achalasia (CPA) is a rare disorder of the upper esophageal sphincter (UES), characterized by failure of the cricopharyngeus muscle to relax during swallowing. Pediatric CPA is particularly uncommon and often associated with comorbidities, such as neurological impairments, developmental delays, and laryngomalacia. The existing literature primarily consists of small case series, limiting insights into its natural history, particularly spontaneous resolution. This case highlights a unique instance of spontaneous improvement in CPA, contributing valuable knowledge to pediatric otolaryngology and gastroenterology. Case Presentation: We report the case of a 38 months male with global motor delay, presenting with feeding difficulties, choking, and aspiration. A videofluoroscopic swallow study (VFSS) confirmed CPA with impaired bolus passage and posterior indentation consistent with a cricopharyngeus bar. Despite multidisciplinary consultations, interventional therapies were deferred due to parental preference and cricopharyngeal EMG findings, showing muscle inhibition during swallowing. Over six months, the patient exhibited a spontaneous resolution of feeding difficulties and aspiration, with the normalization of VFSS findings. This rare case suggests a distinct natural history of CPA in young children. Conclusions: This case emphasizes the role of cricopharyngeal EMG in the differential diagnosis for pediatric feeding difficulties and its potential for spontaneous resolution. It highlights the need for further research into prognostic indicators and management strategies for CPA in children, offering a hopeful perspective for clinicians and caregivers.

1 August 2025 in Acta Otorhinolaryngologica Italica
Verified
Journal Article
Open access
PDF file
FBFederica Di Berardino
Federica Di Berardino
MGMarco Gitto
Marco Gitto
LBLeonardo Braga
Leonardo Braga
NMNoemi Motta
Noemi Motta
VCValeria Castelli
Valeria Castelli
DZDiego Zanetti
Diego Zanetti
Background. Dichotic listening tests, such as the Dichotic Digit Test (DDT) developed by F. Musiek, are vital for assessing auditory processing disorders. There is a lack of validated auditory tests in Italian, necessitating the adaptation of existing tools.Objective. This study aims to provide a preliminary assessment of the reliability and normative data for the newly adapted Italian version of the DDT. It hypothesises that the Italian DDT will show comparable reliability and normative data to the original English version, with a similar Right-Ear Advantage (REA).Methods. The adaptation process involved a pilot study with 20 normal hearing adults, comparing the English and Italian versions of the DDT. Subsequently, the study included 138 children aged 6-10 years, using the Italian version to assess test-retest reliability and gather normative data.Results. The findings revealed a consistent REA across participants that was more pronounced in younger children. The Italian version of DDT demonstrated adequate reliability across age groups and gender, with test-retest stability observed in both adults and children.Conclusions. This preliminary study provides essential data on the reliability and normative scores of the Italian DDT. The findings support its use in clinical and research settings, although further studies are required for comprehensive validation.

29 November 2024 in Clinical Case Reports
Verified
Journal Article
Open access
NMNoemi Motta
Noemi Motta
MGMarco Gitto
Marco Gitto
VCValeria Castelli
Valeria Castelli
Eleonora TobaldiniEleonora Tobaldini
Eleonora Tobaldini
NMNicola Montano
Nicola Montano
FBFederica Di Berardino
Federica Di Berardino
Vestibular syncope is a rare condition in which vertigo may cause syncopal attacks; however, the term has been associated with confusion because it has been ascribed to completely different vestibular and neurological conditions, from dizziness to Menière disease (MD), to the neurovegetative symptoms in benign paroxysmal positional vertigo (BPPV) and central vertebrobasilar hyperfusion. A 75‐year‐old woman with vasodepressive vasovagal syncope, confirmed by a tilt test with trinitrine administration, was referred for an audiological and vestibular assessment showing an acute unilateral peripheral vestibular deficit on the right side. The diagnosis is peripheral acute vestibular deficits. Interventions and outcomes are vestibular treatment and rehabilitation. The patient's vasovagal symptoms immediately improved and were completely resolved. Peripheral vestibular deficits might also trigger syncopal episodes and must be considered and studied by a complete audiological and vestibular evaluation. By restoring the peripheral vestibular function of the right labyrinth after vestibular treatment, a complete long‐term resolution of multiple vasovagal syncopal episodes was observed together with normalization of the tilt test.