Carla Pinto Moura

Prof. Dr. Carla Pinto Moura

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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1 January 2008 in Journal of Voice
Verified
Journal Article
Closed access
CMCarla Pinto Moura
Carla Pinto Moura
LCLuís Miguel Cunha
Luís Miguel Cunha
HVHelena Vilarinho
Helena Vilarinho
MCMaria João Cunha
Maria João Cunha
DFDiamantino Freitas
Diamantino Freitas
MPM. Pais-Clemente
M. Pais-Clemente

25 June 2008 in The Journal of Laryngology & Otology
Verified
Journal Article
Closed access
CMCarla Pinto Moura
Carla Pinto Moura
DAD Andrade
D Andrade
LCL M Cunha
L M Cunha
MTM J Tavares
M J Tavares
MCM J Cunha
M J Cunha
MCM Pais Clemente
M Pais Clemente
Objective: Phenotypical Down syndrome includes pharyngeal and maxillary hypoplasia and, frequently, constricted maxillary arch with nasal obstruction.Study design: This clinical trial assessed the effects of rapid maxillary expansion on ENT disorders in 24 children with Down syndrome randomly allocated to receive either rapid maxillary expansion or not. Each group received ENT and speech therapy assessments before expansion and after the device had been removed.Results: In the rapid maxillary expansion group, the yearly ENT infection rate was reduced when assessed after device removal (p < 0.01). The parents of rapid maxillary expansion children reported a reduction in respiratory obstruction symptoms. Audiological assessment revealed improvements in the rapid maxillary expansion group (p < 0.01). Cephalometry showed increased maxillary width in the rapid maxillary expansion group.Conclusions: Rapid maxillary expansion resulted in a reduction in hearing loss, yearly rate of ENT infections and parentally assessed symptoms of upper airway obstruction, compared with no treatment. These findings are probably related to expanded oronasal space, due to rapid maxillary expansion.

1 August 2017 in International Journal of Pediatric Otorhinolaryngology
Verified
Journal Article
Closed access
FCFilipa Camacho Côrte
Filipa Camacho Côrte
JFJoão Firmino-Machado
João Firmino-Machado
CMCarla Pinto Moura
Carla Pinto Moura
JSJorge Spratley
Jorge Spratley
MSMargarida Santos
Margarida Santos

10 July 2014 in Brazilian Journal of Otorhinolaryngology
Verified
Journal Article
Open access
SCSuzana Boltes Cecatto
Suzana Boltes Cecatto
MSMatilde Monteiro Soares
Matilde Monteiro Soares
Teresa HenriquesTeresa Henriques
Teresa Henriques
EMEurico Monteiro
Eurico Monteiro
CMCarla Pinto Moura
Carla Pinto Moura
Pharyngocutaneous fistula is considered one of the major complications in the postoperative period after total laryngectomy/pharyngolaryngectomy, leading to a severe adverse impact for the patient and society. This study aimed to identify all the described pharyngocutaneous fistula predictive factors and risk classifications. Research was conducted to identify all the studies assessing predictive factors and risk classification for pharyngocutaneous fistula development published until April of 2012 (n = 846). The included studies were analyzed and data regarding their identification, methodological quality and results were recorded. A total of 39 studies were included. The variables consistently reported as associated with fistula development were nutritional deficiency, American Society of Anesthesiologists (ASA) classification, high consumption of alcohol, anemia and hypoalbuminemia, co-morbidities, advanced N stage, location and extent of primary tumor, pre-radiotherapy and pre-chemoradiotherapy treatment, emergency tracheotomy, surgical margin status, surgery's duration, surgeon's experience, local complications of the wound, performance of intraoperative blood transfusion and relationship between nasogastric tube and oral feeding. Several risk factors were associated with pharyngocutaneous fistula formation in the included studies. However, there is still no consensus in the most pertinent selection. Only two classification systems were retrieved and they were not able to accurately predict pharyngocutaneous fistula.

10 June 2015 in Brazilian Journal of Otorhinolaryngology
Verified
Journal Article
Open access
SCSuzana Boltes Cecatto
Suzana Boltes Cecatto
Matilde Monteiro-SoaresMatilde Monteiro-Soares
Matilde Monteiro-Soares
Teresa HenriquesTeresa Henriques
Teresa Henriques
EMEurico Monteiro
Eurico Monteiro
CMCarla Pinto Moura
Carla Pinto Moura
Pharyngocutaneous fistula after larynx and hypopharynx cancer surgery can cause several damages. This study's aim was to derive a clinical decision rule to predict pharyngocutaneous fistula development after pharyngolaryngeal cancer surgery. A retrospective cohort study was conducted, including all patients performing total laryngectomy/pharyngolaryngectomy (n=171). Association between pertinent variables and pharyngocutaneous fistula development was assessed and a predictive model proposed. American Society of Anesthesiologists scale, chemoradiotherapy, and tracheotomy before surgery were associated with fistula in the univariate analysis. In the multivariate analysis, only American Society of Anesthesiologists maintained statistical significance. Using logistic regression, a predictive model including the following was derived: American Society of Anesthesiologists, alcohol, chemoradiotherapy, tracheotomy, hemoglobin and albumin pre-surgery, local extension, N-classification, and diabetes mellitus. The model's score area under the curve was 0.76 (95% CI 0.64-0.87). The high-risk group presented specificity of 93%, positive likelihood ratio of 7.10, and positive predictive value of 76%. Including the medium-low, medium-high, and high-risk groups, a sensitivity of 92%, negative likelihood ratio of 0.25, and negative predictive value of 89% were observed. A clinical decision rule was created to identify patients with high risk of pharyngocutaneous fistula development. Prognostic accuracy measures were substantial. Nevertheless, it is essential to conduct larger prospective studies for validation and refinement.

10 November 2014 in Clinical Genetics
Verified
Journal Article
Closed access
PDF file
MSM.J. Nabais Sá
M.J. Nabais Sá
HSH. Storey
H. Storey
FFF. Flinter
F. Flinter
MNM. Nagel
M. Nagel
SSS. Sampaio
S. Sampaio
JOJoão Paulo Oliveira
João Paulo Oliveira