Karen Barros Parron Fernandes

Dr. Karen Barros Parron Fernandes


Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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1 January 2015 in Journal of Physical Therapy Science
Verified
Journal Article
Open access
HFHebert S. C. Fabre
Hebert S. C. Fabre
RNRicardo L. Navarro
Ricardo L. Navarro
POPaula V.P. Oltramari-Navarro
Paula V.P. Oltramari-Navarro
RORodrigo F. Oliveira
Rodrigo F. Oliveira
DPDeise A. A. Pires-Oliveira
Deise A. A. Pires-Oliveira
KFKaren Barros Parron Fernandes
Karen Barros Parron Fernandes
[Purpose] This study aimed to evaluate the anti-inflammatory and analgesic effects of intraoral application of low-level laser therapy (660 nm) to control pain, swelling and interincisal opening following the extraction of mandibular third molars. [Subjects and Methods] Ten patients underwent removal of lower third molars using the same surgical protocol and pharmacological approach. In the postoperative period, all patients received four consecutive daily sessions of low-level laser therapy, beginning 24 hours after the surgery. Intraoral applications using the diode laser with 660 nm wavelength in the continuous scan mode were performed covering the entire surgical area, which was divided into four quadrants, each of 1 cm(2) area at a distance of 1 cm. The energy applied at each point was 5 J/cm(2) during 8 seconds. [Results] The swelling and interincisal opening returned to normal 24 hours after the first low-level laser therapy application (Friedman test). Moreover, the pain intensity was reduced on the third postoperative day, according to the Friedman test. [Conclusion] Low-level laser therapy (660 nm), at the dosimetry used in this study, was effective in reducing postoperative pain and swelling following oral surgery.

1 January 2016 in Journal of Physical Therapy Science
Verified
Journal Article
Open access
VCVinícius A. Coelho
Vinícius A. Coelho
VPVanessa S. Probst
Vanessa S. Probst
BNBruna M. Nogari
Bruna M. Nogari
DTDenilson C. Teixeira
Denilson C. Teixeira
JFJosiane M. Felcar
Josiane M. Felcar
KFKaren Barros Parron Fernandes
Karen Barros Parron Fernandes
[Purpose] This study aimed to assess the exercise capacity and muscle strength in elderly people using drugs for angiotensin-II blockage. [Subjects and Methods] Four hundred and seven older adults were recruited for this study. Data about comorbidities and medication use were recorded and the individuals were divided into three groups: control group- elderly people with normal exercise capacity (n=235); angiotensin-converting enzyme inhibitor group - individuals using angiotensin-converting enzyme inhibitors (n=140); and angiotensin-II receptor blocker group- patients using angiotensin-II receptor blockers (n= 32). Exercise capacity was evaluated by a 6-minute walking test and muscle strength was measured using a handgrip dynamometer. [Results] Patients from the angiotensin-converting enzyme inhibitor group (mean: 99 ± 12%) and the angiotensin-II receptor blocker group (mean: 101 ± 14%) showed higher predicted values in the 6-minute walking test than the control group patients (mean: 96 ± 10%). Patients from the angiotensin-converting enzyme inhibitor group (mean: 105 ± 19%) and the angiotensin-II receptor blocker group (mean: 105.1 ± 18.73%) showed higher predicted values of muscle strength than control group patients (mean: 98.15 ± 18.77%). [Conclusion] Older adults using angiotensin-converting enzyme inhibitors or angiotensin-II receptor blockers have better functional exercise capacity and muscle strength.

6 May 2015 in International Archives of Otorhinolaryngology
Verified
Journal Article
Open access
PDF file
HTHeloísa Freiria Tsukamoto
Heloísa Freiria Tsukamoto
VCViviane de Souza Pinho Costa
Viviane de Souza Pinho Costa
RSRubens Silva
Rubens Silva
GPGislaine Garcia Pelosi
Gislaine Garcia Pelosi
LMLuciana Lozza de Moraes Marchiori
Luciana Lozza de Moraes Marchiori
KFKaren Barros Parron Fernandes
Karen Barros Parron Fernandes
Introduction Dizziness can be characterized as a balance disorder that causes discomfort, leading to several functional limitations. Currently, vestibular rehabilitation has been highlighted as a possible treatment. Objective Analyze the effects of completing a vestibular rehabilitation treatment protocol on quality of life and postural balance in patients with vestibular complaints, as well as to compare these effects between the patients taking or not taking antivertigo drugs. Methods A nonrandomized controlled trial was performed with 20 patients previously diagnosed with vestibular diseases. Information regarding vertigo symptoms, quality of life as assessed through the Dizziness Handicap Inventory, visual analog scale of dizziness, and stabilometry using force platform was collected. Patients were treated for 12 weeks by a custom protocol. The sample was divided into two groups according to the use (medicated group, n = 9) or not (control group, n = 11) of antivertigo drugs. Results There was improvement in quality of life (p < 0.001) and intensity of dizziness (p = 0.003) with the intervention. An improvement of postural balance was observed through functional tests. However, no statistically significant difference was noted in stabilometry. When both groups were compared, no statistically significant differences between the variations of the variables analyzed were found in the re-evaluation session. Conclusion Quality of life and postural balance are improved with intervention. However, this improvement is not associated with pharmacologic treatment.

1 August 2017 in Acta Ortopedica Brasileira
Verified
Journal Article
Open access
PDF file
CRClaudiane Pedro Rodrigues
Claudiane Pedro Rodrigues
RSRubens Alexandre da Silva
Rubens Alexandre da Silva
ENElias Nasrala Neto
Elias Nasrala Neto
RARodrigo Antonio Carvalho Andraus
Rodrigo Antonio Carvalho Andraus
MFMarcos Tadeu Parron Fernandes
Marcos Tadeu Parron Fernandes
KFKaren Barros Parron Fernandes
Karen Barros Parron Fernandes
Objective: The objective of this study was to analyze the functional status of adult and older adult individuals with lower back pain . Methods: Eighty-three individuals were recruited, 42 older adults (20 with lower back pain and 22 control group) and 41 younger adults (21 with lower back pain and 20 control group). Functional capacity was assessed using the following tests: Timed Up and Go (TUG), Five Times Sit-to-Stand (FTSTS), six-minute walking test (SMWT), and sitting-rising test (SRT) . Results: In the younger adults, there was no difference in functional capacity between the groups (p>0.05). On the other hand, when statistical analysis was adjusted using body mass index (BMI) as a covariate, the lower back pain group performed more poorly on the SRT (p<0.004). Furthermore, poorer physical capacity was seen in the older adults with back pain via the SRT test (p=0.001), and when the BMI was adjusted, a statistical difference was seen in the SRT as well as the SMWT (p<0.05) . Conclusion: Older individuals with lower back pain have poorer physical performance, and the sitting-rising test is the most discerning for assessment of functional status in individuals with lower back pain. Level of Evidence III, Retrospective Comparative Study.

20 August 2022 in Sensors
Verified
Journal Article
Open access
PDF file
CSColince Segning
Colince Segning
JHJessica Harvey
Jessica Harvey
HEHassan Ezzaidi
Hassan Ezzaidi
KFKaren Barros Parron Fernandes
Karen Barros Parron Fernandes
Rubens da SilvaRubens da Silva
Rubens da Silva
SNSuzy Ngomo
Suzy Ngomo
This proof-of-concept study explores the potential of developing objective pain identification based on the analysis of electroencephalography (EEG) signals. Data were collected from participants living with chronic fibromyalgia pain (n = 4) and from healthy volunteers (n = 7) submitted to experimental pain by the application of capsaicin cream (1%) on the right upper trapezius. This data collection was conducted in two parts: (1) baseline measures including pain intensity and EEG signals, with the participant at rest; (2) active measures collected under the execution of a visuo-motor task, including EEG signals and the task performance index. The main measure for the objective identification of the presence of pain was the coefficient of variation of the upper envelope (CVUE) of the EEG signal from left fronto-central (FC5) and left temporal (T7) electrodes, in alpha (8–12 Hz), beta (12–30 Hz) and gamma (30–43 Hz) frequency bands. The task performance index was also calculated. CVUE (%) was compared between groups: those with chronic fibromyalgia pain, healthy volunteers with “No pain” and healthy volunteers with experimentally-induced pain. The identification of the presence of pain was determined by an increased CVUE in beta (CVUEβ) from the EEG signals captured at the left FC5 electrode. More specifically, CVUEβ increased up to 20% in the pain condition at rest. In addition, no correlation was found between CVUEβ and pain intensity or the task performance index. These results support the objective identification of the presence of pain based on the quantification of the coefficient of variation of the upper envelope of the EEG signal.

26 January 2025 in Nutrients
Verified
Journal Article
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CMCláudia Nascimento Montemor
Cláudia Nascimento Montemor
MFMarcos Tadeu Parron Fernandes
Marcos Tadeu Parron Fernandes
AMAudrey de Souza Marquez
Audrey de Souza Marquez
PBPaulo Roberto Bignardi
Paulo Roberto Bignardi
RPRegina Célia Poli
Regina Célia Poli
KFKaren Barros Parron Fernandes
Karen Barros Parron Fernandes
Background: Vitamin D is beneficial for musculoskeletal health. Although low levels of vitamin D are linked to increased pain in knee osteoarthritis (OA), their association with functionality remains understudied. Objective: This study aimed to investigate the association between vitamin D deficiency and functional status in elderly individuals with OA and explore the potential correlation between vitamin D deficiency and plasma levels of tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6). Methods: The study included older adults (≥60 years) from an ageing study, encompassing 105 OA patients and 152 controls. OA diagnosis was confirmed radiographically, and the WOMAC questionnaire assessed functional impairment in these patients. Blood samples were collected to measure 25(OH) vitamin D levels by chemiluminescence and TNF-α and IL-6 levels by ELISA. Results: Patients with vitamin D insufficiency/deficiency exhibited more severe cases of OA compared to those with normal vitamin D levels (p = 0.04). Vitamin D levels were inversely correlated with functional impairment in OA, according to the WOMAC Index (global: rS = −0.25, p = 0.01; pain: rS = −0.21, p = 0.03). Moreover, OA patients with vitamin D deficiency showed significantly higher levels of TNF-α and IL-6 (p < 0.05, Mann−Whitney test). Conclusions: Reduced levels of vitamin D are associated with more severe cases of hip and knee osteoarthritis, increased pain, greater functional impairment, and elevated serum levels of TNF-α and IL-6. Further research is required to elucidate the mechanisms underlying the influence of vitamin D on osteoarthritis and to evaluate the potential benefits of vitamin D supplementation for mitigating disease symptoms and progression.