Aplicação da auriculoterapia verdadeira e sham no tratamento de estresse em enfermeiros.

Prado, Juliana Miyuki do

doi:10.11606/d.7.2014.tde-17042015-124057

Cited by 5 publications

(7 citation statements)

References 15 publications

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“…No que se refere à população estudada, predominaram as produções que abordaram pacientes (n=12; 42,8%) (Chung, 2007;Ruela, 2017;Carpes, 2009;Assis, 2018;Brasileiro, 2018;Souza, 2017;Gonçalo, 2010;Sant'ana, 2015;Franco, 2015;Rodrigues, 2016;Fonseca, 2009;Coutinho, 2018), seguidos de profissionais de enfermagem (Kurebayashi, 2013;Prado, 2014, Figueredo, 2017Silva, 2018) (n=4;14,3%), adultos e idosos (Moura, 2016;Tolentino, 2016; Moura, 2019; Costa, 2019) (n=4; 14,3%); gestantes (Silva, 2016;Mafetoni, 2017) e puérperas (Rodrigues, 2013) (n=3; 10,7%), entre outros (Politti, 2007;Jimenz, 2009; 2014; Marques, 2017; Lopes, 2016) (n=5; 17,9%).…”

Section: Resultsunclassified

“…Constatou-se que a auriculoterapia apresentou resultados positivos no que diz respeito aos aspectos emocionais (Fonseca, 2009;Rodrigues, 2013;Kurebayashi, 2013;Prado, 2014;Lopes, 2016;Figueredo, 2017;Silva, 2018;Silva, 2016). A prática foi efetiva como intervenção para pacientes no pré-operatório, com redução da ansiedade (p=0,001) e da frequência cardíaca (p=0,03) (Fonseca, 2009).…”

Section: Auriculoterapia Como Intervenção Para Promoção Da Saúdeunclassified

“…A auriculoterapia também se mostrou eficaz no enfrentamento e redução de estresse agudo e crônico (burnout). Quando aplicada como intervenção para profissionais de enfermagem, reduziu os níveis de estresse (Lopes, 2016) (p<0,001) (Kurebayashi, 2013;Prado, 2014;Figueredo, 2017), com maior efeito para o grupo sem protocolo (Kurebayashi, 2013), assim como reduziu os níveis mais graves da síndrome de Burnout (p=0,006) (Silva, 2018). Além disso, gestantes diminuíram os níveis de ansiedade (p=0,033) e estresse (p=0,001) (Silva, 2016).…”

Section: Auriculoterapia Como Intervenção Para Promoção Da Saúdeunclassified

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Tendências da produção científica brasileira acerca da auriculoterapia

Morais

Munhoz

Luz

et al. 2020

RSD

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This study intends to analyze the trends of Brazilian productions, based on theses and dissertations, about auriculotherapy. It is a narrative review, developed with theses and dissertations available in the Directory of Theses and Dissertations of the Coordination for the Improvement of Higher Education Personnel. The search took place in January 2020, with the strategy “auriculotherapy” OR “auricular acupuncture”. After applying the selection criteria, 28 studies constituted the corpus of this review. Studies from dissertations (67.9%), concentration area in Nursing (53.6%), with quantitative designs (96.4%) and produced in institutions from southeastern Brazil (75.0%) were predominant. It has highlighted benefits from the practice of auriculotherapy regarding the physical, emotional and neurological health promotion, fighting chronic diseases, besides habits and health improvements. It is concluded that the trends of the Brazilian scientific productions demonstrate the use of auriculotherapy in different aspects, contributing to the promotion and recovery of the health of individuals.

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Section: Resultsunclassified

Section: Auriculoterapia Como Intervenção Para Promoção Da Saúdeunclassified

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Tendências da produção científica brasileira acerca da auriculoterapia

Morais

Munhoz

Luz

et al. 2020

RSD

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“…The existing literature acknowledges the difficulty in establishing protocols to be used as a control because of the high responsiveness and innervation of the auricular pavilion (ie, sham needling is not physiologically inert). [19][20][21] As a control group strategy, our study opted for superficial needling at nonpoints or irrelevant true points, aiming to reach other neural segments. The NSA group points were the external ear, the cheek and face area, and 4 nonspecific points in the helix region (eFigure 3 in Supplement 2), which are points that are not associated with mental health symptoms (eTable 2 in Supplement 2).…”

Section: Nsa Treatmentmentioning

confidence: 99%

Efficacy and Safety of Auricular Acupuncture for Depression

de Oliveira Rodrigues,

Menezes,

Machado Ribeiro Silotto

et al. 2023

JAMA Netw Open

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ImportanceDepression is a leading cause of disability worldwide, and there is increasing interest in nonpharmacological treatments. Auricular acupuncture (AA) is a simple, low-cost, and well-tolerated option, but further studies are needed to establish its efficacy and safety.ObjectiveTo estimate the efficacy and safety of auricular acupuncture as a treatment for depression.Design, Setting, and ParticipantsThis randomized clinical trial was conducted at 4 university research centers in Brazil, from March to July 2023. Eligible patients were adults aged 18 to 50 years whose score on the Patient Health Questionnaire–9 (PHQ-9) indicated moderate depression (score 10-14) or moderately severe depression (score 15-19). Exclusion criteria included previous application of AA, risk of suicidal ideation, or severe depression (PHQ-9 score &gt;20). An intent-to-treat analysis and modified intent-to-treat analysis were conducted.InterventionParticipants were randomized into 2 treatment groups, which included specific AA (SA) and nonspecific AA (NSA). Both groups received 12 sessions of AA with semipermanent needles with daily stimulation twice a week over 6 weeks and were followed-up for 3 months. All participants continued with their usual care for ethical reasons. The SA group’s treatment protocol consisted of 6 acupuncture points on the auricular pavilion chosen according to the diagnosis of depression by traditional Chinese medicine (Shenmen, subcortex, heart, lung, liver, and kidney). The NSA group’s acupuncture points were the external ear, the cheek and face area, and 4 nonspecific points in the helix region unassociated with mental health symptoms. A locator device was used to confirm which areas had neuroreactive points.Main Outcomes and MeasuresThe primary outcome was a reduction of at least 50% in the PHQ-9 score (ie, depression recovery) at 3 months. Secondary outcomes included depression recovery at 4 and 6 weeks; depression remission (PHQ-9 score &lt; 5) at 4 weeks, 6 weeks, and 3 months); and adverse events.ResultsA total of 304 participants were screened, and 74 participants (62 women [84%]; median [IQR] age, 29 [23-27] years) were included in the intention-to-treat analysis, with 37 participants randomized to each group (SA and NSA). A total of 47 participants (64%) were followed-up through 3 months. The results showed no statistically significant difference in depressive recovery between the groups at 3 months (14 of 24 participants in the SA group [58%] vs 10 of 23 participants in the NSA group [43%]; risk ratio [RR], 1.34; 95% CI, 0.76-2.45; P = .38). The proportions of depression recovery and remission at 4 and 6 weeks based on the PHQ-9 were higher in the SA group (except for depression recovery at 6 weeks) with no statistically significant differences. However, a statistically significant difference was observed in symptom remission at 3 months (11 of 24 participants in the SA group [46%] vs 3 of 23 participants in the NSA group [13%]; RR, 1.99; 95% CI, 1.16-3.34; P = .02) in favor of SA. There were no significant differences in adverse event rates between the groups, evidencing the intervention’s safety. Most participants reported mild pain at the needle application site (33 patients [94%] in the SA group vs 32 patients [91%] in the NSA group). Five participants dropped out of the study due to adverse events.Conclusions and RelevanceThe results of this randomized clinical trial suggest that SA over 6 weeks is safe. Although there was no statistically significant difference between groups for the primary efficacy outcome, patients receiving SA did experience greater symptom remission at 3 months. A larger sample size and longer intervention are needed to further evaluate the efficacy of SA for depression.Trial RegistrationClinicalTrials.gov Identifier: NCT05855421

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“…Aquele participante que não retornou após as avaliações dos instrumentos de coleta de dados foi considerado não aderente à pesquisa. Foram toleradas duas faltas no máximo, desde que não tivessem sido consecutivas, pois a acupuntura apresenta bons resultados com o mínimo de uma sessão por semana (88). Foi considerado sem seguimento o participante que não retornou para as avaliações.…”

Section: Adesão E Seguimentounclassified

Eficácia da acupuntura auricular na qualidade do sono em indivíduos com sintomas depressivos: ensaio clínico randomizado

Silotto

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Aplicação da auriculoterapia verdadeira e sham no tratamento de estresse em enfermeiros.

Cited by 5 publications

References 15 publications

Tendências da produção científica brasileira acerca da auriculoterapia

Tendências da produção científica brasileira acerca da auriculoterapia

Efficacy and Safety of Auricular Acupuncture for Depression

Eficácia da acupuntura auricular na qualidade do sono em indivíduos com sintomas depressivos: ensaio clínico randomizado

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