Manejo da dor durante a punção arterial no neonato: estudo descritivo / Manejo del dolor durante la punción arterial en neonatos: estudio descriptivo / Pain management during arterial puncture in newborns: a descriptive study

RESUMO Objetivo descrever as medidas de alívio da dor aplicadas pela equipe de enfermagem durante a punção arterial no neonato e os escores de dor no momento do procedimento. Método estudo descritivo, quantitativo, realizado entre outubro de 2018 e janeiro de 2019, em uma unidade de terapia intensiva neonatal no Noroeste do Paraná, por meio da observação não participantes de 192 punções arteriais, com respectiva mensuração dos escores de dor. O estudo foi aprovado pelo Comitê de Ética em Pesquisa com Seres Humanos. Resultados das 192 punções somente 34 foram analisadas quanto às medidas de alívio e escores de dor, os quais se mostraram elevados. As demais punções foram excluídas, devido perda da monitorização durante o procedimento. Conclusão evidenciou-se pouco uso de intervenções relacionadas ao alívio da dor por parte da equipe. O processo de observação constatou a presença de dor intensa.

RESUMEN Objetivo describir las medidas de alivio del dolor aplicadas por el equipo de enfermería durante la punción arterial en neonatos y las escalas de puntuación de dolor en el momento del procedimiento. Método estudio descriptivo, cuantitativo, realizado entre octubre de 2018 y enero de 2019, en una unidad de cuidados intensivos neonatales del noroeste de Paraná, mediante observación no participante de 192 punciones arteriales, con medición respectiva de puntuaciones de dolor. El estudio fue aprobado por el Comité de Ética para la Investigación con Seres Humanos. Resultados de las 192 punciones, solo 34 fueron analizadas en cuanto a las medidas de alivio y puntuaciones de dolor que fueron elevadas. Se excluyeron las otras punciones debido a la pérdida del monitoreo durante el procedimiento. Conclusión el equipo utilizó poco las intervenciones relacionadas con el alivio del dolor. El proceso de observación verificó la presencia de dolor intenso.

ABSTRACT Objective to describe pain relief measures applied by the nursing team during arterial puncture in neonates, and pain scores during the procedure. Method this descriptive, quantitative study was conducted between October 2018 and January 2019 at a neonatal intensive care unit in northwestern Paraná, by non-participant observation of 192 arterial punctures and measurement of the respective pain scores. The study was approved by the human research ethics committee. Results of the 192 punctures, only 34 were examined for relief measures and pain scores; the latter were found to be high. The other punctures were excluded for loss of monitoring during the procedure. Conclusion pain-relief interventions were little used by the team. The observation process found intense pain.

Post-traumatic stress disorder increases pain sensitivity by reducing descending noradrenergic and serotoninergic modulation.

Exposure to stress might influence pain sensitivity; however, little is known about whether post-traumatic stress disorder (PTSD)-like symptoms alter pain sensitivity and how it can happen. Male rats were exposed to the inescapable footshock paired with either social isolation or a control condition (not exposed to footshock but subjected to social isolation). After 7, 14, or 21 days, memory retention was evaluated. In the following three days, animals underwent the following tests: open-field, social interaction and formalin tests. Another group of animals were subjected to the object recognition test and to von Frey filaments. In other cohorts of animals, saline, fluoxetine, or desipramine were injected intrathecally and immunohistochemistry was performed to investigate whether PTSD-like symptoms alter the expression of c-Fos in serotonergic and noradrenergic neurons. Inescapable footshock induced the development of PTSD-like symptoms. Animals with PTSD-like symptoms showed an increase in the number of flinches in the formalin test and a reduction in mechanical threshold in the von Frey test at both retention intervals. The social interaction was negatively correlated with the nociceptive response in the formalin test. Fluoxetine or desipramine prevented the nociceptive response to chemical stimulus in the formalin test. In addition, in animals with PTSD-like symptoms, there was a reduction in c-Fos expression in serotonergic and noradrenergic neurons. Our results are important for the association of increased sensitivity to pain as one of the clinical manifestations that are present in the development of PTSD, and a possible treatment for increased pain sensitivity in male individuals with PTSD.

Understanding childbirth pain in Brazilian women: A qualitative descriptive study.

BACKGROUND: The pain associated with childbirth is a cause of severe pain, and the literature suggests that it can be influenced by psychosocial influences, the environment, and cognitive processes, creating the overall experience of childbirth. Therefore, the investigation of women's childbirth pain experience is essential. AIM: The purpose of this study is to understand women's childbirth pain and determine which influences can contribute to building different experiences. METHOD: A qualitative descriptive approach was adopted to explore the women's childbirth pain experiences, by understanding the influences on their experiences. Data were collected through in-depth interviews with 21 women in a hospital setting in São Paulo, Brazil, and analysed by thematic analysis. RESULTS: Three major themes emerged from the analysis: (1) experiencing childbirth pain, (2) face-to-face with pain, and (3) empowerment needs. DISCUSSION: Many factors influence how Brazilian women manage pain and shape their experience during childbirth. The findings suggest that when women had a positive experience, they asked for minimal support, demonstrated balance, and expressed that the pain was manageable; when they had unfavourable experiences, they regarded pain as a threat and a punishment and associated it with unpleasant emotions. CONCLUSION: The results outlined concerns that should be addressed in the provision of specific, appropriate care for women, to support them in improving their experience during childbirth.

Effectiveness of hospital clowns for symptom management in paediatrics: systematic review of randomised and non-randomised controlled trials.

OBJECTIVE: To evaluate evidence from randomised controlled trials and non-randomised controlled trials on the effectiveness of hospital clowns for a range of symptom clusters in children and adolescents admitted to hospital with acute and chronic conditions. DESIGN: Systematic review of randomised and non-randomised controlled trials. DATA SOURCES: Medline, ISI of Knowledge, Cochrane Central Register of Controlled Trials, Science Direct, Scopus, American Psychological Association PsycINFO, Cumulative Index to Nursing and Allied Health Literature, and Latin American and Caribbean Health Sciences Literature. STUDY SELECTION: Randomised and non-randomised controlled trials were peer reviewed using the following eligibility criteria: children and adolescents who were admitted to hospital for acute conditions or chronic disorders, studies comparing use of hospital clowns with standard care, and studies evaluating the effect of hospital clowns on symptom management of inpatient children and adolescents as a primary outcome. DATA EXTRACTION AND SYNTHESIS: Two investigators independently screened studies, extracted data, and appraised the risk of bias. Methodological appraisal was assessed by two investigators independently using the Jadad scale, the revised Cochrane risk-of-bias tool for randomised controlled trials (RoB 2), and the risk of bias in non-randomised studies (ROBINS-I) tool for non-randomised controlled trials. RESULTS: 24 studies (n=1612) met the inclusion criteria for data extraction and analysis. Most studies were randomised controlled trials (n=13). Anxiety was the most frequently analysed symptom (n=13), followed by pain (n=9), psychological and emotional responses and perceived wellbeing (n=4), stress (n=4), cancer related fatigue (n=3), and crying (n=2). Five studies used biomarkers, mainly cortisol, to assess stress or fatigue outcome following hospital clowns. Most of the randomised controlled trials (n=11; 85%) were rated as showing some concerns, and two trials were rated with a high risk of bias. Most non-randomised controlled trials (n=6; 55%) were rated with a moderate risk of bias according to ROBINS-I tool. Studies showed that children and adolescents who were in the presence of hospital clowns, either with or without a parent present, reported significantly less anxiety during a range of medical procedures, as well as improved psychological adjustment (P<0.05). Three studies that evaluated chronic conditions showed favourable results for the intervention of hospital clowns with significant reduction in stress, fatigue, pain, and distress (P<0.05). CONCLUSIONS: These findings suggest that the presence of hospital clowns during medical procedures, induction of anaesthesia in the preoperative room, and as part of routine care for chronic conditions might be a beneficial strategy to manage some symptom clusters. Furthermore, hospital clowns might help improve psychological wellbeing in admitted children and adolescents with acute and chronic disorders, compared with those who received only standard care. SYSTEMATIC REVIEW REGISTRATION: PROSPERO CRD42018107099.

El dolor: algunos criterios desde la Psicología / Pain: some psychological criteria

Introducción: El dolor como experiencia subjetiva desagradable es un síntoma frecuente en los pacientes atendidos en el servicio de Hematología. Este afecta al individuo a nivel psicológico y provoca la aparición de dificultades en las áreas laboral, educacional, familiar y en las relaciones interpersonales. La percepción del dolor puede verse distorsionada como resultado de esta alteración provocada en el paciente. Objetivo: Analizar los factores psicológicos que median la percepción del dolor de los pacientes. Métodos: Se realizó una revisión de la literatura, a través del sitio web PubMed y el motor de búsqueda Google Académico. Se emplearon las palabras clave: dolor, manejo del dolor, evaluación del dolor, psicología del dolor, dolor en hematología, dolor en drepanocitosis, dolor en hemofilia, dolor en leucemia. Análisis y síntesis de la información: Se evidencia el carácter multifacético de esta experiencia subjetiva. Los determinantes y mecanismos del dolor son diversos, lo cual implica que su enfrentamiento requiera un enfoque integral que ayude a los pacientes a desarrollar conciencia acerca de los efectos de la enfermedad que padece y los síntomas del dolor. También es necesario guiarlos en la comprensión de los factores que contribuyen a su magnificación, crear estrategias que les ayuden a minimizar la exposición a estos, y orientarlos para que desarrollen métodos personales que les permitan lidiar con el dolor con un mínimo estrés psicológico. Conclusiones: El dolor es un fenómeno complejo que involucra diversas variables y factores en su funcionamiento. Su manejo requiere un enfoque integral para la atención de los pacientes en su enfrentamiento al dolor(AU)

Introduction: Pain as an unpleasant subjective experience is a frequent symptom in patients treated by the Hematology service. This affects the individual on a psychological level and causes the onset of difficulties in the work, educational, family and interpersonal relationships. The perception of pain can be distorted as a result of this alteration caused in the patient. Objective: To analyze the psychological factors that mediate patients' perception of pain. Methods: A literature review was carried out through the PubMed website and the search engine of Google Scholar. The following keywords were used: dolor [pain], manejo del dolor [pain management], evaluación del dolor [pain assessment], psicología del dolor [pain psychology], dolor en hematología [pain in hematology], dolor en drepanocitosis [pain in sickle cell disease], dolor en hemofilia [pain in hemophilia], dolor en leucemia [pain in leukemia]. Information analysis and synthesis: The multifaceted nature of this subjective experience is evidenced. Pain determinants and mechanisms are diverse, which implies that their coping requires a comprehensive approach that helps patients develop awareness about the disease effects and the pain symptoms. It is also necessary to guide them in understanding the factors that contribute to pain magnification, create strategies that help them minimize pain exposure, and guide them to develop personal methods that allow them to deal with pain with minimal psychological stress. Conclusions: Pain is a complex phenomenon involving several variables and factors in its operation. Its management requires a comprehensive approach to patient care regarding coping with pain(AU)

Breakthrough cancer pain: review and calls to action to improve its management.

In this paper, we review the current state of breakthrough cancer pain (BTcP) management. BTcP is a heterogeneous condition and a global problem for cancer patients. It is often managed suboptimally, which results in a negative outcome for patients, healthcare providers, and healthcare systems. Several barriers to the appropriate management of BTcP have been identified. These include, among others, an incomplete definition of BTcP, poor training of healthcare providers and patients alike, a lack of a multidisciplinary approach and the absence of specific protocols and tools. We provide some actions to help physicians and patients improve their approach to BTcP, including specific training, the design of easy-to-use tools for BTcP identification and assessment (such as checklists and pocket-sized cards), individualized treatment, and the use of multidisciplinary teams.

"Waiting for a miracle": Spirituality/Religiosity in coping with sickle cell disease / "Esperando un milagro": Espiritualidad/Religiosidad en el afrontamiento de la enfermedad de célula falciforme / "À espera de um milagre": espiritualidade/religiosidade no enfrentamento da doença falciforme

ABSTRACT Objective: To understand spirituality/religiosity as experienced by people with sickle cell disease, and its influence on coping with the disease. Method: A qualitative, descriptive, and exploratory study conducted in the State of Bahia. Twenty-nine respondents participated in semi-structured interviews. Content analysis was used to analyze the empirical material. Results: Individuals with sickle cell disease experience spirituality/religiosity motivated by their hope for a miracle, and fear of death; among their rites are: reading religious materials, individual and group prayer, and attendance at worship services. The effects on their health include: comfort by means of coping by comparing two evils, anxiety relief, social support, and lifestyle changes; however, spirituality/religiosity may be impaired. Final considerations: This study demonstrates the need to qualify health professionals to address spiritual issues of these individuals during illness, with the aims of diagnosing suffering and anguish, and providing care, comfort and strengthening of the spiritual bonds of these individuals.

RESUMEN Objetivo: Entender la espiritualidad / religiosidad como la experimentan las personas con enfermedad de células falciformes y su influencia en el afrontamiento de la enfermedad. Método: Un estudio cualitativo, descriptivo y exploratorio realizado en el estado de Bahía. Veintinueve encuestados participaron en entrevistas semiestructuradas. Se utilizó análisis de contenido para analizar el material empírico. Resultados: Las personas con enfermedad de células falciformes experimentan espiritualidad / religiosidad motivadas por su esperanza de un milagro y el miedo a la muerte; entre sus ritos se encuentran: lectura de materiales religiosos, oración individual y grupal, y asistencia a los servicios de adoración. Los efectos en su salud incluyen: comodidad mediante el manejo del afrontamiento, alivio de la ansiedad, apoyo social y cambios en el estilo de vida; sin embargo, la espiritualidad / religiosidad puede verse afectada. Consideraciones finales: Este estudio demuestra la necesidad de preparar a los profesionales de la salud para abordar los problemas espirituales de estos individuos durante la enfermedad, con el objetivo de diagnosticar el sufrimiento y la angustia, y de brindar atención, comodidad y fortalecimiento de los vínculos espirituales de estos individuos.

RESUMO Objetivo: Compreender a Espiritualidade/Religiosidade vivenciadas por pessoas com doença falciforme e sua influência sobre o enfrentamento da doença. Método: Estudo qualitativo, descritivo, exploratório, realizado no Estado da Bahia. Participaram 29 pessoas que responderam a entrevistas semiestruturadas. O material empírico foi submetido a análise de conteúdo. Resultados: Pessoas com doença falciforme vivenciam a Espiritualidade/Religiosidade motivadas pela esperança de um milagre e por medo da morte; seus ritos são as leituras de textos religiosos, orações individuais e em grupo, e frequência a cultos; os efeitos sobre sua saúde são: conforto através do coping de comparação, alívio da ansiedade, apoio social, mudança no estilo de vida, porém a Espiritualidade/Religiosidade podem manifestar-se prejudicadas. Considerações finais: Este estudo ressalta a necessidade da qualificação dos profissionais de saúde para a abordagem das questões espirituais dessas pessoas adoecidas, com a preocupação de diagnosticar possíveis sofrimentos, angústias e assim prestar auxílio, conforto e fortalecer os vínculos espirituais desses indivíduos.

Procedimentos dolorosos agudos no recém-nascido pré-termo em uma unidade neonatal / Acute painful procedures pain in the preterm newborn in a neonatal unit / Procedimientos dolorosos agudos en el recién nacido pre-término en una unidad neonatal

Objetivo: analisar o número de procedimentos dolorosos agudos e manejo da dor em recém-nascidos pré-termo em uma unidade neonatal. Método: estudo descritivo, transversal. Teve como campo uma unidade neonatal de uma instituição pública de saúde. Os participantes da pesquisa foram recém-nascidos abaixo de 35 semanas. Resultados: foram incluídos 17 recémnascidos. Foi quantificado um total de 729 procedimentos dolorosos. Em média foram realizados 42,9 procedimentos por recém-nascido durante os primeiros 14 dias de vida, sendo aproximadamente três procedimentos realizados por bebê no serviço diurno. Dentre os procedimentos, o mais frequente foi a punção de calcâneo (23,9%). O manejo predominante foi a contenção facilitada (32,7%). A (re)inserção de pronga foi o segundo procedimento mais realizado. Conclusões: O estudo permitiu apreender que o manejo da dor no recém-nascido pré-termo internado em uma unidade neonatal ainda é um desafio

Objective: to analyze the number of acute painful procedures and pain management in preterm infants in a neonatal unit. Method: a cross-sectional and descriptive study. It was conducted in a neonatal unit of a public health institution. The newborns younger than 35 weeks were the participants in the survey. Results: seventeen preterm newborns were included. A total of 729 painful procedures were quantified. On average, 42.9 procedures per newborn were performed during the first 14 days of birth, and approximately three procedures performed per day service by child. The most common procedure was the hell-stick (23.9%). The predominant management was facilitated tucking (32.7%). The CPAP prongs insertion/reinsertion was the second most performed procedure. Conclusions: The present study showed that the management of pain in the preterm newborns in a neonatal unit is strongly neglected by the professionals

Objetivo: analizar el número de procedimientos dolorosos agudos y manejo del dolor en recién nacidos prematuros en una unidad neonatal. Método: estudio descriptivo, transversal. Tuvo como campo una unidad neonatal de una institución pública de salud. Los participantes de la investigación fueron recién nacidos por debajo de 35 semanas. Resultados: se incluyeron 17 recién nacidos. Se cuantificó un total de 729 procedimientos dolorosos. En promedio se realizaron 42,9 procedimientos por recién nacido durante los primeros 14 días de vida, siendo acerca de tres procedimientos realizados por bebé en el servicio diurno. Entre los procedimientos, el más frecuente fue la punción de calcáneo (23,9%). El manejo predominante fue la contención facilitada (32,7%). La (re) inserción de prong fue el segundo procedimiento más realizado. Conclusiones: El estudio permitió aprehender que el manejo del dolor en el recién nacidos prematuros internado en una unidad neonatal se muestra fuertemente descuidado por el equipo.

"Waiting for a miracle": Spirituality/Religiosity in coping with sickle cell disease.

OBJECTIVE: To understand spirituality/religiosity as experienced by people with sickle cell disease, and its influence on coping with the disease. METHOD: A qualitative, descriptive, and exploratory study conducted in the State of Bahia. Twenty-nine respondents participated in semi-structured interviews. Content analysis was used to analyze the empirical material. RESULTS: Individuals with sickle cell disease experience spirituality/religiosity motivated by their hope for a miracle, and fear of death; among their rites are: reading religious materials, individual and group prayer, and attendance at worship services. The effects on their health include: comfort by means of coping by comparing two evils, anxiety relief, social support, and lifestyle changes; however, spirituality/religiosity may be impaired. FINAL CONSIDERATIONS: This study demonstrates the need to qualify health professionals to address spiritual issues of these individuals during illness, with the aims of diagnosing suffering and anguish, and providing care, comfort and strengthening of the spiritual bonds of these individuals.

Implicaciones del dolor crónico en la calidad de vida de mujeres con fibromialgia / Implicações da dor crônica na qualidade de vida das mulheres com fibromialgia / Implications of chronic pain on the quality of life of women with fibromyalgia

RESUMEN. El objetivo de esta investigación fue comprender las implicaciones del dolor crónico en la calidad de vida de un grupo de mujeres diagnosticadas con fibromialgia. Para ello, se realizó un estudio cualitativo de diseño fenomenológico interpretativo en el que participaron 15 mujeres, con edades comprendidas entre los 23 y los 60 años. El análisis de los datos se realizó con el apoyo del programa Atlas.Ti. Los resultados indican que la intensidad de los síntomas, la interferencia del dolor crónico en actividades cotidianas, las alteraciones emocionales y las cogniciones negativas influyeron en su vida personal, familiar, social y laboral. Las estrategias de afrontamiento que asumieron las participantes facilitaron u obstaculizaron la aceptación de la enfermedad. Se concluye que el impacto de la fibromialgia en la calidad de vida depende más de las estrategias de afrontamiento que de los síntomas de la enfermedad. Las redes de apoyo facilitan el desarrollo de estrategias activas para afrontar la enfermedad.

RESUMO. O objetivo desta pesquisa foi compreender as implicações da dor crônica na qualidade de vida de um grupo de mulheres diagnosticadas com fibromialgia. Para isso, se realizou um estudo qualitativo de cunho fenomenológico interpretativo e envolvendo 15 mulheres, com idades compreendidas entre os 23 e os 60 anos. A análise dos dados se realizou com o apoio do programa Atlas.Ti. Os resultados indicam que a intensidade dos sintomas, a interferência da dor crónica em atividades cotidianas, as alterações emocionais e as cognições negativas influentes em sua vida pessoal, familiar, social e laboral. As estratégias de enfrentamento que assinalaram os participantes em matéria de impedir a aceitação da doença. Se conclui que o impacto da fibromialgia na qualidade de vida depende das estratégias de enfrentamento dos sintomas da doença. As facilidades de acesso ao sistema de saúde, a qualidade de atendimento dos especialistas e o acompanhamento de redes de apoio facilitam o desenvolvimento de estratégias ativas para enfrentar a enfermidade.

ABSTRACT. The aim of this research was to understand the impact of chronic pain on the quality of life of a group of women diagnosed with fibromyalgia. For this, a qualitative study of phenomenological interpretative design was carried out in which 15 women, aged between 23 and 60 years participated. Data analysis was performed with the support of the Atlas.Ti program. The results indicate that the intensity of symptoms, the interference of chronic pain in daily activities, the emotional alterations and the negative cognitions influenced his personal, family, social and work life. The coping strategies assumed by the participants facilitated or hampered the acceptance of the disease. It is concluded that the impact of fibromyalgia on quality of life depends more on coping strategies than on the symptoms of the disease. The support networks facilitate the development of active strategies to confront the disease.

Pain and distress outcomes in infants and children: a systematic review.

The aim of the present study was to systematically review the recent literature about pain and distress outcomes in children and critically analyze the methodological quality of the reports. The systematic review was based on the PRISMA statement and performed by selecting articles that are indexed in scientific databases. The methodological quality of reports was examined using STROBE statement, for observational studies, and CONSORT statement, for randomized controlled trials. The PedIMMPACT consensus was used to evaluate the psychometric quality of pain instruments. We analyzed 23 empirical studies, including 14 randomized controlled trials, seven cross-sectional studies, and two studies with cohort designs. Fourteen studies included preschool- and schoolchildren, and nine studies included infants. Regarding studies with infants, pain responses were evaluated by heart rate, crying and behavioral observation scales, and distress was evaluated only by salivary cortisol. Four-handed care and sensorial saturation interventions were used to evaluate efficacy to reduce pain and distress responses. Concerning studies with children, both pain and distress responses were evaluated by self- and hetero-reports, behavioral observation and/or physiological measures. Distraction was effective for reducing pain and distress during burn dressing changes and needle procedures, and healing touch intervention reduced distress and pain in chronic patients. All of the studies scored at least 60% in the methodological quality assessment. The pain outcomes included measures of validity that were classified as well-established by the PedIMMPACT. This systematic review gathers scientific evidence of distress-associated pain in children. Pain and distress were measured as distinct constructs, and their associations were poorly analyzed.

Pain and distress outcomes in infants and children: a systematic review

The aim of the present study was to systematically review the recent literature about pain and distress outcomes in children and critically analyze the methodological quality of the reports. The systematic review was based on the PRISMA statement and performed by selecting articles that are indexed in scientific databases. The methodological quality of reports was examined using STROBE statement, for observational studies, and CONSORT statement, for randomized controlled trials. The PedIMMPACT consensus was used to evaluate the psychometric quality of pain instruments. We analyzed 23 empirical studies, including 14 randomized controlled trials, seven cross-sectional studies, and two studies with cohort designs. Fourteen studies included preschool- and schoolchildren, and nine studies included infants. Regarding studies with infants, pain responses were evaluated by heart rate, crying and behavioral observation scales, and distress was evaluated only by salivary cortisol. Four-handed care and sensorial saturation interventions were used to evaluate efficacy to reduce pain and distress responses. Concerning studies with children, both pain and distress responses were evaluated by self- and hetero-reports, behavioral observation and/or physiological measures. Distraction was effective for reducing pain and distress during burn dressing changes and needle procedures, and healing touch intervention reduced distress and pain in chronic patients. All of the studies scored at least 60% in the methodological quality assessment. The pain outcomes included measures of validity that were classified as well-established by the PedIMMPACT. This systematic review gathers scientific evidence of distress-associated pain in children. Pain and distress were measured as distinct constructs, and their associations were poorly analyzed.

A Qualitative Study on the Practice of Yoga for Women with Pain-Associated Endometriosis.

OBJECTIVES: To understand the meaning women with pain-associated endometriosis attribute to yoga practice regarding their physical and emotional state at the beginning of the practice; pain management by integrating body and mind; secondary benefits of the practice of yoga, such as self-knowledge, self-care, and autonomy; and the role of the yoga group as psychosocial support. DESIGN: Qualitative study conducted simultaneously with a randomized clinical trial. SETTING: Public university hospital in southeastern Brazil between August 2013 and December 2014. PARTICIPANTS: Fifteen women with pain-associated endometriosis who practiced yoga for 8 weeks. INTERVENTION: After completing the twice-a-week program, all women participated in a single, semi-structured interview. Interviews were recorded and transcribed verbatim, and thematic analyses were performed. OUTCOME MEASURES: The main themes of analysis were women's expectations regarding the practice of yoga, physical and emotional state of women at the beginning of yoga practice, control and pain management through the integration of body and mind, secondary benefits, acquisition of self-knowledge and autonomy, and the role of yoga group as psychosocial support. RESULTS: All participants reported that yoga was beneficial to control pelvic pain. They related that they were aware of the integration of body and psyche during yoga practice and that this helped in the management of pain. Women said they had identified a relationship between pain management and breathing techniques (pranayama) learned in yoga and that breathing increased their ability to be introspective, which relieved pain. The participants have developed greater self-knowledge, autonomy, and self-care and have reduced the use of pain and psychiatric medications. They created ties among themselves, suggesting that the yoga group allowed psychosocial support. CONCLUSIONS: Bodily and psychosocial mechanisms to control pain were identified in women with endometriosis. To reach such control, it is crucial that mind and body integrative techniques are learned.

Effects of animal-assisted activity on self-reported feelings of pain in hospitalized children and adolescents

Animal-assisted intervention (AAI) is an approach recently introduced into the hospital environment to improve the quality of hospitalization and provide important benefits for patients with chronic diseases and long-term hospitalizations. This work aims to verify the effects of animal-assisted activity (AAA) on the expression and quality of self-reported pain in hospitalized children and adolescents, while considering the subjects' subjectivity. The participants were 17 hospitalized children/adolescents of both genders, aged 7 years and older, who complained of pain. Two therapy dogs were selected for the intervention according to the criteria of international protocols. The participants were asked an open question ("How would you describe your pain?"). After the question, an AAA session, which lasted between 5 and 10 min, was held with random activities spontaneously chosen by the subject. The open question was asked again at the end of the session, without the presence of the dog. Positive effects were observed in this population with regard to a decrease in self-reported pain. These results suggest that there is a possible symbolic elaboration of pain by the subject, in which the dog might represent acceptance and affection at a moment of great emotional suffering. (AU)

Hipnose em grupo para pessoas com fibromialgia: considerações clínicas / Hypnosis within groups for people with fibromyalgia: clinical considerations

A síndrome dolorosa crônica conhecida como fibromialgia possui etiologia desconhecida e tem tido um número crescente de diagnósticos, desafiando sistemas tradicionais de cuidado. Diante disso, ainda que prevaleça a hegemonia do modelo biomédico, tratamentos que buscam uma compreensão complexa da experiência da dor têm contribuído significativamente para o tratamento dessa população. A hipnose se constitui como uma ferramenta importante para o tratamento da dor e tem sido representada em diversas pesquisas. Entretanto, partindo de uma perspectiva qualitativa, grande parte delas estudam apenas atendimentos individuais, ocasionando uma grande escassez de estudos relativos à hipnose em grupo. Dessa forma, devido a consagrada efetividade de grupos terapêuticos e da hipnose no tratamento da dor, essa pesquisa intenciona analisar o impacto de intervenções hipnóticas em grupos terapêuticos nas configurações subjetivas da dor vivida por pessoas com fibromialgia. Por conceber a dor como uma experiência subjetiva, foi utilizada a metodologia construtiva-interpretativa, com base da Epistemologia Qualitativa de González Rey, a fim de desenvolver a compreensão dessas configurações subjetivas. Foram realizados dois grupos, cada um com doze encontros no CAEP (UnB), nos quais foram utilizadas temáticas baseadas na metodologia de hipnose ericksoniana chamada "Grupo de Crescimento" de Tereza Robles. Nos casos estudados, diversos elementos relacionados a processos subjetivos relativos às dores das participantes denunciaram a complexidade dessas experiências. A vivência da hipnose e das trocas no contexto do grupo, impactaram em alguns desses elementos, indicando reconfigurações subjetivas relativas à autonomia, a experiências traumáticas e aos modos de relação dos sujeitos. A vivência do transe proporciona alterações de referências que se apresentaram de forma específica no contexto de grupo. A construção e interpretação dos indicadores propiciaram reflexões que demonstraram a importância de reconhecer a dor como uma experiência subjetiva, da hipnose em grupo como uma ferramenta importante para pessoas com fibromialgia, além de outras questões sociais e clínicas.(AU)

The chronic pain syndrome known as fibromyalgia has an unknown etiology and has an increasing number of diagnoses, challenging traditional care systems. Therefore, although the prevalence of the biomedical model, treatments that seek a complex understanding of the pain experience have contributed significantly to treating cases of this disease. Hypnosis is an important tool for the treatment of pain as has been shown in several studies. However, from a qualitative perspective, most of them approached only sessions conducted individually, which explain the severe shortage of studies on the use of hypnosis within groups. Thus, due to the effectiveness of therapeutic groups and hypnosis itself in the treatment of pain, this research analyses the impact of hypnotic interventions in therapeutic groups in the subjective configuration of pain experienced by people with fibromyalgia. Acknowledging pain as a subjective experience, this research adopts a constructive-interpretative methodology supported by the principles of the Qualitative Epistemology by González Rey, in order to develop an understanding of these subjective configurations. Two separate groups were conducted, each with twelve meetings in CAEP (UNB), in which were adopted themes based on Ericksonian hypnosis methodology called "Growth Group" by Theresa Robles. In the cases analyzed, several elements related to subjective processes related to pain felt by the participants indicated the complexity of these experiences. The hypnotic experience, as well as the sharing of experiences within the groups, affected some of these elements, pointing to subjective reconfigurations related to autonomy, traumatic experiences and the subject's relations. The trance provides reference shifts which were detected specifically in the group context. The development and interpretation of these indicators have led to reflections that demonstrated the importance of recognizing pain as a subjective experience, group hypnosis as an important tool for people with fibromyalgia, besides other social and clinical issues.(AU)

Prevalence of suicidal ideation in patients with chronic non-cancer pain referred to a behaviorally based pain program.

BACKGROUND: Patients with chronic pain often experience co-occurring depression and in some cases suicidal ideation. It is critical to discover risk factors for suicide in this vulnerable patient population. OBJECTIVE: To assess the prevalence of suicidal ideation and identify potential risk factors in patients with chronic non-cancer pain. STUDY DESIGN: Retrospective chart review. SETTING: Four hundred and sixty-six patients with chronic non-cancer pain referred to a behaviorally based pain program in a community health system. METHODS: Data collected included pain intensity and level of pain interference (Brief Pain Inventory), pain duration, pain site, depression level (Beck Depression Inventory Fast Screen for Medical Patients), anxiety (Beck Anxiety Inventory), personal and family psychiatric and substance use disorder history, level of isolation, and demographic data. Univariate and logistic regression analyses were performed. RESULTS: Results showed a high rate of suicidal ideation in this patient population (28%). Univariate analyses stratified by level of suicide (no suicidal ideation or passive/active suicidal ideation) revealed statistically significant group differences on pain location (extremity P = 0.046, generalized P = 0.047), work disruption (P = 0.049), social withdrawal (P < 0.001), pre-pain history of depression (P < 0.001), family history of depression (P < 0.001), and history of sexual/physical abuse (P < 0.001). Logistic regression revealed that history of sexual/physical abuse (Beta = 0.825; P = 0.020; OR = 2.657 [95% CI = 1.447 - 4.877]), family history of depression (Beta = 0.471; P = 0.006; OR = 1.985 [95% CI = 1.234 - 3.070]), and being socially withdrawn (Beta = 0.482; P < 0.001; OR = 2.226 [95% CI = 1.431 - 3.505]) were predictive of suicidal ideation. LIMITATIONS: Measure of depression was not included in data analysis to reduce effect of co-linearity. Also the study population was a specialty pain clinic allowing for possible subject selection bias. CONCLUSIONS: Results of this study are consistent with the prevailing literature on pain and suicide demonstrating a high prevalence of suicidal ideation in the chronic pain population. Novel predictive variables were also identified that will provide the basis for developing a risk stratification model that can be further tested prospectively in chronic pain patients.

Psychosocial and pharmacological management of pain in pediatric sickle cell disease.

For children with sickle cell disease (SCD), pain is associated with significant current and future morbidity and mortality. Unfortunately, few evidence-based guidelines exist for the management of pain episodes in children with SCD. To inform empirically based treatment strategies for pain management in pediatric SCD, this review integrates and evaluates the extant literature on psychosocial and pharmacological approaches to the management of pain. Findings reveal a paucity of rigorous investigations of psychosocial and pharmacological pain management interventions in children with SCD. Psychosocial interventions included were primarily cognitive-behavioral in nature, whereas pharmacological approaches targeted non-opioid analgesics (ie, nonsteroidal anti-inflammatory drugs and corticosteroids) and opioid medications (ie, morphine and oxycodone). However, to date there is not a "gold standard" for pain management among children with SCD. Because psychosocial and physiological processes each play a role in the etiology and experience of pain, effective pain management requires multidimensional, comprehensive treatment approaches. Considering the significant impact of pain on functional outcomes and quality of life among children with SCD, additional clinical trials are warranted to ensure that interventions are safe and efficacious.

Treatment expectations among adolescents with chronic musculoskeletal pain and their parents before an initial pain clinic evaluation.

OBJECTIVES: To understand expectations regarding treatment recommendations among treatment-seeking adolescents with chronic musculoskeletal pain and their parents. METHODS: A total of 102 adolescent-parent dyads were recruited at the time of initial contact with a multidisciplinary pain management clinic. Each participant completed reports of adolescent pain intensity and disability, biopsychosocial perspective of pain, and treatment expectations related to recommendations and feedback for a vignette description of an adolescent presenting at an initial multidisciplinary pain clinic evaluation. RESULTS: Descriptive findings for individual treatment expectations and adolescent-parent dyad agreement statistics were examined. Slight to fair levels of agreement occurred for 50% of the expectations assessed. The strongest shared expectations were for recommendations to return to school, pursue psychological counseling, and pursue PT/OT treatment. Stronger agreement occurred for items reflecting alternative, emotional, behavioral, and activity recommendations with weaker agreement for medical interventions (eg, medication and surgery). Correlations emerged between individual expectations and adolescent pain intensity, disability, with the greatest number of significant relationships found for adolescent and parent expectations and biopsychosocial perspectives of pain. DISCUSSION: Our results document that adolescents and parents show modest levels of agreement on expectations for treatment at the time of an initial pain clinic evaluation. This may relate to expectations being internal perspectives not clearly expressed within families; thus, the initial treatment consultation may provide an important opportunity to create and align appropriate expectations. Implications of our findings are considered with respect to education, treatment, and future research to understand factors that contribute to treatment adherence and outcomes.

Pain beliefs and readiness to change among adolescents with chronic musculoskeletal pain and their parents before an initial pain clinic evaluation.

OBJECTIVES: To understand relationships between pain-related beliefs and readiness to change among treatment-seeking adolescents with chronic musculoskeletal pain and their parents. METHODS: A total of 102 adolescent-parent dyads were recruited at the time of initial evaluation at a multidisciplinary pain management clinic. Dyads completed self-report measures to assess pain, catastrophizing, endorsement of a biopsychosocial perspective of pain, and readiness to change/motivation to adopt a self-management approach to pain coping. RESULTS: Agreement between adolescent-parent dyad reports of pain catastrophizing and readiness to change was found; however, adolescents were less likely to view pain as "affected by feelings and emotions" than parents. The hypothesis that greater pain catastrophizing would be correlated with less readiness to change was partially supported. Adolescent and parents who reported lower levels of endorsement of a biopsychosocial perspective were less willing to adopt a self-management approach to pain coping. Endorsement of a biopsychosocial perspective of pain aligned with readiness to change stages more consistently for parents. DISCUSSION: This study documents initial relationships among pain catastrophizing, biopsychosocial perspectives of pain, and readiness to engage in a self-management approach to pain coping for adolescents with chronic pain and their parents. Although agreement exists between dyads regarding catastrophizing and readiness to change, differences were noted in biopsychosocial perspective and dominant readiness to change stage before an initial pain clinic encounter. Findings are considered in terms of future research to advance knowledge regarding the role these factors may play in treatment adherence and outcomes.