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[PMID]:28830215
[Au] Autor:Liu Y; Tang WPY; Gong S; Chan CWH
[Ad] Endereço:* The Nethersole School of Nursing, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N. T., Hong Kong SAR.
[Ti] Título:A Systematic Review and Meta-Analysis of Acupressure for Postoperative Gastrointestinal Symptoms among Abdominal Surgery Patients.
[So] Source:Am J Chin Med;45(6):1127-1145, 2017.
[Is] ISSN:0192-415X
[Cp] País de publicação:Singapore
[La] Idioma:eng
[Ab] Resumo:Postoperative ileus is a common and often life-threatening gastrointestinal complication with few management methods available for patients. Integrating acupressure into perioperative care promises to bring benefits into preventing postoperative ileus. This systematic review and meta-analysis aims to evaluate the efficacy of acupressure in identifying the signs and symptoms of postoperative ileus among patients undergoing abdominal surgery. The MEDLINE, EMBASE, Web of Science, CINAHL, China Journal Net and Wanfang databases were searched for high-quality RCTs using keywords such as acupressure, postoperative ileus, abdominal surgery, etc. A total of six studies ([Formula: see text]) were included in this review and meta-analysis. The quality of the literature was found to be uniformly moderate by the Effective Public Health Practice Project (EPHPP) assessment tool. The results of meta-analyses revealed that acupressure could significantly reduce risks for postoperative nausea (OR 0.52, 95% CI 0.39-0.70, [Formula: see text]) and vomiting (OR 0.54, 95% CI 0.39-0.75, [Formula: see text]) compared with the control group, without significant heterogeneity among studies. Meta-analysis of the need for antiemetic drugs suggested that the OR was 0.39 (95% CI 0.20-0.78, [Formula: see text]) with significant heterogeneity among studies. Our results suggested that acupressure might be effective in reducing the incidence of postoperative nausea and vomiting and the need for antiemetic drugs among patients undergoing abdominal surgery. Considering the substantial risk of bias in the articles included, future high-quality RCTs with a rigorous methodology are desirable to provide solid evidence. Furthermore, other signs and symptoms of postoperative ileus should be explored in future.
[Mh] Termos MeSH primário: Abdome/cirurgia
Acupressão
Íleus/prevenção & controle
Complicações Pós-Operatórias/prevenção & controle
Náusea e Vômito Pós-Operatório/prevenção & controle
[Mh] Termos MeSH secundário: Bases de Dados Bibliográficas
Seres Humanos
Ensaios Clínicos Controlados Aleatórios como Assunto
[Pt] Tipo de publicação:JOURNAL ARTICLE; META-ANALYSIS; REVIEW
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171005
[Lr] Data última revisão:
171005
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170824
[St] Status:MEDLINE
[do] DOI:10.1142/S0192415X17500616


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[PMID]:28816951
[Au] Autor:Zhang B; Dong JN; Sun P; Feng C; Liu YC
[Ad] Endereço:aDepartment of Oncology, The Affiliated Hongqi Hospital of Mudanjiang Medical University bDepartment of Rehabilitation Comprehensive Laboratory cDepartment of Anatomy, Mudanjiang Medical University dDepartment of Ultrasound, The Affiliated Hongqi Hospital of Mudanjiang Medical University, Mudanjiang, China.
[Ti] Título:Effect of therapeutic care for treating fatigue in patients with breast cancer receiving chemotherapy.
[So] Source:Medicine (Baltimore);96(33):e7750, 2017 Aug.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: This study aimed to evaluate the effect of therapeutic care (TC) for fatigue in breast cancer patients receiving chemotherapy. METHODS: A total of 48 breast cancer patients receiving chemotherapy were randomly divided into the intervention group and the control group, with 24 patients in each group. The patients in the intervention group were treated with TC, while the participants in the control group received the sham intervention. The interventions in both groups were for 30 min/d, 3 days weekly for 12 weeks. The primary outcome of fatigue was measured by the multidimensional fatigue inventory (MFI). The secondary outcomes were measured by the Hospital Anxiety and Depression Scale (HADS) and Pittsburgh Sleep Quality Index (PSQI). All outcomes were assessed before and after 6 and 12 weeks of the intervention. RESULTS: The intervention with TC showed greater efficacy than sham TC in decreasing the MFI score after week 6 (P < .05) and week 12 (P < .01) of treatment. Significant differences were also found in the HADS and PSQI between the 2 groups after 12 weeks of treatment (P < .01). CONCLUSION: This study demonstrated that TC might decrease fatigue and relieve the anxiety and depression of breast cancer patients receiving chemotherapy.
[Mh] Termos MeSH primário: Acupressão/métodos
Antineoplásicos/efeitos adversos
Neoplasias da Mama/tratamento farmacológico
Fadiga/etiologia
Fadiga/terapia
[Mh] Termos MeSH secundário: Adulto
Antineoplásicos/uso terapêutico
Ansiedade/psicologia
Neoplasias da Mama/psicologia
Depressão/psicologia
Método Duplo-Cego
Feminino
Seres Humanos
Meia-Idade
Sono/fisiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; RANDOMIZED CONTROLLED TRIAL
[Nm] Nome de substância:
0 (Antineoplastic Agents)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170908
[Lr] Data última revisão:
170908
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170818
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000007750


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[PMID]:28714769
[Au] Autor:Jung GS; Choi IR; Kang HY; Choi EY
[Ad] Endereço:1 Department of Nursing, Hanlyo University , Gwangyang-si, Republic of Korea.
[Ti] Título:Effects of Meridian Acupressure Massage on Body Composition, Edema, Stress, and Fatigue in Postpartum Women.
[So] Source:J Altern Complement Med;23(10):787-793, 2017 Oct.
[Is] ISSN:1557-7708
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: This study aims to investigate the effects of meridian acupressure massage on body composition, edema, stress, and fatigue in postpartum women. DESIGN: A quasi-experimental design with a nonequivalent control group was utilized. SETTINGS/LOCATION: The Postpartum Care Center of Women's Hospital in Gwangju City, Republic of Korea. SUBJECTS: The study group consisted of 39 postpartum women, 19 in the experimental group and 20 in the control group, recruited from the postpartum care center of Women's Hospital in Gwangju city, South Korea. INTERVENTIONS: The experimental group was provided with meridian acupressure massage for 90 min daily over 5 days as an experimental therapy. OUTCOME MEASURES: Body composition (body weight, BMI, total body water, ECW ratio, LBM, and body fat) Edema (subjective edema, average girth of the upper limbs, and average girth of the lower limbs), Stress (psychological stress and physical stress), and Fatigue. RESULTS: The experimental group demonstrated a significantly larger decrease compared with the control group in measures of body composition, edema, total subjective stress, psychological stress, and subjective fatigue. CONCLUSIONS: Meridian acupressure massage can hasten the return to original body composition after childbirth.
[Mh] Termos MeSH primário: Acupressão
Composição Corporal/fisiologia
Edema/terapia
Fadiga/terapia
Massagem
Período Pós-Parto/fisiologia
[Mh] Termos MeSH secundário: Adulto
Peso Corporal
Feminino
Seres Humanos
Meridianos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171113
[Lr] Data última revisão:
171113
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170718
[St] Status:MEDLINE
[do] DOI:10.1089/acm.2016.0362


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[PMID]:28682918
[Au] Autor:Xu JH; Mi HY
[Ad] Endereço:Department of Neurology, Beijing ChaoYang Hospital, Capital Medical University, Beijing, China.
[Ti] Título:A randomized controlled trial of acupressure as an adjunctive therapy to sodium valproate on the prevention of chronic migraine with aura.
[So] Source:Medicine (Baltimore);96(27):e7477, 2017 Jul.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: The primary objective of the present study was to evaluate the efficacy and safety of using acupressure as an adjunctive therapy to sodium valproate (SV) combined with acupressure (ASV) on the prevention of chronic migraine with aura (CMA). METHODS: A total of 98 patients with CMA were randomly divided into an intervention group and a control group, with 49 patients in each group. The patients in the intervention group received ASV, while the participants in the control group received SV alone. The primary outcome was measured by the numeric rating scale (NRS). The secondary outcomes including frequency of migraine attacks, the times of using analgesics, and quality of life, measured by the short-form 36 Health Survey Scale (SF-36) score. In addition, adverse events (AEs) were also recorded throughout the trial. The outcomes were measured at the end of the 8-week treatment, and 4-week follow-up. RESULTS: After the 8-week treatment and 4-week follow-up, ASV efficacy was not greater than that of SV alone regarding pain relief, as measured using the NRS, and frequency of migraine attacks, consumption of analgesics, and quality of life, as measured using the SF-36. However, ASV can significantly reduce the nausea when compared with SV (P = .04). CONCLUSION: The present results indicate that ASV can decrease migraine-related nausea during treatment, but cannot relieve pain or enhance quality of life in patients with CMA.
[Mh] Termos MeSH primário: Acupressão
Fármacos do Sistema Nervoso Central/uso terapêutico
Enxaqueca com Aura/terapia
Ácido Valproico/uso terapêutico
[Mh] Termos MeSH secundário: Adulto
Analgésicos/uso terapêutico
Terapia Combinada
Feminino
Seguimentos
Seres Humanos
Masculino
Medição da Dor
Qualidade de Vida
Resultado do Tratamento
[Pt] Tipo de publicação:JOURNAL ARTICLE; RANDOMIZED CONTROLLED TRIAL
[Nm] Nome de substância:
0 (Analgesics); 0 (Central Nervous System Agents); 614OI1Z5WI (Valproic Acid)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170724
[Lr] Data última revisão:
170724
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170707
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000007477


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[PMID]:28653963
[Au] Autor:Macznik AK; Schneiders AG; Athens J; Sullivan SJ
[Ad] Endereço:*Centre for Health, Activity, and Rehabilitation Research, School of Physiotherapy, University of Otago, Dunedin, New Zealand;†School of Human, Health and Social Sciences, Central Queensland University, Bundaberg, Australia; and‡Department of Preventive and Social Medicine, University of Otago, Dunedin, New Zealand.
[Ti] Título:Does Acupressure Hit the Mark? A Three-Arm Randomized Placebo-Controlled Trial of Acupressure for Pain and Anxiety Relief in Athletes With Acute Musculoskeletal Sports Injuries.
[So] Source:Clin J Sport Med;27(4):338-343, 2017 Jul.
[Is] ISSN:1536-3724
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: Injuries are a common consequence of sports and recreational activity. The optimal management of symptoms is a crucial element of sports injury management. Acupressure has previously been shown to effectively decrease symptoms of musculoskeletal injury, thus may be considered a potentially useful intervention in the management of sport-related injuries. Therefore, this study was conducted to examine the effectiveness of acupressure in decreasing pain and anxiety in acutely injured athletes. DESIGN: A prospective 3-arm randomized placebo-controlled trial. SETTING: A sports injury clinic, Dunedin, New Zealand. PATIENTS: Seventy-nine athletes who sustained a sport-related musculoskeletal injury on the day. INTERVENTION: Three minutes of either acupressure, sham acupressure, or no acupressure. MAIN OUTCOME MEASURES: The primary outcomes of pain and anxiety intensity were measured before and immediately after the intervention on a 100-mm visual analog scale (VAS). Pain and anxiety relief, satisfaction with treatment, willingness to repeat a similar treatment, and belief in the effect of acupressure were secondary outcomes measured on Likert scales after the intervention. RESULTS: The acupressure group reported 11 mm less pain (95% CI: 5-17) on average than the sham acupressure group, and 9 mm less (95% CI: 3-16) than the control group as a result of the intervention (P < 0.05). There was no difference between groups in: anxiety levels, or in any of the secondary outcome measures. CONCLUSIONS: Three minutes of acupressure was effective in decreasing pain intensity in athletes who sustained an acute musculoskeletal sports injury when measured on the VAS, but did not change anxiety levels.
[Mh] Termos MeSH primário: Acupressão
Ansiedade/terapia
Traumatismos em Atletas/terapia
Manejo da Dor/métodos
[Mh] Termos MeSH secundário: Adolescente
Adulto
Atletas
Feminino
Seres Humanos
Masculino
Nova Zelândia
Medição da Dor
Estudos Prospectivos
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE; RANDOMIZED CONTROLLED TRIAL
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171030
[Lr] Data última revisão:
171030
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170628
[St] Status:MEDLINE
[do] DOI:10.1097/JSM.0000000000000378


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[PMID]:28504569
[Au] Autor:Kao YH; Huang YC; Chung UL; Hsu WN; Tang YT; Liao YH
[Ad] Endereço:1 Graduate Institute of Health Allied Education, National Taipei University of Nursing and Health Sciences , Taipei City, Taiwan .
[Ti] Título:Comparisons for Effectiveness of Aromatherapy and Acupressure Massage on Quality of Life in Career Women: A Randomized Controlled Trial.
[So] Source:J Altern Complement Med;23(6):451-460, 2017 Jun.
[Is] ISSN:1557-7708
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: This study was aimed to compare the effectiveness of aromatherapy and acupressure massage intervention strategies on the sleep quality and quality of life (QOL) in career women. DESIGN: The randomized controlled trial experimental design was used in the present study. One hundred and thirty-two career women (24-55 years) voluntarily participated in this study and they were randomly assigned to (1) placebo (distilled water), (2) lavender essential oil (Lavandula angustifolia), (3) blended essential oil (1:1:1 ratio of L. angustifolia, Salvia sclarea, and Origanum majorana), and (4) acupressure massage groups for a 4-week treatment. The Pittsburgh Sleep Quality Index and Short Form 36 Health Survey were used to evaluate the intervention effects at pre- and postintervention. RESULTS: After a 4-week treatment, all experimental groups (blended essential oil, lavender essential oil, and acupressure massage) showed significant improvements in sleep quality and QOL (p < 0.05). Significantly greater improvement in QOL was observed in the participants with blended essential oil treatment compared with those with lavender essential oil (p < 0.05), and a significantly greater improvement in sleep quality was observed in the acupressure massage and blended essential oil groups compared with the lavender essential oil group (p < 0.05). CONCLUSIONS: The blended essential oil exhibited greater dual benefits on improving both QOL and sleep quality compared with the interventions of lavender essential oil and acupressure massage in career women. These results suggest that aromatherapy and acupressure massage improve the sleep and QOL and may serve as the optimal means for career women to improve their sleep and QOL.
[Mh] Termos MeSH primário: Acupressão
Aromaterapia
Transtornos do Sono-Vigília/terapia
Mulheres Trabalhadoras
[Mh] Termos MeSH secundário: Adulto
Feminino
Seres Humanos
Meia-Idade
Qualidade de Vida
Sono/fisiologia
Inquéritos e Questionários
Mulheres Trabalhadoras/psicologia
Mulheres Trabalhadoras/estatística & dados numéricos
[Pt] Tipo de publicação:JOURNAL ARTICLE; RANDOMIZED CONTROLLED TRIAL
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170626
[Lr] Data última revisão:
170626
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170516
[St] Status:MEDLINE
[do] DOI:10.1089/acm.2016.0403


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[PMID]:28438274
[Au] Autor:Yeganeh M; Baradaran HR; Qorbani M; Moradi Y; Dastgiri S
[Ad] Endereço:Department of Epidemiology, Tabriz University of Medical Sciences, Tabriz, Iran.
[Ti] Título:The effectiveness of acupuncture, acupressure and chiropractic interventions on treatment of chronic nonspecific low back pain in Iran: A systematic review and meta-analysis.
[So] Source:Complement Ther Clin Pract;27:11-18, 2017 May.
[Is] ISSN:1873-6947
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Low back pain (LBP) is one of the most common health problems in adults. The impact of LBP on the individual can cause loss of health status and function related to pain in the back. To reduce the impact of LBP on adults, drug therapy is the most frequently recommended intervention. But over the last decade, a substantial number of randomized clinical trials of non-pharmacological intervention for LBP have been published. OBJECTIVE: To determine the effectiveness of acupuncture, acupressure and chiropractic (non-pharmacological) interventions on the treatment of chronic nonspecific low back pain in Iran. STUDY DESIGN: Systematic review and meta-analysis. METHODS: A systematic literature search was completed without date restrictions up to May 2013 in five major databases (Medline, CINAHL, Science Direct, CAJ Full-text Database, and Cochrane databases). Only randomized controlled trials published in Persian (Farsi) or English languages were included. Two independent reviewers extracted the data. The quality of the papers was assessed using the Cochrane Back Review Risk of Bias criteria. RESULTS: Initial searches revealed 415 papers, 382 of which were excluded on the basis of abstract alone. After excluding 23 papers due to duplication, the remaining 10 trial papers were subjected to a more detailed analysis of the full text, which resulted in three being excluded. The seven remaining trials had a lack of methodological and clinical homogeneity, precluding a meta-analysis. The trials used different comparators with regards to the primary outcomes, the number of treatments, the duration of treatment and the duration of follow-up. CONCLUSION: This systematic review demonstrates that acupuncture, acupressure and chiropractic may have a favorable effect on self-reported pain and functional limitations on NSCLBP. However, the results should be interpreted in the context of the limitations identified, particularly in relation to the heterogeneity in the study characteristics and the low methodological quality in many of the included studies.
[Mh] Termos MeSH primário: Acupressão
Terapia por Acupuntura
Dor Crônica/terapia
Dor Lombar/terapia
Manipulação Quiroprática
[Mh] Termos MeSH secundário: Adolescente
Adulto
Feminino
Seres Humanos
Irã (Geográfico)
Masculino
Meia-Idade
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE; META-ANALYSIS; REVIEW
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170626
[Lr] Data última revisão:
170626
[Sb] Subgrupo de revista:N
[Da] Data de entrada para processamento:170426
[St] Status:MEDLINE


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[PMID]:28434473
[Au] Autor:Bazarganipour F; Taghavi SA; Allan H; Beheshti F; Khalili A; Miri F; Rezaei M; Mojgori M; Imaninasab F; Irani F; Salari S
[Ad] Endereço:Hormozgan Fertility & Infertility Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
[Ti] Título:The effect of applying pressure to the LIV3 and LI4 on the symptoms of premenstrual syndrome: A randomized clinical trial.
[So] Source:Complement Ther Med;31:65-70, 2017 Apr.
[Is] ISSN:1873-6963
[Cp] País de publicação:Scotland
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: To evaluate the effect of simple acupressure protocol in LIV3, LI4 and placebo points on the quality of life (QOL) in women with premenstrual syndrome (PMS). METHOD: This paper reports a randomized, single blinded clinical trial. 97 participants (students in of Hormozgan University of Medical Sciences, Iran) with PMS were allocated to three groups to receive 20min acupressure on different acupoints for 14days before menstruation for three consecutive menstrual cycles (training and then two cycles self applied acupressure). The acupoints were LIV3 and LI4; one group received acupressure at a placebo point. Each participant completed the PSST scale (to determine PMS severity), HADS scale (for depression and anxiety), and quality of life SF12. RESULTS: The number of people with moderate/severe PMS decreased in LIV3 and LI4 acupressure groups by the second and third cycles compared with the placebo group (p<0.04). Moreover, depression and anxiety scores significantly decreased in the LIV3 and LI4 groups by the second and third cycles compared with the placebo group (p<0.05).Analyzing the score of SF12 fields in the second and third cycles showed a significant difference in all dimensions between the intervention and placebo groups. There was no significant difference between LIV3 and LI4 acupressure groups in decrease of PMS symptoms, anxiety and depression and improving SF12scores (p<0.05). CONCLUSION: Performing the simple acupressure protocol at LIV3 and LI4 is an effective method to decrease the severity of PMS symptoms, anxiety and depression, and to improve the QOL. Pressure at LIV3 and LI4 appears to be equally effective.
[Mh] Termos MeSH primário: Acupressão
Pontos de Acupuntura
Síndrome Pré-Menstrual/terapia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Ansiedade/terapia
Depressão/terapia
Feminino
Seres Humanos
Irã (Geográfico)
Meia-Idade
Qualidade de Vida
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE; RANDOMIZED CONTROLLED TRIAL
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170626
[Lr] Data última revisão:
170626
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170425
[St] Status:MEDLINE


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[PMID]:28418209
[Au] Autor:Adlan AS; Chooi KY; Mat Adenan NA
[Ad] Endereço:Department of Obstetrics and Gynaecology, Faculty of Medicine, University Malaya Medical Centre, Kuala Lumpur, Malaysia.
[Ti] Título:Acupressure as adjuvant treatment for the inpatient management of nausea and vomiting in early pregnancy: A double-blind randomized controlled trial.
[So] Source:J Obstet Gynaecol Res;43(4):662-668, 2017 Apr.
[Is] ISSN:1447-0756
[Cp] País de publicação:Australia
[La] Idioma:eng
[Ab] Resumo:AIM: To evaluate the efficacy of acupressure at the Neiguan point (Pericardium [P]6) as adjuvant treatment during inpatient management of severe nausea and vomiting in pregnancy. METHODS: Low risk, spontaneously conceived singleton pregnancies were randomly assigned to a treatment group, who received an acupressure band placed at the Neiguan point (P6) or a placebo group who received an otherwise identical non-stimulating wristband. Participants wore the band for 12 h daily for the first three days of admission. The primary outcome measure was the severity of symptoms of nausea, vomiting and retching, recorded according to Pregnancy-Unique Quantification of Emesis and Nausea score. RESULTS: There was a statistically significant improvement in Pregnancy-Unique Quantification of Emesis and Nausea scores from day 1 until day 3 of admission in the treatment group compared with the placebo. Patients who received Neiguan point acupressure also showed a significant improvement in their ketonuria scores. The treatment group required a shorter hospital stay compared with the placebo. The only reported side effect of the acupressure band was redness on the wrist. CONCLUSIONS: The use of the acupressure band at the Neiguan point (P6) for 12 h daily for three days for inpatients with hyperemesis gravidarum significantly reduced the symptoms of nausea, vomiting and retching and ketonuria and led to a reduction in hospital stay. We recommend the use of the acupressure band at the Neiguan point (P6) as an adjunct/supplementary therapy to co-exist with the standard care of management for hyperemesis gravidarum, particularly in low-risk pregnant women.
[Mh] Termos MeSH primário: Acupressão/métodos
Êmese Gravídica/terapia
Avaliação de Processos e Resultados (Cuidados de Saúde)
[Mh] Termos MeSH secundário: Acupressão/instrumentação
Adulto
Método Duplo-Cego
Feminino
Seres Humanos
Gravidez
[Pt] Tipo de publicação:JOURNAL ARTICLE; RANDOMIZED CONTROLLED TRIAL
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170807
[Lr] Data última revisão:
170807
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170419
[St] Status:MEDLINE
[do] DOI:10.1111/jog.13269


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[PMID]:28406870
[Au] Autor:Hamlaci Y; Yazici S
[Ad] Endereço:Faculty of Health Science, Eskisehir Osmangazi University, Eskisehir, Turkey (Ms Hamlaci); and Faculty of Health Science, Istanbul University (Dr Yazici), Istanbul, Turkey.
[Ti] Título:The Effect of Acupressure Applied to Point LI4 on Perceived Labor Pains.
[So] Source:Holist Nurs Pract;31(3):167-176, 2017 May/Jun.
[Is] ISSN:1550-5138
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Controlling labor pain is one of the basic goals for caregivers during the birthing process. There are many pharmacological and nonpharmacological methods that are used for controlling pain and helping the mother to cope with pain and have a favorable labor. The study was planned as a randomized, controlled experimental study to detect the effect of acupressure applied to Point LI4 on perceived labor pains. The study sample comprised 88 pregnant women (44 acupressure group, 44 control group), who complied with the study guidelines, agreed with the conditions of the study, and signed the informed consent. Acupressure was applied to the study group when cervical dilatation reached 4 to 5 cm and again when cervical dilation was 7 to 8 cm. Acupressure was applied to Point LI4 on both the hands at the same time from the beginning to the end of the contraction (16 times). Evaluation with the visual analog scale was made 6 times: when the pregnant woman was first admitted to the hospital, before and after acupressure, and within 2 hours after delivery. The control group received routine care. There were statistically significant differences between the groups in subjective labor pain scores (P < .0001). There was a significant difference between the groups in terms of total duration of labor. As shown from our study, applying acupressure to Point LI4 was found to be effective in decreasing the perception of labor pains and shortening the labor (P < .05). Mothers were pleased with this treatment, but they found it insufficient to control their pain.
[Mh] Termos MeSH primário: Acupressão/normas
Dor do Parto/terapia
Manejo da Dor/métodos
Parto/psicologia
Complicações na Gravidez/terapia
[Mh] Termos MeSH secundário: Acupressão/métodos
Pontos de Acupuntura
Adolescente
Adulto
Terapias Complementares/normas
Feminino
Seres Humanos
Dor do Parto/enfermagem
Manejo da Dor/normas
Percepção
Gravidez
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170918
[Lr] Data última revisão:
170918
[Sb] Subgrupo de revista:N
[Da] Data de entrada para processamento:170414
[St] Status:MEDLINE
[do] DOI:10.1097/HNP.0000000000000205



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