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1.
BMJ Open Qual ; 9(2)2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-32327423

RESUMO

INTRODUCTION: The UK Department of Health have targeted a reduction in stillbirth by 50% by 2025; to achieve this, the first version of the Saving Babies' Lives Care Bundle (SBLCB) was developed by NHS England in 2016 to improve four key areas of antenatal and intrapartum care. Clinical practice guidelines are a key means by which quality improvement initiatives are disseminated to front-line staff. METHODS: Seventy-five clinical practice guidelines covering the four areas of antenatal and intrapartum care in the first version of SBLCB were obtained from 19 maternity providers. The content and quality of guidelines were evaluated using the Appraisal of Guidelines for Research and Evaluation (AGREE II) tool. Maternity health professionals in participating organisations were invited to participate in an anonymous survey to determine perceptions toward and experiences of the use of clinical practice guidelines using a series of Likert scales. RESULTS: Unit guidelines showed considerable variation in quality with median scores of 50%-58%. Only 4 (5.6%) guidelines were recommended for use in clinical practice without modifications, 54 (75.0%) were recommended for use subject to modifications and 12 (16.7%) were not recommended for use. The lowest scoring domains were 'rigour of development', 'stakeholder involvement' and 'applicability'. A significant minority of unit guidelines omitted recommendations from national guidelines. The majority of staff believed that clinical practice guidelines standardised and improved the quality of care but over 30% had insufficient time to use them and 24% stated they were unable to implement recommendations. CONCLUSION: To successfully implement initiatives such as the SBLCB change is needed to local clinical practice guidelines to reduce variation in quality and to ensure they are consistent with national recommendations . In addition, to improve clinical practice, adequate time and resources need to be in place to deliver and evaluate care recommended in the SBLCB.


Assuntos
Serviços de Saúde Materna/normas , Pacotes de Assistência ao Paciente/instrumentação , Qualidade da Assistência à Saúde/normas , Natimorto/psicologia , Adulto , Inglaterra/epidemiologia , Feminino , Hospitais/estatística & dados numéricos , Humanos , Serviços de Saúde Materna/estatística & dados numéricos , Pacotes de Assistência ao Paciente/normas , Pacotes de Assistência ao Paciente/estatística & dados numéricos , Gravidez , Melhoria de Qualidade , Qualidade da Assistência à Saúde/estatística & dados numéricos , Natimorto/epidemiologia , Inquéritos e Questionários
2.
Am J Reprod Immunol ; 73(1): 36-55, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25283845

RESUMO

PROBLEM: Inflammation is a driver of labor in myometrium and cervix; however, the involvement of decidua is poorly defined. We have reported decidual leukocyte infiltration prior to and during labor; the regulators of these inflammatory processes are unknown. METHOD OF STUDY: Choriodecidua RNA obtained after term labor or elective cesarean delivery was applied to Affymetrix GeneChips. Pathway analysis and gene validation were performed. RESULTS: Extensive inflammatory activation was identified in choriodecidua following labor, predominantly upregulation of genes regulating leukocyte trafficking and cytokine signalling. Genes governing cell fate, tissue remodelling, and translation were also altered. Upregulation of candidate genes (ICAM1, CXCR4, CD44, TLR4, SOCS3, BCL2A, and IDO) was confirmed. NFκB, STAT1&3, HMGB1, and miRNA-21, miRNA-46, miRNA-141, and miRNA-200 were predicted upstream regulators. CONCLUSION: This study confirms inflammatory processes are major players in labor events in choriodecidua, as in other gestational tissues. Suppressing uterine inflammation is likely to be critical for arresting premature labor.


Assuntos
Córion/fisiologia , Decídua/fisiologia , Inflamação/imunologia , Trabalho de Parto/imunologia , Leucócitos/imunologia , Movimento Celular/genética , Citocinas/metabolismo , Feminino , Perfilação da Expressão Gênica , Humanos , Inflamação/genética , Mediadores da Inflamação/metabolismo , Início do Trabalho de Parto/imunologia , Trabalho de Parto/genética , MicroRNAs/genética , MicroRNAs/metabolismo , Análise em Microsséries , Gravidez , Transdução de Sinais/genética , Transdução de Sinais/imunologia , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo , Regulação para Cima
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