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Dive into the research topics where Holly Bacon is active.

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Featured researches published by Holly Bacon.


Rheumatology | 2014

The relationship between benign joint hypermobility syndrome and psychological distress: a systematic review and meta-analysis

Toby O. Smith; Victoria Easton; Holly Bacon; Emma Jerman; Kate Armon; Fiona Poland; Alex J. MacGregor

OBJECTIVE This study examines the reported evidence of an association between benign joint hypermobility syndrome (BJHS) and psychological symptoms. METHODS A systematic review of published (AMED, CINAHL, MEDLINE, EMBASE, PubMed, Cochrane Library) and unpublished research databases (OpenGrey, the World Health Organization (WHO) International Clinical Trials Registry Platform, Current Controlled Trials, the UK National Research Register Archive) was performed from their inception to January 2013. Studies assessing the prevalence and incidence of psychological conditions for people diagnosed with BJHS were included. Meta-analysis assessing the odds ratio (OR) and standardized mean difference in severity of psychological conditions was performed. Methodological quality was assessed using the Critical Appraisal Skills Programme (CASP) appraisal tools. RESULTS Fourteen papers including 3957 participants, 1006 people with and 2951 controls without BJHS were eligible. The overall methodological quality was moderate. The results indicated that people with BJHS experience significantly greater perceptions of fear and more intense fear (P < 0.05) and have a higher probability of demonstrating agoraphobia (P < 0.05), anxiety (OR 4.39, 95% CI 1.92, 10.40), depression (OR 4.10, 95% CI 1.79, 9.41) and panic disorders (OR 6.72, 95% CI 2.22, 20.35) than those without BJHS (P ≤ 0.005). Neither anxiety nor depression have been assessed in childhood populations. CONCLUSION People with BJHS commonly exhibit a range of symptoms related to anxiety and depression. Considerable emotional symptoms accompany BJHS. Further study is warranted to explore how these results relate to non-Mediterranean populations and children. However, the data suggest that targeting psychological symptoms could be an important approach to managing the range of symptoms reported in these patients.


Disability and Rehabilitation | 2014

Physiotherapy and occupational therapy interventions for people with benign joint hypermobility syndrome: a systematic review of clinical trials

Toby O. Smith; Holly Bacon; Emma Jerman; Vicky Easton; Kate Armon; Fiona Poland; Alex J. MacGregor

Abstract Purpose: This study assessed the literature to determine the efficacy and effectiveness of physiotherapy and occupational therapy interventions in the treatment of people with benign joint hypermobility syndrome (BJHS). Methods: Published literature databases including: AMED, CINAHL, MEDLINE, EMBASE, PubMed and the Cochrane Library, in addition to unpublished databases and trial registries were searched to October 2012. All clinical trials comparing the clinical outcomes of Occupational Therapy and Physiotherapy interventions compared to non-treatment or control intervention for people with BJHS were included. Results: Of the 126 search results, 3 clinical studies satisfied the eligibility criteria. The data provides limited support for the use of wrist/hand splints for school children. While there is some support for exercise-based intervention, there is insufficient research to determine the optimal mode, frequency, dosage or type of exercise which should be delivered. Conclusions: The current evidence-base surrounding Occupational Therapy and Physiotherapy in the management of BJHS is limited in size and quality. There is insufficient research exploring the clinical outcomes of a number of interventions including sensory integration, positioning and posture management and education. Longer term, rigorous multi-centre randomised controlled trials are warranted to begin to assess the clinical and cost-effectiveness of interventions for children and adults with BJHS. Implications for Rehabilitation There is an evidence-base to support clinician’s use of proprioceptive-based exercises in adults, and either tailored or generalised physiotherapy regimes for children with BJHS. Clinicians should be cautious when considering the prescription of hand/wrist splints for school age children with BJHS, based on the current research. Until further multi-centre trials are conducted assessing the clinical and cost-effectiveness of interventions for children and adult with BJHS, clinical decision-making should be based on theoretical rather than evidence-based grounds for this population.


Archives of Disease in Childhood | 2015

G282 The efficacy of a multidisciplinary intervention strategy for the treatment of benign joint hypermobility syndrome (bjhs) in childhood. a randomised, single centre parallel group trial (the bendy study)

Pj Bale; Victoria L. Easton; Holly Bacon; Emma Jerman; K Armon; Alex J. MacGregor

Introduction Joint hypermobility is common in childhood and can be associated with musculoskeletal pain and dysfunction. Current management is delivered by a multidisciplinary team but evidence of efficacy is limited. This clinical trial aimed to determine whether a structured multidisciplinary intervention resulted in improved clinical outcomes compared with standard care. Method A prospective randomised, single centre parallel group trial comparing an 8-week individualised multidisciplinary intervention programme with current standard management (advice and a physiotherapy appointment). Children and young people (CYP) were assessed for pain, function, coordination and strength at baseline, 3 and 12 months. Results 119 children, aged 5 to 16 years, with symptomatic hypermobility were randomised to receive targeted multidisciplinary intervention (I) (n = 59) or standard management (S) (n = 60). Of these, 105 were followed to 12-months. There was a significant improvement in child and parent reported pain, coordination and strength. However, no added benefit could be shown from the intervention (Table 1). The number of CYP showing significant pain reduction (>=40%) was 27 (50.0%) (I) vs 21 (41.1%) (S). Those pain free at 12 months were 29 (56.9%) (I) vs 20 (45.5%) (S). The response was independent of the degree of hypermobility. Abstract G282 Table 1 The rate of change in primary and secondary outcomes over 12 month follow-up period, this data includes analysis from multilevel modelling Conclusions This is the first RCT to compare a structured multidisciplinary intervention with standard care in symptomatic childhood hypermobility. The study demonstrates significant improvement among subjects but no additional benefit from targeted intervention. The findings emphasise the benefit of informed diagnosis and management according to clinical need, but highlight the difficulty in demonstrating subtle benefit from specific interventions without better tools for case definition and outcomes assessment.


Pediatric Rheumatology | 2014

The efficacy and cost effectiveness of a multidisciplinary intervention strategy for the treatment of benign joint hypermobility syndrome (BJHS) in childhood. a randomised, single centre parallel group trial. (The bendy study)

Pj Bale; Vicky Easton; Holly Bacon; Emma Jerman; Kate Armon

Joint hypermobility is common in childhood and can be associated with musculoskeletal pain and dysfunction. Current management is delivered by a multidisciplinary team but evidence of efficacy is limited.


Rheumatology International | 2013

Do people with benign joint hypermobility syndrome (BJHS) have reduced joint proprioception? A systematic review and meta-analysis

Toby O. Smith; Emma Jerman; Victoria Easton; Holly Bacon; Kate Armon; Fiona Poland; Alex J. MacGregor


Arthritis & Rheumatism | 2014

A89: The Relationship Between Benign Joint Hypermobility Syndrome and Developmental Coordination Disorders in Children

Victoria L. Easton; Pj Bale; Holly Bacon; Emma Jerman; Kate Armon; Alex J. MacGregor


Rheumatology | 2014

The relationship between benign joint hypermobility syndrome and developmental coordination disorders in children

Victoria L. Easton; Holly Bacon; Kate Armon; Alex J. MacGregor


Rheumatology | 2015

OP2. The efficacy of a multidisciplinary intervention strategy for the treatment of benign joint hypermobility syndrome in childhood: a randomized, single centre parallel group trial (The BENDY Study)

Peter Bale; Vicky Easton; Holly Bacon; Emma Jerman; Kate Armon; Alex J. MacGregor


Rheumatology | 2014

296. The Relationship Between Benign Joint Hypermobility Syndrome and Motor Difficulties in Children

Victoria L. Easton; Holly Bacon; Emma Jerman; Kate Armon; Peter Bale; Alex J. Macregor


Rheumatology | 2014

288. The Brighton Criteria Fail to Capture the Clinical Characteristics of Benign Joint Hypermobility Syndrome in Children: Data from the Bendy Study

Peter Bale; Alex J. MacGregor; Kate Armon; Vicky Easton; Holly Bacon; Jerman Emma

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Kate Armon

Norfolk and Norwich University Hospital

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Emma Jerman

University of East Anglia

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Vicky Easton

Norfolk and Norwich University Hospital

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Peter Bale

Norfolk and Norwich University Hospital

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Victoria L. Easton

Norfolk and Norwich University Hospital

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Emma Jerman

University of East Anglia

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Pj Bale

University of East Anglia

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