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    Worcester City Hospital

    79论文总数
    1,041引用总数

    Worcester City Hospital was a public hospital in Worcester, Massachusetts from 1871 to 1991. It was established by an act of the Massachusetts state legislature and initially funded with a $200,000 donation from Worcester philanthropist George Jacques. The hospital was initially run out of the Abijah Bigelow house (at the corner of Front and Church Streets). As of 1988, the 271-bed hospital had an occupancy rate of only 39 percent. The hospital was closed in 1991 due to financial difficulty and its campus at 26 Queen Street now houses a non-profit community health center called the Family Health Center of Worcester.

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    论文(79)

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    1Hyperbaric Oxygen Therapy in Children with Brain Injury: A Retrospective Case Series
    Michal Hajek, Ondrej Jor,Jakub Tlapak,Dittmar Chmelar

    Introduction and Importance: Some experimental studies on brain injury associated with traumatic brain injury (TBI) and hypoxic-ischaemic encephalopathy (HIE) reveal a positive effect of hyperbaric oxygen therapy (HBOT). However, in clinical medicine, most of the scientific evidence available in the current literature relates only to TBI. Methods: The primary objective is to empirically assess the efficacy of HBOT in mitigating the symptoms of disability associated with brain injury in children, with a view to elucidating its therapeutic potential and clinical benefits. Outcomes: A total of 21 patients have been treated with HBOT. The mean age was 6±4.6 years. There were 12 cases (57%) of TBI, 8 cases (38%) of HIE and 1 case (5%) of ischaemic stroke. The mean initial Glasgow Coma Scale (GCS) at hospital admission immediately after accident was 3.3±0.9. The mean time from injury to HBOT was 5.2 ± 3.8 weeks. The mean number of HBOT exposures was 10±4.3. The mean GCS pre-HBOT was 10.7±3.7 and 12.3±3.4 (p=0.004) after post-HBOT, respectively. The mean Glasgow Outcome Scale (GOS) was 3.3±0.8 pre-HBOT, and 3.9±1.1 (p<0.001) after post-HBOT, respectively. Eighteen cases were included in response to HBOT assessment. Six cases (33%) were evaluated as large clinically significant response (CSR), 7 cases (39%) were evaluated as partial response with minimally important difference (MID). Five cases (28%) were evaluated as non-response. The results showed better response to HBOT in cases of starting HBOT up to 4 weeks (p=0.02) after the injury. There was no serious HBOT-related complication or injury. Conclusion: Results of our study demonstrate both clinical and statistically significant patient response to HBOT. Our data also suggest that the earlier HBOT started after diagnosis up to 4 weeks, the more pronounced patients' response to HBOT was achieved. The provision of HBOT to pediatric patients is feasible in large regional hyperbaric centers.

    2025International journal of medical sciences(2025)引用:2
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    2The Effectiveness of Hyperbaric Oxygen Treatment in Patients with Complex Regional Pain Syndrome: A Retrospective Case Series
    Michal Hajek,Dittmar Chmelar,Jakub Tlapak,Miloslav Klugar

    Background: Complex regional pain syndrome (CRPS) presents as persistent regional pain, both spontaneous and triggered. The demand persists for innovative treatments that patients can endure with minimal adverse effects. Hyperbaric oxygen therapy (HBOT) emerges as a possible intervention in this regard. Methods: The main objective of this work is to retrospectively analyse a case series of patients diagnosed with CRPS treated in the Centre of Hyperbaric Medicine Ostrava over two years (period 2018-2019). The HBOT was applied at 2.0-2.4 absolute atmosphere (ATA) once a day. Results: A total of 83 patients with CRPS were treated with HBOT. 98% of cases reported pain, 92% reported limitation of movement of the affected limb, 87% had swelling of the limb, 41% had lividity and 70% had sensory problems. The mean number of HBOT exposures was 22.0 +/- 7.1. At the end of HBOT treatment, 86% of cases had symptoms relief. The mean VAS value of pain at rest before the start of HBOT was 3.2 +/- 3.0, after treatment it was 1.6 +/- 1.9 (p<0.001). In a pain at activity it was 6.1 +/- 2.4 and 3.7 +/- 2.4 (p<0.001), respectively, at the end of HBOT. The value of the functional assessment of the limb was 7.0 +/- 2.0 and 4.3 +/- 2.4 (p<0.001), respectively, at the end of treatment. 79 cases were included in the end-of-treatment assessment. 23 cases (29%) were evaluated as large clinically significant response, 48 cases (61%) were evaluated as partial response with minimally important difference. The results showed larger clinical HBOT effect in cases of disease duration up to 3 and 6 months (p=0.029). Conclusions: The majority of patients improved pain and functional state of the affected limb. Our data also suggests the sooner after diagnosis of CRPS is HBOT started, the treatment has larger clinical effect. There was no serious HBOT-related complication or injury.

    2024International Journal of Medical Sciences(2024)引用:3
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    3Feasibility of Conducting a Military-Relevant Multicenter Cohort Study to Assess Outcomes of Early Trauma Resuscitative Interventions in a Prolonged Care Civilian Setting.
    Nee-Kofi Mould-Millman,Julia M. Dixon,Hendrick J. Lategan,Brenda Beaty,Bailey Fosdick,Chelsie Fleischer,Shaheem de Vries,Steven G. Schauer,Elmin Steyn,Janette Verster,Lesley Hodsdon,Suzan Mukonkole,

    BACKGROUND:The Epidemiology and Outcomes of Prolonged Trauma Care (EpiC) study is a 4-year, prospective, observational, large-scale epidemiologic study in South Africa. It will provide novel evidence on how early resuscitation impacts postinjury mortality and morbidity in patients experiencing prolonged care. A pilot study was performed to inform the main EpiC study. We assess outcomes and experiences from the pilot to evaluate overall feasibility of conducting the main EpiC study. METHODS:The pilot was a prospective, multicenter, cohort study at four ambulance bases, four hospitals, and two mortuaries from March 25 to August 27, 2021. Trauma patients 18 years or older were included. Data were manually collected via chart review and abstraction from clinical records at all research sites and inputted into Research Electronic Data Capture. Feasibility metrics calculated were as follows: screening efficiency, adequate enrollment, availability of key exposure and outcome data, and availability of injury event date/time. RESULTS:A total of 2,303 patients were screened. Of the 981 included, 70% were male, and the median age was 31.4 years. Six percent had one or more trauma relevant comorbidity. Fifty-five percent arrived by ambulance. Forty percent had penetrating injuries. Fifty-three percent were critically injured. Thirty-three percent had one or more critical interventions performed. Mortality was 5%. Four of the eight feasibility metrics exceed the predetermined threshold: screening ratio, monthly enrollment, percentage with significant organ failure, and missing injury date/time for emergency medical services patients. Two feasibility metrics were borderline: key exposure and primary outcome. Two feasibility metrics fell below the feasibility threshold, which necessitate changes to the main EpiC study: percentage with infections and missing injury date/time for walk-in patients. CONCLUSION:The EpiC pilot study suggests that the main EpiC study is overall feasible. Improved data collection for infections and methods for missing data will be developed for the main study. LEVEL OF EVIDENCE:Prognostic and Epidemiological; Level V.

    2023JOURNAL OF TRAUMA AND ACUTE CARE SURGERY(2023)引用:4
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    4Reviewing the Impact of Antenatal Pelvic Floor Training Using a Novel Vaginal Balloon Device on the Childbirth-Related Health Outcomes in Czech Women
    Karel Fousek

    Vaginal delivery is a known risk factor for various negative outcomes significantly influencing both short-term and long-term aspects of women’s health. Many methods and techniques mitigating these negative outcomes are being studied.

    2023Journal of Reproductive Medicine, Gynaecology &amp Obstetrics(2023)引用:1
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    5COVID-19 Infection Prevention and Control Management During Hyperbaric Oxygen Therapy: a Best Practice Implementation Project.
    Michal Hajek,Dittmar Chmelar,Miroslav Rozloznik,Alexandra Lochmanova,Jakub Tlapak,Tereza Vrbova,Miloslav Klugar,Jitka Klugarova

    OBJECTIVE:This implementation project compared standard operating procedures, accepted preventive measures, and disinfection procedures between the initial stage of the COVID-19 pandemic (first wave: March 15 to May 31, 2020) and the later stages of the pandemic (second and third waves: September 1, 2020 to January 31, 2021).INTRODUCTION:This project sought to improve compliance with international evidence-based guidelines and clinical standards for the prevention and control of COVID-19 infection during hyperbaric oxygen therapy taking into account the conditions of the local hospital.METHODS:Guided by the JBI evidence implementation framework, seven evidence-based audit criteria were developed for the prevention and control of COVID-19 infection during hyperbaric oxygen therapy. A questionnaire was used to measure compliance in baseline and follow-up audits.RESULTS:Differences between the baseline and follow-up audits were noted for criteria 6 and 7. Criterion 6 increased from 0% to 100% as the hyperbaric facility was equipped with certified ultraviolet-C radiation for air disinfection during the later period, but this equipment was not available in the initial period of the pandemic. Criterion 7 dropped from 100% in the baseline audit to 0% in the follow-up audit because of a significant increase in the operational burden of the treatment capacity of the facility, which made it impossible to comply with the recommended distancing between patients.CONCLUSIONS:Differences were found in preventive measures, disinfection procedures, work organization, and approach to care strategy. The project objectives were met and the implementation strategies proved effective. Larger sample sizes would need be needed to confirm the reproducibility of the results.

    2023JBI EVIDENCE IMPLEMENTATION(2023)引用:1
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    合作机构(34)

    斯泰伦博斯大学合作论文 4
    开普敦大学合作论文 4
    University Hospital Ostrava合作论文 3
    奥斯特拉发大学合作论文 3
    帕拉茨基大学合作论文 2
    Victoria Hospital (Saint Lucia)合作论文 2
    马萨诸塞大学合作论文 2
    伯明翰大学合作论文 2
    Western Health合作论文 2
    塔夫茨大学合作论文 1

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