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1.
Res Pract Thromb Haemost ; 5(7): e12602, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34667923

ABSTRACT

INTRODUCTION: In 2017, all people with severe hemophilia B in Ireland switched to recombinant factor IX Fc fusion protein concentrate (rFIXFc) prophylaxis. Patient-reported outcomes (PROs) and health-related quality of life (HRQoL) are important to evaluate with new treatments. AIMS: To assess HRQoL in people with severe hemophilia B and their experience after switching to rFIXFc prophylaxis. METHODS: Participants completed a Patient Reported Outcomes Burden and Experience (PROBE) questionnaire on initiation and following two years of rFIXFc prophylaxis. The PROBE questionnaire has four domains: demographics, general health, haemophilia-specific, and European Quality of Life 5-Dimensions (EQ-5D-5L) questionnaire. RESULTS: Twenty-three participants completed the questionnaire at both time points. The number of activities where chronic pain occurred and interfered with the activity was reduced by 25% and 33%, respectively (P < .001), following two years of rFIXFc prophylaxis. There was a 9% decrease in chronic pain during the second year of rFIXFc prophylaxis compared to baseline, but the rate remained high, at 74%. A 25% reduction in the number of affected activities of daily living (ADLs) was reported following 2 years of rFIXFc prophylaxis (P = .007). The most common health problems were arthritis, hypertension, anxiety/depression, and gingivitis. The median EQ-5D-5L score was similar following two years of rFIXFc prophylaxis, 0.76 (range, -0.01 to 0.95), compared to 0.77 (range, 0.36-1) at baseline. CONCLUSION: This study of real-world patient experience using PROs demonstrates a reduction in chronic pain and improvement in ADLs in participants after switching to rFIXFc prophylaxis. It provides important insights into patient-identified health care needs and living with severe hemophilia B.

2.
Haemophilia ; 27(6): e690-e697, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34614282

ABSTRACT

INTRODUCTION: Recombinant factor IX fusion protein concentrate (rFIXFc) is increasingly used for prophylaxis in people with haemophilia B (PWHB), but experience in the perioperative setting is limited. AIMS: To evaluate real-world perioperative factor usage, bleeding and complications in PWHB (≥18 years) who received rFIXFc for surgical haemostasis and to describe the treatment regimens used. METHODS: Single centre, retrospective review of all PWHB who underwent a major or minor surgical procedure between June 2017 and July 2020 and received rFIXFc perioperatively for maintenance of surgical haemostasis. RESULTS: A total of 56 PWHB (45 male and 11 female), including people with mild (n = 32), moderate (n = 4) and severe (n = 20) haemophilia B, underwent 11 major and 131 minor procedures with rFIXFc for surgical haemostasis. Haemostasis was rated as excellent (9/11) or good (2/11) in all major procedures. Median total rFIXFc consumption for orthopaedic surgeries was 972 IU/kg (range 812-1031 IU/kg) and for other major (non-orthopaedic) surgeries was 323 IU/kg (range 167-760 IU/kg). The median number of perioperative rFIXFc infusions was 19 (range 17-26) for orthopaedic surgery and 7 (range 5-17) for other major surgeries. The number of infusions in the postoperative period was determined by procedure and patient factors. Complications included bowel ileus and wound infection. Most minor procedures were managed with single infusion of rFIXFc, with no bleeding complications in 95% of minor procedures. There were no thromboembolic events or inhibitor formation. CONCLUSION: This unique data provides real-world evidence that rFIXFc is safe and effective in achieving haemostasis in PWHB undergoing surgery.


Subject(s)
Hemophilia A , Hemophilia B , Adult , Factor IX/therapeutic use , Female , Hemophilia B/drug therapy , Humans , Male , Minor Surgical Procedures , Recombinant Fusion Proteins , Retrospective Studies
3.
J STEM Educ ; 22(2): 46-51, 2021.
Article in English | MEDLINE | ID: mdl-34413711

ABSTRACT

The motivational outcome of undergraduate research experiences is an increasingly common component of STEM education practices. Student benefits associated with these experiences include increased interest and retention in STEM and/or research fields. Across the country, many institutional research activities in twenty-three states and Puerto Rico are supported through the National Institutes of Health's Institutional Development Award (IDeA) Networks of Biomedical Research Excellence (INBRE) Program. INBREs are statewide collaborations of research intensive and primarily undergraduate institutions that are designed to support the biomedical research pipeline as well as faculty research. Most INBREs offer summer undergraduate research experiences to meet their program goals. While the structure and focus of these programs are tailored to state-specific needs, they typically include 10-15 week sessions and many emphasize participation from underrepresented student populations. In summer 2019, eleven INBREs collaborated to explore the collective reach and impact of their summer undergraduate research programs (SURPs). A common set of survey items were identified and added to pre- and/or post-program surveys. These items focused on the reach of the programs (e.g. demographics of participating students) and the impact of the programs on educational goals for students. In total, data from 461 students across 11 states were included in the project. One third of participating students were from underrepresented racial/ethnic groups; 28% were first-generation college students and 34% were Pell grant eligible. After the program, 72% of participants reported that they hoped to earn a doctoral-level degree. Our results suggest that INBRE-supported SURPs are successfully reaching underrepresented students and that INBRE-supported students widely anticipate pursuing graduate level study in STEM fields.

4.
Haemophilia ; 27(4): 618-625, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33939224

ABSTRACT

INTRODUCTION: In 2017, all people with severe haemophilia B (PWSHB) in Ireland switched from standard half-life (SHL) recombinant FIX (rFIX) to rFIX Fc fusion protein (rFIXFc) prophylaxis. AIMS: To evaluate prophylaxis regimens, bleeding rates and factor usage for two years of rFIXFc prophylaxis in a real-world setting. METHODS: Data collected retrospectively from electronic diaries and medical records of PWSHB for a two-year period on rFIXFc prophylaxis were compared with paired baseline data on SHL rFIX treatment. RESULTS: 28 PWSHB (≥18 years) were enrolled, and at switchover 79% were receiving prophylaxis and 21% episodic treatment with SHL rFIX. At 24 months following switchover, all remained on rFIXFc prophylaxis with reduced infusion frequency; median dose per infusion once weekly (55 IU/kg, 20/28), every 10 days (63 IU/kg, 2/28) or every 14 days (98 IU/kg, 6/28). Median annualised bleed rate improved significantly on rFIXFc prophylaxis (2.0 versus 3.3 on SHL FIX) (p = 0.01). Median FIX trough level with once-weekly infusions was 0.09 IU/ml (0.06-0.14 IU/ml). Management of bleeding episodes was similar with rFIXFc and SHL rFIX; one infusion was sufficient to treat 74% and 77% of bleeds, respectively, with similar total median treatment per bleeding episode. Factor consumption reduced by 28% with rFIXFc prophylaxis (57 IU/kg/week, range 40-86 IU/kg/week) compared with SHL rFIX (79 IU/kg/week, range 44-210 IU/kg/week) (p = 0.002). CONCLUSION: This study provides important insights into real-world experience of switching to rFIXFc prophylaxis in an adult population, demonstrating high rates of prophylaxis, with reduced infusion frequency, bleeding and FIX consumption.


Subject(s)
Factor IX , Hemophilia B , Adult , Factor IX/therapeutic use , Follow-Up Studies , Hemophilia B/drug therapy , Humans , Immunoglobulin Fc Fragments/therapeutic use , Recombinant Fusion Proteins , Retrospective Studies
5.
Haemophilia ; 26(6): 984-990, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32997849

ABSTRACT

INTRODUCTION: The COVID-19 pandemic caused an unprecedented impact to haemophilia healthcare delivery. In particular, rapid implementation of telehealth solutions was required to ensure continued access to comprehensive care. AIMS: To explore patient and healthcare provider (HCP) experience of telehealth in a European Haemophilia Comprehensive Care Centre. METHOD: A systematic evaluation was performed to survey patient and HCP experience and compare clinical activity levels with telehealth to in-person attendances. RESULTS: Public health measures implemented in March 2020 to reduce COVID-19 spread resulted in a 63% decrease in medical/nursing clinic consultation activity compared to the same period in 2019. Implementation of digital care pathways resulted in marked increase in activity (52% greater than 2019). Importantly, enhanced patient engagement was noted, with a 60% reduction in non-attendance rates. Survey of patients who had participated in medical/nursing teleconsultations demonstrated that teleconsultations improved access (79%), reduced inconvenience (82%), was easy to use (94%) and facilitated good communication with the HCP (97%). A survey exploring the telemedicine experience of HCPs, illustrated that HCPs were satisfied with teleconsultation and the majority (79%) would like to continue to offer teleconsultation as part of routine patient care. In addition to medical/nursing reviews, continued access to physiotherapy with virtual exercise classes for people with haemophilia and teleconsultation for acute dental issues was equally successful. CONCLUSION: During an unprecedented public health emergency, telehealth has enabled continued access to specialized haemophilia comprehensive care. Our novel findings show that this alternative is acceptable to both patients and HCPs and offers future novel opportunities.


Subject(s)
COVID-19/epidemiology , Delivery of Health Care/statistics & numerical data , Hemophilia A/epidemiology , SARS-CoV-2/physiology , Telemedicine/statistics & numerical data , Adolescent , Adult , Aged , Aged, 80 and over , Comprehensive Health Care , Female , Humans , Ireland/epidemiology , Male , Middle Aged , Pandemics , Young Adult
6.
Nurse Educ ; 45(5): 261-264, 2020.
Article in English | MEDLINE | ID: mdl-32251248

ABSTRACT

BACKGROUND: Some schools and nursing care organizations have implemented 12-hour shifts for students' clinical experiences. PURPOSE: The aim of this review was to identify how student 12-hour shifts compared to shifts of less than 12 hours influence patient safety, care quality, learning outcomes, and student, faculty, and staff satisfaction. METHODS: Searches for academic literature using electronic databases resulted in 13 primary research articles covering the period between 1982 and 2018. RESULTS: During longer clinical shifts, no change in patient safety events occurred. Students and clinical staff perceived care quality was maintained or influenced positively. Faculty were undecided or minimally did not believe care quality improved. While students perceived meeting learning outcomes, faculty perceptions were divided. Students were satisfied with longer shifts; however, the satisfaction of faculty and clinical staff was mixed. CONCLUSIONS: Within realms of patient safety, care quality, learning outcomes, and student, faculty, and clinical staff satisfaction, research has been insufficient and inconclusive regarding 12-hour student shifts.


Subject(s)
Education, Nursing , Learning , Personal Satisfaction , Quality of Health Care , Students, Nursing , Education, Nursing/standards , Education, Nursing/statistics & numerical data , Humans , Quality of Health Care/statistics & numerical data , Students, Nursing/psychology , Students, Nursing/statistics & numerical data , Time Factors
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