By E. Deckard. Sterling College, Kansas. 2018.
R51 Concurrent prescription of drugs known to promote hyperkalaemia is not a contraindication to the use of ACEI/ARBs but be aware that more frequent monitoring of serum potassium concentration may be required buy generic levitra super active 40 mg online. R52 Stop ACEI/ARB therapy if the serum potassium concentration rises to above 6 generic levitra super active 40mg overnight delivery. R54 If there is a fall in eGFR or rise in plasma creatinine after starting or increasing the dose of ACEI/ARB generic levitra super active 20mg free shipping, but it is less than 25% (eGFR) or 30% (serum creatinine) of baseline buy levitra super active 40mg with visa, the test should be repeated in a further 1–2 weeks levitra super active 40mg low price. Do not modify the ACE/ARB dose if the change in eGFR <25% or change in plasma creatinine is <30%. R55 If the eGFR change is ≥25% or change in plasma creatinine is ≥30%: q investigate other causes of a deterioration in renal function such as volume depletion or concurrent medication (e. The older population are also more prone to reduced volume status and sodium depletion, have greater comorbidity and are more likely to be taking concurrent medications making them potentially more susceptible to the adverse effects of ACEI/ARBs. Indeed, there is a perception that ACEI or ARB treatment puts the older person at greater risk for adverse events such as acute kidney failure/injury, hypotension, falls, and reduced quality of life. Few studies have described the progression of CKD in older community based individuals, and none have confirmed the widely held belief that low GFR is associated with a rapid progression of kidney dysfunction in older people. Is there a greater potential risk of further deterioration of renal function because of the high prevalence of renal stenotic atherosclerotic lesions and very frequent concomitant use of diuretics and nonsteroidal anti-inflammatory drugs? Although this study lacked the statistical power necessary to assess efficacy of losartan treatment in each of the three increasing age ranges, it did analyse the interaction between age and losartan treatment for the outcomes of death, hyperkalaemia, and adverse events such as acute renal failure. The oldest participant in the study was 74 years old, and thus this study lacks data on very elderly people. A retrospective cohort analysis of people >65 years of age was conducted to investigate whether receiving an ACE inhibitor at hospital discharge following an acute myocardial infarction increased one year survival rates in people with poor renal function (serum creatinine >3 g/dl, N=1582) compared with people with better renal function (serum creatinine ≤3 mg/dl, N=19,320). In all three age groups (people ≤57 years, age >57 to 65 years, or >65 years) there was NS difference in risk of death between losartan and placebo. In people without a previous history of CVD, there was NS difference between candesartan and conventional treatment for the incidence of congestive heart failure. The receipt of an ACE inhibitor at hospital discharge was associated with a 16% increase in 1-year survival for patients with better renal function (serum creatinine ≤3 mg/dl, N=19,320, mean age 75, HR 0. In all three age groups (people ≤57 years, age 57–65 years, or >65 years) there was NS difference in incidence of adverse events between losartan or placebo. Thus, increasing age did not significantly increase the risk of hyperkalaemia from losartan. None of the people in the studies were over 75 years of age. Thus there is a lack of evidence for changes in the risk/benefit of ACEI/ARB therapy in people over this age; however, the GDG felt that in the absence of evidence of harm people above this age should not be denied the benefits of ACEI/ARB therapy. Studies in experimental rat models showed that aldosterone may contribute to the progression of kidney disease and antagonists of aldosterone may reduce proteinuria and retard the progression of kidney disease independently of effects on blood pressure. Haemodynamic and humoral actions of aldosterone have important clinical implications for the pathogenesis of progressive renal disease and consequently may influence future antihypertensive strategies. Although ACEI/ARBs are effective in preventing disease progression, there may be additional benefit from concurrent aldosterone-receptor blockade. There were no studies that investigated spironolactone in adults with non-proteinuric CKD. Three double-blind RCTs examined the effects of spironolactone in addition to treatment with ACE inhibitors and/or ARBs in adults with diabetic nephropathy281,282 and in a mixed population of diabetic and nondiabetic nephropathy. None of the studies reported cardiovascular outcomes, mortality, or progression to ESRD. The reduction in proteinuria was significantly greater in people with GFR <60 ml/min/1. By contrast, proteinuria did not change from baseline in people treated with ACEI or ARB therapy alone. Compared with the ramipril + irbesartan group, there was a greater reduction in 24-hour proteinuria in the ramipril + irbesartan + spironolactone group. There was NS difference in proteinuria reduction between ramipril + spironolactone group and ramipril + irbesartan + spironolactone groups. The spironolactone-induced decrease in proteinuria was similar regardless of presence of diabetes. Four people receiving spironolactone + conventional therapy and two people receiving conventional therapy alone developed hyperkalaemia (no p value stated).
Applications for commercial reproduction should be addressed to: NIHR Journals Library buy discount levitra super active 20mg line, National Institute for Health Research generic levitra super active 40 mg fast delivery, Evaluation purchase levitra super active 40 mg free shipping, Trials and Studies Coordinating Centre levitra super active 20mg mastercard, Alpha House cheap levitra super active 20mg otc, University of Southampton Science Park, Southampton SO16 7NS, UK. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that xvii suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK. Large numbers of children and young people live with LTCs and the NHS is under pressure to find more efficient ways of caring for them. Self-care support describes techniques that help young people and their families gain the confidence, skills and knowledge they need to manage their condition and get the most out of health services. Self-care support is often provided by a health professional, but could also be given by another person who is able to help (e. To answer this question, we identified all studies that reported the effects of self-care support for children and young people (aged < 18 years) with long-term physical or mental health conditions. We included studies that reported effects on QoL or health symptoms and service use. Ninety-seven studies were included, evaluating 114 interventions. Most interventions were for children and young people with asthma and provided over 2 hours per four sessions of self-care support. Future studies should test different types of self-care support over a wider range of conditions. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that xix suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK. Health-care providers are faced with the growing need to deliver high-quality services in a way that maximises available financial resources without compromising care quality or health outcomes for children and young people. Self-care support interventions offer a potential solution to this problem and are intended to enhance the self-care capacities of children, young people and their families, while simultaneously reducing the fiscal burden facing contemporary health-care systems. Self-care can be defined as the actions that people take to maintain their physical and mental health; meet social and psychological needs; prevent illness or accidents; and maintain their health and well-being. Self-care support refers to the role played by health-care professionals (or other self-care support agents, such as teachers or peers), in supporting the individual and/or their families to take control of a health condition through developing their confidence, knowledge and skills, and their psychological and social resources. Children diagnosed with LTCs face a lifetime of symptom management, and the extent to which they and their families negotiate this in childhood is likely to influence their longer-term health outcomes, life chances and subsequent patterns of health service utilisation. Providing optimal, evidence-based support for self-care thus has the potential to make significant and sustained contributions to NHS efficiency, as well as improving quality of care and health outcomes. Objectives To determine which models of self-care support for LTC management are associated with significant reductions in health services utilisation and cost, without compromising quality of life (QoL) or health status outcomes for children and young people. Methods We conducted a systematic review with meta-analysis. Our review inclusion criteria were as follows: l population – children and young people aged 0–18 years with a long-term physical or mental health condition l intervention – self-care support delivered in a health, social care, educational or community setting l comparator – usual care, including more intensive usual care (e. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that xxi suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK. SCIENTIFIC SUMMARY To identify relevant literature, we searched multiple electronic databases: MEDLINE, EMBASE, PsycINFO, Cumulative Index to Nursing and Allied Health Literature, ISI Web of Science (including Social Sciences Citation Index and Science Citation Index Expanded), NHS Economic Evaluation Database, The Cochrane Library (including Cochrane Database of Systematic Reviews, Database of Abstracts of Reviews of Effects and Cochrane Central Register of Controlled Trials), Health Technology Assessment database, Paediatric Economic Database Evaluation and IDEAS. All databases were searched from inception to March 2015. Additional search strategies included scanning the bibliographies of all relevant retrieved articles, targeted author searches and forward citation searching. Data were extracted on populations, interventions, study quality and outcomes. We conducted meta-analyses and presented the results of the included studies according to a permutation plot, simultaneously plotting the effect of interventions on service utilisation and health. Each plot gives a visual impression of the distribution of studies across the cost-effectiveness plane, distinguishing between studies that reduce costs without compromising outcomes and those that reduce costs but also compromise outcomes, or those that compromise both outcomes and costs.
It should be noted that some study participants were members of more than one stakeholder group (e discount 20mg levitra super active free shipping. These participants were categorised according to our primary reason for seeking to recruit them to the study discount levitra super active 40 mg otc. However purchase levitra super active 20mg with visa, we were cognisant of these multiple roles discount levitra super active 20mg mastercard, and the interview topic guides were adjusted according levitra super active 20 mg low price. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals 5 provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK. Recruitment and consenting In building the overall sample, within each stakeholder group the research team adopted a purposive sampling approach that aimed to ensure a balance of representatives of physiotherapists, occupational therapists and speech and language therapists, as well as representation from different parts of the country. The target sample sizes for each stakeholder group are shown in Table 2. Recruitment took place in two overlapping stages: a first stage to recruit individual interview participants, and a second stage to recruit group interview participants. Recruitment materials, including study information sheets and consent forms, can be found in Appendices 1–3. TABLE 2 Target sample size for each participant group Stakeholder group Sample size, (n) Clinical academics and researchers ≈10 Representatives of national professional groups ≈6 Therapy practitioners 8 × ≈7 group participants (N = ≈55) Consultant paediatricians and paediatric neurologists ≈6 Parents 4×≈8 group participants (N = ≈32) Children and young people 4 × ≈6 group participants (N = ≈25) 6 NIHR Journals Library www. This involved searches of the NIHR funding database and high-impact therapy journals for academic clinicians and researchers currently (or recently) active in the field of therapy interventions. The research team then used a snowballing method, whereby existing recruits were asked for suggestions of other relevant people to include in the study from among their colleagues and professional networks. This iterative recruitment process continued until, from initial analyses and discussions within the research team, data saturation on key or critical themes had been achieved. All individual interview participants were sent an e-mail invitation to take part in the study. This e-mail introduced the research, the nature of the interview and the topics for exploration. If no response was received, a member of the research team followed this up by telephone or a further e-mail. Arrangements were then made with those who responded positively for a suitable date and time to conduct the interview. Finally, a confirmation e-mail was sent, to which was attached an additional information sheet setting out the scope of the interview and giving final details about the interview. For those taking part in a telephone interview, also attached to the confirmation e-mail was a consent form outlining the protocols of the interview so that participants could familiarise themselves with these before giving their recorded verbal consent at the beginning of the interview. The three people who were interviewed in person gave written consent before the interview took place. Stage 2: recruitment to focus groups In the second stage of recruitment, we sought groups of frontline practitioners, parents, and children and young people to take part in focus group discussions. Recruitment methods varied according to the group in question. Practitioner groups were recruited through direct representations to the lead practitioners and heads of therapy services we had recruited to individual interviews, or by securing a workshop slot at forthcoming professional conferences. This included sending the co-ordinator an information sheet with details about the study to forward to all those taking part. This sheet also explained that, at the start of the meeting, participants would be asked to give their written consent to take part in the study. All practitioner focus group participants were also asked to complete a brief pro forma regarding their professional backgrounds. Those attending focus groups were offered a personalised certificate of attendance to include in their career portfolios. In the case of parents and children and young people, we aimed to recruit pre-existing groups in the belief both that this would be more time efficient and that pre-existing groups can move more quickly onto the particular task or discussion and, within the context of a single data collection event, are therefore more likely to yield high-quality data. For parents, we were able to use an established parent group co-ordinated by our own research unit. The study topic was introduced as an agenda item and discussed accordingly at a regular meeting. We then approached several condition-specific voluntary organisations for potential parent groups as well as local groups of the National Network of Parent Carer Forums (www. A flier was designed and distributed for this purpose.
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