Abstract 3148: Self Reported Quality of Life After Intracerebral Hemorrhage: Is a Modified Rankin Scale Score of 4 Worth it?

Stroke ◽  
2012 ◽  
Vol 43 (suppl_1) ◽  
Author(s):  
Jonathan T Kleinman ◽  
Ryan W Snider ◽  
Irina Eyngorn ◽  
Demi Thai ◽  
Sevan R Komshian ◽  
...  

Background: Intracerebral hemorrhage (ICH) trials often define poor outcome as a modified Rankin Scale Score (mRS) ≥4. While mRS score thresholds are important for demonstrating treatment effect, they do no tell physicians if a treatment outcome is “worth it.” Little self-reported quality of life (QOL) data exists to guide physicians, so opinions during academic discussions and/or family meetings may be driven by personal bias. We sought to describe both self and surrogate reported QOL in ICH survivors in relation to mRS score. Methods: Consecutive ICH patient were prospectively enrolled in the NIH-funded DiAgnostic Utility of MRI in Spontaneous Intracerebral Hemorrhage (DASH) study. Survivors were followed up at 3 months in clinic and at 12 months by telephone. At each time point, patients or surrogates were asked to rate the patient’s QOL as: excellent, good, fair, or poor. mRS scores were determined by an investigator through a semi-structured interview. Results: Self reported QOL was available in 95 patients with 143 QOL ratings, and surrogate reported QOL in 66 patients with 84 QOL ratings. Of self-reporters with a mRS of 4, 29% reported at least a good QOL, and 93% rated at least a fair QOL ( Figure 1). Of self-reporters with a mRS of 3, 58% reported at least a good QOL, and 97% rated at least a fair QOL. Patients with a mRS of 4 were less likely to report a poor QOL than surrogate raters (χ 2 =3.9, p=0.05, Figure 2). In all patients, both self-reported and surrogate reported QOL were only loosely associated with mRS (R 2 =0.25 and R 2 =0.12, respectively). Forty-eight patients had self-reported QOL at 3 and 12 months. In these patients mRS improved in 16 (33%) patients without an associated improvement in QOL. Seven patients (15%) reported an improvement in QOL, but only 3 had an improvement in their mRS between 3 and 12 months. In 3 (6%) patients, the mRS worsened while QOL remained unchanged. No change in mRS was seen in 8 (17%) patients who reported worse QOL at 12 than at 3 months. Conclusions: Self reported QOL is only loosely correlated with mRS for the individual patient. Patient surrogates are more prone to rate QOL of patients with a mRS of 4 as poor than patients themselves. These data are clinically relevant as mRS alone may not capture the satisfaction of the individual patient with their outcome.

2020 ◽  
Vol 26 (2) ◽  
pp. 122-134
Author(s):  
Maria P. M CHAIM ◽  
Sebastião B. C. NETO, ◽  
Aminn y F. PEREIRA, ◽  
Virgínia E. S. M. COSTA

The quality of life (QOL) of mothers of children with autism spectrum disorder (ASD) is related to the symptomatic and idiopathic characteristics of the existential condition of the child and is determined by the subjective understandings attributed according to the individual experience. The primary objective of this article is to describe and understand the subjective constructs about the self-referenced QOL of mothers of children with ASD. It is an empirical study, qualitative and based on a reading of phenomenological psychopathology. Participated 10 mothers of children with ASD, users of public health services in Goiânia. The following instruments were used: a sociodemographic and clinical data questionnaire and a semi-structured interview script about QOL. The interviews were submitted to the construction of thematic categories, according to the methodology of Giorgi (1985), and later were correlated with the existential categories of Augras (2004). It was observed that although a standard is sought to understand QOL, each mother has subjective factors that reflect in her way of experiencing the condition of being a mother of a child with special needs. It is concluded that it is the science, when seeking to understand the quality of life of people with similar characteristics, to consider the relevance of the subjective aspects and the meaning that each mother constructs of its own reality.


Neurology ◽  
2018 ◽  
Vol 91 (1) ◽  
pp. e26-e36 ◽  
Author(s):  
Ching-Jen Chen ◽  
Dale Ding ◽  
Thomas J. Buell ◽  
Fernando D. Testai ◽  
Sebastian Koch ◽  
...  

ObjectiveTo compare the functional outcomes and health-related quality of life metrics of restarting vs not restarting antiplatelet therapy (APT) in patients presenting with intracerebral hemorrhage (ICH) in the ERICH (Ethnic/Racial Variations of Intracerebral Hemorrhage) study.MethodsAdult patients aged 18 years and older who were on APT before ICH and were alive at hospital discharge were included. Patients were dichotomized based on whether or not APT was restarted after hospital discharge. The primary outcome was a modified Rankin Scale score of 0–2 at 90 days. Secondary outcomes were excellent outcome (modified Rankin Scale score 0–1), mortality, Barthel Index, and health status (EuroQol–5 dimensions [EQ-5D] and EQ-5D visual analog scale scores) at 90 days.ResultsThe APT and no APT cohorts comprised 127 and 732 patients, respectively. Restarting APT was associated with lower rates of good functional outcome (36.5% vs 40.8%; p = 0.021) and lower Barthel Index scores at 90 days (p = 0.041). The 2 cohorts were then matched in a 1:1 ratio, and the matched cohorts each comprised 107 patients. No difference in primary outcome was observed between restarting vs not restarting APT (35.5% vs 43.9%; p = 0.105). There were also no differences between the secondary outcomes of the 2 cohorts.ConclusionRestarting APT in patients with ICH of mild to moderate severity after acute hospitalization is not associated with worse functional outcomes or health-related quality of life at 90 days. In patients with significant cardiovascular risk factors who experience an ICH, restarting APT remains the decision of the treating practitioner.


Author(s):  
Emily Basquille ◽  
Verna McKenna ◽  
Ailish Houlihan ◽  
Kate Molony ◽  
Dr. Veronica McInerney ◽  
...  

Context: The aim of this study was to profile a cardiac rehabilitation population in the West of Ireland and establish Subjective Quality of Life (SQoL), using The Schedule for Evaluation of Individual Quality of Life-Direct Weighting (SEIQoL-DW), a validated subjective QoL measure. Bothersome symptoms (SB) and Symptom Interference in SQoL (SBIQoL) were also assessed using a using a modified SEIQoL-DW. Objectives: QoL is a difficult concept to define, therefore the medical profession often premise QoL on health and illness. The focus of this study was to explore the QoL needs of a cardiac population, with a view to informing the development of a newly formed cardiac rehabilitation support group. The SEIQoL-DW was developed to overcome the limitations of quantitative questionnaires, as it is based on the individual’s personal view of life and its quality. Methods: SQoL, symptoms and SBIQoL, of 22 individuals, who had suffered a cardiac event were explored. SEIQoL-DW is a semi-structured interview, enabling the individual to convert their perspectives into scientific values. QoL areas of importance to patients are called ‘cues’. A modified SEIQoL-DW was used to assess SB and SBIQoL. Data were analysed using both quantitative analysis and qualitative descriptive analysis. Findings: Participants highlighted a range of QoL cues; findings from this study showed that 45% of participants did not rate ‘health’ in the first five QoL cues. A significant number of participants experienced symptoms; a medium negative correlation was found between symptom interference and QoL, rho = -0.353, with high levels of symptom interference associated with low levels of QoL. Conclusions: The range of QoL cues and bothersome symptoms identified in this study had implications for the development of the group, with participants eager to participate and talk candidly about their needs. SEIQoL-DW proved to be an acceptable, reliable and valid technique for measuring both individual QoL, SB and SBIQoL, taking greater consideration of individual perspectives compared with traditional measurement approaches. The significance of nominated symptoms and SBIQoL warrants further attention, especially if these symptoms are reversible.


Author(s):  
Amélie Gabet ◽  
Valérie Olié ◽  
Yannick Béjot

Background Atrial fibrillation (AF) represents a major indication for oral anticoagulants (OAC) that contribute to spontaneous intracerebral hemorrhage (ICH). This study evaluated AF prevalence among patients with ICH, temporal trends, and early functional outcomes and death of patients. Methods and Results Patients with first‐ever ICH were prospectively recorded in the population‐based stroke registry of Dijon, France, (2006–2017). Association between AF and early outcome of patients with ICH (ordinal modified Rankin Scale score and death at discharge) were analyzed using ordinal and logistic regressions. Among 444 patients with ICH, 97 (21.9%) had AF, including 65 (14.6%) with previously known AF treated with OAC, and 13 (2.9%) with newly diagnosed AF. AF prevalence rose from 17.2% (2006–2011) to 25.8% (2012–2017) ( P ‐trend=0.05). An increase in the proportion of AF treated with OAC (11.3% to 17.5%, P ‐trend=0.09) and newly diagnosed AF (1.5% to 4.2%, P ‐trend=0.11) was observed. In multivariable analyses, after adjustment for premorbid OAC, AF was not significantly associated with ordinal modified Rankin Scale score (odds ratio [OR], 1.29; 95% CI, 0.69–2.42) or death (OR, 0.89; 95% CI, 0.40–1.96) in patients with ICH. Nevertheless, adjusted premorbid OAC use remained highly associated with a higher probability of death (OR, 2.53; 95% CI, 1.11–5.78). Conclusions AF prevalence and use of OAC among patients with ICH increased over time. Premorbid use of OAC was associated with poor outcome after ICH, thus suggesting a need to better identify ICH risk before initiating or pursuing OAC therapy in patients with AF, and to develop acute treatment and secondary prevention strategies after ICH in patients with AF.


Author(s):  
Maria Silva Santana

RESUMO:Evidencia-se a atividade física como recurso importante para amenizar a degeneração provocada pelo envelhecimento, bem como possibilitar  ao idoso manter uma qualidade de vida ativa. O objetivo do estudo foi conhecer e descrever o significado da atividade física para a terceira idade. Ele consistiu em um estudo transversal com base na Teoria das Representações Sociais, cuja forma de conhecimento socialmente elaborado e partilhado tem um objetivo prático e contribui para a construção de uma realidade comum a um conjunto social. A amostra foi não-probabilística e por conveniência. Participaram do estudo 70 pessoas, do sexo masculino e do feminino, com média de idade de 62 anos, integrantes do Programa Saúde e Cidadania na Terceira Idade, do CEFET/RN, Brasil, que ensina pessoas a fazer atividade física, visando o auto-cuidado com a saúde a partir dos 50 anos. Na coleta de dados, foi utilizada a técnica da entrevista estruturada em situação individual contendo questões sócio-demográficas sobre a percepção da importância da atividade física para a saúde e uma questão aberta.  Constataram-se os diferentes entendimentos compartilhados dos indivíduos do estudo sobre os benefícios da atividade física, representados pelos campos semânticos fuga dos problemas, auto-estima, felicidade, qualidade de vida e integração social. O fenômeno, identificado no âmbito psicossocial, foi capaz de esclarecer aspectos importantes da necessidade da atividade física para as práticas de saúde em geral para idosos.PALAVRAS-CHAVE: Qualidade de vida. Saúde do idoso. Psicologia Social. ABSTRACT: The physical activity is evidenced as an important resource to alleviate the degeneration caused by aging, and enable the elderly to maintain an active quality of life. This study aims to present and describe the significance of physical activity for elderly. It consisted of a cross sectional study based on the Theory of Social Representations, whose socially established and shared form of knowledge has a practical objective and contributes to the construction of a common reality to a social conjunct. The sample was non-probabilistic and for convenience. Study participants were 70 people, males and females, with a mean age of 62 years old, all members of the Health and Citizenship in the Third Age Program, of CEFET / RN, Brazil, which teaches people to do physical activity, aiming the self-health care starting from  the 50 years old. In data collecting, it was used the technique of individual structured interview containing socio-demographic questions   about the importance of the perception of physical activity to health and an opened question.   There are different understandings about the individual components of the study about the benefits of physical activity, which are represented by the semantic fields of problems escapade, self-esteem, happiness, quality of life and social integration. The phenomenon, identified in thepsychosocial ambit, was able to clarify important aspects about the necessity of physical activity for the general health practices for elderly. KEYWORDS: Quality of life. Elderly Health. Social Psychology.


2019 ◽  
Vol 4 (1) ◽  
pp. 20
Author(s):  
Machiko Higuchi ◽  
Chandani Liyanage

Objectives: This study aimed at gaining an understanding of senior citizens’ lifestyles from childhood and clarifying the factors important in sustaining their quality of life (QOL).Methods: Using purposive sampling, in-depth interviews by semi-structured interview guide were conducted among five senior citizens in a Sri Lankan community. The interviews were analysed narratively.Results: Three males and two females over the age of 70 were interviewed. All had obtained a decent level of education and lived with extended family. They had sound relationships with their children and were engaged in social roles, keeping them occupied and giving their lives a sense of meaning. They made use of both Western and traditional medicine, including religious activities, depending on their ailments.Conclusion and further research: The QOL of independent community-dwelling senior citizens in Sri Lanka was related to education, psychological independence, sustaining daily life, engagement in social activities, and satisfaction with children’s support, house sitting for their children, and engaging in multiple health activities to prevent and treat symptoms. Further narrative research is suggested to highlight the individual experiences of senior citizens, which will help develop an effective strategy for sustaining the QOL of this population in Sri Lanka.


1999 ◽  
Vol 17 (11) ◽  
pp. 3603-3611 ◽  
Author(s):  
Dympna Waldron ◽  
Ciaran A. O'Boyle ◽  
Michael Kearney ◽  
Michael Moriarty ◽  
Desmond Carney

PURPOSE: Despite the increasing importance of assessing quality of life (QoL) in patients with advanced cancer, relatively little is known about individual patient's perceptions of the issues contributing to their QoL. The Schedule for the Evaluation of Individual Quality of Life (SEIQoL) and the shorter SEIQoL–Direct Weighting (SEIQoL-DW) assess individualized QoL using a semistructured interview technique. Here we report findings from the first administration of the SEIQoL and SEIQoL-DW to patients with advanced incurable cancer. PATIENTS AND METHODS: QoL was assessed on a single occasion using the SEIQoL and SEIQoL-DW in 80 patients with advanced incurable cancer. RESULTS: All patients were able to complete the SEIQoL-DW, and 78% completed the SEIQoL. Of a possible score of 100, the median QoL global score was as follows: SEIQoL, 61 (range, 24 to 94); SEIQoL-DW, 60.5 (range, 6 to 95). Psychometric data for SEIQoL indicated very high levels of internal consistency (median r = .90) and internal validity (median R2 = 0.88). Patients' judgments of their QoL were unique to the individual. Family concerns were almost universally rated as more important than health, the difference being significant when measured using the SEIQoL-DW (P = .002). CONCLUSION: Patients with advanced incurable cancer were very good judges of their QoL, and many patients rated their QoL as good. Judgments were highly individual, with very high levels of consistency and validity. The primacy given to health in many QoL questionnaires may be questioned in this population. The implications of these findings are discussed with regard to clinical assessment and advance directives.


2003 ◽  
Vol 128 (1) ◽  
pp. 17-26 ◽  
Author(s):  
David J. Kay ◽  
Richard M. Rosenfeld

OBJECTIVE: The goal was to validate the SN-5 survey as a measure of longitudinal change in health-related quality of life (HRQoL) for children with persistent sinonasal symptoms. DESIGN AND SETTING: We conducted a before and after study of 85 children aged 2 to 12 years in a metropolitan pediatric otolaryngology practice. Caregivers completed the SN-5 survey at entry and at least 4 weeks later. The survey included 5 symptom-cluster items covering the domains of sinus infection, nasal obstruction, allergy symptoms, emotional distress, and activity limitations. RESULTS: Good test-retest reliability ( R = 0.70) was obtained for the overall SN-5 score and the individual survey items ( R ≥ 0.58). The mean baseline SN-5 score was 3.8 (SD, 1.0) of a maximum of 7.0, with higher scores indicating poorer HRQoL. All SN-5 items had adequate correlation ( R ≥ 0.36) with external constructs. The mean change in SN-5 score after routine clinical care was 0.88 (SD, 1.19) with an effect size of 0.74 indicating good responsiveness to longitudinal change. The change scores correlated appropriately with changes in related external constructs ( R ≥ 0.42). CONCLUSIONS: The SN-5 is a valid, reliable, and responsive measure of HRQoL for children with persistent sinonasal symptoms, suitable for use in outcomes studies and routine clinical care.


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