Quality of life in schizophrenia and bipolar disorder: The impact of symptomatic remission and resilience

AbstractBackground:Health-related quality of life (HRQOL) is significantly affected in individuals with schizophrenia or bipolar I disorder (BD-I). The current study investigated whether symptomatic remission and resilience might differently impact HRQOL in these patients.Methods:Fifty-two patients with schizophrenia and 60 patients suffering from BD-I from outpatient mental health services as well as 77 healthy control subjects from the general community were included into a cross-sectional study. HRQOL and resilience were assessed using the WHOQOL-BREF and the Resilience Scale. In patients, psychopathology was quantified by the Positive and Negative Syndrome Scale or the Montgomery Asberg Depression Rating Scale and the Young Mania Rating Scale, respectively.Results:Notably, both patient groups showed lower HRQOL and resilience compared to control subjects, non-remitted patients indicated lower HRQOL than remitted ones. The effect of remission on HRQOL was significantly larger in patients with BD-I than in those with schizophrenia but did not explain the difference in HRQOL between groups. Resilience predicted HRQOL in all three groups. When accounting for the effect of resilience among remitted patients, only the difference in HRQOL between schizophrenia patients and control subjects was significant.Conclusion:These findings demonstrate the impact of symptomatic remission and resilience on HRQOL of both patients suffering from schizophrenia and BD-I and indicate that these factors are especially relevant for HRQOL of patients with BD-I.

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Quality of Life in Patients with Psoriasis Seen in the Department of Dermatology, Antananarivo, Madagascar

BioMed Research International ◽

10.1155/2020/9292163 ◽

2020 ◽

Vol 2020 ◽

pp. 1-5

Author(s):

Fandresena Arilala Sendrasoa ◽

Naina Harinjara Razanakoto ◽

Volatantely Ratovonjanahary ◽

Onivola Raharolahy ◽

Irina Mamisoa Ranaivo ◽

...

Keyword(s):

Quality Of Life ◽

Negative Impact ◽

Young Patients ◽

The Body ◽

University Hospital ◽

Medical Decision ◽

Cross Sectional ◽

The Difference ◽

The Impact

Background. Psoriasis is a chronic, inflammatory, and multifactorial dermatosis that impairs quality of life (QoL). Health-related QoL has become an important element in medical decision-making along with the effectiveness and the harmlessness of the treatments. Objective. To assess the impact of psoriasis in the QoL of patients with psoriasis by using the DLQI scales. Methods. A cross-sectional study from January to June 2018 was conducted in the Department of Dermatology of the University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar, including patients more than 18 years old with mild to severe psoriasis. The severity of psoriasis was assessed using the “Psoriasis Area and Severity Index (PASI)”. QoL of patients with psoriasis was evaluated by using the DLQI scales. Results. 80 patients were included, their mean age was 36.5 years, and the male to female was 1.5 : 1. The mean DLQI score was 13.8. Symptoms, feelings, and psychic were the most altered dimensions. QoL was impaired in young patients, single, having medium level education. Even though patients with disease duration more than 5 years had higher DLQI score than other patients, the difference was not statistically significant (p=0.36). Furthermore, the clinical presentation of psoriasis did not influence the patient’s QoL (p=0.73). Patients with nail involvement had QoL impaired but the difference with another localization was not statistically significant (p=0.2). The quality of life was influenced by body area involved. The higher the body surface area involved, the more QoL is impaired (p=0.002). Furthermore, the higher the PASI, the more QoL is altered (p=0.002). Conclusion. Psoriasis has a negative impact in the quality of life in Malagasy patients with psoriasis, especially in younger and single patients. Worse quality of life is correlated to severity of psoriasis.

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Evaluation of Somnoplasty using Snoring Symptom Inventory

Otolaryngology ◽

10.1016/j.otohns.2008.05.264 ◽

2008 ◽

Vol 139 (2_suppl) ◽

pp. P82-P82 ◽

Cited By ~ 2

Author(s):

Venkat R Srinivasan ◽

Christopher Low ◽

Paul W A Goodyear ◽

Steve Derbyshire ◽

Aneesh Veetil

Keyword(s):

Quality Of Life ◽

Cross Sectional Study ◽

Sleep Apnoea ◽

Long Term Results ◽

Cross Sectional ◽

The Difference ◽

The Impact ◽

Radiofrequency Volumetric Tissue Reduction ◽

Tissue Reduction

Objective To assess whether radiofrequency volumetric tissue reduction of the palate can improve patients’ snoring symptoms and quality of life. Methods A prospective cross-sectional study was undertaken. Over an 18-month period, consecutive habitual snorers without sleep apnoea were asked to complete a validated Snoring Symptoms Inventory (SSI) questionnaire before and 3–6 months after radiofrequency surgical treatment. It contained 25 questions on the impact of snoring symptoms, including social, work, physical and emotional aspects. Most patients underwent 2 operations (Somnoplasty® Somnus device) with a 2-month interval. A scale of 0 (no snoring) to 10(extremely loud snoring) was used to assess partners’ perception of the snoring intensity. Paired T-test was used to compare the mean difference in the SSI before and after surgery. Partners’ scores were analysed with Wilcoxon signed ranks test. Results 26 patients (19 male, 7 female) aged between 33 and 74 (mean=48) were recruited. Preoperative BMI scores ranged from 19 to 35 (mean=28). Pre- and postoperative mean SSI scores were 60.5 (SD 12.3) and 42.8 (SD 17.4). The difference between the 2 means is 17.6 (95% Confidence Interval, 11.0 to 24.2), P<0.0001. The median for pre- and postoperative partners’ scores is 10 and 5 respectively. and the difference is statistically significant (P<0.0001). Conclusions Radiofrequency volumetric tissue reduction can improve habitual snorers’ snoring symptoms, snoring-related quality of life, and partner's perception of their snoring. Long-term results of this procedure need to be ascertained with further studies.

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Pruritus and Malodour in Patients with Hidradenitis Suppurativa: Impact on Quality of Life and Clinical Features Associated with Symptom Severity

Dermatology ◽

10.1159/000502139 ◽

2019 ◽

Vol 236 (1) ◽

pp. 59-65 ◽

Cited By ~ 2

Author(s):

Alejandro Molina-Leyva ◽

Carlos Cuenca-Barrales

Keyword(s):

Quality Of Life ◽

Clinical Features ◽

Hidradenitis Suppurativa ◽

Rating Scale ◽

Life Quality ◽

Numeric Rating Scale ◽

Cross Sectional Study ◽

Cross Sectional ◽

The Impact

Background: Patients with hidradenitis suppurativa (HS) suffer from symptoms such as pruritus and malodour which can significantly impair their quality of life. Objectives: (1) To analyse the impact of pruritus and malodour on the quality of life of patients with HS and (2) to explore the potential association between clinical features and the severity of these symptoms. Patients and Methods: This is a cross-sectional study. The Numeric Rating Scale (NRS) was used to assess pruritus and malodour. Quality of life was assessed by means of the Dermatology Life Quality Index (DLQI). Results: Two hundred and thirty-three patients were included in the study. Both pruritus and malodour positively correlated with worse quality of life (p < 0.05). Pruritus intensity was associated with the number of regions affected by HS, female sex, the intensity of suppuration, and the presence of comorbid Crohn’s disease. Statin use was associated with lower levels of pruritus. Malodour intensity was associated with higher body mass index, disease duration, the number of regions affected, Hurley stage, and intensity of suppuration. Conclusions: The results of our study show that pruritus and malodour are key symptoms in patients with HS which have a great impact on their quality of life. We have identified clinical features potentially associated with the intensity of these symptoms which could be useful to identify higher-risk patients and may influence treatment decisions.

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The Impact Of Death Anxiety On Quality Of Life Among Cancer Patients: A Case Of Bahawalpur And Multan District

Psychology and Education Journal ◽

10.17762/pae.v58i1.2162 ◽

2021 ◽

Vol 58 (1) ◽

pp. 5473-5477

Author(s):

Siraj Hussain Et al.

Keyword(s):

Quality Of Life ◽

Cancer Patients ◽

Death Anxiety ◽

Negative Impact ◽

Sampling Technique ◽

Cross Sectional Survey ◽

Cross Sectional ◽

The Difference ◽

The Impact

The current study aimed to carved the impact of death anxiety on quality of life among cancer patients. The study focused to find out the difference of death anxiety in the context of gender and socio-demographic factors; and to seek out the impact of death anxiety on the quality of life of cancer patients. Purposive sampling technique was opted to collect the N= 110 cancer patients from Victoria hospital Bahawalpur and the Minar hospital Multan though the cross-sectional survey research design. The instrument was adopted from Lemming fear of death anxiety scale and WHOQOL. To cognizant the study Correlation t-test was computed which put forth that women cancer patients have a positive correlation between death anxiety and the quality of life. The conclusion is there is an impact of death anxiety on quality of life among patients who were hospitalized. Death anxiety has a negative impact on quality of life among cancer patients. Patients both male and female experience death anxiety at a certain level that may impact their quality of life, cancer patients who were hospitalized they have more death anxiety than other cancer patients. Septate Psychological counseling sessions can assist to decline the death anxiety among cancer patients.

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Quality of life in patients with psoriasis seen in the Department of Dermatology, Antananarivo Madagascar.

10.21203/rs.2.23219/v3 ◽

2020 ◽

Author(s):

Fandresena Arilala Sendrasoa ◽

Ratovonjanahary Volatantely ◽

Razanakoto Naina Harinjara ◽

Raharolahy Onivola ◽

Rakotoarisaona Mendrika Fifaliana ◽

...

Keyword(s):

Quality Of Life ◽

Negative Impact ◽

Young Patients ◽

The Body ◽

University Hospital ◽

Medical Decision ◽

Cross Sectional ◽

The Difference ◽

The Impact

Abstract BACKGROUND: Psoriasis is a chronic, inflammatory and multifactorial dermatosis that impairs quality of life (QoL). Health-related QoL has become an important element in medical decision making along with the effectiveness and the harmlessness of the treatments.OBJECTIVE: To assess the impact of psoriasis in the QoL of patients with psoriasis by using the DLQI scales.METHODS: A cross-sectional study, during ten months, was conducted in the Department of Dermatology of the University Hospital Joseph Raseta Befelatanana Antananarivo Madagascar including patients more than 15 years-old with moderate to severe psoriasis. The severity of psoriasis was assessed using the “Psoriasis Area and Severity Index (PASI)”. QoL of patients with psoriasis was evaluated by using the DLQI scales.RESULTS: 80 patients were included, their mean age was 36.52 years and the male to female was 1.5:1. The mean DLQI score was 13.85. Symptoms, feelings and psychic were the most altered dimensions. QoL was impaired in young patients, single, having medium level education. Even though patients with disease duration more than 5 years had higher DLQI score than other patients, the difference was not statistically significant (p=0.36). Furthermore, clinical presentation of psoriasis didn’t influence patient’s QoL (p=0.73). Patients with nail involvement had QoL impaired but the difference with another localization was not statistically significant (p=0.2).The quality of life was influenced by body area involved. The higher the body surface area involved, the more QoL is impaired (p=0.002). Furthermore, the higher the PASI, the more QoL is altered (p=0.002).CONCLUSION: Psoriasis has a negative impact in the quality of life in Malagasy patients with psoriasis, especially in younger and single patients. Worse quality of life is correlated to severity of psoriasis.

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Quality of Life in Patients With Psoriasis Seen in the Department of Dermatology, Antananarivo Madagascar.

10.21203/rs.2.23219/v1 ◽

2020 ◽

Author(s):

Fandresena Arilala Sendrasoa ◽

Ratovonjanahary Volatantely ◽

Razanakoto Naina Harinjara ◽

Raharolahy Onivola ◽

Rakotoarisaona Mendrika Fifaliana ◽

...

Keyword(s):

Quality Of Life ◽

Negative Impact ◽

Young Patients ◽

The Body ◽

University Hospital ◽

Medical Decision ◽

Cross Sectional ◽

The Difference ◽

The Impact

Abstract BACKGROUND: Psoriasis is a chronic, inflammatory and multifactorial dermatosis that impairs quality of life (QoL). Health-related QoL has become an important element in medical decision making along with the effectiveness and the harmlessness of the treatments.OBJECTIVE: To assess the impact of psoriasis in the QoL of patients with psoriasis by using the DLQI scales.METHODS: A cross-sectional study, during ten months, was conducted in the Department of Dermatology of the University Hospital Joseph Raseta Befelatanana Antananarivo Madagascar including patients more than 15 years-old with moderate to severe psoriasis. The severity of psoriasis was assessed using the “Psoriasis Area and Severity Index (PASI)”. QoL of patients with psoriasis was evaluated by using the DLQI scales.RESULTS: 80 patients were included, their mean age was 36,52 years and the male to female was 1,5:1. The mean DLQI score was 13,85. Symptoms, feelings and psychic were the most altered dimensions. QoL was impaired in young patients, single, having medium level education. Even though patients with disease duration more than 5 years had higher DLQI score than other patients, the difference was not statistically significant (p=0,36). Furthermore, clinical presentation of psoriasis didn’t influence patient’s QoL (p=0,73). Patients with nail involvement had QoL impaired but the difference with another localization was not statistically significant (p=0,2).The quality of life was influenced by body area involved. The higher the body surface area involved, the more QoL is impaired (p=0,002). Furthermore, the higher the PASI, the more QoL is altered (p=0,002).CONCLUSION: Psoriasis has a negative impact in the quality of life in Malagasy patients with psoriasis, especially in younger and single patients. Worse quality of life is correlated to severity of psoriasis.

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Quality Of Life In Patients With Psoriasis Seen In The Department of Dermatology, Antananarivo Madagascar.

10.21203/rs.2.23219/v2 ◽

2020 ◽

Author(s):

Fandresena Arilala Sendrasoa ◽

Ratovonjanahary Volatantely ◽

Razanakoto Naina Harinjara ◽

Raharolahy Onivola ◽

Rakotoarisaona Mendrika Fifaliana ◽

...

Keyword(s):

Quality Of Life ◽

Negative Impact ◽

Young Patients ◽

The Body ◽

University Hospital ◽

Medical Decision ◽

Cross Sectional ◽

The Difference ◽

The Impact

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Subthreshold symptoms in bipolar disorder: Impact on quality of life

European Psychiatry ◽

10.1016/j.eurpsy.2016.01.153 ◽

2016 ◽

Vol 33 (S1) ◽

pp. S122-S122

Author(s):

R. Khemakhem ◽

W. Homri ◽

D. Karoui ◽

H. Belhadj ◽

L. Mouelhi ◽

...

Keyword(s):

Quality Of Life ◽

Bipolar Disorder ◽

Rating Scale ◽

Cross Sectional Study ◽

Poor Quality ◽

Average Score ◽

Young Mania ◽

Cross Sectional ◽

Sf 36

IntroductionSeveral studies have analyzed the influence of bipolar disorder (BD) related to many kinds of functioning. Even if it is obvious that patients in relapse have poor quality of live (QoL), what's about it in interictal phases with subthreshold symptoms?AimsTo study the potential relationship between QoL and subthreshold symptoms in bipolar I patients in remission.ObjectiveTo evaluate the above relationship, we hypothesized that subsyndromic BD phases can be related to worse subjectively QoL.MethodsThis was a cross-sectional study. Forty-four BD patients were enrolled. The subthreshold symptoms were evaluated by Hamilton Depression Rating Scale (HDRS) and Young Mania Rating Scale (YMRS). Patients with HDRS lower than 7 and YMSR lower than 6 were the successful applicants. Then, we run the Tunisian version of SF-36 to measure the QoL.ResultsTwenty-seven men and seventeen women with an average age of 39.3 years were selected. Age of beginning of BD was 31.5 years and patients were in relapse since 1.56 years. The HDRS's average score was 2.73. Twenty patients (45.5%) have an HDRS upper than 4. The YMRS's average score was 2.25 and twenty-nine BD's patients have a score between 1 and 6. The overall average score at SF-36 scale were 64.2 and 25% of BD patient with subthreshold symptoms had a poor QoL.ConclusionsSubsyndromic interictal phases affect the QoL of BD patients and it's necessary to introduce therapy adapted according to troubles in order to improve patient's quality of life and functioning.Disclosure of interestThe authors have not supplied their declaration of competing interest.

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Quality of life in Hungarian polio survivors

Journal of Public Health ◽

10.1007/s10389-020-01459-w ◽

2021 ◽

Author(s):

Erika Viktória Miszory ◽

Melinda Járomi ◽

Annamária Pakai

Keyword(s):

Quality Of Life ◽

Mental Health ◽

Sample Selection ◽

Cross Sectional Study ◽

Two Dimensions ◽

Cross Sectional ◽

Emotional Role ◽

The Difference ◽

Polio Survivors

Abstract Aim The number of Hungarian polio patients can be estimated at approximately 3000. Polio infection is currently affecting people 56–65 years of age. The aim of the study was to reveal the quality of life of patients living with polio virus in Hungary. Subject and methods The quantitative cross-sectional study was conducted in January–April 2017 among polyomyelitis patients living in Hungary. In the non-random, targeted, expert sample selection, the target group was composed of patients infected with poliovirus (N = 268). We have excluded those who refused to sign the consent statement. Our data collection method was an SF-36 questionnaire. Using the IBM SPSS Statistics Version 22 program, descriptive and mathematical statistics (χ2-test) were calculated (p < 0.05). Results The mean age of the members of the examined population is 63.5 years; 68.1% were women and 31.90% were men. The majority of the respondents were infected by the polyovirus in 1956 (11.9%), 1957 (24.3%), and 1959 (19.5%). Polio patients, with the exception of two dimensions (mental health, social operation), on the scale of 100 do not reach the “average” quality of life (physical functioning 23 points, functional role 36 points, emotional role 47 points, body pain 48 points, general health 42 points, vitality 50 points, health change 31 points). Conclusion The quality of life of polio patients is far below the dimensions of physical function, while the difference in mental health compared to healthy people is minimal. It would be important to educate health professionals about the existing disease, to develop an effective rehabilitation method.

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Quality of life and perceived health status in surviving adults with univentricular heart

Heart ◽

10.1136/hrt.86.1.69 ◽

2001 ◽

Vol 86 (1) ◽

pp. 69-73

Author(s):

Z Saliba ◽

G Butera ◽

D Bonnet ◽

P Bonhoeffer ◽

E Villain ◽

...

Keyword(s):

Quality Of Life ◽

Normal Population ◽

Psychosocial Problems ◽

Perceived Health ◽

Univentricular Heart ◽

Cross Sectional ◽

Clinical Variables ◽

Health Measures ◽

The Impact

OBJECTIVETo evaluate the quality of life in patients with univentricular heart and to determine the impact of sociodemographic and clinical characteristics.DESIGN AND SETTINGRetrospective, cross sectional study conducted in a regional paediatric cardiology centre.PATIENTSThe health records of 89 survivors with univentricular heart (median age 21 years; range 17–49 years) were reviewed. Sixty seven answered the Duke questionnaire. Sociodemographic and clinical variables were similar in the responders and non-responders. The impact of sociodemographic and clinical variables on individual Duke's measures was assessed.RESULTSThe Duke scores of adults with univentricular heart were similar to the normal population. Cyanosis predicted a worse score for physical (p = 0.05) and perceived health measures (p = 0.02). A higher educational level predicted a better score for physical (p = 0.004), mental (p = 0.01), and general health measures (p = 0.02). Orthopaedic problems worsened the social score (p = 0.05). Psychosocial problems worsened the pain score (p = 0.04). In comparison with the other anatomical types, mitral atresia worsened the perceived health score (p = 0.02). Patients younger than 23 years scored better for almost all health and dysfunction measures.CONCLUSIONSDespite repeated interventions and other disease related everyday stresses, a selected group of adults with univentricular heart had a satisfying quality of life.

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