Quality of Life among Multiple Sclerosis Patients
Regarding relatively high prevalence of MS in Mazandaran province, this study was designed to measure the quality of life in multiple sclerosis patients living in Mazandaran province. MS is one of the progressive and chronic demyelinative disorders involving active members of society. In this descriptive study, the community of research included members of Mazandaran Multiple sclerosis Association (MMSA). The census sampling method was used. The volunteers (101 patients) were assessed from October 2005 to March 2006. Assessment tool for data collection was standard questionnaire SF-36. The questionnaire consists of 36 questions and its validity has already been determined in many countries including Iran and it has high reliability (alpha chronbach 0/77- 0/90). Clinical manifestations and the severity of the disease were evaluated with history and physical examination taken by neurologists and using EDSS criteria. The results showed that 76% of the patients were females and 26% were males. The age range was 18-60 years (33/27±8/31). The emergence of disease was at age 12-54 years (27/12±8/03). About 7% of the patients had positive family history of multiple sclerosis. The mean score (based on 100) of general health, physical health, mental health, vivacity, social health and physical pain were, respectively, 41/34±10/22, 54/75±30/25, 53/25±22/03, 54/75±24/44, 56/62±20/96 and 35/75±31/68. In this study, the quality of life was relatively good in all aspects. This may be due to mildness of disease in majority of patients, low age at time of disease emergence and shorter duration of disease.
Received: March 01, 2010;
Accepted: May 08, 2010;
Published: June 10, 2010
MS is one of the progressive and chronic demyelinative disorders with unknown
origin. Based on researches, the injury of myelin is a primary involvement of
viral infection in early of life that produces immunity process later years
(Green, 2003; Phipps and Long, 2003).
Some studies have shown relationship between MS and variety of class I HLA
(Zabihi et al., 2004). MS is one of the most
disabling chronic neurological disorders in young adults (18 to 40 years old).
Clinical manifestations depends on the location of nerve involvement. Optic
nerves with relation to cerebrum, brain stem, cerebellum and spinal cord involve
more than other parts of central nervous system (Polaski et
al., 1998). The most common signs of MS consists of fatigue, weakness,
numbness, unharmonious movements and ataxia (Pugliatti et
al., 2006; Etemadifar et al., 2006; Turk
Boru et al., 2006). Other signs include bladder, bowel and sexual
problems (Lewis et al., 2004; Brunner
and Sudarth, 2004; Ignanavicious and Workman, 2004). The total prevalence
of MS in past 3 decads was 83 in 100/000 and the woman to the man ratio is 2
(Pugliatti et al., 2006). High prevalence of
MS (more than 30 in 100/000) in North Europe, North America, South Canada, South
Australia, Newzealand, Iran and Turkey and low prevalence of MS (lower than
5 in 100/000) in south Europe, Japan, China and south America has been reported
(Etemadifar et al., 2006; Turk-Boru
et al., 2006). This may be related to differences of race, weather
or both. Incidence of MS in the moderate weather is 5 times more than tropic
zones (Brunner and Sudarth, 2004; Ignatavicious
and Workman, 2004). There isn't exact statistics about the prevalence of
MS in Iran. But based on one study in Kerman, the prevalence of MS was reported
30-60 in 100/000 and based on another study in Isphahan was 35/5 in 100/000
(Zabihi et al., 2004; Etemadifar
et al., 2006; Allaedini, 2005).
The results of many studies such as Patti et al.
(2003) in Italy, Pittock et al. (2004) in
America, Turpin et al. (2007) in Canada, Beiske
et al. (2007) in Norway shows, the quality of life is an important
factor in evaluation of both the effects of disease and measurement of the results
of clinical trials about MS. Patients with MS during progress of the disease,
experience both physical and mental problems (Nortvedt
et al., 2000; Morales-Gonzales et al., 2004).
Based on results of the studies such as Janardhan and Bakshir
(2002) in America, Montel and Bungener (2007) in
France, Thompton et al. (2006) in England, fatigue
and depression due to MS, are common problems that can affect on the quality
of life. Regarding to low age at time of disease emergence and involving active
members of society, evaluation of the quality of life in these patients seems
essential. The study of quality of life in these patients could decrease relieve
some disabilities and promotes residual abilities to maximal levels. Regarding
relatively high prevalence of MS in moderate weather such as Mazandaran province,
this study was designed to measure the quality of life in multiple sclerosis
patients living in Mazandaran province.
MATERIALS AND METHODS
In this descriptive study, the community of research included members of Mazandaran Multiple sclerosis Association (MMSA). The census sampling method was used. The volunteers (101 patients) were assessed from October 2005 to March 2006. At first the patients was called by principles of association and asked them if they intend to take part in research. Then they was referred to association office in Sari on three days a week (Saturday, Monday, Wednesday).
Assessment tool for data collection was standard questionnaire SF-36. It was
used by Sweden first time and then translated in many countries (Benito-Leon
et al., 2002; Miller et al., 2000;
Pfennings et al., 1999; Nortvedt
et al., 2001; Nichol et al., 2001).
The validity of questionnaire was already ascertained by Motamed
et al. (2005) on Shiraz university staff, by Montazeri
et al. (2005) on health persons over 15 years old in Tehran and by
Mohammadpour et al. (2007) on population over
40 years old of Mazandaran and chronbach alpha was reported 0/77 to 0/90. This
questionnaire consists of 6 questions about general health, 10 questions about
physical health, 4 questions about vivacity, 5 questions about mental health,
2 questions about social relationships, 4 questions about physical limitation,
3 questions about mental limitation and 2 questions about pain.
In this questionnaire, some questions was scored 1-5, some 1-3 and the others
1-2. Total of scores analyzed based on 100. Some of the characteristics of patients
such as age, sex, state of marriage, duration of disease, history of other disease,
job, primary clinical manifestation and severity of disease was determined by
taking history and physical exam by neurologists and using Krutzke Expanded
Disability Status Scale (EDSS), that is the most common assessment tool for
MS disability (McMillan and Moor, 2006; Krutzke,
1983; Basil et al., 1999; Hobart
et al., 2000) and scored 0-10 (the higher number shows the more disability).
The questionnaire was completed by cooperation of two nurses with baccalaureate
degree. Data were analyzed by using the mean, standard deviation, T test and
The age range of patients was 18-40 years old (33/27±8/31). The duration of disease was 1-25 years (6/15±4/49) and the emergence of disease was at 12-54 years (27/12±8/03). Seventy two percent of patients were married. There was family history in 7% of patients. Nine percent of patients had past history of other disease (2% heart disease, 2% respiratory disease, 5% diabetes). Thirty nine percent of patients were employed and 26% had lost their job because of their disease.
The results of this study showed the most common clinical manifestation of MS patients were fatigue (78%); motor disorders (76%) and sensory disorders (74%), respectively (Table 1).
The severity of disease was assessed by EDSS that was scored from 0-10 and the higher number shows the more disability (Table 2). In this study the range of disability was 1-8 (2/96±1/77). The disability scores of majority of patients (63%) was mild (1-3) and the minority of patients (6%) was severe (>7).
The mean of physical health (54/75±30/25); vivacity (54/75±24/24) and social relationships (52/62±20/96) were higher than other quality of life indexes.
T test didn't show significant relationship between the quality of life and age, duration of disease, sex and marriage state. It might be related to shortage of samples in this study (Table 3). T-test showed significant relationship between fatigue and the quality of life (physical limitations, mental limitations and mental health indexes) p = 0/001.
||Primary clinical manifestations of MS among members of MMSA
||Disability scores among members of MMSA
||The mean and standard deviation of the quality of life indexes
among members of MMSA
The results of t test showed significant relationship between motor disorders and the quality of life (physical limitations and mental health index) p = 0/004, sensory disorders and the quality of life (physical limitations) p = 0/005, visual disorders and the quality of life (mental health index) p = 0/001, ataxia and the quality of life (physical limitations and mental health index) p = 0/006and p = 0/002, respectively, sexual disorders and the quality of life (physical limitations and mental health) p = 0/008 and p = 0/000, respectively.
T test showed significant relationship between disability scores and the quality of life (general health, physical health and physical limitations) p = 0/004, p = 0/001 and p = 0/000, respectively.
The levene's test showed significant different between disability scores and social relationship (p = 0/0003).
In this study, the mean of age of the emergence of disease was 27/12±8/03.
In European countries, the age of emergence of MS is higher than Middle East.
The mean of age of the emergence of MS is 31/7 in England, 29/6 in Jordan, 25/9
in Arabia, 26/6 in Iran and 32/4 in Tunisia (Ammar et
al., 2006; Wasay et al., 2006). The results
of this study showed the woman to the man ratio is 1/7. This ratio makes difference
in different countries and even different locations of the same country. It
has reported 2/6 in England, 1/9 in Jordan, 1/3 in Arabia, 1/5 in Iran (Wasay
et al., 2006; Etemadifar et al., 2006).
Family history of MS has been %3-23 in different studies.
In this study, it was 7%. It adjusts with one study in Kerman (7/8 %) (Zabihi
et al., 2004).
The majority of patients Had Moderate physical health (54/75±30/25),
mental health (53/25±22/03), vivacity (54/75±24/44) and social
relationship (52/62±20/96). In addition, the results of this study showed
26% of patients had lost their job. In comparison with Morales-Gonzales
et al. (2004) in spain (65/8%), that wasn't high. It might be related
to the lower disability scores of patients in this study.
In Patti et al. (2003) study on 180 patients
with MS, the quality of life showed the lower of mean in all indexes (p = 0/001).
In other study by Nortvedt et al. (2000) in
Norway on 194 patients with MS, the quality of life in subgroup of mental health
was moderate (0/2 SD) and in subgroup of physical health was decreased significantly.
In Nichol et al. (2001) study on 96 patients
with MS, physical health was also low. But the results of Benito-Leon
et al. (2002) in spain on 209 patients with MS, showed anexiety and
depression has higher mean versus other indexes of the quality of life. Thompton
et al. (2006) in England also compared 39 patients with MS and 40
health persons. The scores, both in the anexiety and depression were higher
than in patients with MS.
The results of this study showed significant relationship between fatigue and
physical limitations and mental health (p = 0/001). Janardhan
and Bakshi (2002) in assessment of 60 patients with MS in America reported
fatigue resulted in impairment of health concept (p = 0/03) and sexual dysfunction
(p = 0/008) and mental health impairment (p = 0/006).
Although the pathopysiology of MS is controversial, studies shows fatigue is
not only the most common complaint of MS, but also one of the most common causes
of physical and mental limitations. Some of the surveys shows the effects of
fatigue on the physical state of patients, is independent. So, evaluation of
fatigue, provides more information about disability and it's effects on therapeutic
decision making (Mohammadpour et al., 2007; Bethoux,
2006). In this study, there was significant relationship between disability
state and general health (p = 0/004), physical health (p = 0/001) and social
relationships (p = 0/003) that adjusts with Nortvedt et
al. (2000) study.
But in Patti et al. (2003) Study, there was
only correlation between disability scores and physical health index (p = 0/001).
In this study, the quality of life of members of MMSA was moderate in all aspects. This may be due to mildness of disease in majority of patients, low age at time of disease emergence and shorter duration of disease.
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