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Intest Res > Volume 15(3); 2017 > Article
Kim, Jung, Lee, Park, Kim, Choi, Kim, Moon, Moon, Song, Na, Yang, and Korean Association for the Study of Intestinal Diseases (KASID): Impact of inflammatory bowel disease on daily life: an online survey by the Korean Association for the Study of Intestinal Diseases

Abstract

Background/Aims

Inflammatory bowel disease (IBD) is a chronic disabling gastrointestinal disorder that diminishes the quality of life of the affected individuals. Limited data are available regarding the impact of IBD on the daily life of Koreans.

Methods

Self-administered, computer-aided, internet-based questionnaires were distributed to members of a Korean patient organization for IBD from March to April 2013, by the Korean Association for the Study of Intestinal Diseases.

Results

A total of 599 patients with IBD (387 with Crohn's disease [CD] and 212 with ulcerative colitis [UC]) were enrolled. The majority of patients (81%) expressed feelings of fatigue, weakness, and being worn out in their daily lives during times of flare; this percentage was reduced to 61% during remission. Respondents were absent from work or school for an average period of 18 days because of illness, within the first 6 months; the majority of respondents (64%) felt stressed about their absence. Forty-six percent of the respondents reported having received unfair comments at work, or having suffered discrimination. Forty-seven percent of the respondents felt that IBD had negatively affected their income and earnings. Compared with patients with UC, those with CD reported a more frequent negative impact of IBD on work, or more economic burden. More than half of the respondents (61%) reported that IBD had prevented them from making or keeping friends.

Conclusions

IBD significantly impacts daily life, including work, education, and social relationships. Treatment that addresses the full spectrum of life of a patient would be more effective.

INTRODUCTION

Although the incidence rate of IBD in Asian countries is considerably lower than the rate in Western countries, the burden of IBD has been rapidly increasing in Korea.1,2,3 However, public awareness about IBD is still low in Korea. Delay in the diagnosis of IBD could delay therapy, which can worsen the outcome.4,5,6,7
IBD mainly consists of UC and CD. These are chronic disabling gastrointestinal disorders that diminish the quality of life (QOL) of the patient.5,8,9,10 Patients with IBD more frequently receive disability allowances than those received by age-matched individuals from the general population,5,6,10 which proves the detrimental effects of IBD on healthrelated QOL and productivity.5,8 A recent large-scale study (comprising 4,670 patients with IBD from 25 countries) conducted by the European Federation of Crohn's and Ulcerative Colitis Associations (EFCCA) reported the detrimental effects of IBD on intimate relationships, and the unfair comments received by the patients with regard to their work performance. 8
However, limited studies have assessed the impact of IBD on the life of patients in Korea, with the majority of studies having been conducted in Western cohorts.5,6,8,9,10 In addition, there is little public knowledge regarding IBD and the chronic suffering of patients in Korea.
To overcome these issues, the Korean Association for the Study of Intestinal Diseases (KASID) has been conducting the “Happy Bowel Campaign” since 2013 to raise public awareness of IBD in general and to provide accurate information regarding the importance of early diagnosis and proper treatment to patients with IBD. In addition, the KASID is a promoter of World IBD Day, held every year on May 19.
This study reports the findings of a KASID-sponsored survey that aimed to investigate the impact of IBD on the daily lives of patients in Korea.

METHODS

1. Study Population

Patients with UC or CD were enrolled. Self-administered, computer-aided, internet-based questionnaires were distributed to them by the KASID, from March to April 2013. The KASID advertised the study through the Korean IBD patient advocacy and support group newsletter and website, and through online advertisements during the Happy Bowel Campaign. The purpose of the study was explained to patients at the time of enrollment. The survey was anonymous and the data were analyzed without revealing the personal details of the patients. Patients who had no Internet access were excluded, since the survey was only available online. Responding to the survey questions was considered consent to participate.

2. Survey

The survey was designed by KASID members of the International Affairs Committee Secretary of Liaison & Public Relations in cooperation with a communications company “Communication Works.” The survey was based primarily on the IMPACT survey of the EFCCA and on previously published reports8 on the QOL of patients with IBD. The survey consisted of 68 questions divided into 6 categories: (1) demographics, (2) experience with IBD, (3) overall impact on life, (4) overall impact on work, (5) overall economic impact, and (6) impact on relationships (Supplementary Material 1).
Some questions regarding “flare” and “remission” were short-answer questions. Most questions were closed ended, and participants were allowed to select one applicable option. The extent of “flare” and “remission” was open to patient interpretation. The questions concerning the overall impact of IBD were measured using a 5-point Likert scale (strongly agree, 5; agree, 4; neither agree nor disagree, 3; disagree, 2; strongly disagree, 1). In these cases, disagree or strongly disagree represented “no” and the other responses represented “yes.”

3. Statistical Analysis

The collected data were analyzed using SPSS for Windows version 22.0 statistical software (IBM Corp., Armonk, NY, USA). With regard to statistical accuracy, a range of ±2.53% (95% CI limits) was set. Descriptive statistics and multiple linear regression analysis were used to analyze the responses, with subanalyses of patients with CD and UC. Subgroup differences were calculated using the chi-square test.

4. Ethics

The study was approved by the Seoul National University Ethics Committee (number: E-1403-037-563), with the completion and return of the survey implying consent to participate.

RESULTS

1. Demographics

A total of 599 patients with IBD (387 [64.6%] with CD and 212 [35.4%] with UC) completed the survey. Demographic and baseline data for all respondents are shown in Fig. 1. The majority of respondents were male (69.6%) in both the CD and UC subgroups. The majority of participants (59%) reported a period of more than 5 years since the diagnosis of IBD (60% of the patients in the CD subgroup and 57% of the patients in the UC subgroup).

2. Experience with IBD

Most respondents (84%) from the CD and UC groups reported IBD being chronically active, whereas 16% reported being in remission. Sixty-five percent of the patients had been admitted to a hospital for IBD within the 5 years preceding the study; however, the proportion of patients with CD was significantly higher than the proportion of patients with UC (76%, P <0.001), with regard to the hospitalization. Thirty-eight percent of the patients received emergency care before being diagnosed with IBD. Eighteen percent of the respondents had experienced a surgical procedure because of IBD. More patients with CD than with UC reported this experience (P <0.001) (Table 1).
Forty-one percent of the respondents reported visiting a hospital 6 months after they noticed the first symptoms related to IBD. The time before the first hospital visit was significantly longer in patients with CD (P <0.001). The reasons for delayed hospital visit were lack of knowledge about IBD (75%), mild symptoms (13%), inconvenient hospital access (3%), economic burden (3%), and others (6%). Most respondents (75%) received a final diagnosis within a year after they first noticed the symptoms. The other 25% patients received a final diagnosis after more than a year; in 3% of these, IBD was diagnosed after 5 years from their first symptoms. The time required for final diagnosis was also significantly longer in patients with CD (P <0.001) (Table 1).
About three-quarters of the respondents reported undergoing current treatment by a gastroenterologist (75%), while 13% reported undergoing current treatment by a primary physician. The most commonly taken drug among the respondents was 5-aminosalicylates (69%), followed by immunosuppressive agents (48%), corticosteroids (15%), and biological drugs (11%). More patients with CD than with UC were being treated with biological drugs (15% and 5%, respectively) at the time of conducting the study. Sixty-one percent of the patients had experienced side effects from corticosteroids, and 87% of the patients were concerned about the long-term effects of corticosteroids.

3. Overall Impact of IBD on Life

The majority of patients (81%) expressed feelings of fatigue, weakness, and being worn out in their daily lives during times of flare; this percentage was reduced to 61% during remission. Most patients (68%) felt stressed and were psychologically affected even during remission. Thirty-seven percent of the patients reported that they felt like committing suicide (CD 41% vs. UC 30%, P =0.01). Multiple linear regression analysis revealed that previous emergency care (P =0.021), previous hospitalizations (P =0.036), previous surgeries (P =0.035), experience of abdominal pain (P=0.008), and using biologics (P =0.020) were associated with the feeling of committing suicide. Most patients (74%) were anxious about their future (Table 2). Young age (P =0.047), low income (P =0.026), and experience of abdominal pain (P <0.001) were associated with anxiety about the future, as per multivariable regression analysis.

4. Overall Impact of IBD on Work

More than half (52%) of the respondents reported absence from work or school because of illness within the past 6 months (mean, 18 days). Younger patients and patients with CD had had more sick days; the mean period absence owing to sickness was 10 days for those >40 years of age and 23 days for those <40 years of age (P <0.001), and 20 days versus 14 days for patients with CD and UC, respectively (P <0.001). The absence from work/school owing to IBD caused stress in 64% of the respondents. Compared to patients with UC, those with CD reported a more frequent negative impact of IBD on work (Table 3). The use of biologics (P =0.007) and steroids (P =0.001), previous hospitalization (P =0.043), previous surgeries (P =0.009), and abdominal pain (P =0.001) were associated with the negative impact of IBD on work, as per multiple linear regression analysis.

5. Overall Economic Impact of IBD

Forty-one percent of the respondents reported decreased QOL owing to the economic burden caused by IBD. Twenty-one percent of the respondents had stopped medical treatment because of the economic burden. Those with CD reported an economic burden more often than those with UC (Table 4). Male gender (P =0.001), old age (P =0.011), low income (P =0.008), use of steroids (P =0.039) and biologics (P =0.023), previous hospitalization (P =0.048), and previous surgeries (P =0.002) were associated with high economic burden, as per multivariable regression analysis.

6. Impact of IBD on Relationships

Sixty-one percent of the patients reported that IBD had prevented them from making or keeping friends. Nearly half of the respondents (47%) reported having had to end an intimate relationship owing to IBD. Most of the respondents (70%) reported that the patient association had a beneficial impact on their life (Table 5). Young age (P =0.002), previous surgeries (P =0.003), and previous hospitalization (P =0.038) were associated with the negative impact of IBD on relationships, as per multivariable regression analysis.

DISCUSSION

IBD is typically diagnosed in childhood or early adulthood, and is a lifelong condition.5,8,9,10 Although IBD does not reduce life expectancy, it has a substantial impact on health-related QOL.8,11,12 The present study reports the experience of IBD among Korean patients and the impact of IBD on their daily life. Most patients with IBD were tired, weak and worn out in their daily life during a remission as well as during flareups. A large number of patients reported that IBD adversely affected their QOL. This negative impact of IBD was more severe in patients with CD than in those with UC. A previous experience of surgeries, and hospitalization due to IBD were associated with this negative impact. In general, chronic fatigue has been found to be more prevalent in patients with IBD than in healthy subjects,9,13,14 which, in turn, diminishes the health-related QOL in IBD.9 Accordingly, physicians should remember that fatigue is an important symptom of IBD that impacts the health-related QOL of the patients.
In this study, the time from onset of symptoms of IBD to hospital visit was long; over 41% of the patients had been symptomatic for at least 6 months before visiting a clinician. The most common cause of delayed hospital visit was lack of patient's knowledge about the disease. In addition, although most responders reported establishment of a final diagnosis within 12 months after noticing the first symptoms, 25% of the patients waited for more than a year for the final diagnosis. The delay in meeting a specialist and emergency department visit was more striking for patients with CD than for those with UC. Population-based cohort studies reported that one-fifth to one-third of the patients with CD have complications such as stricture, abscess and/or fistula at the time of diagnosis.15,16 Functional gastrointestinal disorders such as IBS often mimic early manifestations of IBD, and infectious diseases such as intestinal tuberculosis, which mimic IBD, can hinder accurate assessment of the disease in Korea, thereby delaying hospital visit or referral to IBD specialists.7,17,18 In the IMPACT survey, only 54% of the 4,670 patients received a final diagnosis within 1 year after noticing the first symptoms. About 20% of the patients received a final diagnosis after more than 5 years. The majority of patients (67%) had visited an emergency department at least once before their diagnosis.8 Timely diagnosis and treatment would help reduce the health care burden of hospitals, including prediagnosis hospital visits or admissions.8,19 Patients with IBD tend to require emergency room or primary clinic care prior to diagnosis; thus, awareness about IBD is necessary among emergency care staff or primary physicians. 8
About 15% of the respondents received corticosteroid therapy, which was a concern for most of them. Corticosteroid use should be consistent with the guidelines, and the advantages and possible detrimental effects should be discussed with patients.8,20,21,22
The fluctuations and unpredictable exacerbations of IBD symptoms have a significant psychological impact on the patient's life. Fears related to the long-term effects of treatments, and the progression of the disease can exacerbate anxiety and depression.11,23,24,25 In the present study, 37% of the patients reported having felt like committing suicide. Most patients were anxious about their future. The prevalence of anxiety and/or depression in patients with IBD has been reported to be 35% during remission;24 the prevalence of anxiety and depression during relapse has been reported to be 80% and 60%, respectively.25 In a recent study, Korean patients with IBD showed higher levels of depression and impaired health-related QOL than those shown by healthy controls.26 The negative perceptions of IBD among patients and the depressive mood can increase treatment nonadherence, leading to a poorer outcome.19 Integrating psychological interventions with conventional medical treatment seems prudent.11
IBD had a considerable impact on work and economic burden in the present study. Many patients, especially young respondents and those with CD, had missed school or work in the 6 months prior to the study, consistent with other reports,8,27 which, for many patients, is a source of stress and can be the basis for hurtful comments or employment problems. Accordingly, medical discussions should consider work and economic burden as important facets of treatment among Korean patients with IBD.
With regard to building human relationships, IBD can lead to decreased physical intimacy and social activity.28,29 Being able to talk about IBD-related problems in a supportive group setting was helpful for many respondents, as was the awareness created by health care professionals regarding the influence of IBD on these aspects of life.
This study had several limitations. Firstly, the survey was a self-completed instrument and was only available online, so individuals without Internet access could not participate. Thus, the results cannot be generalized to the entire population. Secondly, the survey questionnaire was not validated. Finally, self-assessment introduces the possibility of recall bias concerning aspects such as medication use and emergency care. Some patients might have overestimated the negative impact of IBD on their lives.
Despite the limitations, our study is meaningful because it is the first large-scale study to investigate the effects on IBD on the daily life of Korean patients. The results would be valuable in devising strategies of care, and campaigns to increase the awareness of IBD in Korea.
In conclusion, IBD considerably affects the daily life of the patients, including their work, school, and social relationships. Treatment that addresses that full spectrum of a patient's life would be more effective.

NOTES

Financial support: None.

Conflict of interest: None.

Supplementary Material 1

A Survey of Patients with Inflammatory Bowel Disease (IBD)
ir-15-338-s001.pdf

References

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Fig. 1

Baseline characteristics of patients with IBD. aP <0.05, compared with patients with UC.

ir-15-338-g001.jpg
Table 1

Experience with IBD

Values are presented as number (%).

CD (n=387) UC (n=212) P-value
Current status of IBD
 Chronically active condition 325 (84) 178 (84) 1.000
 In remission 62 (16) 34 (16) 1.000
Hospitalization in the past 5 yr 294 (76) 98 (46) <0.001
Emergency care before diagnosis of IBD 186 (48) 40 (19) <0.001
Previous surgeries owing to IBD 190 (49) 13 (6) <0.001
Time to hospital visit since noticing first symptoms (mo)
 <6 208 (54) 145 (68) <0.001
 ≥6 179 (46) 67 (32) <0.001
Time required to receive the final diagnosis since noticing the first symptoms (mo)
 <6 199 (51) 144 (68) <0.001
 6–12 77 (20) 29 (14) 0.058
 >12 112 (29) 38 (18) 0.003
Table 2

Overall Impact of IBD on Daily Life

Values are presented as number (%).

CD (n=387) UC (n=212) P-value
Felt tired, weak, and worn out in daily life during flare-ups 311 (80) 174 (81) 0.664
Felt tired, weak, and worn out in daily life during remission 238 (61) 127 (60) 0.727
Felt stressed and psychologically affected during remission 270 (69) 137 (64) 0.201
Having felt like committing suicide 158 (41) 64 (30) 0.010
Having felt anxiety about the future 302 (78) 141 (67) 0.003
Table 3

Overall Impact of IBD on Work

Values are presented as number (%).

CD (n=387) UC (n=212) P-value
Cancelled or rescheduled an appointment 238 (62) 121 (57) 0.297
Left office or school early 220 (57) 80 (38) <0.001
Absence from work or school 228 (59) 83 (39) <0.001
Felt stress about taking time off work or school 271 (70) 112 (53) <0.001
Received unfair comments at work or school 155 (40) 52 (25) <0.001
Suffered discrimination or were ostracized 52 (14) 14 (7) 0.010
Decline in income or academic ability 200 (52) 80 (38) 0.010
Unable to perform to their full potential 252 (66) 119 (56) 0.035
Table 4

Overall Economic Impact of IBD

Values are presented as number (%).

CD (n=387) UC (n=212) P-value
Stopped medical treatment owing to economic burden 96 (25) 30 (14) 0.002
IBD had negatively affected the income 201 (52) 180 (38) <0.001
Sorry for the family bearing treatment cost 244 (63) 79 (37) <0.001
Decreased quality of life owing to the economic burden 170 (44) 77 (36) 0.082
Table 5

Impact of IBD on Relationships

Values are presented as number (%).

CD (n=387) UC (n=212) P-value
Prevented from making or keeping friends 237 (62) 126 (59) 0.663
Had to end an intimate relationship end owing to IBD 182 (47) 100 (47) 1.000
Felt stressed about keeping intimate family relationships 155 (40) 85 (40) 1.000
Meeting others with IBD made them more optimistic 120 (31) 67 (32) 0.927
Patient association had a beneficial impact on their life 258 (67) 161 (76) 0.020


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