Assessment of health-related quality of life in individuals with interstitial lung diseases in a tertiary care hospital in south India

Material & Methods

This study was undertaken from June 2022 to December 2023 at the department of Pulmonary Medicine, St. John’s National Academy of Health Sciences, Bengaluru, after obtaining approval from Institutional Ethics Review Board. Individuals presenting to the pulmonary medicine outpatient and ILD clinic consecutively were recruited in this study. Consenting individuals aged >18 yr, diagnosed with ILD as per standard guidelines and multidisciplinary discussions were recruited in the study. Illiterate individuals who lacked the competence to complete the questionnaires were excluded. Pregnant women, individuals with ILDs with significant extrapulmonary manifestations which could affect HRQoL, those with an exacerbation of ILD in the preceding four weeks, and those having any terminal illness were excluded from this study.

After obtaining a written informed consent, clinical, demographic information and self-reported comorbidities were collated. Spirometry was performed using Smart PFT (Peso Medicare, India) as per ATS/ ERS recommendations⁵ and forced vital capacity (FVC) per cent predicted was noted. A six-minute walk test (6MWT) was performed as per ATS/ ERS guidelines⁶, the distance walked, and desaturation were noted. HRQoL assessment was done using the ILD specific King’s Brief Interstitial Lung Disease (K-BILD) questionnaire and the generic 5-level EQ-5D version (EQ-5D-5L) questionnaire. Permission was sought from the copyright owners of these questionnaires for use in the study. We also wanted to assess the patient related experience with the treatment prescribed. The Patient Experiences and Satisfaction with Medications (PESaM) questionnaire did not have an English version. Hence after obtaining permission from the developers, an adapted version of the validated questionnaire (Dutch) was used⁷. This was chosen with an intent to gain a comprehensive perspective on the impact of the disease and the treatment on patients’ lives. Details of the questionnaires and the adaptations made are mentioned in the supplementary material.

Results

A hundred and fifty-nine individuals with ILD participated in this study were recruited, with a mean (SD) age of 53.2 (12.9) yr which predominantly included females (64.15%). The most common etiology of ILD was connective tissue disease associated ILD (40.8%) followed by hypersensitivity pneumonitis (11.3%) and idiopathic pulmonary fibrosis (10.6%). The median (IQR) duration of illness was 5 (3, 25) months. Co-morbidities were present in 105 (66%) patients with hypertension (37.1%) and diabetes mellitus (33.9%) being the commonest, followed by hypothyroidism, ischemic heart disease and obstructive airway disease. Baseline characteristics of the patients are summarized in Table I.

The mean ± SD score for K-BILD was 55.7 ± 9.8 with the lowest mean scores for the ‘breathlessness and activity’ domain (40.1 ± 18.2) followed by ‘psychological impact’ (55.5 ± 11.7) and ‘chest symptoms’ (76.5 ± 18.8) respectively. The mean ± SD score for EQ-5D-5L was 66.2 ± 16.3 and 0.6 ± 0.3 for the EQ VAS and EQ-5D-5L index, respectively. The adapted version of the PESaM questionnaire showed that majority of the population was satisfied with medications (88.6%), thought that medications were effective (64.1%), had a positive impact on social life (61.6%), and were easy to consume (89.9%). Findings of the information provided in results of the questionnaires are summarized in Table II and the Figure. Descriptive questions of PESaM (adapted version) showed that additional cost incurred for medications was the usual reason for dissatisfaction. Common side effects mentioned were weight gain, swelling and puffiness of the face, gastric discomfort, loose stools, altered taste, decreased appetite and sleep disturbances. Participants were often found citing weight gain and change in physical appearance as being discomforting during social interactions.

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Figure.

Results of health-related quality of life questionnaires. EQ VAS, EuroQol Visual Analog Scale; K-BILD, King’s Brief Interstitial Lung Disease - B&A, breathlessness and activity domain, Chest, chest symptoms domain, Psych, Psychological domain.

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On assessing correlation of HRQoL with lung function parameters, both the questionnaires had a significant correlation with 6-min walk distance and desaturation during 6MWT. However, the correlation of all the domains was weak with FVC per cent predicted (Table III). On analyzing the correlation between EQ-5D-5L and K-BILD questionnaires, total K-BILD score had a strong correlation with the EQ-5D-5L index (r = 0.84; P<0.001) and EQ-VAS (r=0.73; P<0.001). Analysis of the correlation between different domains of both the questionnaires are presented in Table IV.

Linear regression analysis was performed to assess the relationship between demographic variables, lung function parameters and HRQoL domains. Univariate analysis was initially performed to identify significant predictors of HRQoL, providing a preliminary understanding of each variable’s individual impact. Baseline characteristics such as age, sex, presence of comorbidities, duration of illness and type of ILD were not found to be significant in the univariate analysis and were excluded in the regression model.

A multivariate analysis was then conducted to assess the association between lung function parameters and HRQoL. The analysis was adjusted to account for the potential confounding effects of different lung function parameters on each other, ensuring that the association between each parameter and HRQoL was examined independently. In multivariate analysis, it was found that FVC per cent predicted was significantly associated with the K-BILD ‘chest symptom’ domain; six-min walk distance was significantly associated with EQVAS, K-BILD total, ‘psychological’ and ‘breathlessness and activity’ domains; and desaturation during 6MWT with EQVAS, K-BILD and K-BILD ‘breathlessness and activity’ domain (Table V).

Discussion

The measurement of one’s own subjective well-being that is impacted by an illness or its treatment is known as health-related quality of life (HRQoL)⁸. Interstitial lung diseases (ILD) are a group of chronic respiratory diseases typified by progressive dyspnea and cough. Current treatment options depend on the type of ILD and essentially include steroids, immunosuppressants and antifibrotics. Although progress has been made in the last decade with newer therapies, a significant proportion of affected individuals continue to experience progressive decline in lung functions, disturbing symptoms and become dependent for activities of daily living. Treatment for ILD also has financial implications and as the disease progresses, the requirement of long-term oxygen therapy further limits activities. All the above result in social isolation and have a psychological impact which affects the HRQoL⁹.

High quality clinical care can only be delivered by employing a patient-centric approach. It has been increasingly agreed upon by clinicians, researchers, and patients that disease management and research studies should focus on patient related outcomes (PROs) as an important endpoint³. PROs are patient-reported outcomes that are not interpreted by a clinician and address how an illness or treatment affects a person’s quality of life¹⁰. HRQoL is difficult to evaluate owing to its subjective and dynamic nature with multiple domains and varying perception among patients with similar disease severity. These idiosyncrasies are augmented by social, cultural, and religious differences which affect the value ascribed to each domain.

Traditionally treatment of ILD has focused on tangible outcomes like change in lung function, exercise capacity and radiological findings. Although HRQoL is being included as an important endpoint in therapeutic decision making and research studies, it is still given a low priority¹¹. HRQoL in individuals with ILD was initially assessed using questionnaires validated in other chronic diseases like St. George Respiratory questionnaire (SGRQ)¹². However, these questionnaires may not capture the nuances which are unique to ILD. Hence, ILD specific questionnaires were developed including King’s Brief Interstitial Lung Disease (K-BILD), A Tool to Assess Quality of life in Idiopathic Pulmonary Fibrosis (ATAQ-IPF), Living with IPF (L-IPF) and Chronic Hypersensitivity Pneumonitis Health Related Quality of Life (CHP-HRQoL).

Impaired HRQoL in individuals with ILD has been reported in studies using various questionnaires. Many of these studies have been done on individuals with idiopathic pulmonary fibrosis (IPF). HRQoL assessed by SGRQ was reported to be impaired in IPF and disease duration, co-morbidities, FVC and need for long term oxygen therapy were the prime drivers of the impairment¹³. A systematic review reported that IPF had a negative impact on HRQoL by predominantly affecting the physical health domains. Various instruments were used to assess the same and standardization of these tools could harmonize the findings and make comparisons possible across the globe¹⁴.

K-BILD questionnaire was developed as a disease specific tool to assess HRQoL in individuals with ILD. The questionnaire has previously been translated and validated in European and South American countries^15,16. It has been found to be a useful tool in assessing HRQoL in ILDs and is responsive to interventions^17-19. The ‘breathlessness and activity’ subscale of K-BILD was found to have high internal consistency and reliability and is recommended as the best PRO measure for dyspnea in individuals with ILD²⁰.

Representation of Asians is reportedly <20 per cent in literature¹⁴ with infinitesimal data available from Indians. In our study, we chose to use a combination of generic (EQ-5D-5L) and ILD specific (K-BILD) questionnaires as per recommendations to assess the HRQoL comprehensively among Indians ²¹. Since we believed that treatment offered also influences HRQoL, we also used an adapted version of the PESaM questionnaire to assess patient experience and satisfaction with the treatment. Our study population predominantly included females with CTD-ILD. Compared to other studies our participants had a lower mean FVC per cent predicted indicating a more severe spectrum of ILD. In concordance with the other studies, the mean K-BILD scores were comparable with ‘breathlessness and activity’ domain affected more than ‘psychological’ and ‘chest symptoms’ domain^18,22.

Consistent with other studies, a strong correlation was found between the questionnaires specifically in the ‘breathlessness and activity’ domain. Our study showed a weak correlation between the HRQoL measures and FVC per cent predicted. This reinforces the fact that physiological testing may not completely capture the impact of the disease. The 6MWT, being a submaximal exercise testing, showed a strong correlation with HRQoL. Since most of the activities of daily living are performed at submaximal levels of exertion, it may reflect the exercise capacity better and thus correlate better with the health status⁶.

Results of the adapted version of the PESaM questionnaire provide insights into effects and side-effects of medications prescribed and stress the importance of considering patient experience-related outcomes as well.

This study was not without limitations. As it is a single-center study, with a small sample size, the results cannot be generalized. The population included had varied subtypes of ILD and owing to smaller numbers, a subgroup analysis of the HRQoL based on the type of ILD could not be performed. Illiterate individuals had to be excluded due to the self-administered nature of most of the questionnaires. Interview based assessment of these questionnaires still needs validation. We were unable to perform a comprehensive lung function testing including diffusion capacity and lung volumes in all patients. The appropriateness of the treatment offered and the effect of each medication on HRQoL was not analyzed. It also remains to be seen if these measures are sensitive to changes with treatment during follow up.

It was also found during the study that aspects like disturbing cough, poor sleep quality and financial burden were not adequately captured by these questionnaires. Many of our participants found it difficult to comprehend and answer a few questions and required assistance for the same. Though symptom and domain specific questionnaires are available, it is the need of the hour to have a comprehensive tool which can evaluate all aspects of HRQoL relevant to patients with ILD in the right social and cultural framework to enable them to handle their disease better.

Overall, the findings of this study suggest that FVC, six-min walk distance and exercise induced desaturation were independent predictors of HRQoL in patients with ILD.