Ultrasound Applicability in the Assessment of Patients With Fibrosing Interstitial Lung Disease

NCT ID: NCT06844331

Last Updated: 2025-08-07

Basic Information

• Recruitment Status: ENROLLING_BY_INVITATION
• Total Enrollment: 117 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-10-21
• Study Completion Date: 2026-05-31

Brief Summary

In this study the investigators want to examine the different ultrasound techniques to assess the patients with lung fibrosis.

The investigators want to followup these patients in 1 year to see the changes in lungs, pleura, diaphragm and measurments of overarm and thigh muscles to see that the investigators can identify the patients with lung fibrosis with this methods and monitor the progression.

Now a days the CT scan in the lungs needs to monitor these participants, but the investigators want to see the ultrasound can use insted for CT scanning to minitor these pateints.

These patient group has very bad prognosis, so it is necessary to identify these patients as early as possible to treatments.

Detailed Description

Introduction Fibrosing interstitial lung diseases (F-ILD) represent a heterogeneous disease category involving many subtypes with different clinical, radiological and histological characteristics . Idiopathic pulmonary fibrosis (IPF) is the most common subtype of F-ILD, and IPF is the prototype of other F-ILD phenotypes, known as progressive pulmonary fibrosis (PPF). Despite their diverse presentation, the common denominator defining them as F-ILD patients is due to similarities regarding irreversible symptom worsening, decline in lung physiological parameters and progression of pulmonary fibrosis on thoracic imaging . Accomplishment of early F-ILD diagnosis and disease progression is crucial to initiate treatment at early stage of disease. Chest high-resolution computed tomography (HRCT) is considered the golden standard to diagnose and quantify pulmonary fibrosis. However, repeated HRCT performance is time-consuming, and repeated HRCT scanning is hampered by the cumulated radiation exposure with the increasing risk of cancer development.

Therefore, it is necessary to propose new modalities for the early identification and monitoring of disease progression in F-ILD patients.

Thoracic ultrasound (TUS) is superior to diagnose various conditions of the lung parenchyma and pleura compared to chest X-ray (CXR) . B-line artefacts (BLA) and the interstitial syndrome (IS) are well described TUS indicators related to ILD, and several studies have described a linear correlation between an increasing number of BLAs and the severity degree of fibrotic HRCT findings based on a Warrick score . Additionally, a significant negative correlation between an increased distance between BLAs and decreasing lung physiological parameters has also been demonstrated. Not only parenchymal, but also pleural abnormalities (PA) occur in patients with F-ILD. Several studies have proposed that increasing thickness and irregularity of the pleura can be used as a tool to assess disease severity in patients with F-ILD.

Less investigated ultrasound (US) modalities within F-ILD are diaphragm excursion (DE) and lung ultrasound share wave elastography (LUSWE). Different methods have been used to evaluate DE . According to current evidence, IPF patients were found to have a lower DE compared to healthy individuals, and restrictive ventilation pattern with lower values of forced vital capacity (FVC) was also associated with lower DE . These findings may be explained by a combination of lung compliance reduction ("lung stiffness") and development of diaphragm muscle atrophy over time in patients presenting with F-ILD traits where further development of hypoxemia and immobilization in severe disease stages may develop to sarcopenia.

LUSWE is based on measuring the velocity of the US waves' propagation along the lung surface from a given surface point (intercostal space), where the velocity is dependent on the change in wave phase with distance. The velocity of the US waves increases with tissue stiffness as consequence of reduced elastic properties. In two observational studies distinct higher LUSWE velocities were found in ILD patients compared to healthy individuals, and furthermore a negative correlation between LUSWE velocities and FVC and interstitial lung abnormalities was observed . Therefore, LUSWE may be a valuable supplementary and clinical tool not only to identify F-ILD but also to separate F-ILD from non-fibrotic ILD.

As previously described patients with F-ILD will in addition to increased dyspnea over time, also develop weight loss due to sarcopenia. Sarcopenia is defined as loss of muscle strength, endurance (muscle quality), and muscle mass (muscle quantity), and part of the frailty syndrome defined by a combined loss of functional reserves across different domains (e.g. physical ability, cognition, and energy) resulting in negative implications on health status in multimorbid and especially older patients . The European Working Group on Sarcopenia in Older People 2 (EWGSOP-2) has established diagnostic consensus criteria in which the diagnosis of sarcopenia is made by assessing 1) physical function either by chair stand test or hand-grip strength, by hand dynamometer and 2) estimating the appendicular lean mass. The latter can be done by using B-mode US and anthropometric measurements the appendicular lean mass (ALM) can be estimated. The established thresholds for ALM for men and women have been defined (<20 kg and <7, 0 kg/m2 for men and <15 kg and < 5,5kg/m2 for women).

The main challenge in comparing study results on TUS/US in patients with F-ILD is the heterogeneity in the methodology with use of different TUS/US protocols in incomparable cohorts with a mixture of different ILD subtypes, where some subtypes present with a more fibrotic pattern than others. In this context, it is problematic to determine the diagnostic value of TUS/US for a specific F-ILD category. Some studies have investigated on TUS use in patients with IPF , but most of the studies on patients with F-ILD are of observational nature with cross-sectional designs and primarily performed in patients with underlying autoimmune rheumatic diseases . At present, no studies have accomplished real-life prospective TUS/US follow-up, including promptly investigated TUS/US modalities such as BLA, IS, and PA, and less investigated TUS/US modalities such as DE, LUSWE and ALM, and dealt with these TUS/US modalities as a monitoring tool for F-ILD disease activity or treatment response, and is thus an area encumbered with a significant knowledge gap. The latter was emphasized in the recent European Respiratory Society statement on TUS that warrants studies assessing the impact of these points as areas of future TUS/US research .

Hypotheses The investigators hypothesize that TUS/US modalities such as BLA, IS, PA, DE, LUSWE, and ALM are clinically valuable, both individually and in combination for identifying F-ILD and monitoring disease activity. These modalities are expected to correlate with FVC, diffusion capacity of the lung for carbon monoxide (DLCO), HRCT findings, and clinical symptoms. In such, F-ILD patients with severe disease are hypothesized to present with TUS/US findings as increased number of BLAs, increased pleura thickness with irregularity, decreased DE, higher LUSWE velocities, and lower ALM values. Furthermore, these parameters are proposed to serve as dynamic indicators of F-ILD disease activity over time.

Statistical analyses To assess the reproducibility of our sample the investigators conducted descriptive statistics. Categorical outcomes were presented as numbers and percentages and non-categorical outcomes were presented as either median and interquartile range or mean and standard deviation, depending on the normality of the variable.

The primary objective where to evaluate the predictive value of the longitudinal measured TUS/US modalities on the outcomes HRCT, Warrick score and its subscales, PFT, 6MWT and PROMs. Hence the investigators utilize a mixed effect model including a random intercept. The evaluation of the model predictive performance will be assessed by way of reliability (including intra and inter rater reliability) based on the intra class correlation coefficient and agreement evaluated by Bland-Altman plots with 95% limits of agreement. The discrepancy will be defined as the difference between the predictive and true value of the outcome based on the mixed effect model.

For sensitivity purposes the investigators will also assess the predictive of specific characteristics of HRCT by way of descriptive statistics.

Missing data will be assumed to be missing either completely at random or at random, and thus will handled implicitly by maximum likelihood estimation.

All analyses will be performed using either Stata SE 16.1 (StataCorp, College Station, TX, USA) or the statistical software R, 95% confidence intervals will be reported and a p-value less than 0.05 will be considered statistically significant.

Ethics The study will be conducted in accordance with the Declaration of Helsinki with written patient consent of included patients after prior oral and written project information. The patient can withdraw her/his statement of commitment at any time. The law on the processing of personally identifiable information will be complied with and data from the project will be stored in accordance with Odense University Hospital's guidelines. The project is approved by the Danish Data Protection Agency (Ref. no. 22/45135) and the Science Ethics Committee for the Region of Southern Denmark (Ref. no. S-20220036).

Patient recruitment Respiratory physicians from SCILS, Department of Respiratory Medicine at Odense University Hospital will recruit patients who prior to follow-up in SCILS have received recruitment material. Patients, who are willing to participate in LORD study will be contacted by the PhD student, where an agreement for information and obtainment of detailed oral and written consent will be planned. This meeting will take place in the outpatient clinic of SCILS under quiet circumstances, and the patient will be given 24 hours to consider participation. The patients who are willing to participate will be included after obtain their oral and written consent. Other patients, who are not willing to participate will follow up in the rutine SCILS clinic.

HRCT A standard HRCT scan with inspiratory and expiratory image sections on average results in the patient having a radiation dose of approx. 6-7 mSv (Sievert definition: SI unit for the dosage of ionizing radiation equal to 100 rems. 1 Sv = 1 Sievert = 100 rem = 1 J/kg ((this is based on calculations from The National Institute of Radiation Hygiene (Danish: "Statens Institut for Strålehygiejne")). It is theoretically calculated that such a radiation dose entails a risk of developing cancer of 0.01-0.1%, meaning that the total lifetime risk of developing a cancer disease increases from 25% (which applies to the entire population) to 25.1%. In this population of patients this risk is considered negligible.

TUS/US In TUS/US examinations, sound waves are converted into images on a TV screen. No side effects have been reported with the use of US. Apart from a slight pressure experienced when the ultrasound head touches the chest, the US examination is painless with minimal discomfort for the patient (37). As there are no immediate disadvantages or risks associated with TUS/US, the study only seems to contribute with advantages in form of clinically relevant information.

Sample size The endpoint used for sample size calculation is the ability of TUS performed at 12 months follow-up to detect disease progression using HRCT findings at 12 months as the golden standard. With an expected overall prevalence of the F-ILD phenotype of 14-32% among patients with ILD(38, 39), significance level of 0.05, power of 80%, an expected TUS sensitivity of 70-80%, and assuming the clinical use of US would be as a screening test prior to HRCT confirmation, the calculated sample size is estimated to be between 31 (sensitivity 70%) and 107 patients (sensitivity 80%) (40). Patients with F-ILD are associated with increased mortality, why some patients will not be alive at 12 months follow-up. A conservative estimate is that 10% of the patients will not complete or have died within the 1-year follow-up following inclusion. Adjusting for a 10% drop-out at 12 months follow-up will increase the total sample size to be between 34 and 117 patients with F-ILD. Since the study is performed as part of a PhD programme and 12 months follow up time is needed, the inclusion period necessities to be restricted to 12 months to ensure feasibility within the three year time frame of the PhD programme. Based on the sample-size calculations and the inclusion period restrictions the study will aim to include up to 117 patients or as many as possible with at least 34 patients within the inclusion period of 12 months.

Patient involvement Our study will actively involve patients and their relatives in all aspects of the research process which involves that protocol details, recruitment material and information documents have presented and been discussed with patients in our clinic prior to their final editions. The project group consider it essential to include patients as early in the research process as possible to adjust their needs and experiences, which may have crucial impact on how the projects are being planned. The project group responsible for this project in SCILS at the Department of Respiratory Medicine will orally inform the relevant group of potential patients about the project and provide written information materials. Written consent will be obtained prior to inclusion.

Discussion The LORD study is a single-center, real life, prospective observational study examining patients with F-ILD three times over a follow-up period of 12 months according to whether several different US modalities (BLA, IS, PA, DE with area-method and M-mode, LUSWE and ALM) can be used to diagnose and identify disease progression. To the best of our knowledge, this is the first study to explore multiple TUS/US modalities within this patient category in a longitudinal set-up.

The investigatrs plan to examine not only most conventional investigated TUS modalities such as BLA and PA , but also less investigated US modalities such as LUSWE and diaphragm excrusion on basis of the above mentioned methods. Additionally, the ALM modality has the potential to monitor changes in muscle quality and quantity over time in these often fragile patients, an area that has not been thoroughly investigated in patients with F-ILD.

Thought TUS/US has been increasingly used in the past two decades, the overall evidence in this area is heterogeneous in nature, both regarding to F-ILD subtypes but also applied TUS/US protocols . Therefore, our study intend to clarify a detailed and enhanced perspective on the application of TUS/US modalities in patients with F-ILD, both single but also composite for identification of diagnosis and disease progression.

The diagnostic delay of F-ILD is considerable high approximating two years, and further the mortality rate is high in this patient group compared to other chronic lung diseases. Up to now no curative medicine have been found for F-ILD, but two antifibrotic therapies are available, Pirfenidon and Nintedanib, which delay the disease progression and in such indirectly increases survival. This emphasizes the importance of early detection and prompt treatment initiation in patients with F-ILD, why the investigators await our results in anticipation.

Several strengths and limitations should be addressed:

TUS has already described as a relevant screening modality in other F-ILD and with other US modalities (LUSWE, DE and ALM) it can use to screen patients with F-ILD in a better and promising way. Our study aims to show that TUS/US modalities is feasible and useful method that can use to monitor and early detect disease activity in F-ILD patients.

TUS/US are radiation free modalities that can performed in same day of consultation, and it is easily accessible.

Patients that are included in our study are assessed in MDT conferences in tertiary ILD center in Denmark, and it reduced the selection bias and false classification on diagnosis (information bias) as well as a homogeneous group of F-ILD.

The investigators planned to follow-up patients in baseline, after 180 and 365 days performing PFT, 6MWT, clinical examination and TUS/US on same day.

All the TUS/US findings validated HRCT as golden standard, and HRCT examined by a subspecialized HRCT radiologist , who is blinded from clinical, paraclinical and TUS/US data. It gives low intraobserver variability to our study.

The PhD student perform TUS/US scanning to all the included patients. It also gives low intraobserver variability.

The main limitation in our study is that unable to carry out the HRCT scanning and TUS/US in same day. According to hospital setup in Denmark, it is not possible to carry out HRCT in same day with TUS/US. This may interferer the correlation between HRCT and ultrasound. However, PFT, 6MWT, clinical examination and US examination will conducted in same day.

HRCT is performing in several centers can also be a limitation. The patients referred to our center from the peripheral hospitals with HRCT scanning. There can be differences in scan machines, setup and scanning protocols. However, as mentioned earlier all the HRCT scanning assessed by the subspecialized HRCT radiologist who is blinded from US results and other data.

Our study is a single center study and not 100% generalized to other F-ILD cohorts. There can be an intrainstitutional bias.

Furthermore, performing several different TUS/US modalities require training, can be examiner dependent, and there are 3 clinicians that report TUS/US findings apart from the PhD student. This can give high interobserver variability.

Apart from those, the mortality rate is high in F-ILD patients and will be expected high dropout rate. Therefore, the investigators are expecting to include patients according to our sample size calculation (34-117 patients).

Finally, the LORD study will contribute with knowledge on innovative methods to identification and prediction of F-ILD development over time due the study's follow-up design. Investigating a combination of different TUS/US modalities as single or composite markers of F-ILD disease dynamics is original and not previously conformed for this disease category. The observations from this study will not only fill out the existing knowledge gap, but also be able to point-out which future TUS/US markers to be used in order determine F-ILD disease severity, and thus be clinical implementable.

Conditions

Fibrosing Interstitial Lung Diseases; Thoracic Ultrasound

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

F-ILD patients

The investigators including the patients with fibrosing interstitial lunge disease (F-ILD) as cohort.

Both the patients with idiopathic interstitial lung diseases and progressive pulmnoary fibrosis will include.

Thoracic ultrasound

Intervention Type: DEVICE

The investigators want to investigate that TUS/US can use to identify and to monitir the disease progression in the patients with F-ILD

Interventions

Thoracic ultrasound

The investigators want to investigate that TUS/US can use to identify and to monitir the disease progression in the patients with F-ILD

Intervention Type: DEVICE

Other Intervention Names

Ultrasound

Eligibility Criteria

Inclusion Criteria

• Patients must be over 18 years.
• Diagnosis of IPF obtained on a multidisciplinary team conference .
• Diagnosis of PPF according to 2022 ATS/ERS/JRS/ALAT Clinical Practice Guideline.
• Ability for subject to comply with the requirements of the study.
• Informed consent.

Exclusion Criteria

• Patients not willing to or able to give informed consent.
• Acute exacerbation in F-ILD < 4 weeks.
• Pregnant and breastfeeding mothers

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Odense University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jesper R Davidsen, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Respiratory Medicine, Odense University Hospital

Locations

Odense University Hospital

Odense, Southern Denmark, Denmark

Countries

Denmark

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Other Identifiers

S-20220036

Identifier Type: -

Identifier Source: org_study_id