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Aug 2018




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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
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On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
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On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
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On Jan 2020

Important Notice

Original article / research
Year : 2022 | Month : February | Volume : 16 | Issue : 2 | Page : KC08 - KC12 Full Version

Role of Infrared Imaging for Detection of Subclinical Inflammation of Joints: A Prospective Cohort Study


Published: February 1, 2022 | DOI: https://doi.org/10.7860/JCDR/2022/49612.16029
Satyabrata Nath, Kakali Das, Mrinal Kanti Bhowmik

1. Assistant Professor, Department of Physical Medicine and Rehabilitation Department (PMR), Agartala Government Medical College, Agartala, Tripura, India. 2. Student, Department of Computer Science and Engineering, Tripura University, Agartala, Tripura, India. 3. Assistant Professor, Department of Computer Science and Engineering, Tripura University, Agartala, Tripura, India.

Correspondence Address :
Satyabrata Nath,
Agartala Government Medical Research, Agartala, Tripura, India.
E-mail: sbnathpmr@gmail.com

Abstract

Introduction: The detection of inflammation is important for diagnosis of inflammatory joint diseases and its severity. There are clinically doubtful cases of inflammation of joints. Advanced thermal cameras are able to detect the presence of inflammation. Hence, thermal imaging technology has been used for detection of this type of subclinical inflammation of joints.

Aim: To study the efficacy of infrared imaging to detect the subclinical inflammation of joints in doubtful cases of arthritis.

Materials and Methods: A prospective cohort study was conducted for a period of one year from January 2016 to June 2017. The study comprised of 60 patients of all age groups. Patients with joint pain attending Outpatient Department (OPD) of Physical Medicine and Rehabilitation Department (PMR), Agartala Government Medical College (AGMC) and Govind Ballav Pant Hospital (GBPH), Agartala, India, irrespective of the duration of illness and diseases were selected considering inclusion and exclusion criteria. They were evaluated clinically (swelling, tenderness, redness, increased temperature and the presence of restriction of movement) for presence of inflammation in the joint. Blood tests were done for Acute Phase Reactant (APR) namely Erythrocyte Sedimentation Rate (ESR) and C-Reactive Protein (CRP) and infrared imaging of the respective joints were taken. On the basis of clinical examination, all these patients were divided in three groups: (i) patients with inflamed joint; (ii) non inflamed joint; and (iii) doubtful inflammation of joints. Infrared imaging of all the respective joints of all the patients were compared with the respective results of APR for presence of inflammation. Values more than the normal range of APR were considered as positive marker for inflammation. The data was analysed statistically by calculating sensitivity, specificity, Positive Predictive Value (PPV) and Negative Predictive Value (NPV) using Matrix Laboratory (MATLAB) 2013b software.

Results: Out of 60 cases, 37 (61.66%) patients showed clinically inflamed joints, 10 (16.66%) showed no inflammation and 13 (21.66%) showed clinically doubtful cases of inflammation. The results were statistically analysed and the sensitivity, specificity, PPV and NPV of infrared imaging for detection of joint inflammation were 91%, 80%, 94% and 72%, respectively.

Conclusion: Infrared imaging is a very sensitive tool for the detection of inflammation of joints and is very useful for detection of subclinical inflammation of joint.

Keywords

C-reactive protein, Erythrocyte sedimentation rate, Sensitivity, Specificity

The most important aspect in the management of arthritis is to establish the diagnosis of inflammation. Clinicians are dependent on clinical measures like joint tenderness, swelling, redness, restriction of movement and warmth of joint surface, which are all subjective identifiers for the diagnosis of the arthritis (1). Along with these subjective measures some blood tests like ESR (2) and CRP (3) are considered for detection of inflammation in the joint. More than the normal values of either ESR (normal value in adult male is 10-12 mm in one hour and in adult female is 12-19 mm in one hour) or CRP (normal value in adult is <5 mg/dL) or both is considered to be positive evidence for inflammation of joint (4) and when both ESR and CRP values are negative, the condition is considered as negative inflammation of joint. There is no gold standard for identifying the synovitis of joints (5).

In some cases these clinical parameters collectively cannot detect the synovitis, commonly known as subclinical inflammation of joints. Imaging with Ultrasonography (USG) and Magnetic Resonance Imaging (MRI) has increased the clinicians ability to detect the effusion earlier when there is clinically doubtful synovitis (i.e., joint inflammation) (5),(6). These imaging methods are costlier. Thermal imaging has recently emerged as an important medical diagnostic tool for different disease conditions. Different research works related to thermal imaging have been mentioned in (Table/Fig 1) which provides an insight on the ability of thermal imaging in the detection of inflammation of joint (10),(11),(12),(13),(14),(15),(16). From these studies it can be concluded that there is a relationship between the surface temperature (detected by thermograms) and radiographs of the osteosrthritis patients. Using that correlation, it was concluded that thermograms are efficient in the detection of the severity of osteoarthritis (10),(11),(12). Wherein, (14),(15),(16) considering Rheumatoid Arthritis (RA) and to determine the applicability of thermaography in the early diagnosis of arthritis patients, its severity and disease activity. In the above mentioned studies, diagnosis of subclinical inflammation has not been considered. Whereas, the diagnosis of early subclinical inflammation may help clinicians in the initial clinical examination of patients. With this background the present study was conducted with an aim to evaluate the efficiency and accuracy of infrared imaging in the detection of inflammation of joints, particularly the subclinical inflammation.

Material and Methods

A prospective cohort study was conducted in the OPD of PMR Department, Agartala Government Medical College (AGMC) and Govind Ballav Pant Hospital (GBPH), Agartala, India from January 2016 to June 2017. The study was approved by the Institutional Ethical Committee of Agartala Government Medical College vide Ethics Committee approval number Ref. no. 4 (6-11)- AGMC/Medical Education/ Ethics Com/2018/15136, dated 31st December, 2018) and written consent from all the patients was obtained.

Patients with joint pain were screened irrespective of their duration of illness considering the inclusion and exclusion criteria and a total of 60 patients were selected for the study. On the basis of clinical examination all these patients were divided in three groups; (i) 37 (61.66%) patients with inflamed joint; (ii) 10 (16.66%) non inflamed joint; and 13 (21.66%) doubtful inflammation of joints.

Inclusion criteria: Patient in the age group between 18-60 years of either gender with joint pain, irrespective of the diseases and the duration of illness were included.

Exclusion criteria: Patients with post-traumatic joint swelling, known of malignancy, mental illness, poor general condition, fever, severe anaemia, presence of metal implant in the joint to be evaluated and presence of skin infection in or around the joint to be studied were excluded from the study.

Study Procedure

The randomly selected patients were clinically evaluated and infrared imaging of concerned joints were captured along with necessary biochemical blood tests. The infrared camera used in this study was FLIR T650sc with resolution of 640×480. The infrared images were captured from knee, ankle, elbow and wrist joints as per clinical presentation. The patients included in this study were having one among the following diagnosis namely Osteoarthritis (OA), Rheumatoid Arthritis (RA), Seronegative Spondyloarthopathy (SSpA), Ankylosing Spondylitis (AS), Reactive Arthritis (ReA), and gout (Table/Fig 2) (17),(18),(19),(20),(21),(22),(23),(24) precisely maintaining all the protocols to create the dataset.

A number of factors can affect the thermogram acquisition adversely (24) which are categorised into four groups namely infrared camera specification, infrared camera positioning, environmental condition and patient preparation (23). Camera specification, camera positioning and patient preparation are easy to handle manually compared to environmental condition. But the control of environmental conditions is not in the hands of human. Radiation of objects present in the surrounding environment of acquisition setup can degrade the quality of Infrared image. Other objects having radiation property may produce the artifacts on the temperature profile of the actual object during capturing, such as electric wires, pipes, outlets etc. Field of View (FOV) and required distance between object and camera with respect to the size of the room were identical for all patients. Authors also tried to control other factors such as room temperature and room humidity. The room temperature was fixed in between 220oC to 250oC and the humidity was between 40% to 60% (25).

A dark room made of black clothes and black coloured wood with closed windows in a closed room for acquisition of Infrared image to avoid these interferences (11). The room was also protected from direct sunlight and air drifts (26). To find the efficiency of thermal imaging in the above mentioned categories, a state-of-the-art experimentation framework was adopted (13),(22). Among these, it was found that the mean temperature is the most common feature used to detect arthritis from thermograms. The mean temperature can be calculated by the following formula:

mean±sum(x)/size(x)

Where, ‘x’ is the respective joint part extracted from the thermograms. Sum(x) is the sum of the intensity values present in ‘x’ and size(x) is the total number of pixel present in ‘x’. According to the previous research works in thermal images from healthy subjects, the mean temperature of the anterior knee was 29.5±1.6°C whereas, 30.5±0.8°C and 30.7±1.3°C in thermal images from RA and OA effected subjects (26),(27).

Clinical examinations, ESR and CRP were incorporated here for validation of infrared thermal imaging. Wherein, clinical examination can be defined by the subjective measures used by clinician for diagnosing inflammation. The subjective measures considered during clinical examination were swelling, tenderness, redness, increased temperature of the joints and restriction of movement of the affected joint. Among these three factors (clinical examination, ESR, CRP), if all of them were found positive then it was considered as positive and vice-versa for negative cases. If either ESR or CRP was positive, then the condition of subclinical inflammation of joint was considered when clinical examination could not assess the inflammation clinically and ESR or CRP was found inconclusive (22).

Statistical Analysis

Four factors such as, sensitivity, specificity, PPV and NPV were used for analysis of the data statistically. MATLAB 2013b software (8.2 version) was used. In MATLAB, the mean values were calculated from the images. The mean value was considered as an indicator of the arthritis. Afterwards, with this mean value authors diagnose subclinical inflammation. Sensitivity, specificity, PPV and NPV are used to assess the efficacy of the mean feature and thermal imaging in detection of subclinical inflammation. In the first step, the mean feature is a dependent variable, whereas pixel values were independent variables. In the second step, specificity, sensitivity, PPV and NPV are the dependent variable and True Positive (TP), False Positive (FP), True Negative (TN) and False Negative (FN) are the independent variables.

Results

The study population was 60 cases with 37 females (61.7%) and 23 males (38.3%). The highest proportions of study participants were found to be suffering from OA i.e., 22 (36.67%) cases (Table/Fig 3).

In (Table/Fig 4), left image shows the positive thermogram of knee with rheumatoid arthritis and right image shows the knee thermogram of normal subject.

(Table/Fig 5) showing two samples of osteoarthritis, (Table/Fig 6) present samples of knee and ankle affected by Reactive Arthritis (ReA). Hands and wrist of rheumatoid arthritis patient are shown in (Table/Fig 7).

A total of 37 (61.66%) patients with clinical presence of inflammation and the average ESR and CRP values were 55.19 mm and 9.03 mg/L, respectively. Out of these cases thermal imaging was able to detect inflammation in 34 cases (91.89%). Thermal imaging failed in 3 (8.10%) cases, where it was unable to detect inflammation.

A total of 10 (16.66%) cases of clinically non inflammatory joint pain with average ESR and CRP values are 13.96 mm and 3.82 mg/L respectively. Out of these cases thermal imaging showed absence of inflammation in eight cases (80%) and failed in two (20%) cases. It is worth noting that in most of the osteoarthritis cases inflammation was absent.

There were 13 (21.66%) subclinical cases in the studied population and the average ESR and CRP of these patients were 27.46 mm and 5.52 mg/L, respectively. Thermal imaging detected inflammation in 11 (84.61%) cases which is compatible with the higher value of average ESR of this group of patients (Table/Fig 8).

(Table/Fig 9) shows the performance of thermal imaging in detection of positive and negative inflammation. It shows that thermal imaging have 91% sensitivity, 80% specificity, PPV of 94% and NPV of 72%.

Discussion

Increase or decrease in temperature has a direct relation with aggravation or reduction of inflammation. Acute inflammatory changes with high heat dissipation can be detected clinically but mild inflammation of joint may not give rise to significant heat to be detected by clinical examination. As a result subclinical features pose several difficulties to the clinicians in accurately diagnosing arthritis. There were number of cases having subclinical inflammation (13),(14).

The observed results also indicated that thermal imaging methodology has the potential in aiding clinicians during clinical examination of the inflammation. The performance of thermal imaging in detection of positive and negative inflammation showed thermal imaging of 91% sensitivity, 80% specificity, PPV 94% and NPV 72%. More specifically, thermal imaging have high sensitivity and specificity which inturn means that thermal imaging is effective in the detection of positive inflammation and negative inflammation with lower rate of FP and FN. The PPV and NPV also showed the efficacy of thermal imaging in detection of positive and negative inflammation. Hence, authors can conclude that thermal imaging has the potential in the detection of subclinical inflammation.

There are several reported literatures regarding thermal imaging in detection of arthritis listed in (Table/Fig 1). Although, there are several studies (10),(11),(12),(13),(14),(15),(16),(28), but according to the authors’ knowledge no work concentrates on detection of subclinical inflammation using thermal imaging. Thermal imaging is an effective tool that can help the clinicians in diagnosis of subclinical inflammation. Hence, clinicians can make use of thermal imaging technology along with their observation to assess the doubtful inflammation.

Limitation(s)

In the present study, though the sample size was small, more study will be helpful to establish the role of thermal imaging in the detection of doubtful inflammation of joints.

Conclusion

The comparison of ESR and CRP values with the infrared thermal imaging implied that thermal imaging can be considered as a tool for detection of inflammation of joint including the subclinical inflammation of joint.

References

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DOI and Others

DOI: 10.7860/JCDR/2022/49612.16029

Date of Submission: Mar 25, 2021
Date of Peer Review: May 15, 2021
Date of Acceptance: Oct 09, 2021
Date of Publishing: Feb 01, 2022

AUTHOR DECLARATION:
• Financial or Other Competing Interests: Funded under Grant No. 5/7/1516/2016- RCH, Dated 20/06/2017 by
ICMR, Government of India.
• Was Ethics Committee Approval obtained for this study? Yes
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Mar 27, 2021
• Manual Googling: Oct 08, 2021
• iThenticate Software: Jan 15, 2022 (19%)

ETYMOLOGY: Author Origin

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