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Abstract Number: 0545

Referral Pattern and Factors Associated with Time to Diagnosis for Lupus in India- multicentric Data from the SLE Special Interest Group (SIG) of the Indian Rheumatology Association (IRA)

Vineeta Shobha1, Liza Rajasekhar2, Shaleni V1, Arul Rajamurgan3, VijayKR Rao4, Subramanian Nallasivan5, Dr Yogesh Preet Singh6, Avinash Jain7, Aradhana Singh8, Franciosalgeo George1, Sourabh Malviya9, Deepak Yadav10, John Mathew11 and Amita Aggarwal10, 1St. John's National Academy of Health Science, Bangalore, India, 2Nizam's Institute of Medical Sciences, Madhapur, India, 3Madras Medical College, Chennai, India, 4Divisha Arthritis and Medical Center, Bangalore, India, 5Velammal Medical College Hospital, Madurai, India, 6Himalayan Institute of Medical Sciences, Dehradun, India, 7SMS Medical College, Lucknow, India, 8SMSMC&H, Jaipur, India, 9Medanta super speciality Hospital, Indore, India, 10Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Lucknow, India, 11Christian Medical College Vellore, Vellore, India

Meeting: ACR Convergence 2023

Keywords: Demographics, Epidemiology, Health Care, socioeconomic factors, Systemic lupus erythematosus (SLE)

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Session Information

Date: Sunday, November 12, 2023

Title: (0543–0581) SLE – Diagnosis, Manifestations, & Outcomes Poster I

Session Type: Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Early diagnosis remains an unmet need for SLE patients across the world. Reasons for delay in diagnosis differ in various geographic regions and largely depend on accessibility to medical care. We report the time to diagnosis, its determinants and the referral pattern from India.

Methods: Members of the Lupus special interest group developed a questionnaire including a pilot run to understand the referral pattern and variables affecting time to diagnosis of Lupus. Patients fulfilling the SLICC criteria for SLE diagnosed after Jan 2022 were included. All patients provided written informed consent. All centres received permission from their ethics committees. Their socio demographic profile as per modified Kuppuswamy scale(2022), health care referral pattern, organ systems affected and disease related parameters at diagnosis were recorded. The data was categorised into early and late diagnosis based on median time taken for diagnosis and the differences were explored using Chi-square, univariate and multivariate logistic regression.

Results: Nine centres provided data for 348 patients for this study, four were Government university teaching hospitals(n=191), 3 private university teaching hospitals (n=116) and 2 from single specialty clinics (n=41). Figure 1 represents an overview of centres which participated in the current study and the home states from where the patients were enrolled. Patients originated from both rural (48%) as well as urban areas(52%).

The mean age of SLE patients was 28.48±10.92 years, 93% were women and 57% were married. The median time to diagnosis was 7 months(IQR 3::18), about one third [92(30.4%)] were diagnosed within 3 months and 55(18.2%) within one month. In about 38%, the diagnosis was beyond 12 months. Renal involvement at diagnosis was observed in 19.3% (69/348).The mean SLEDAI-2k at diagnosis (n=232) was 12.13+ 6.85 and in 33/232(14.2%) SLEDAI was <4.

The mean Kuppuswamy scale was 12.39+6.55 reflective of lower middle class patient population. In the univariate analysis, illiteracy (uOR=1.81, 95%CI:0.99,3.35), renal involvement (uOR=1.87,95%CI:0.90,3.93) and lower family income (p=0.05) were found to be associated with delayed diagnosis.(table1) However, in the multivariate analysis only illiteracy (AOR=2.36,95%CI:1.02,5.66) remained significantly associated with delayed diagnosis.(table2)

The referring practitioners were largely another graduate or postgraduate doctor (87%). No referral was made by a medical field worker. The family size, employment and marital status did not influence the time to diagnosis, however, the regional differences were evident.(p=0.001) Almost half patients were self-financing (56.6%) ,with one-third (36.9%) utilising private medical insurance and < 2% receiving government health insurance.

Conclusion: Very early diagnosis (within 3 months of symptom onset) was made in about a third of SLE patients. Time taken for diagnosis was longer in those with low literacy and differed in geographic regions of our country.

Supporting image 1

Abbreviations: NPSLE- Neuropsychiatric systemic lupus erythematosus, SLEDAI 2K- SLE disease activity Index.

Supporting image 2

Supporting image 3


Disclosures: V. Shobha: None; L. Rajasekhar: None; S. V: None; A. Rajamurgan: None; V. Rao: None; S. Nallasivan: None; D. Singh: None; A. Jain: None; A. Singh: None; F. George: None; S. Malviya: None; D. Yadav: None; J. Mathew: None; A. Aggarwal: None.

To cite this abstract in AMA style:

Shobha V, Rajasekhar L, V S, Rajamurgan A, Rao V, Nallasivan S, Singh D, Jain A, Singh A, George F, Malviya S, Yadav D, Mathew J, Aggarwal A. Referral Pattern and Factors Associated with Time to Diagnosis for Lupus in India- multicentric Data from the SLE Special Interest Group (SIG) of the Indian Rheumatology Association (IRA) [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 9). https://acrabstracts.org/abstract/referral-pattern-and-factors-associated-with-time-to-diagnosis-for-lupus-in-india-multicentric-data-from-the-sle-special-interest-group-sig-of-the-indian-rheumatology-association-ira/. Accessed .
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