Literature DB >> 17718102

Subspecialty evaluation of chronically ill hospitalized patients with suspected immune defects.

Ami Mehra1, Peter Sidi, John Doucette, Lissette Estrella, Helen Rouvelas, Charlotte Cunningham-Rundles.   

Abstract

BACKGROUND: The diagnosis of primary immunodeficiency is suggested by recurrent or unusual infections and inflammatory and autoimmune conditions. Because the diversity of immune defects and clinical presentations poses a diagnostic challenge in hospital populations, a computer algorithm was devised to help identify patients.
OBJECTIVE: To assess use of pertinent subspecialty clinics by patients with clinical features of immunodeficiency.
METHODS: Using a validated algorithm based on International Classification of Diseases, Ninth Revision (ICD-9), codes applied to The Mount Sinai Hospital billing records, we investigated hospitalized patients, 60 years or younger, who had been diagnosed as having conditions associated with immunodeficiency, excluding those with confounding medical conditions. Immunodeficiency-related disease codes were given a weighted score based on relative severity and expressed as a sum for admissions between January 1, 1999, and December 31, 2003. Demographic features, subspecialty care, and clinic attendance were determined.
RESULTS: The 296 computer-identified patients with illnesses characteristic of immunodeficiency were 35.8% Hispanic, 27.0% African American, and 21.6% white; their median age was 13.3 years. Patients were hospitalized 1,261 times, or a median of 4.2 times each (range, 1-42 times), and had 5,700 diagnoses. Of the patients, 75.0% received primary care at The Mount Sinai Hospital. Although the most common diagnosis was pneumonia (n = 243), 45% of patients never received allergy/immunology or pulmonary subspecialty care.
CONCLUSION: Despite receiving primary medical care at the same hospital, many frequently hospitalized subjects with features of immunodeficiency do not receive medical care in appropriate subspecialty clinics.

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Year:  2007        PMID: 17718102     DOI: 10.1016/S1081-1206(10)60638-2

Source DB:  PubMed          Journal:  Ann Allergy Asthma Immunol        ISSN: 1081-1206            Impact factor:   6.347


  4 in total

Review 1.  Common variable immunodeficiency: etiological and treatment issues.

Authors:  Sean Deane; Carlo Selmi; Stanley M Naguwa; Suzanne S Teuber; M Eric Gershwin
Journal:  Int Arch Allergy Immunol       Date:  2009-07-01       Impact factor: 2.749

Review 2.  The Importance of Primary Immune Deficiency Registries: The United States Immunodeficiency Network Registry.

Authors:  Joao Pedro Lopes; Charlotte Cunningham-Rundles
Journal:  Immunol Allergy Clin North Am       Date:  2020-06-07       Impact factor: 3.479

3.  Examining the use of ICD-9 diagnosis codes for primary immune deficiency diseases in New York State.

Authors:  Elena S Resnick; Priyanka Bhatt; Peter Sidi; Charlotte Cunningham-Rundles
Journal:  J Clin Immunol       Date:  2012-09-01       Impact factor: 8.317

Review 4.  Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice.

Authors:  Beatriz Tavares Costa-Carvalho; Anete Sevciovic Grumach; José Luis Franco; Francisco Javier Espinosa-Rosales; Lily E Leiva; Alejandra King; Oscar Porras; Liliana Bezrodnik; Mathias Oleastro; Ricardo U Sorensen; Antonio Condino-Neto
Journal:  J Clin Immunol       Date:  2013-11-16       Impact factor: 8.317

  4 in total

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