Hospitalization in amyotrophic lateral sclerosis
- 27 March 2001
- journal article
- Published by Wolters Kluwer Health in Neurology
- Vol. 56 (6) , 753-757
- https://doi.org/10.1212/wnl.56.6.753
Abstract
Objective: As ALS progresses, extensive supportive care is required, including multidisciplinary outpatient care and hospitalization. The authors studied the causes, health care utilization, and outcomes for hospitalized patients with ALS. Methods: With use of the 1996 Nationwide Inpatient Sample, an administrative database representing 20% of U.S. hospitals, 1,600 hospitalizations in patients with ALS were identified and compared with 5,364,728 non-ALS hospitalizations. Results: The most common concurrent diagnoses in patients with ALS were dehydration and malnutrition (574 patients, 36%), pneumonia (507 patients, 32%), and respiratory failure (398 patients, 25%). Only 38% of patients with ALS were discharged to home without home health care compared with 73% of patients with non-ALS. Fifteen percent of patients with ALS died in the hospital compared with 3% of non-ALS patients. The average length of hospital stay and charges were greater for patients with ALS than for non-ALS patients (8.4 days and $19,810 for ALS patients and 5.4 days and $11,924 for non-ALS patients). Mortality was significantly associated with emergency room admission (versus nonemergency admission; OR = 1.60), increasing age (per year; OR = 1.03), respiratory failure (OR = 3.37), and pneumonia (OR = 2.02) (p < 0.01 for all comparisons). Conclusions: Patients with ALS have lengthy and costly hospital admissions, a high in-hospital mortality rate, and few routine discharges. Recognition of the issues that precipitate hospitalization may allow development of preventive strategies.Keywords
This publication has 21 references indexed in Scilit:
- The ALS Patient Care DatabaseNeurology, 2000
- Home mechanical ventilation for amyotrophic lateral sclerosis: nasal compared to tracheostomy-intermittent positive pressure ventilationJournal of the Neurological Sciences, 1996
- Percutaneous endoscopic gastrostomy in patients with amyotrophic lateral sclerosis and impaired pulmonary functionGastrointestinal Endoscopy, 1994
- A comparison of administrative versus clinical data: coronary artery bypass surgery as an exampleJournal of Clinical Epidemiology, 1994
- Adult onset motor neuron disease: worldwide mortality, incidence and distribution since 1950.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Effects of an Expanding Home Care Program for the Terminally IIIMedical Care, 1987
- Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in managementAnnals of Neurology, 1985
- Spirometry in Amyotrophic Lateral SclerosisArchives of Neurology, 1979
- STUDIES ON EPIDEMIOLOGICAL, CLINICAL AND ETIOLOGICAL ASPECTS OF ALS DISEASE IN SARDINIA, SOUTHERN ITALYActa Neurologica Scandinavica, 1977
- Functional studies of the parotid and pancreas glands in amyotrophic lateral sclerosisJournal of Neurology, Neurosurgery & Psychiatry, 1974