Predictors of emergent feeding tubes and tracheostomies in amyotrophic lateral sclerosis (ALS)

Abstract Predictable decline in ALS makes unplanned gastrostomy and tracheostomy avoidable. We determined whether gastrostomy or tracheostomy insertion during emergent hospitalization is associated with patient or hospital characteristics, changed Medicare policy in 2001, or proximity to specialized ALS care. We performed a retrospective analysis of hospitalizations and procedures for ALS/MND patients in Pennsylvania between 1996 and 2009. We identified predictors of gastrostomy/tracheostomy during emergent hospitalization and trends over time. Patients underwent 1748 gastrostomies and 373 tracheostomies. Thirty-two percent of gastrostomies and 67% of tracheostomies were placed emergently. Emergent hospitalizations involving gastrostomy were more expensive with fewer home discharges. Black patients and Medicaid patients had higher odds of emergent gastrostomy placement. Conversely, academic hospital affiliation decreased odds of emergent gastrostomy or tracheostomy placement (AOR 0.49, AOR 0.37, p < 0.001). After Medicare policy changes, gastrostomy use increased, while emergent gastrostomies decreased. Surprisingly, proximity to specialized care was associated with increased emergent gastrostomy placement. In conclusion, black patients and Medicaid patients were more likely to undergo emergent gastrostomy insertion. Patients receiving gastrostomy during emergent admissions had fewer home discharges and higher costs. Academic hospital affiliation decreased odds of emergent gastrostomy or tracheostomy. After Medicare changes broadening access, while gastrostomy use increased, the proportion of emergent procedures decreased.

[1]  C. Steiner,et al.  Comorbidity measures for use with administrative data. , 1998, Medical care.

[2]  W. Knaus,et al.  Influence of Patient Preferences and Local Health System Characteristics on the Place of Death , 1998, Journal of the American Geriatrics Society.

[3]  R. Sufit,et al.  Practice parameter: The care of the patient with amyotrophic lateral sclerosis (An evidence‐based review) , 1999, Muscle & nerve.

[4]  Steven M. Albert,et al.  Prospective study of palliative care in ALS: choice, timing, outcomes , 1999, Journal of the Neurological Sciences.

[5]  R. Sufit,et al.  Practice parameter: The care of the patient with amyotrophic lateral sclerosis (an evidence-based review) , 1999, Neurology.

[6]  T L Munsat,et al.  Practice Parameter: The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology , 1999, Neurology.

[7]  M. Borum,et al.  The Effects of Patient Race on Outcomes in Seriously Ill Patients in SUPPORT: An Overview of Economic Impact, Medical Intervention, and End‐Of‐Life Decisions , 2000, Journal of the American Geriatrics Society.

[8]  M. Leavitt Medscape's response to the Institute of Medicine Report: Crossing the quality chasm: a new health system for the 21st century. , 2001, MedGenMed : Medscape general medicine.

[9]  Adriano Chiò,et al.  Validity of hospital morbidity records for amyotrophic lateral sclerosis. A population-based study. , 2002, Journal of clinical epidemiology.

[10]  O. Hardiman,et al.  Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000 , 2003, Journal of neurology, neurosurgery, and psychiatry.

[11]  R. Sufit,et al.  Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunction , 2003, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

[12]  S. Tang,et al.  Determinants of Congruence between the Preferred and Actual Place of Death for Terminally Ill Cancer Patients , 2003, Journal of palliative care.

[13]  S H Appel,et al.  Prevalence and patterns of cognitive impairment in sporadic ALS , 2005, Neurology.

[14]  L. H. van den Berg,et al.  Multidisciplinary ALS care improves quality of life in patients with ALS , 2005, Neurology.

[15]  R. Olney,et al.  The effects of executive and behavioral dysfunction on the course of ALS , 2005, Neurology.

[16]  A. Chiò,et al.  Positive effects of tertiary centres for amyotrophic lateral sclerosis on outcome and use of hospital facilities , 2006, Journal of Neurology, Neurosurgery & Psychiatry.

[17]  Richard L Street,et al.  Racial differences in doctors' information‐giving and patients' participation , 2006, Cancer.

[18]  R. Olney,et al.  Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. , 2006, The Cochrane database of systematic reviews.

[19]  P. Maciejewski,et al.  Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment. , 2008, JAMA.

[20]  Haiden A Huskamp,et al.  Health care costs in the last week of life: associations with end-of-life conversations. , 2009, Archives of internal medicine.

[21]  H. Mitsumoto,et al.  Outcomes research in amyotrophic lateral sclerosis: Lessons learned from the amyotrophic lateral sclerosis clinical assessment, research, and education database , 2009, Annals of neurology.

[22]  N. Keating,et al.  Place of death: correlations with quality of life of patients with cancer and predictors of bereaved caregivers' mental health. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.