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  • Measure Summary
  • NQMC:010267
  • Jul 2012

Amyotrophic lateral sclerosis (ALS): percentage of patients diagnosed with ALS and dysphagia, weight loss, or impaired nutrition who were offered at least once annually dietary or enteral nutrition support via percutaneous endoscopic gastrostomy or radiographic inserted gastrostomy.

American Academy of Neurology (AAN). Amyotrophic lateral sclerosis performance measurement set. St. Paul (MN): American Academy of Neurology (AAN); 2012 Jul 31. 75 p.

View the original measure documentation External Web Site Policy

This is the current release of the measure.

Primary Measure Domain

Clinical Quality Measures: Process

Secondary Measure Domain

Does not apply to this measure

Description

This measure is used to assess the percentage of patients diagnosed with amyotrophic lateral sclerosis (ALS) and dysphagia, weight loss, or impaired nutrition who were offered at least once annually dietary or enteral nutrition support via percutaneous endoscopic gastrostomy (PEG) or radiographic inserted gastrostomy (RIG).

Rationale

There is supportive evidence that implementation of enteral feeding will result in improved survival. Studies compared survival in patients receiving percutaneous endoscopic gastrostomy (PEG) (n=585) vs. those without PEG (n=1619). One study demonstrated a survival advantage vs. control with multivariate analysis (p equals 0.02), but not with univariate analysis (p equals 0.09) (Chio et al., 1999). A population-based study from Italy found improved survival with PEG compared to patients with oral intake, also based on a multivariate analysis (3.89-fold; p equals 0.0004) (Chiò et al., 2002). Two studies demonstrated prolonged survival in the PEG group vs. PEG refusers similar results when patients with PEG were compared to nasogastric-fed controls (p equals 0.03). However, 4 studies failed to find a significant survival benefit with PEG (Chiò et al., 1999; Chiò et al., 2002; Desport et al., 2000; Mitsumoto et al., 2003). All but one (Forbes, Colville, & Swingler, 2004) of the negative studies included patients not needing PEG as a control group. The positive studies used controls that refused PEG (Del Piano et al., 1999; Mazzini et al., 1995) or used a risk model and multivariate analysis based on factors that predicted survival (statistically controlling for confounders) (Chiò et al., 1999; Chiò et al., 2002). Studies using appropriate controls or multivariate analysis demonstrated that PEG is probably effective in prolonging survival in amyotrophic lateral sclerosis (ALS), although insufficient data exist to quantitate the survival advantage (Katzberg & Benatar, 2011).

The following clinical recommendation statements are quoted verbatim from the referenced clinical guidelines and represent the evidence base for the measure:

  • In patients with ALS with impaired oral food intake, enteral nutrition via PEG/radiologically inserted gastrostomy (RIG) should be considered to stabilize body weight (Miller et al., 2009).
  • PEG or RIG should be considered for prolonging survival in patient with ALS (Miller et al., 2009).
  • When PEG is indicated, patient and carers should be informed: (i) of the benefits and risks of the procedure; (ii) that it is possible to continue to take food orally as long as it is possible; (iii) that deferring PEG to a late disease stage may increase the risk of the procedure (Andersen et al., 2005).
  • The timing of PEG/RIG is based on an individual approach taking into account bulbar symptoms, malnutrition (weight loss greater than 10%), respiratory function and the patient's general condition. Thus, early operation is highly recommended (Andersen et al., 2005).

Evidence for Rationale

American Academy of Neurology (AAN). Amyotrophic lateral sclerosis performance measurement set. St. Paul (MN): American Academy of Neurology (AAN); 2012 Jul 31. 75 p.

Andersen PM, Borasio GD, Dengler R, Hardiman O, Kollewe K, Leigh PN, Pradat PF, Silani V, Tomik B, EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral. EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relatives. Eur J Neurol. 2005 Dec;12(12):921-38. [122 references] PubMed External Web Site Policy

Chiò A, Finocchiaro E, Meineri P, Bottacchi E, Schiffer D. Safety and factors related to survival after percutaneous endoscopic gastrostomy in ALS. ALS Percutaneous Endoscopic Gastrostomy Study Group. Neurology. 1999 Sep 22;53(5):1123-5. PubMed External Web Site Policy

Chiò A, Mora G, Leone M, Mazzini L, Cocito D, Giordana MT, Bottacchi E, Mutani R, Piemonte and Valle d'Aosta Register for ALS (PARALS). Early symptom progression rate is related to ALS outcome: a prospective population-based study. Neurology. 2002 Jul 9;59(1):99-103. PubMed External Web Site Policy

Del Piano M, Occhipinti P, Orsello M, Ballare M. Percutaneous endoscopic gastrostomy (PEG) reduces complications and improves survival in amyotrophic lateral sclerosis (ALS). Gastrointest Endosc. 1999;49:AB192.

Desport JC, Preux PM, Truong CT, Courat L, Vallat JM, Couratier P. Nutritional assessment and survival in ALS patients. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Mar;1(2):91-6. PubMed External Web Site Policy

Forbes RB, Colville S, Swingler RJ, Scottish Motor Neurone Disease Research Group. Frequency, timing and outcome of gastrostomy tubes for amyotrophic lateral sclerosis/motor neurone disease--a record linkage study from the Scottish Motor Neurone Disease Register. J Neurol. 2004 Jul;251(7):813-7. PubMed External Web Site Policy

Katzberg HD, Benatar M. Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database Syst Rev. 2011;(1):CD004030. PubMed External Web Site Policy

Mazzini L, Corra T, Zaccala M, Mora G, Del Piano M, Galante M. Percutaneous endoscopic gastrostomy and enteral nutrition in amyotrophic lateral sclerosis. J Neurol. 1995 Oct;242(10):695-8. PubMed External Web Site Policy

Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W, Kalra S, Katz JS, Mitsumoto H, Rosenfeld J, Shoesmith C, Strong MJ, Woolley SC, Quality Standards Subcommittee of the American Academy of Neurology. Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2009 Oct 13;73(15):1218-26. [40 references] PubMed External Web Site Policy

Mitsumoto H, Davidson M, Moore D, Gad N, Brandis M, Ringel S, Rosenfeld J, Shefner JM, Strong MJ, Sufit R, Anderson FA, ALS CARE Study Group. Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunction. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):177-85. PubMed External Web Site Policy

Primary Health Components

Amyotrophic lateral sclerosis (ALS); dysphagia; weight loss; impaired nutrition; dietary nutrition support; enteral nutrition support; percutaneous endoscopic gastrostomy (PEG); radiographic inserted gastrostomy (RIG)

Denominator Description

All patients with a diagnosis of amyotrophic lateral sclerosis (ALS) and dysphagia, weight loss or impaired nutrition (see the related "Denominator Inclusions/Exclusions" field)

Numerator Description

Patients who were offered at least once annually dietary or enteral nutrition support via percutaneous endoscopic gastrostomy (PEG) or radiographic inserted gastrostomy (RIG)

Type of Evidence Supporting the Criterion of Quality for the Measure

  • A clinical practice guideline or other peer-reviewed synthesis of the clinical research evidence
  • A formal consensus procedure, involving experts in relevant clinical, methodological, public health and organizational sciences
  • A systematic review of the clinical research literature (e.g., Cochrane Review)
  • One or more research studies published in a National Library of Medicine (NLM) indexed, peer-reviewed journal

Additional Information Supporting Need for the Measure

Importance of Topic

Prevalence and Incidence

  • Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a type of motor neuron disease that is a rapidly progressive and fatal neurological disease (National Institute of Neurological Disorders and Stroke [NINDS], 2013).
  • Twenty thousand to 30,000 people in the United States (U.S.) have ALS (NINDS, 2013).
  • Five thousand people are diagnosed with ALS in the U.S. annually (NINDS, 2013).
  • ALS is one of the most common neuromuscular diseases worldwide (NINDS, 2013).
  • In 90% to 95% of all ALS cases the disease occurs apparently at random with no clearly associated risk factors (NINDS, 2013).
  • Five percent to 10% of all ALS cases are inherited (NINDS, 2013).
  • Twenty percent of all familial cases result from a specific genetic defect that leads to mutation of the enzyme known as superoxide dismutase 1 (SOD1) (NINDS, 2013).
  • No cure exists for ALS. Newer pharmacotherapy agents have been found to reduce the progression, but not halt the disease development (NINDS, 2013).
  • The prevalence of ALS is said to be between six and eight cases per 100,000 in the population. Using the higher prevalence estimate and data from the 2000 U.S. census, nearly 22,600 Americans are living with ALS at any one time. Since ALS is a disease of aging, as the U.S. population increases and ages, an increase in the prevalence of ALS can be anticipated (ALS Association, 2012)
  • Cognitive dysfunction is seen in 20% to 50%, while only 3% to 5% develop dementia that is usually of frontotemporal type (Strong et al., 2009). Consensus criteria for diagnosis have recently been reported (Strong et al., 2009).
  • Death due to respiratory failure follows on average 2 to 4 years after onset, but a small group may survive for a decade or more (Haverkamp, Appel, & Appel, 1995).
  • The mean age of onset is 47 to 52 years in familial cases (FALS) and 58 to 63 years in sporadic (SALS) cases (Bobowick & Brody, 1973).
  • The lifetime risk for developing ALS for individuals aged 18 years has been estimated to be 1 in 350 for men and 1 in 420 for women (Armon, 2007) with male sex, increasing age and hereditary disposition being the main risk factors (Heffernan et al., 2006).

Mortality and Morbidity

  • Most patients with ALS die within 2 to 5 years of onset (Lechtzin et al., 2002). Only 10% of ALS patients survive for 10 years or more (Miller et al., "Drug, nutritional," 2009).
  • Treatment of respiratory insufficiency improves survival, quality of life and respiratory symptoms (Lechtzin et al., 2002; Miller et al., "Drug, nutritional," 2009). The diagnosis and management of respiratory insufficiency is critical because most deaths from ALS are due to respiratory failure (Lechtzin et al., 2002; Miller et al., "Drug, nutritional," 2009; EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis et al., 2012; Laird et al., 2001).
  • Falls surveillance will lead to interventions to prevent falls and decrease fall related deaths in ALS patients. Falls are an independent predictor of adverse health outcomes (Gil et al., 2008). Fall related deaths occur in 1.7% of ALS patients (Rubenstein & Josephson, 2002). Several specific risk factors for falls have been identified, including muscle weakness, deficits in gait or balance, visual deficits, arthritis, impairments in activities of daily living, depression, and cognitive impairment (Ringholz et al., 2005).
  • Studies confirm the presence of cognitive impairment in 50% of patients with ALS and particularly implicate executive dysfunction and mild memory decline in the disease process (Laird et al., 2001). More severe impairment occurs in a subset of patients with ALS and has features consistent with frontal temporal dementia (FTD) (Phukan, Pender, & Hardiman, 2007; Gordon et al., 2007). Recent studies have demonstrated the feasibility of screening patients in a busy specialized ALS clinic (Flaherty-Craig et al., 2009; Woolley & Katz, 2011), but this is still not routinely practiced. A fuller characterization of the extent of cognitive and behavioral dysfunction in ALS has important implications given that it shortens survival (Elamin et al., 2011), and the burden and stress for carers of patients with FTD is very great. It also has relevance to effective communication, legal issues and end-of-life decision making by patients with motor neuron disease (MND) (Elamin et al., 2011).
  • Pseudobulbar affect (PBA), excessive laughing or crying, or involuntary emotional expression disorder affects 20% to 50% of patients with ALS, especially in pseudobulbar palsy (McCullagh et al., 1999). Patients are embarrassed and isolated by these symptoms, which in turn greatly diminishes the patients' quality of life.
  • Sialorrhea, or drooling, is embarrassing, socially isolating, and is associated with aspiration pneumonia. The prevalence is estimated at 50%, and 70% of patients receiving oral medications for treatment reported benefit (Laird et al., 2001; Miller et al., "Multi-disciplinary," 2009)
  • Fatigue may be a symptom of depression, poor sleep, abnormal muscle activation, immobility, or respiratory dysfunction. Fatigue diminishes quality of life for patients with ALS. Fatigue was a side effect of therapy in 26% of patients taking riluzole vs. 13% taking placebo (Bensimon, Lacomblez, & Meininger, 1994). Asthenia occurred in 18% of patients taking riluzole vs. 12% of patients taking placebo in a larger study (Lacomblez et al., 1996).
  • The prevalence of depression in ALS ranges from 0% to 44%, although systematic studies suggest 10% in advanced ALS (Laird et al., 2001; Wicks et al., 2007). Depression shortens survival and lowers quality of life for patients with ALS (Phukan, Pender, & Hardiman, 2007). There is consensus among experts that depression should be treated in patients with ALS (Laird et al., 2001); however, there are no controlled studies of benefit or harm.
  • Insomnia is common in ALS and may be a symptom of early respiratory weakness, underlying anxiety, depression, or pain (Hetta & Jansson, 1997). There is a concern that sedative/hypnotic agents may suppress the respiratory drive in patients with ALS.
  • Weight loss is a key prognostic indicator for ALS with the risk of death increased 7-fold when body mass index is less than 18.5 kg/m2 (Marin et al., 2011; Lehéricey et al., 2012; Spataro et al., 2011; Desport et al., 1999; Vaisman et al., 2009; Dupuis et al., 2008).
  • ALS patients have dysarthria in nearly all bulbar onset patients and nearly 40% of ALS patients with spinal onset. More than 95% of ALS patients cannot speak before death and patients who accept gastrostomy tube, non-invasive ventilation or tracheostomy-ventilation have a greater need for augmentative alternative communication as the disease progresses (Ball, Beukelman, & Pattee, "Communication," 2004; Ball, Beukelman, & Pattee, "Acceptance," 2004; Mathy, Yorkston, & Gutmann, 2000; Beukelman, Fager, & Nordness, 2011).
  • End of life discussions will improve patient decision making with respect to disease management (NINDS, 2013; ALS Association, 2012; Strong et al., 2009; Haverkamp, Appel, & Appel, 1995; Bobowick & Brody, 1973; Heffernan et al., 2006). Pain in ALS should be treated following accepted guidelines (Oliver et al., 2011; Albert et al., 1999, Mitsumoto et al., 2005; Nolan et al., 2008; Albert et al., 2005; Albert et al., 2009).

Office Visits and Hospital Stays

  • One study's significant findings were that common morbidities increased over time (pneumonia [38.1% to 47.3%], respiratory failure [26.9% to 35.5%], and nutritional deficiency [43.0% to 56.3%]); the median length of stay dropped from 6 to 4 days; mean hospital charges increased from $21,574 to $24,314; the proportion of hospital deaths decreased over time (17.6% to 14.6%), whereas the proportion discharged to home health/hospice care (14.0% to 18.2%) and to long-term care facilities (13.2% to 27.9%) increased. The odds ratio (OR) of death was 5.03 (95% CI: 4.57 to 5.54) for those admitted with respiratory failure, 1.36 (1.24 to 1.50) for those with pneumonia, and 0.84 (0.77 to 0.92) for those with nutritional deficiency. The high OR of death in patients admitted for pneumonia or respiratory failure is likely associated with more advanced disease, whereas the protective effect of admission for nutritional deficiency is consistent with the predominance of bulbar symptoms and admission earlier in the disease. The trends during the 15 years of this administrative data set were for increasing comorbidities and higher utilization of end-of-life care (Dubinsky, Chen, & Lai, 2006).

Family Caregiving

  • Caregiver burden was correlated to their level of depression and quality of life and, differently from other chronic disorders, increased with the worsening of patients' disability. ALS patients have a good objective perception of their impact on caregivers (Chiò et al., 2005).
  • Recent studies assessing caregivers' burden in chronic neurologic disorders have found some features shared by caregivers: the perceived burden exceeds the objective measures of patients' impairment, the amount of burden is independent of diagnosis, and the patients' cognitive functioning is an important factor in determining the level of burden (Thommessen et al., 2002).

Cost

  • ALS is a difficult to diagnose, fatal, progressive degenerative disease with an average survival time of 2 to 5 years. Percutaneous endoscopic gastrostomy (PEG) and bi-level intermittent positive pressure (BIPAP) ventilation may be the major interventions leading to longer survival of patients with ALS. Riluzole has been shown to have modest effects on survival (as opposed to functional) gains and is currently the only drug approved for the treatment of ALS. Mechanical ventilation (via a tracheostomy tube) is expensive, but is widely used in later stage patients with ALS in the U.S. A review of nine cost-effectiveness studies of riluzole found the following: drug costs and survival gains are the major drivers of cost effectiveness; survival gains are estimated from truncated databases with a high degree of uncertainty; more accurate stage-specific utility weights based on patients who agreed to treatment are needed; case incidence-based evaluations should be carried out; cost-effectiveness ratios are insensitive to discount rates; employment and caregiver issues or externalities have been widely ignored; threshold acceptance cost-effectiveness values are ill-defined and evaluations are not generalizable to other countries because of cost and treatment style differences. On account of the high degree of uncertainty pertaining to survival gains and the relatively high costs per life years or quality-adjusted life-years gained, and while acknowledging that not every therapy has to be cost effective (e.g., orphan drugs), it is still inconclusive as to whether or not riluzole can be considered as cost-effective therapy for ALS (Ginsberg & Lowe, 2002).

Disparities

  • All races and ethnic backgrounds are affected by ALS (NINDS, 2013).
  • ALS most common in individuals 40 to 60 years old, but younger and older people can develop the disease (NINDS, 2013).
  • Men are more likely to develop ALS than women. Studies suggest an overall ratio of about 1.5 men to every woman who develops ALS in Western countries (ALS Association, 2012).

Opportunity for Improvement

  • Not all patients who should have enteral feeding receive this treatment with only 43% of ALS patients who met guideline indications for gastrostomy tube placement undergoing the procedure (Miller et al., "Outcomes," 2009). Increasing proportions of patients who would most likely benefit are now receiving treatment but not all (Bradley et al., 2004; Mitsumoto et al., 2003; Albert et al., 2001; Rabkin, Wagner, & Del Bene, 2000).
  • Poor respiratory function increases the risk of the procedure (Miller, "Outcomes," 2009). Early detection of impaired nutrition and referral to a gastroenterologist will increase the safety and utilization of percutaneous endoscopic gastrostomy (PEG) and radiographic inserted gastrostomy (RIG) (Bradley et al., 2004; Mitsumoto et al., 2003; Albert et al., 2001).

Evidence for Additional Information Supporting Need for the Measure

Albert SM, Murphy PL, Del Bene M, Rowland LP, Mitsumoto H. Incidence and predictors of PEG placement in ALS/MND. J Neurol Sci. 2001 Oct 15;191(1-2):115-9. PubMed External Web Site Policy

Albert SM, Murphy PL, Del Bene ML, Rowland LP. Prospective study of palliative care in ALS: choice, timing, outcomes. J Neurol Sci. 1999 Oct 31;169(1-2):108-13.

Albert SM, Rabkin JG, Del Bene ML, Tider T, O'Sullivan I, Rowland LP, Mitsumoto H. Wish to die in end-stage ALS. Neurology. 2005 Jul 12;65(1):68-74. PubMed External Web Site Policy

Albert SM, Whitaker A, Rabkin JG, del Bene M, Tider T, O'Sullivan I, Mitsumoto H. Medical and supportive care among people with ALS in the months before death or tracheostomy. J Pain Symptom Manage. 2009 Oct;38(4):546-53. PubMed External Web Site Policy

ALS Association. Epidemiology of ALS and suspected clusters. [internet]. Washington (DC): ALS Association; [accessed 2012 Apr 06].

American Academy of Neurology (AAN). Amyotrophic lateral sclerosis performance measurement set. St. Paul (MN): American Academy of Neurology (AAN); 2012 Jul 31. 75 p.

Armon C. Sports and trauma in amyotrophic lateral sclerosis revisited. J Neurol Sci. 2007 Nov 15;262(1-2):45-53. PubMed External Web Site Policy

Ball LJ, Beukelman DR, Pattee GL. Acceptance of augmentative and alternative communication technology by persons with amyotrophic lateral sclerosis. Augmentative Altern Commun. 2004;20(2):113-22.

Ball LJ, Beukelman DR, Pattee GL. Communication effectiveness of individuals with amyotrophic lateral sclerosis. J Commun Disord. 2004 May-Jun;37(3):197-215. PubMed External Web Site Policy

Bensimon G, Lacomblez L, Meininger V. A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. N Engl J Med. 1994 Mar 3;330(9):585-91. PubMed External Web Site Policy

Beukelman D, Fager S, Nordness A. Communication support for people with ALS. Neurol Res Int. 2011;2011:714693. PubMed External Web Site Policy

Bobowick AR, Brody JA. Epidemiology of motor-neuron diseases. N Engl J Med. 1973 May 17;288(20):1047-55. PubMed External Web Site Policy

Bradley WG, Anderson F, Gowda N, Miller RG, ALS CARE Study Group. Changes in the management of ALS since the publication of the AAN ALS practice parameter 1999. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Dec;5(4):240-4. PubMed External Web Site Policy

Chiò A, Gauthier A, Calvo A, Ghiglione P, Mutani R. Caregiver burden and patients' perception of being a burden in ALS. Neurology. 2005 May 24;64(10):1780-2. PubMed External Web Site Policy

Desport JC, Preux PM, Truong TC, Vallat JM, Sautereau D, Couratier P. Nutritional status is a prognostic factor for survival in ALS patients. Neurology. 1999 Sep 22;53(5):1059-63. PubMed External Web Site Policy

Dubinsky R, Chen J, Lai SM. Trends in hospital utilization and outcome for patients with ALS: analysis of a large U.S. cohort. Neurology. 2006 Sep 12;67(5):777-80. PubMed External Web Site Policy

Dupuis L, Corcia P, Fergani A, Gonzalez De Aguilar JL, Bonnefont-Rousselot D, Bittar R, Seilhean D, Hauw JJ, Lacomblez L, Loeffler JP, Meininger V. Dyslipidemia is a protective factor in amyotrophic lateral sclerosis. Neurology. 2008 Mar 25;70(13):1004-9. PubMed External Web Site Policy

EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis, Andersen PM, Abrahams S, Borasio GD, de Carvalho M, Chio A, Van Damme P, Hardiman O, Kollewe K, Morrison KE, Petri S, Pradat PF, Silani V, Tomik B, Wasner M, Weber M. EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS) -- revised report of an EFNS task force. Eur J Neurol. 2012 Mar;19(3):360-75. [186 references] PubMed External Web Site Policy

Elamin M, Phukan J, Bede P, Jordan N, Byrne S, Pender N, Hardiman O. Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia. Neurology. 2011 Apr 5;76(14):1263-9. PubMed External Web Site Policy

Flaherty-Craig C, Brothers A, Dearman B, Eslinger P, Simmons Z. Penn State screen exam for the detection of frontal and temporal dysfunction syndromes: application to ALS. Amyotroph Lateral Scler. 2009 Apr;10(2):107-12. PubMed External Web Site Policy

Gil J, Funalot B, Verschueren A, Danel-Brunaud V, Camu W, Vandenberghe N, Desnuelle C, Guy N, Camdessanche JP, Cintas P, Carluer L, Pittion S, Nicolas G, Corcia P, Fleury MC, Maugras C, Besson G, Le Masson G, Couratier P. Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study. Eur J Neurol. 2008 Nov;15(11):1245-51. PubMed External Web Site Policy

Ginsberg G, Lowe S. Cost effectiveness of treatments for amyotrophic lateral sclerosis: a review of the literature. PharmacoEconomics. 2002;20(6):367-87. PubMed External Web Site Policy

Gordon PH, Wang Y, Doorish C, Lewis M, Battista V, Mitsumoto H, Marder K. A screening assessment of cognitive impairment in patients with ALS. Amyotroph Lateral Scler. 2007 Dec;8(6):362-5. PubMed External Web Site Policy

Haverkamp LJ, Appel V, Appel SH. Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. Brain. 1995 Jun;118 (Pt 3):707-19. PubMed External Web Site Policy

Heffernan C, Jenkinson C, Holmes T, Macleod H, Kinnear W, Oliver D, Leigh N, Ampong MA. Management of respiration in MND/ALS patients: an evidence based review. Amyotrophic Lateral Sclerosis. 2006 Mar;7(1):5-15. PubMed External Web Site Policy

Hetta J, Jansson I. Sleep in patients with amyotrophic lateral sclerosis. J Neurol. 1997 Apr;244(4 Suppl 1):S7-9. PubMed External Web Site Policy

Lacomblez L, Bensimon G, Leigh PN, Guillet P, Meininger V. Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II. Lancet. 1996 May 25;347(9013):1425-31. PubMed External Web Site Policy

Laird RD, Studenski S, Perera S, Wallace D. Fall history is an independent predictor of adverse health outcomes and utilization in the elderly. Am J Manag Care. 2001 Dec;7(12):1133-8. PubMed External Web Site Policy

Lechtzin N, Rothstein J, Clawson L, Diette GB, Wiener CM. Amyotrophic lateral sclerosis: evaluation and treatment of respiratory impairment. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Mar;3(1):5-13. PubMed External Web Site Policy

Lehéricey G, Le Forestier N, Dupuis L, Gonzalez-Bermejo J, Meininger V, Pradat PF. [Nutritional management in amyotrophic lateral sclerosis: A medical and ethical stake]. Presse Med. 2012 Jun;41(6 Pt 1):560-74. PubMed External Web Site Policy

Marin B, Desport JC, Kajeu P, Jesus P, Nicolaud B, Nicol M, Preux PM, Couratier P. Alteration of nutritional status at diagnosis is a prognostic factor for survival of amyotrophic lateral sclerosis patients. J Neurol Neurosurg Psychiatry. 2011 Jun;82(6):628-34. PubMed External Web Site Policy

Mathy P, Yorkston K, Gutmann M. AAC for individuals with amyotrophic lateral sclerosis. Augment Disord. 2000;:183-231.

McCullagh S, Moore M, Gawel M, Feinstein A. Pathological laughing and crying in amyotrophic lateral sclerosis: an association with prefrontal cognitive dysfunction. J Neurol Sci. 1999 Oct 31;169(1-2):43-8. PubMed External Web Site Policy

Miller RG, Anderson F, Brooks BR, Mitsumoto H, Bradley WG, Ringel SP, ALS CARE Study Group. Outcomes research in amyotrophic lateral sclerosis: lessons learned from the amyotrophic lateral sclerosis clinical assessment, research, and education database. Ann Neurol. 2009 Jan;65 Suppl 1:S24-8. PubMed External Web Site Policy

Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W, Kalra S, Katz JS, Mitsumoto H, Rosenfeld J, Shoesmith C, Strong MJ, Woolley SC, Quality Standards Subcommittee of the American Academy of Neurology. Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2009 Oct 13;73(15):1218-26. [40 references] PubMed External Web Site Policy

Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W, Kalra S, Katz JS, Mitsumoto H, Rosenfeld J, Shoesmith C, Strong MJ, Woolley SC, Quality Standards Subcommittee of the American Academy of Neurology. Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multi-disciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee [TRUNC]. Neurology. 2009 Oct 13;73(15):1227-33. [40 references] PubMed External Web Site Policy

Mitsumoto H, Bromberg M, Johnston W, Tandan R, Byock I, Lyon M, Miller RG, Appel SH, Benditt J, Bernat JL, Borasio GD, Carver AC, Clawson L, Del Bene ML, Kasarskis EJ, LeGrand SB, Mandler R, McCarthy J, Munsat T, Newman D, Sufit RL, Versenyi A. Promoting excellence in end-of-life care in ALS. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Sep;6(3):145-54. PubMed External Web Site Policy

Mitsumoto H, Davidson M, Moore D, Gad N, Brandis M, Ringel S, Rosenfeld J, Shefner JM, Strong MJ, Sufit R, Anderson FA, ALS CARE Study Group. Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunction. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):177-85. PubMed External Web Site Policy

National Institute of Neurological Disorders and Stroke (NINDS). Amyotrophic lateral sclerosis (ALS) fact sheet. [internet]. Bethesda (MD): National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH); 2013 Jun [6 p].

Nolan MT, Kub J, Hughes MT, Terry PB, Astrow AB, Carbo CA, Thompson RE, Clawson L, Texeira K, Sulmasy DP. Family health care decision making and self-efficacy with patients with ALS at the end of life. Palliat Support Care. 2008 Sep;6(3):273-80. PubMed External Web Site Policy

Oliver D, Campbell C, Sykes N, Tallon C, Edwards A. Decision-making for gastrostomy and ventilatory support for people with motor neurone disease: variations across UK hospices. J Palliat Care. 2011;27(3):198-201. PubMed External Web Site Policy

Phukan J, Pender NP, Hardiman O. Cognitive impairment in amyotrophic lateral sclerosis. Lancet Neurol. 2007 Nov;6(11):994-1003. PubMed External Web Site Policy

Rabkin JG, Wagner GJ, Del Bene M. Resilience and distress among amyotrophic lateral sclerosis patients and caregivers. Psychosom Med. 2000 Mar-Apr;62(2):271-9. PubMed External Web Site Policy

Ringholz GM, Appel SH, Bradshaw M, Cooke NA, Mosnik DM, Schulz PE. Prevalence and patterns of cognitive impairment in sporadic ALS. Neurology. 2005 Aug 23;65(4):586-90. PubMed External Web Site Policy

Rubenstein LZ, Josephson KR. The epidemiology of falls and syncope. Clin Geriatr Med. 2002 May;18(2):141-58. PubMed External Web Site Policy

Spataro R, Ficano L, Piccoli F, La Bella V. Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: effect on survival. J Neurol Sci. 2011 May 15;304(1-2):44-8. PubMed External Web Site Policy

Strong MJ, Grace GM, Freedman M, Lomen-Hoerth C, Woolley S, Goldstein LH, Murphy J, Shoesmith C, Rosenfeld J, Leigh PN, Bruijn L, Ince P, Figlewicz D. Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis. Amyotroph Lateral Scler. 2009 Jun;10(3):131-46. PubMed External Web Site Policy

Thommessen B, Aarsland D, Braekhus A, Oksengaard AR, Engedal K, Laake K. The psychosocial burden on spouses of the elderly with stroke, dementia and Parkinson's disease. Int J Geriatr Psychiatry. 2002 Jan;17(1):78-84. PubMed External Web Site Policy

Vaisman N, Lusaus M, Nefussy B, Niv E, Comaneshter D, Hallack R, Drory VE. Do patients with amyotrophic lateral sclerosis (ALS) have increased energy needs?. J Neurol Sci. 2009 Apr 15;279(1-2):26-9. PubMed External Web Site Policy

Wicks P, Abrahams S, Masi D, Hejda-Forde S, Leigh PN, Goldstein LH. Prevalence of depression in a 12-month consecutive sample of patients with ALS. Eur J Neurol. 2007 Sep;14(9):993-1001. PubMed External Web Site Policy

Woolley SC, Katz JS. Review article: utility of the ALS Cognitive Behavioral Screen. Neurodegener Dis Manag. 2011;1(6):473-9.

Extent of Measure Testing

This measure is being made available without any prior testing. The American Academy of Neurology (AAN) recognizes the importance of testing of all of its measures and encourages testing of the amyotrophic lateral sclerosis (ALS) measurement set for feasibility and reliability by organizations or individuals positioned to do so. The AAN welcomes the opportunity to promote the initial testing of these measures and to ensure that any results available from testing are used to refine the measures before implementation.

Evidence for Extent of Measure Testing

American Academy of Neurology (AAN). Amyotrophic lateral sclerosis performance measurement set. St. Paul (MN): American Academy of Neurology (AAN); 2012 Jul 31. 75 p.

State of Use

Current routine use

Current Use

Internal quality improvement

Professional certification

Measurement Setting

Ambulatory/Office-based Care

Home Care

Hospital Outpatient

Skilled Nursing Facilities/Nursing Homes

Professionals Involved in Delivery of Health Services

Physicians

Least Aggregated Level of Services Delivery Addressed

Individual Clinicians or Public Health Professionals

Statement of Acceptable Minimum Sample Size

Does not apply to this measure

Target Population Age

Unspecified

Target Population Gender

Either male or female

National Quality Strategy Aim

Better Care

National Quality Strategy Priority

Person- and Family-centered Care
Prevention and Treatment of Leading Causes of Mortality

IOM Care Need

Living with Illness

IOM Domain

Effectiveness

Patient-centeredness

Case Finding Period

Unspecified

Denominator Sampling Frame

Patients associated with provider

Denominator (Index) Event or Characteristic

Clinical Condition

Denominator Time Window

Does not apply to this measure

Denominator Inclusions/Exclusions

Inclusions
All patients with a diagnosis of amyotrophic lateral sclerosis (ALS) and dysphagia, weight loss or impaired nutrition

Note: Refer to the original measure documentation for International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) diagnosis codes and Current Procedural Terminology (CPT) Evaluation and Management (E/M) service codes.

Exclusions
Documentation of a medical reason for not offering dietary or enteral nutritional support (e.g., patient already on percutaneous endoscopic gastrostomy/radiographic inserted gastrostomy [PEG/RIG]; patient cannot tolerate the procedure)

Exclusions/Exceptions

Medical factors addressed

Numerator Inclusions/Exclusions

Inclusions
Patients who were offered at least once annually dietary or enteral nutrition support via percutaneous endoscopic gastrostomy (PEG) or radiographic inserted gastrostomy (RIG)

Exclusions
Unspecified

Numerator Search Strategy

Fixed time period or point in time

Data Source

Administrative clinical data

Electronic health/medical record

Paper medical record

Type of Health State

Does not apply to this measure

Instruments Used and/or Associated with the Measure

Unspecified

Measure Specifies Disaggregation

Does not apply to this measure

Scoring

Rate/Proportion

Interpretation of Score

Desired value is a higher score

Allowance for Patient or Population Factors

Unspecified

Standard of Comparison

Internal time comparison

Original Title

Measure #8: ALS nutritional support offered.

Measure Collection Name

Amyotrophic Lateral Sclerosis Performance Measurement Set

Submitter

American Academy of Neurology - Medical Specialty Society

Developer

American Academy of Neurology - Medical Specialty Society

Funding Source(s)

Unspecified

Composition of the Group that Developed the Measure

Work Group Members Amyotrophic Lateral Sclerosis

Co-Chairs: Robert G. Miller, MD; Benjamin Rix Brooks, MD

American Academy of Neurology Representatives: Steven Ringel, MD; Hiroshi Mitsumoto, MD; Carlayne Jackson, MD; Christen Shoesmith, MD, BSc; Edward Kasarskis, MD, PhD

Pulmonologist: Robert C. Basner, MD

Gastroenterologist: Nicholas Procaccini, MD

American Academy of Physical Medicine and Rehabilitation: Gregory Carter, MD

Nurse: Dallas Forshew, RN, BSN

Physical Therapy/Occupational Therapy: Mohammed Sanjak, PhD, PT, MBA; Pat Casey, MS, CRCC

Hospice/Palliative Care Specialist: Bob Osborne, RN

Muscular Dystrophy Association: Valerie Cwik, MD

Patient Representative: Christine Jasch, OTR/L

Insurance Representatives: Fredrik Tolin, MD, MBA (Humana)

American Academy of Neurology Staff: Rebecca J. Swain-Eng, MS; Gina Gjorvad

Methodologist: Rebecca Kresowik

Quality Measurement and Reporting Subcommittee Facilitators & Liaisons: Richard Dubinsky, MD (Facilitator); Joel Kaufman, MD (Facilitator); Adam Cohen, MD (Facilitator); Christopher Bever, MD (QMR Chair); Eric Cheng, MD, MS (QMR Vice-Chair)

Financial Disclosures/Other Potential Conflicts of Interest

Unspecified

Adaptation

This measure was not adapted from another source.

Date of Most Current Version in NQMC

2012 Jul

Measure Maintenance

Unspecified

Date of Next Anticipated Revision

Unspecified

Measure Status

This is the current release of the measure.

Source(s)

American Academy of Neurology (AAN). Amyotrophic lateral sclerosis performance measurement set. St. Paul (MN): American Academy of Neurology (AAN); 2012 Jul 31. 75 p.

Measure Availability

Source available from the American Academy of Neurology (AAN) Web site External Web Site Policy.

For more information, contact AAN at 201 Chicago Avenue, Minneapolis, MN 55415; Phone: 800-879-1960; Fax: 612-454-2746; Web site: www.aan.com External Web Site Policy.

NQMC Status

This NQMC summary was completed by ECRI Institute on March 8, 2016. The information was not verified by the measure developer.

Copyright Statement

This NQMC summary is based on the original measure, which is subject to the measure developer's copyright restrictions.

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