Nutritional Diagnosis Grid - Alabama Medicaid Agency
Nutritional Diagnosis Grid - Alabama Medicaid Agency
Nutritional Diagnosis Grid - Alabama Medicaid Agency
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Nutrition Plus > 12 months Adult<br />
Inadequate oral intake, voluntary (anorexia 783.0) and involuntary (barriers to normal ingestion):<br />
Dysphagia (787.2); Malignancy of lip, oral cavity & pharyngeal cavity (140.0-149.9); Alzheimer’s<br />
disease (331.0); Huntington’s chorea (334.0); Jakob-Creutzfeldt disease (046.1); MS (340); Other<br />
demyelinating disease of CNS (341.9); Pick’s disease (331.0); Profound mental retardation (318.2);<br />
Coma (780.01, 780.09); Persistent vegetative state (780.03); Leukodystrophy (330.0); Cerebral<br />
Lipidosis (330.1); Other specific cerebral degeneration in childhood (Rett’s syndrome) (330.8);<br />
Cerebral degeneration in generalized lipidoses (330.2, with underlying disease code); Cerebral<br />
degeneration of childhood in other diseases classified elsewhere (330.3, with underlying disease<br />
code); Parkinson’s disease (332.0, 332.1); Supranuclear Palsy (333.0); ALS (335.20); Motor neuron<br />
disease (335.2); Progressive muscular atrophy (335.21); Progressive bulbar palsy (335.22);<br />
Psuedobulbar palsy (335.23); Encephalopathy (348.3); Senile dementia (290.0); Malnutrition (261);<br />
Post-op feeding, within 4 weeks of surgery (579.3)<br />
<strong>Nutritional</strong> Drink > 2 Adult<br />
For patients unable to maintain their nutrition from normal foods: Dysphagia (787.2); Malignancy<br />
of lip, oral cavity & pharyngeal cavity (140.0-149.9); Jakob-Creutzfeldt disease (046.1); Other<br />
demyelinating disease of CNS (341.8, 341.9); Pick’s disease (331.0); Profound mental retardation<br />
(318.2); Coma (780.01, 780.09); Persistent vegetative state (780.03); Leukodystrophy (330.0);<br />
Cerebral Lipidosis (330.1); Other specific cerebral degeneration in childhood (Rett’s syndrome)<br />
(330.8); Cerebral degeneration in generalized lipidoses (330.2, with underlying disease code);<br />
Cerebral degeneration of childhood in other diseases classified elsewhere (330.3, with underlying<br />
disease code); Supranuclear Palsy (333.0); Motor neuron disease (335.2); Progressive muscular<br />
atrophy (335.21); Progressive bulbar palsy (335.22); Pseudobulbar palsy (335.23); Encephalopathy<br />
(348.3); Malnutrition (261); Post-op feeding, within 4 weeks of surgery (579.3), CRF (ESRD) (585,<br />
586)<br />
<strong>Nutritional</strong> Liquid<br />
"nutri-drink"<br />
> 2 Adult<br />
For patients unable to maintain their nutrition from normal foods: Dysphagia (787.2); Malignancy<br />
of lip, oral cavity & pharyngeal cavity (140.0-149.9); Jakob-Creutzfeldt disease (046.1); Other<br />
demyelinating disease of CNS (341.8, 341.9); Pick’s disease (331.0); Profound mental retardation<br />
(318.2); Coma (780.01, 780.09); Persistent vegetative state (780.03); Leukodystrophy (330.0);<br />
Cerebral Lipidosis (330.1); Other specific cerebral degeneration in childhood (Rett’s syndrome)<br />
(330.8); Cerebral degeneration in generalized lipidoses (330.2, with underlying disease code);<br />
Cerebral degeneration of childhood in other diseases classified elsewhere (330.3, with underlying<br />
disease code); Supranuclear Palsy (333.0); Motor neuron disease (335.2); Progressive muscular<br />
atrophy (335.21); Progressive bulbar palsy (335.22); Pseudobulbar palsy (335.23); Encephalopathy<br />
(348.3); Malnutrition (261); Post-op feeding, within 4 weeks of surgery (579.3), CRF (ESRD) (585,<br />
586)<br />
<strong>Nutritional</strong> Supplement<br />
"nutri-drink"<br />
> 2 Adult<br />
For patients unable to maintain their nutrition from normal foods: Dysphagia (787.2); Malignancy<br />
of lip, oral cavity & pharyngeal cavity (140.0-149.9); Jakob-Creutzfeldt disease (046.1); Other<br />
demyelinating disease of CNS (341.8, 341.9); Pick’s disease (331.0); Profound mental retardation<br />
(318.2); Coma (780.01, 780.09); Persistent vegetative state (780.03); Leukodystrophy (330.0);<br />
Cerebral Lipidosis (330.1); Other specific cerebral degeneration in childhood (Rett’s syndrome)<br />
(330.8); Cerebral degeneration in generalized lipidoses (330.2, with underlying disease code);<br />
Cerebral degeneration of childhood in other diseases classified elsewhere (330.3, with underlying<br />
disease code); Supranuclear Palsy (333.0); Motor neuron disease (335.2); Progressive muscular<br />
atrophy (335.21); Progressive bulbar palsy (335.22); Pseudobulbar palsy (335.23); Encephalopathy<br />
(348.3); Malnutrition (261); Post-op feeding, within 4 weeks of surgery (579.3), CRF (ESRD) (585,<br />
586)<br />
<strong>Nutritional</strong> Supplement<br />
Plus "nutri-drink plus"<br />
> 2 Adult<br />
For children unable to maintain their nutrition from normal foods: Dysphagia (787.2); Malignancy<br />
of lip, oral cavity & pharyngeal cavity (140.0-149.9); Jakob-Creutzfeldt disease (046.1); Other<br />
demyelinating disease of CNS (341.8, 341.9); Pick’s disease (331.0); Profound mental retardation<br />
(318.2); Coma (780.01, 780.09); Persistent vegetative state (780.03); Leukodystrophy (330.0);<br />
Cerebral Lipidosis (330.1); Other specific cerebral degeneration in childhood (Rett’s syndrome)<br />
(330.8); Cerebral degeneration in generalized lipidoses (330.2, with underlying disease code);<br />
Cerebral degeneration of childhood in other diseases classified elsewhere (330.3, with underlying<br />
disease code); Supranuclear Palsy (333.0); Motor neuron disease (335.2); Progressive muscular<br />
atrophy (335.21);<br />
OA 1 < 3 For propionic acidemia and methylmalonic acidemia (270.7)<br />
OA 2 > 12 months Adult Propionic or Methylmalonic Acidemia (270.3) (Should this be 270.7?)<br />
12 10/1/11