Disease staging: CliniCal anD CoDeD Criteria - HCUP

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Clinical <strong>Criteria</strong> with Description, Diagnostic Findings and ICD-9-CM codes DXCat Number: PED08 MultiStage: No DXCat Label: Anomaly: Integument (Genodermatoses) Specificity: A Etiology: Genetic (or hereditary) Stage Description Diagnostic findings ICD-9-CM Codes 1.01 Congenital dermatoses, Ichthyosis, Congenital dermatoses [operative/pathology report] DX 3348, 75683, 7570-7579, 7788; Keratosis palmaris et plantaris, OR Ichthyosis [operative/pathology report] Pachyonychia congenita, Dyskeratosis OR Keratosis palmaris et plantaris [operative/pathology report] congenita, Porokeratosis, Xeroderma OR Pachyonychia congenita [operative/pathology report] pigmentosum, Ectodermal dysplasia, Focal OR Dyskeratosis congenita [operative/pathology report] dermal hypoplasia syndrome, Aplasia cutis OR Porokeratosis [operative/pathology report] congenita, Poikiloderma congenitale, OR Xeroderma pigmentosum [operative/pathology report] Bloom's syndrome, Ataxia-telangiectasia, OR Ectodermal dysplasia [operative/pathology report] Epidermolysis bullosa, Familial benign OR Focal dermal hypoplasia syndrome [operative/pathology report] pemphigus, Keratosis follicularis, OR Aplasia cutis congenita [operative/pathology report] Acrokeratosis verruciformis of hopf, OR Poikiloderma congenitale [operative/pathology report] Psuedoxanthoma elasticum, Connective OR Bloom’s syndrome [operative/pathology report] tissue nevus, Ehlers-danlos syndrome, OR Ataxia-telangiectasia [operative/pathology report] Cutis laxa, Urticaria pigmentosa, OR Epidermolysis bullosa [operative/pathology report] Incontinentia pigmenti, or Hypomelanosis OR Familial benign pemphigus [operative/pathology report] of ito OR Keratosis follicularis [operative/pathology report] OR Acrokeratosis verruciformis of hopf [operative/pathology report] OR Pseudoxanthoma elasticum [operative/pathology report] OR Connective tissue nevus [operative/pathology report] OR Ehlers-danlos syndrome [operative/pathology report] OR Cutis laxa OR Urticaria pigmentosa [operative/pathology report] OR Incontinentia pigmenti [operative/pathology report] OR Hypomelanosis of ito [operative/pathology report] 2.01 Bullous congenital ichthyosiform erythroderma, Harlequin ichthyosis, Epidermolysis bullosa dystrophicans, recessive type Bullous congenital [operative/pathology report] OR ichthyosiform erythroderma [operative/pathology report] OR Harlequin ichthyosis [operative/pathology report] OR Epidermolysis bullosa dystrophicans, recessive type [operative/pathology report] NO; References: Harper JI. Genetics and genodermatoses. In: Champion RH, Burton JL, Burns DA, Breathnach SM. Rook/Wilkson/Ebling Textbook of Dermatology. 6th ed. Oxford: Blackwell Science Ltd.; 1998:357-436. Johnson B Jr., Honig P. Congenital diseases (Genodermatoses). In: Elder D, Elnitsas R, Jaworsky C, Johnson B Jr. Lever’s Histopathology of the skin. 8th ed. Philadelphia, PA: Lippincott; 1997:117-150. Thursday, January 07, 2010 9:22:56 AM ©2010 Thomson Reuters. All rights reserved.
Clinical <strong>Criteria</strong> with Description, Diagnostic Findings and ICD-9-CM codes DXCat Number: PED09 MultiStage: No DXCat Label: Anomaly: Neural Tube Defects Specificity: A Etiology: Congenital; Genetic (or hereditary) Stage Description Diagnostic findings ICD-9-CM Codes 1.01 Dermal sinus Dermal sinus, lumbosacral defect with connection to the subarachnoid [operative/pathology report] NO; 1.02 Spina bifida occulta Spina bifida occulta, failure of fusion of vertebral laminae without protrusion of the spinal cord or meninges [operative/pathology report or lumbosacral x-ray report or CT scan or MRI or myelogram report] DX 75617; 1.03 Spina bifida occulta with tethered umbilical cord Stage 1.02 AND tethered umbilical cord 1.04 Spinal bifida occulta with diastematomyelia Stage 1.02-1.03 AND diastematomyelia 2.01 Meningocele Meningocele, failure of fusion of vertebral laminae with protrusion of the meninges [operative/pathology report or lumbosacral x-ray report or CT scan or MRI or myelogram report] 2.02 Defects of the neural tube with Stage 1.01-2.01 hemiparesis or paraparesis AND hemiparesis OR paraparesis 2.03 Defects of the neural tube with bladder dysfunction 2.04 Defects of the neural tube with urinary tract infection Stage 1.01-2.02 AND bladder dysfunction [urology report] Stage 1.01-2.03 AND UTI: 2.05 Syringomyelia Syringomyelia [operative/pathology report] 2.06 Defects of the neural tube with paralysis Stage 1.01-2.05 AND quadriplegia OR hemiplegia OR paraplegia NO; DX 74251; DX 74190-74193; STAGE 1.01-2.01 + (DX 3430- 3431, 3434); STAGE 1.01-2.02 + (DX 34461, 5965, 59651-59659); STAGE 1.01-2.04 + DXCAT GUS10; DX 3360; STAGE 1.01-2.05 + DX 34400- 34409; 3.01 Myelomeningocele Myelomeningocele, failure of fusion of vertebral laminae with protrusion of the meninges and spinal cord [operative/pathology report or lumbosacral x-ray report or CT scan or MRI report] 3.02 Encephalocele Encephalocele, cyst or cavity in the cerebral hemispheres with a ventricle connection [CT scan report] 3.03 with meningitis Stage 1.01-3.02 AND meningitis: 3.04 with hydrocephalus Stage 1.01-3.03 AND hydrocephalus, ventricular dilatation [CT scan report or operative/pathology report] 3.05 Hydrocephalus with herniation of the Stage 1.01-3.03 medulla and cerebellar tonsils ("Chiari AND hydrocephalus, ventricular dilatation [CT scan report or operative/pathology report] crisis") or respiratory failure NO; DX 7420; STAGE 1.01-3.02 + (GROUP MENGIT__BACT OR GROUP MENING__VIR); DX 74100-74103, 7423; STAGE 3.04 + (DX 3484 OR GROUP RESP_FAIL); Thursday, January 07, 2010 9:22:56 AM ©2010 Thomson Reuters. All rights reserved.
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Disease Staging: Clinical and Coded
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Copyright © 1999-2010 Thomson Reut
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present edition, are documented in
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Salvatore Mangione, M.D. Associate
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Bryce Templeton, M.D. Professor of
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acterial meningitis). And some may
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substage level. Different integer s
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choose to undergo an elective surgi
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Disease Staging can also be used as
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may occur? Does this vary depending
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16. Taroni F, Repetto F, Louis DZ e
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References 1. Nuland SB. Doctors: T
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Clinical Criteria with Description,
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Acute renal failure: Onset within o
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Anemia: Hemoglobin Decreased: Cord
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Aspartate aminotransferase, serum (
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Chronic renal failure: Small kidney
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Convalescent/Acute Phase serology:
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CSF Reference values: CSF Cell coun
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Down’s syndrome: Cytogenetics rep
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Fractional excretion of sodium (FEN
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Hepatitis: Serum bilirubin > 3 mg/d
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Hypernatremia: Increased: Serum sod
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Hypoxemia: pO2 < 60 mmHg with patie
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Lipase, serum: Increased: Serum lip
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Myocardial infarction, acute (AMI):
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Pneumonia: New pulmonary infiltrate
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Rheumatoid arthritis: Five of the f
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Sepsis: Sepsis syndrome OR Viremia:
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Thrombocytopenia: Decreased: Platel
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Vitamin B 12 binding capacity, unsa
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Disease staging: CliniCal anD CoDeD Criteria - HCUP

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