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3. Present On Admission Exempt ICD-10-CM Codes

Present On Admission Exempt ICD-10-CM Codes

Present On Admission is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA. The following 37,297 ICD-10-CM codes are considered exempt from POA reporting.

Displaying codes 501-600 of 37,297:

• Q16.2
  Absence of eustachian tube
• Q16.3
  Congenital malformation of ear ossicles
• Q16.4
  Other congenital malformations of middle ear
• Q16.5
  Congenital malformation of inner ear
• Q16.9
  Congenital malformation of ear causing impairment of hearing, unspecified
• Q17.0
  Accessory auricle
• Q17.1
  Macrotia
• Q17.2
  Microtia
• Q17.3
  Other misshapen ear
• Q17.4
  Misplaced ear
• Q17.5
  Prominent ear
• Q17.8
  Other specified congenital malformations of ear
• Q17.9
  Congenital malformation of ear, unspecified
• Q18.0
  Sinus, fistula and cyst of branchial cleft
• Q18.1
  Preauricular sinus and cyst
• Q18.2
  Other branchial cleft malformations
• Q18.3
  Webbing of neck
• Q18.4
  Macrostomia
• Q18.5
  Microstomia
• Q18.6
  Macrocheilia
• Q18.7
  Microcheilia
• Q18.8
  Other specified congenital malformations of face and neck
• Q18.9
  Congenital malformation of face and neck, unspecified
• Q20.0
  Common arterial trunk
• Q20.1
  Double outlet right ventricle
• Q20.2
  Double outlet left ventricle
• Q20.3
  Discordant ventriculoarterial connection
• Q20.4
  Double inlet ventricle
• Q20.5
  Discordant atrioventricular connection
• Q20.6
  Isomerism of atrial appendages
• Q20.8
  Other congenital malformations of cardiac chambers and connections
• Q20.9
  Congenital malformation of cardiac chambers and connections, unspecified
• Q21.0
  Ventricular septal defect
• Q21.1
  Atrial septal defect
• Q21.2
  Atrioventricular septal defect
• Q21.3
  Tetralogy of Fallot
• Q21.4
  Aortopulmonary septal defect
• Q21.8
  Other congenital malformations of cardiac septa
• Q21.9
  Congenital malformation of cardiac septum, unspecified
• Q22.0
  Pulmonary valve atresia
• Q22.1
  Congenital pulmonary valve stenosis
• Q22.2
  Congenital pulmonary valve insufficiency
• Q22.3
  Other congenital malformations of pulmonary valve
• Q22.4
  Congenital tricuspid stenosis
• Q22.5
  Ebstein's anomaly
• Q22.6
  Hypoplastic right heart syndrome
• Q22.8
  Other congenital malformations of tricuspid valve
• Q22.9
  Congenital malformation of tricuspid valve, unspecified
• Q23.0
  Congenital stenosis of aortic valve
• Q23.1
  Congenital insufficiency of aortic valve
• Q23.2
  Congenital mitral stenosis
• Q23.3
  Congenital mitral insufficiency
• Q23.4
  Hypoplastic left heart syndrome
• Q23.8
  Other congenital malformations of aortic and mitral valves
• Q23.9
  Congenital malformation of aortic and mitral valves, unspecified
• Q24.0
  Dextrocardia
• Q24.1
  Levocardia
• Q24.2
  Cor triatriatum
• Q24.3
  Pulmonary infundibular stenosis
• Q24.4
  Congenital subaortic stenosis
• Q24.5
  Malformation of coronary vessels
• Q24.6
  Congenital heart block
• Q24.8
  Other specified congenital malformations of heart
• Q24.9
  Congenital malformation of heart, unspecified
• Q25.0
  Patent ductus arteriosus
• Q25.1
  Coarctation of aorta
• Q25.21
  Interruption of aortic arch
• Q25.29
  Other atresia of aorta
• Q25.3
  Supravalvular aortic stenosis
• Q25.40
  Congenital malformation of aorta unspecified
• Q25.41
  Absence and aplasia of aorta
• Q25.42
  Hypoplasia of aorta
• Q25.43
  Congenital aneurysm of aorta
• Q25.44
  Congenital dilation of aorta
• Q25.45
  Double aortic arch
• Q25.46
  Tortuous aortic arch
• Q25.47
  Right aortic arch
• Q25.48
  Anomalous origin of subclavian artery
• Q25.49
  Other congenital malformations of aorta
• Q25.5
  Atresia of pulmonary artery
• Q25.6
  Stenosis of pulmonary artery
• Q25.71
  Coarctation of pulmonary artery
• Q25.72
  Congenital pulmonary arteriovenous malformation
• Q25.79
  Other congenital malformations of pulmonary artery
• Q25.8
  Other congenital malformations of other great arteries
• Q25.9
  Congenital malformation of great arteries, unspecified
• Q26.0
  Congenital stenosis of vena cava
• Q26.1
  Persistent left superior vena cava
• Q26.2
  Total anomalous pulmonary venous connection
• Q26.3
  Partial anomalous pulmonary venous connection
• Q26.4
  Anomalous pulmonary venous connection, unspecified
• Q26.5
  Anomalous portal venous connection
• Q26.6
  Portal vein-hepatic artery fistula
• Q26.8
  Other congenital malformations of great veins
• Q26.9
  Congenital malformation of great vein, unspecified
• Q27.0
  Congenital absence and hypoplasia of umbilical artery
• Q27.1
  Congenital renal artery stenosis
• Q27.2
  Other congenital malformations of renal artery
• Q27.30
  Arteriovenous malformation, site unspecified
• Q27.31
  Arteriovenous malformation of vessel of upper limb