Valid for Submission
I45.81 is a billable diagnosis code used to specify a medical diagnosis of long qt syndrome. The code I45.81 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code I45.81 might also be used to specify conditions or terms like acquired long qt syndrome, andersen tawil syndrome, congenital conduction defect, congenital long qt syndrome, congenital long qt syndrome , jervell and lange-nielsen syndrome, etc.
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code I45.81 are found in the index:
- - Jervell-Lange-Nielsen syndrome - I45.81
- - Romano-Ward (prolonged QT interval) syndrome - I45.81
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Acquired long QT syndrome
- Andersen Tawil syndrome
- Congenital conduction defect
- Congenital long QT syndrome
- Congenital long QT syndrome
- Jervell and Lange-Nielsen syndrome
- Long QT syndrome
- Long QT syndrome
- Long QT syndrome caused by drug
- Prolonged QT interval
- QT interval - finding
- Romano-Ward syndrome
- LONG QT SYNDROME-. a condition that is characterized by episodes of fainting syncope and varying degree of ventricular arrhythmia as indicated by the prolonged qt interval. the inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. the two major forms are romano ward syndrome and jervell lange nielsen syndrome.
- ROMANO WARD SYNDROME-. a form of long qt syndrome that is without congenital deafness. it is caused by mutation of the kcnq1 gene which encodes a protein in the voltage gated potassium channel.
- ANDERSEN SYNDROME-. a form of inherited long qt syndrome or lqt7 that is characterized by a triad of potassium sensitive periodic paralysis ventricular ectopic beats and abnormal features such as short stature low set ears and scoliosis. it results from mutations of kcnj2 gene which encodes a channel protein inward rectifier potassium channels that regulates resting membrane potential.
Diagnostic Related Groups - MS-DRG Mapping
Convert I45.81 to ICD-9 Code
Information for Patients
Also called: Irregular heartbeat
An arrhythmia is a problem with the rate or rhythm of your heartbeat. It means that your heart beats too quickly, too slowly, or with an irregular pattern. When the heart beats faster than normal, it is called tachycardia. When the heart beats too slowly, it is called bradycardia. The most common type of arrhythmia is atrial fibrillation, which causes an irregular and fast heart beat.
Many factors can affect your heart's rhythm, such as having had a heart attack, smoking, congenital heart defects, and stress. Some substances or medicines may also cause arrhythmias.
Symptoms of arrhythmias include
- Fast or slow heart beat
- Skipping beats
- Lightheadedness or dizziness
- Chest pain
- Shortness of breath
Your doctor can run tests to find out if you have an arrhythmia. Treatment to restore a normal heart rhythm may include medicines, an implantable cardioverter-defibrillator (ICD) or pacemaker, or sometimes surgery.
NIH: National Heart, Lung, and Blood Institute
- Arrhythmias (Medical Encyclopedia)
- Atrial fibrillation or flutter (Medical Encyclopedia)
- Cardiac ablation procedures (Medical Encyclopedia)
- Ectopic heartbeat (Medical Encyclopedia)
- Electrocardiogram (Medical Encyclopedia)
- Exercise stress test (Medical Encyclopedia)
- Heart palpitations (Medical Encyclopedia)
- Holter monitor (24h) (Medical Encyclopedia)
- Paroxysmal supraventricular tachycardia (PSVT) (Medical Encyclopedia)
- Ventricular tachycardia (Medical Encyclopedia)
- Wolff-Parkinson-White syndrome (Medical Encyclopedia)
Jervell and Lange-Nielsen syndrome Jervell and Lange-Nielsen syndrome is a condition that causes profound hearing loss from birth and a disruption of the heart's normal rhythm (arrhythmia). This disorder is a form of long QT syndrome, which is a heart condition that causes the heart (cardiac) muscle to take longer than usual to recharge between beats. Beginning in early childhood, the irregular heartbeats increase the risk of fainting (syncope) and sudden death.
Romano-Ward syndrome Romano-Ward syndrome is a condition that causes a disruption of the heart's normal rhythm (arrhythmia). This disorder is a form of long QT syndrome, which is a heart condition that causes the heart (cardiac) muscle to take longer than usual to recharge between beats. The term "long QT" refers to a specific pattern of heart activity that is detected with an electrocardiogram (ECG or EKG), which is a test used to measure the electrical activity of the heart. In people with long QT syndrome, the part of the heartbeat known as the QT interval is abnormally long. Abnormalities in the time it takes to recharge the heart lead to abnormal heart rhythms.The arrhythmia associated with Romano-Ward syndrome can lead to fainting (syncope) or cardiac arrest and sudden death. However, some people with Romano-Ward syndrome never experience any health problems associated with the condition.Fifteen types of long QT syndrome have been defined based on their genetic cause. Some types of long QT syndrome involve other cardiac abnormalities or problems with additional body systems. Romano-Ward syndrome encompasses those types that involve only a long QT interval without other abnormalities.