The ICD-10 code for Glanzmann's thrombasthenia is D69.1. In the ICD-9 coding system, the corresponding code for this condition is 287.1. Glanzmann's thrombasthenia is a rare inherited bleeding disorder characterized by a deficiency or dysfunction of platelet glycoprotein IIb/IIIa, leading to impaired platelet aggregation. It can result in prolonged bleeding and easy bruising. Proper diagnosis and management are crucial for individuals with this condition.
Glanzmann's thrombasthenia is a rare inherited bleeding disorder characterized by impaired platelet function, specifically the lack or dysfunction of a glycoprotein called integrin alpha-IIb beta-3, which plays a crucial role in platelet aggregation and clot formation. Due to this deficiency, affected individuals may experience prolonged bleeding episodes, easy bruising, and excessive bleeding following injury or surgery.
In the International Classification of Diseases, 10th Revision (ICD-10), Glanzmann's thrombasthenia is classified under the code D69.1. This code specifically denotes "Qualitative platelet defects" and further specifies "Glanzmann's thrombasthenia" as the condition. The ICD-10 coding system is widely used globally for the classification of diseases and medical conditions.
On the other hand, in the previous version of the International Classification of Diseases, 9th Revision (ICD-9), Glanzmann's thrombasthenia was classified under the code 286.2. This code represents "Other and unspecified coagulation defects," with a subcategory specifying "Glanzmann's disease." ICD-9 was used prior to the implementation of ICD-10 and has been largely replaced by the newer coding system.
It is important to note that ICD codes are used for medical billing, research, and statistical purposes, allowing healthcare providers and organizations to accurately document and communicate diagnoses. They aid in the organization and analysis of health data, ensuring appropriate treatment and management for patients with Glanzmann's thrombasthenia.