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PATIENTThe Non Arthroplasty Hip Surgery Register (NAHR)Patient StickerThe British Hip Society 3543 Lincolns Inn Fields, London WC2A 3PN www.britishhipsociety.com/NAHRNon Arthroplasty Hip Surgery Register

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How to fill out non arthroplasty hip registry

01

Access the non arthroplasty hip registry form

02

Fill in patient demographic information such as name, date of birth, and contact information

03

Record details of the hip surgery performed, including the type of procedure and any complications

04

Include information about the pre-operative and post-operative care provided to the patient

05

Submit the completed form to the designated registry organization

Who needs non arthroplasty hip registry?

01

Patients who have undergone non arthroplasty hip surgery

02

Healthcare providers and researchers interested in tracking outcomes of non arthroplasty hip procedures

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What is non arthroplasty hip registry?

The non arthroplasty hip registry is a database designed to collect and analyze data regarding non-surgical hip procedures and treatments, aimed at improving patient outcomes and understanding the effectiveness of various interventions.

Who is required to file non arthroplasty hip registry?

Healthcare providers performing non-surgical hip interventions, including physicians and clinics involved in hip management, are generally required to file the non arthroplasty hip registry.

How to fill out non arthroplasty hip registry?

To fill out the non arthroplasty hip registry, providers must collect relevant patient data, treatment details, and outcome measures, and then input this information into the designated registry system or platform as per the provided guidelines.

What is the purpose of non arthroplasty hip registry?

The purpose of the non arthroplasty hip registry is to track treatment outcomes, enhance clinical practice, support research, and facilitate the continuous improvement of non-surgical hip treatment methods.

What information must be reported on non arthroplasty hip registry?

Information that must be reported includes patient demographics, specific diagnoses, treatment details, outcomes, complications, and follow-up data.

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