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Paper Title

An Overview of Rhabdomyolysis

Article Identifiers

Registration ID: IJNRD_221880

Published ID: IJNRD2405501

: http://doi.one/10.1729/Journal.39557

Keywords

Rhabdomyolysis, Myalgia, Creatinine kinase, Pigmenturia, Skeletal muscles.

Abstract

A clinical condition known as rhabdomyolysis involves the breakdown of skeletal muscle tissue and intracellular muscle fluid being released into the bloodstream. An overview of rhabdomyolysis is the aim of this thorough analysis of the literature. When there is a history of rhabdomyolysis, it is a dangerous illness that can pose a life-threatening threat. Although there are no universally accepted diagnostic criteria for rhabdomyolysis, it is appropriate to define it as an increase in a minimum 10-fold increase in serum creatine kinase activity, the maximum permitted by normal, after which a sharp drop in sCK levels to (or close to) normal levels. Myalgia, weakness, and pigmenturia are traditional aspects of the clinical presentation, which might vary greatly. Rhabdomyolysis treatment is dependent on an early diagnosis. Maintaining renal function, treating compartment syndrome, addressing metabolic imbalances, and fluid replacement should be the main goals of treatment throughout the acute period. Most individuals only have one rhabdomyolysis episode, which is typically brought on by drug addiction, prescription side effects, trauma, or epileptic seizures.

How To Cite (APA)

Mayur Bagul, Dr. Sarika Kamble , Chanchal Bhalerao , Prachi Birari, & Nikita Aware (May-2024). An Overview of Rhabdomyolysis . INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 9(5), f1-f9. http://doi.one/10.1729/Journal.39557

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Paper Reg. ID: IJNRD_221880

Published Paper Id: IJNRD2405501

Downloads: 000122255

Research Area: Medical Science

Author Type: Indian Author

Country: Dhule, Maharashtra , India

Published Paper PDF: https://ijnrd.org/papers/IJNRD2405501.pdf

Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2405501

Crossref DOI: http://doi.one/10.1729/Journal.39557

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Call For Paper - Volume 10 | Issue 12 | December 2025

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