IN'WHEN'TION

  INTRODUCTION   The Acute Respiratory Distress Syndrome (ARDS) is a prevalent cause of respiratory failure among critically ill patients, characterized by the sudden onset of noncardiogenic pulmonary edema, hypoxemia, and the requirement for mechanical ventilation. ARDS commonly manifests in the context of pneumonia, sepsis, aspiration of gastric contents, or severe trauma, affecting around 10% of all patients in intensive care units globally. Despite advancements, the mortality rate remains high at 30–40% in most research studies. Pathological examinations of ARDS patients frequently indicate widespread alveolar damage, while laboratory investigations have revealed injury to both alveolar epithelial and lung endothelial cells, leading to the accumulation of protein-rich inflammatory edematous fluid in the alveolar space. The diagnosis is predicated on consensual syndromic criteria, with adjustments for under-resourced settings and pediatric patients. Therapy primarily centers on

                                                                      Artificial Hands Patients with limited hand function due to various medical conditions such as hand injuries, strokes, or spinal cord injuries (SCI) which often result in hand paralysis need artificial hands. Types of Artificial Hands Body-Powered Artificial Hands : Controlled by cables linked to a harness worn on the opposite shoulder of the amputated limb. Movement is driven by the user's shoulder and upper arm muscles. Limitations: Limited range of motion due to potential derailment of the cable system. Myoelectric Artificial Hands : Use electromyography (EMG) sensors placed on the skin over residual limb muscles. Detects electrical signals from muscle contractions, which are then processed to control hand movements. Limitations: Expensive, requires regular maintenance, sensitive to sweat and moisture affecting sensor performance. C

  Introduction This article is to analyze the new technology invented by the National Institute of Technology, PATNA, INDIA. The invention as describes by the patent specification is a "Disposable Crockery Crusher." This device is designed to crush disposable crockery, such as plastic and paper-based cups, plates, and utensils, to make their disposal more efficient and environmentally friendly. The preeminent plastic consumer products in production encompass packaging crafted from LDPE (e.g., bags, containers, food packaging film), containers fabricated from HDPE (e.g., milk bottles, shampoo bottles, ice cream tubs), and PET (e.g., bottles for water and other beverages). Collectively, these items represent approximately 36% of plastic manufacturing. Additionally, the utilization of plastics in the realms of building and construction, textiles, transportation, and electrical equipment constitutes a substantial segment of the plastics market. [1] The invention which is relat

  The Medical Entrance Examination (NEET-UG) 2024 has been the subject of numerous allegations of anomalies, leading to controversy surrounding the exam. Take a look at what we now know, which includes students calling for ‘reneet’, pleading for a CBI investigation, grace marks, paper leaks, and now a political controversy. The ‘reneet’ campaign is trending all over India.   FACTUAL REASON FOR THE CONTROVERSY   The National Testing Agency (NTA) has used a normalizing formula in the valuation of the NEET exam occurred on May 5 th,   2024. The normalizing formula means, giving compensatory marks or grace mark to the students. Here in the case of 2024 NEET, NTA has provided a grace mark to 1563 students, who attended the exam. The reason for such distribution is that those students were not allowed to write   the exam for the full duration of time, from the centres. For compensating the time loss NTA provided grace mark to such number of students. This decision of NTA have caused