scholarly journals CLINICAL PROFILE OF MAXILLO FACIAL FRACTURES IN A TERTIARY CARE HOSPITAL IN UTTAR PRADESH

2018 ◽  
Vol VOLUME 6 (VOLUME 6 NUMBER 2 DECEMBER 2018) ◽  
pp. 1-10
Author(s):  
Helena Babu

Introduction- Trauma from external causes poses one of the greatest challenges for public health services in different parts of the world. Maxillofacial fractures are the most common outcome of trauma. Several factors which are contributing to these can be managed well after careful examination of the clinical profile of the patients. Aim - This study was done to find the clinical profile of maxilla facial fractures in a tertiary care hospital in Uttar Pradesh. Materials and methods -A retrospective study was conducted in Department of Otolaryngology and Head and Neck Surgery, SRMS IMS from May 2016 - October 2018. Medical records of 53 patients in and around west Uttar Pradesh with maxillofacial injuries admitted in our hospital were studied. Results –Males in age group in 20-40 yr were mostly involved in RTA which was most common cause of fmaxillofacial injuries. Fracture mandible was the most commonly fractured bone. Conclusion - There has to be strict regulations installed by the government to ensure compliance of rules regarding use of seat belts while driving and use of helmet while riding two-wheeler. Better compliance of traffic rules is an important factor in reducing the incidents of this trauma. KEYWORDS -Maxillofacial trauma, RTA , Fracture mandible

2020 ◽  
Vol 13 (2) ◽  
pp. 69-72
Author(s):  
Manchala Pratap Reddy ◽  
◽  
Pogula Nagarjuna Reddy ◽  
G.Vijaya Kumar ◽  
◽  
...  

2019 ◽  
Vol 11 (1) ◽  
pp. 45-47
Author(s):  
Sanjay Anarase ◽  
◽  
Yogita Sanjay Anarase ◽  

2017 ◽  
Vol 2 (4) ◽  
pp. S40
Author(s):  
D. Sree Bhushan Raju ◽  
B. Vijay Kiran ◽  
N. Vamsi krishna ◽  
B.N.R. Ramesh ◽  
G. Anvesh ◽  
...  

2021 ◽  
Vol 8 (15) ◽  
pp. 968-971
Author(s):  
Sadiq Yunus Mulla ◽  
Sachin Sitaram Pandit ◽  
Sachin Kisan Shivnitwar

BACKGROUND Haemophilia’s are X-linked hereditary blood clotting disorders due to deficiency of factor VIII (haemophilia A) or factor IX (haemophilia B) & also has identical clinical manifestations, screening tests abnormalities and sex-linked genetic transmission. Haemophilia’s result from defects in the factor VIII / IX gene that lead to decreased amount of factor VIII / IX protein, the presence of a functionally abnormal protein, or combination of both. Haemophilia A is a classic example of an X-linked recessive trait. The severity of their bleeding depends on their factor VIII activity level; and, rarely, a woman can have very low factor VIII activity, and present with symptoms of moderate or even severe haemophilia. We wanted to study the clinical profile of patients of haemophilia admitted in a tertiary care hospital. METHODS This is a cross-sectional study enrolling 60 known cases of haemophilia A & B admitted in wards & ICU / attending OPD of a tertiary care hospital. History was obtained in detail & thorough clinical examination was carried out. Precipitating factors for bleeding (spontaneous / minor trauma / major trauma / surgical operation / dental procedure / others), family h / o bleeding were studied in detail. RESULTS Of the total 60 cases of haemophilia, majority (49) of cases were of haemophilia A and 11 cases were of haemophilia B. In the study, majority (28.33 %) of cases belonged to 12 - 20 years age group and the most common presentation was haemarthrosis (61.67 %). 6 patients had factor VIII inhibitor antibodies and all of them were of haemophilia A. CONCLUSIONS Haemarthrosis is the most common clinical presentation of haemophilia and most common cause for haemarthrosis is spontaneous bleeding. Most common joint involved in bleeding was knee joint (target joint). Presence of factor VIII inhibitor antibodies specially in haemophilia A patients is not uncommon. KEYWORDS Haemophilia, Factor VIII, Factor IX


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