Professional Documents
Culture Documents
Submitted by,
Junior resident
Department of Otorhinolaryngology
Ph: 7559921014
Junior Resident
Department of Otorhinolaryngology
To,
The Secretary
Thanking You,
Yours faithfully,
Junior Resident
Department of Otorhinolaryngology
Place: Thiruvananthapuram Sree Uthradom Thirunal Academy of
Date: Medical Science, Thiruvananthapuram
DECLARATION BY THE GUIDE
Department: Otorhinolaryngology
Title of the Study: A descriptive cross sectional study on the etiological factors and
I take the full responsibility and accountability for planning, execution, and adverse events
occurring during the study .The data collected and records will be retained by myself for a
4. Month and year of appearing in final examination for completing the course: 2025
5. Name(s) ,designations(s) & address of guide and co-guide (s) with mobile number and
Email ID
Assistant Professor
Department of ENT
Sree Uthradom Thirunal Academy of Medical Science,
Signature of PG student
commonest and most difficult to treat emergencies 1. Approximately 60% of population are
affected by epistaxis at some point in their lifetime, with 6% requiring medical attention 2. It
affects all age groups and both sexes. Epistaxis can be classified as anterior and posterior
based on the site of origin 3. Anterior epistaxis is more common than posterior epistaxis 4.
Anterior epistaxis arises either from Kiesselbach’s plexus, a rich vascular anastomotic area
formed by end arteries in Little’s area or from retrocolumellar vein. It is more common in
children and young adults. It is rarely severe and can be controlled by local pressure or
anterior nasal packing. Posterior epistaxis arises commonly from Woodruff’s plexus, a plexus
of prominent blood vessels lying just inferior to the posterior end of inferior turbinate 5 . It is
more common in elderly. Usually the bleeding will be profuse and requires posterior nasal
The causes of epistaxis can be divided into local, general systemic, medication induced.
The local causes includes: infection, trauma, deviated nasal septum, septal spur , digital
manipulation , foreign body , chemicals , neoplasm , etc. The general systemic causes
Medications causing epistaxis includes: NSAIDs, Anticoagulants, topical nasal steriods etc .
For the effective management of patients with epistaxis, it is important to know the blood
supply of nasal cavity. Nasal cavity is supplied by branches of internal and external carotid
arteries. Majority of the nasal cavity is supplied by the sphenopalatine artery, which is a
general first aid, chemical cauterization , anterior and posterior nasal packing . In cases of
REVIEW OF LITERATURE
Literature search was done and the role of identification of different aetiological factors for
A study was conducted by Ramesh Parajuli in 2015 among 84 patients with epistaxis in a
tertiary care hospital in central Nepal. Out of 84 patients, 52 were males and 32 were females.
The most common cause of epistaxis was idiopathic (38.09%) followed by hypertension
(27.38%), trauma (15.47%) and coagulopathy (8.33%). Regarding treatment methods, most
(52.38%) of patient required anterior nasal packing. Chemical cautery was sufficient to stop
bleeding in 14.28% of patients; electrocautery and posterior nasal packing were performed in
2.38% and 16.66% patients. Two patients (2.38%) required endoscopic sphenopalatine
arterial ligation. Anterior nasal packing was the most common treatment method used for
epistaxis in a tertiary care hospital Mangalore. Out of these 65% were males and 35% were
females. Most of the cases were aged more than 50 years (31.7%) with the mean age of 38.56
years. Most common aetiology of epistaxis in this study was hypertension (20%), followed
by acute rhino sinusitis (15%). Commonest cause in children was deviated nasal septum and
acute rhino sinusitis, while in young adults trauma was the most common cause. Most
common cause in elderly was hypertension. Medical management was given in most of the
cases (65%) while anterior and posterior nasal packing was done in 20% and 10% cases
respectively. Three cases underwent electro cauterization of bleeding point 9.
A retrospective study was conducted by Shweta (2019) among 96 patients with epistaxis in a
tertiary care hospital Himachal Pradesh. Out of the total 96 cases, 58.3% were males and
41.6% were females. Most of the patients were over 40 years of age. The maximum,
19(19.79) were in the age group of 51-60 years and minimum 2 (2.08%) were in the age
group of 90-100 years. In the study of 96 cases , common group in this series was of
trauma 12 (12.5%) , 7 cases (7.29) had blood dyscrasias , DNS with spur in 3 (3.12%) ,
METHODOLOGY
Research question: How far the identification of aetiological factors help in the effective
Duration of study: 2 year after Institutional Research Committee and Ethical Committee
approval.
Study setting: Department of Otorhinolaryngology, Sree Uthradom Thirunal Academy of
Sample size: 94
n= Zα 2 p q /d2
Inclusion criteria
1. Patients presenting with epistaxis in the out patients and emergency department of
ENT in the age group of 0 to 80 years who gives consent for the study
Exclusion criteria
An informed consent will be obtained from the patients and parents of children in the study
population. The first priority will be given to arrest the bleeding by first aid measures or
anterior nasal packing. Then a detailed medical and surgical history will be taken. This will
examination will include anterior rhinoscopy using Thudicum or Killian’s nasal speculum
and posterior rhinoscopy using St. Clair Thompson’s postnasal mirror. Complete blood
examination will also be carried out in order to rule out systemic causes and
Study tool
1. Nasal speculum
Data obtained will be entered in Microsoft office excel sheet. Statistical analysis will be done
with the help of SPSS version 27. Categorical variables will be expressed in frequency and
Study will be conducted only after getting approval from the ethical committee of the
institution and KUHS. Written informed consent will be obtained from all the patients. When
the subject is younger than 18years, written informed consent will be obtained from their
parents. Privacy and confidentiality will be maintained. Study results will be used only for
The expected outcome of the study is to find out how identification of aetiological factors
REFERENCES
1582,2002.
Surg .2018
10. Shaweta , Rajnish Sharma , Nisha Sharma, “ Epistaxis : A retrospective clinical study”.
● Name:
● Age:
● Sex:
● Occupation:
● Phone no:
● Address:
Presenting complaint
● Onset:
● Duration:
● Unilateral/bilateral:
● Quantity:
● History of trauma:
● History of allergy:
● Any medical / surgical treatment taken for similar complaints in the past:
GENERAL EXAMINATION
● Systemic examination:
● Cardiovascular system:
● Respiratory system:
● Gastrointestinal system:
EXTERNAL APPEARANCE
● Vestibule:
● Anterior rhinoscopy:
● Nasal septum:
● Nasal passage:
● Nasal mucosa:
● Floor:
● Lateral wall:
● Posterior rhinoscopy:
● If yes, specify:
INVESTIGATIONS
● BRE
● BT
● CT
● PT INR
● APTT
● RFT
● LFT
● BLOOD GROUP
● PERIPHERAL SMEAR
● NASAL ENDOSCOPY
● TREATMENT GIVEN
PATIENT INFORMATION SHEET
study, I will be doing detailed interview of the patient. By participating in the study, you will
not have to incur any additional expenses. The outcome of the study will be used for
academic purposes and for publishing articles. But the details of the individuals will be kept
confidential. Participating in the study will not result in any harm to the subjects. You can
withdraw from the study at any point of time without any reason, which will not affect your
Department of Otorhinolaryngology
I have fully read and understood the information given to me by Dr. Lekshmi Devi .V. I am
adequately informed about various aspects of the study. I am aware that I have the right to
withdraw from this study at any time and it will not affect my treatment at any cost. I
understood that there is no financial liability on me. I understood that result of the study will
study.
Name : Name:
consent )
I (Relative / Guardian) of
have fully read and understood the information given to me by Dr.Lekshmi Devi .V. I am
adequately informed about various aspects of the study. I have understood that i have the
right to refuse the consent or withdraw it at any time during the study without adversely
understood that the result of the study will be published maintaining the patient
എന്ന്
ഗവേഷക :
ജൂനിയർ റസിഡന്റ്
ഇ.എൻ.ടി വിഭാഗം
മെഡിക്കൽസയൻസ്, തിരുവനന്തപുരം
ഒപ്പ്:
രോഗിയുടെ പേര്:
ഒപ്പ്:
ബന്ധുവിന്റെ പേര്:
ഒപ്പ്:
Dr Lekshmi Devi V
PG resident
Department of ENT
”. I am going to give you information and invite you to be a part of the research study. You
can choose whether or not to participate in this. We have discussed the research with
your parents/guardian and they knew that we are also asking you for your
also have to agree. But if you don’t wish to take part in the research, you do not
have to, even if your parents have agreed. You may discuss anything this with your
parents or friends or anyone else you feel comfortable talking to. You can decide
whether to participate or not after you have discussed it over. You don’t have to
decide immediately. There may be some words you don’t understand or things that
you want me to explain more about . Please ask me to stop at any time and i will
explain them slowly. If you decide not to be in this research it is okay and nothing
changes. Even if you say yes you can change your mind later if you feel otherwise
After you say yes to the study, relevant history will be taken from your
parents/guardians ,You can ask me to explain again at any time and I will explain
more about the process. I have checked with the child and they understood the
procedures. This study is not going to cause any harm to you as I am just collecting
some data of you and is not giving you any new drug/vaccine or is not altering your
clinical treatment. I have checked with the child and they understood the benefits.
We will not tell other people that you are in this research and we won’t share
information about you to anyone. Afterwards I will publish them by writing but
keeping your details confidential. No one will be mad /disappointed with you. If you
say no it's your choice. You can think about it and tell me later. If you want you can
say yes now and can change your mind later and it’s still ok. You can ask me
questions now or later. I have written a number and address where you can reach me
or if you are nearby you can come with your parents and see me. If you choose to be
a part of this study I will also give you a copy of this paper to keep for yourself.
I have read this information (or had the information read to me. I have had my questions
answered and I know that I can ask questions later if I want. I agree to take part in
this research. OR I do not wish to take part in this research and I have not signed
Date.................
In case of illiterate, I have witnessed the accurate reading of the assent form to the child and
the individual has had the opportunity to ask questions. I confirm that the individual
Date..........
I have accurately read or witnessed the accurate reading of the assent form to the potential
participant, and the individual has had the opportunity to ask questions. I confirm
Date:
പിജി റസിഡന്റ്
ഇ ൻ ടി വിഭാഗം
തിരുവനന്തപുരം
പ്രസിദ്ധികരിക്കാൻ സാധ്യതയുണ്ട്.
അറിവോടെയുള്ള സമ്മതം
അല്ലെങ്കിൽ
ഈ ഗവേഷണത്തിന്റെ ഭാഗമാകാൻ എനിക്ക് സമ്മതമല്ല
പേര്
ഒപ്പ്
തിയതി
നിരക്ഷരർക്കു
മൽകിയിരുന്നു
സാക്ഷിയുടെപേര് ഒപ്പ്
തിയതി
കുട്ടിയുടെ
കൈയ്യൊപ്പ്