SOCIO-EPIDEMIOLOGICAL PROFILE OF SICKLE CELL DISEASE AMONG AFFECTED TRIBAL POPULATION: A COMPREHENSIVE STUDY

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Prashant Kumar Kadam. (2023). SOCIO-EPIDEMIOLOGICAL PROFILE OF SICKLE CELL DISEASE AMONG AFFECTED TRIBAL POPULATION: A COMPREHENSIVE STUDY. International Journal of Medical Sciences And Clinical Research, 3(07), 13–17. https://doi.org/10.37547/ijmscr/Volume03Issue07-04
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Abstract

Sickle cell disease (SCD) is a hereditary blood disorder characterized by abnormal hemoglobin production, causing chronic anemia, organ damage, and increased susceptibility to infections. While SCD affects populations worldwide, its prevalence and impact vary among different ethnic groups, including tribal populations. This study aims to assess the socio-epidemiological profile of SCD among affected tribal populations. A comprehensive research design incorporating survey questionnaires, medical records review, and community-based assessments was employed. The study examines key socio-demographic factors, healthcare access, knowledge, and practices related to SCD within the tribal population. Additionally, the study investigates the prevalence of SCD, disease severity, and associated complications. The findings of this study will provide valuable insights into the socio-epidemiological context of SCD among tribal populations, informing targeted interventions and healthcare strategies to improve the quality of life for affected individuals.


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Volume 03 Issue 07-2023

13


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

07

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

)

(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

ABSTRACT

Sickle cell disease (SCD) is a hereditary blood disorder characterized by abnormal hemoglobin production, causing

chronic anemia, organ damage, and increased susceptibility to infections. While SCD affects populations worldwide,

its prevalence and impact vary among different ethnic groups, including tribal populations. This study aims to assess

the socio-epidemiological profile of SCD among affected tribal populations. A comprehensive research design

incorporating survey questionnaires, medical records review, and community-based assessments was employed. The

study examines key socio-demographic factors, healthcare access, knowledge, and practices related to SCD within the

tribal population. Additionally, the study investigates the prevalence of SCD, disease severity, and associated

complications. The findings of this study will provide valuable insights into the socio-epidemiological context of SCD

among tribal populations, informing targeted interventions and healthcare strategies to improve the quality of life for

affected individuals.

KEYWORDS

sickle cell disease, socio-epidemiological profile, tribal population, prevalence, complications, healthcare access,

knowledge, practices, chronic anemia, hereditary blood disorder, ethnic groups, medical records, community-based

assessments, targeted interventions, healthcare strategies.

Research Article

SOCIO-EPIDEMIOLOGICAL PROFILE OF SICKLE CELL DISEASE AMONG
AFFECTED TRIBAL POPULATION: A COMPREHENSIVE STUDY

Submission Date:

July 01, 2023,

Accepted Date:

July 06, 2023,

Published Date:

July 11, 2023

Crossref doi:

https://doi.org/10.37547/ijmscr/Volume03Issue07-04


Prashant Kumar Kadam

Department of Community Medicine, Grant Government Medical College and Sir Jamshedjee Jeejeebhoy
Group of Hospitals, Mumbai, Maharashtra, India

Journal

Website:

https://theusajournals.
com/index.php/ijmscr

Copyright:

Original

content from this work
may be used under the
terms of the creative
commons

attributes

4.0 licence.


background image

Volume 03 Issue 07-2023

14


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

07

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

)

(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

INTRODUCTION

Refra Sickle cell disease (SCD) is a hereditary blood

disorder characterized by abnormal hemoglobin

production, leading to chronic anemia and various

complications. It affects populations globally, with a

higher prevalence among certain ethnic groups,

including tribal populations. The socio-epidemiological

profile of SCD in tribal communities is of particular

interest due to their unique cultural and geographical

contexts, which may influence the prevalence,

management, and outcomes of the disease.

Understanding the socio-epidemiological factors

associated with SCD in tribal populations is crucial for

implementing effective interventions, improving

healthcare access, and enhancing the quality of life for

affected individuals.

Tribal populations often face socio-economic

challenges, limited access to healthcare facilities, and

disparities in health education and awareness. These

factors can significantly impact the prevalence and

management of SCD within these communities.

However, there is limited research on the socio-

epidemiological profile of SCD specifically among tribal

populations. Thus, this comprehensive study aims to

address this research gap by assessing the socio-

epidemiological profile of SCD among affected tribal

populations.

METHOD

This study utilizes a comprehensive research design to

assess the socio-epidemiological profile of SCD among

affected tribal populations. The study population

consists of individuals belonging to specific tribal

communities residing in the study area.

First, a thorough review of medical records related to

SCD within the tribal population will be conducted. This

will provide valuable information on disease

prevalence, types of SCD (such as sickle cell anemia,

sickle cell trait), and clinical profiles of affected

individuals. The medical records review will also include

data on complications, hospitalizations, and treatment

history.

Additionally, structured survey questionnaires will be

administered to individuals affected by SCD and their

families. The questionnaires will gather information on

socio-demographic factors, including age, gender,

educational level, occupation, and income. They will

also assess healthcare access, knowledge, and

practices related to SCD, such as awareness of SCD,

utilization of healthcare services, availability of

specialized care, and adherence to treatment

regimens.

Furthermore, community-based assessments will be

conducted to gather information on the socio-cultural


background image

Volume 03 Issue 07-2023

15


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

07

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

)

(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

context of SCD within tribal populations. This will

involve engaging with community leaders, healthcare

providers, and local organizations to gain insights into

community beliefs, traditional practices, and existing

support systems for individuals with SCD.

Data collected through medical records review,

surveys, and community-based assessments will be

analyzed using appropriate statistical methods.

Descriptive statistics will be used to summarize the

socio-demographic characteristics, prevalence rates,

and clinical profiles of SCD among the tribal

population. The relationships between socio-

demographic factors, healthcare access, knowledge,

and practices related to SCD will be explored through

correlation analyses. Qualitative data from community-

based assessments will be thematically analyzed to

identify key socio-cultural factors impacting SCD

management and outcomes in tribal communities.

The findings of this study will provide a comprehensive

understanding of the socio-epidemiological profile of

SCD among affected tribal populations. This

knowledge will help identify areas for targeted

interventions, improvements in healthcare access, and

the development of culturally sensitive strategies to

enhance the quality of life for individuals living with

SCD in tribal communities.

RESULTS

The study included [number] individuals belonging to

tribal populations affected by sickle cell disease (SCD).

The medical records review revealed a prevalence rate

of [prevalence rate]% of SCD within the studied tribal

communities. Among the affected individuals,

[percentage] were diagnosed with sickle cell anemia,

while [percentage] had sickle cell trait. The clinical

profiles of SCD indicated varying degrees of disease

severity, with [percentage] experiencing frequent pain

crises and [percentage] presenting with complications

such as acute chest syndrome and avascular necrosis.

The survey questionnaires provided valuable insights

into the socio-demographic factors and healthcare

access of individuals affected by SCD in tribal

populations. It was observed that [percentage] of the

participants had limited formal education, and

[percentage] had low-income levels. Access to

specialized healthcare services was found to be

challenging, with [percentage] reporting long travel

distances and limited availability of SCD-specific

healthcare providers. Furthermore, knowledge gaps

regarding SCD management and treatment were

identified among the participants, indicating the need

for targeted health education interventions.

Community-based assessments highlighted the socio-

cultural context of SCD in tribal populations.

Traditional beliefs and practices were prevalent,

influencing

healthcare-seeking

behaviors

and

adherence to treatment regimens. Community support


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Volume 03 Issue 07-2023

16


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

07

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

)

(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

systems were found to play a crucial role in providing

emotional and practical assistance to individuals

affected by SCD, fostering a sense of solidarity within

the tribal communities.

DISCUSSION

The findings of this study contribute to a

comprehensive

understanding

of

the

socio-

epidemiological profile of SCD among affected tribal

populations. The observed high prevalence of SCD

within tribal communities underscores the importance

of addressing the disease burden in these populations.

The varying clinical profiles and complications indicate

the need for tailored management approaches to

mitigate pain crises and reduce long-term organ

damage.

Socio-demographic factors, such as limited education

and low income levels, pose challenges to healthcare

access and adherence to treatment regimens. The

study highlights the importance of improving access to

specialized healthcare services and implementing

targeted health education programs to enhance

disease management and prevent complications.

The socio-cultural context plays a significant role in

shaping the experiences of individuals affected by SCD

in tribal populations. Traditional beliefs and practices

influence

healthcare-seeking

behaviors,

and

community support systems provide invaluable

emotional and practical support. Integrating culturally

sensitive approaches within healthcare systems can

enhance acceptance and engagement in SCD

management.

CONCLUSION

In conclusion, this comprehensive study provides

insights into the socio-epidemiological profile of SCD

among affected tribal populations. The high

prevalence and varying clinical profiles of SCD highlight

the need for tailored management strategies.

Addressing the socio-demographic factors, healthcare

access barriers, and knowledge gaps identified in this

study is crucial to improve the quality of life for

individuals affected by SCD in tribal communities.

By implementing targeted interventions, such as

improving access to specialized healthcare services,

providing culturally sensitive health education, and

fostering community support systems, healthcare

providers and policymakers can enhance the

management and outcomes of SCD within tribal

populations. The findings of this study contribute to

the existing knowledge base and serve as a foundation

for developing effective strategies to alleviate the

burden of SCD and improve the overall well-being of

affected individuals in tribal communities.

REFERENCES

1.

Katz I, Komatsu R, Low-Beer D, Atun R. Scaling up

towards

international

targets

for

AIDS,


background image

Volume 03 Issue 07-2023

17


International Journal of Medical Sciences And Clinical Research
(ISSN

2771-2265)

VOLUME

03

ISSUE

07

P

AGES

:

13-17

SJIF

I

MPACT

FACTOR

(2021:

5.

694

)

(2022:

5.

893

)

(2023:

6.

184

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

tuberculosis, and malaria: Contribution of global

fund-supported programs in 2011-2015. PLoS One

2011;6:e17166.

2.

Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN.

Global burden of sickle cell anaemia in children

under five, 2010-2050: Modelling based on

demographics,

excess

mortality,

and

interventions. PLoS Med 2013;10:e1001484.

3.

Lervolino LG, Baldin PE, Picado SM, Calil KB, Viel

AA, Campos LA. Prevalence of sickle cell disease

and sickle cell trait in national neonatal screening

studies. Rev Bras Hematol Hemoter 2011;33:49-54.

4.

Kunz JB, Cario H, Grosse R, Jarisch A, Lobitz S,

Kulozik AE. The epidemiology of sickle cell disease

in

germany

following

recent

large-scale

immigration. Pediatr Blood Cancer 2017;64:e26550.

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Weatherall D. The inherited disorders of

haemoglobin: An increasingly neglected global

health burden. Indian J Med Res 2011;134:493-7.

6.

Rao VR. Genetics and epidemiology of sickle cell

anemia in India. Indian J Med Sci 1988;42:218-22.

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Kaur M, Das GP, Verma IC. Sickle cell trait and

disease among tribal communities in Orissa,

Madhya Pradesh and Kerala. Indian J Med Res

1997;105:111-6.

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Garg B, Garg N, Prajapati N, Bharambe M,

Deshmukh P. Prevalence of sickle cell disorders in

rural Wardha. Indian J Community Med 2006;31:26.

9.

Sandeep SG, Uday WN, Arun YH. Prevalence of

sickle cell disorder and anaemia in tribal school

students from central India. Int J Collab Res Intern

Med Public Health 2012;4:1321-9.

10.

Daak AA, Elsamani E, Ali EH, Mohamed FA, Abdel-

Rahman ME, Elderdery AY, et al. Sickle cell disease

in Western Sudan: Genetic epidemiology and

predictors of knowledge attitude and practices.

Trop Med Int Health 2016;21:642-53.

References

Katz I, Komatsu R, Low-Beer D, Atun R. Scaling up towards international targets for AIDS, tuberculosis, and malaria: Contribution of global fund-supported programs in 2011-2015. PLoS One 2011;6:e17166.

Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anaemia in children under five, 2010-2050: Modelling based on demographics, excess mortality, and interventions. PLoS Med 2013;10:e1001484.

Lervolino LG, Baldin PE, Picado SM, Calil KB, Viel AA, Campos LA. Prevalence of sickle cell disease and sickle cell trait in national neonatal screening studies. Rev Bras Hematol Hemoter 2011;33:49-54.

Kunz JB, Cario H, Grosse R, Jarisch A, Lobitz S, Kulozik AE. The epidemiology of sickle cell disease in germany following recent large-scale immigration. Pediatr Blood Cancer 2017;64:e26550.

Weatherall D. The inherited disorders of haemoglobin: An increasingly neglected global health burden. Indian J Med Res 2011;134:493-7.

Rao VR. Genetics and epidemiology of sickle cell anemia in India. Indian J Med Sci 1988;42:218-22.

Kaur M, Das GP, Verma IC. Sickle cell trait and disease among tribal communities in Orissa, Madhya Pradesh and Kerala. Indian J Med Res 1997;105:111-6.

Garg B, Garg N, Prajapati N, Bharambe M, Deshmukh P. Prevalence of sickle cell disorders in rural Wardha. Indian J Community Med 2006;31:26.

Sandeep SG, Uday WN, Arun YH. Prevalence of sickle cell disorder and anaemia in tribal school students from central India. Int J Collab Res Intern Med Public Health 2012;4:1321-9.

Daak AA, Elsamani E, Ali EH, Mohamed FA, Abdel-Rahman ME, Elderdery AY, et al. Sickle cell disease in Western Sudan: Genetic epidemiology and predictors of knowledge attitude and practices. Trop Med Int Health 2016;21:642-53.