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This reference provides an update on current therapies to treat neglected diseases, a class of diseases that primarily affect tropical regions where investment in research and development is limited.
The book starts with an introduction to neglected diseases followed by reviews of therapeutic strategies to overcome the impact of neglected diseases. This is followed by updated information for handling leprosy, dengue, lymphatic filariasis, dracunculiasis, helminthiasis, Chagas’ disease, neurocysticercosis, leishmaniasis, rabies, trematodiasis, buruli ulcer and trachoma in 10 focused chapters, respectively. The chapters provide information on disease mechanism, transmission and management protocols, along with scientific references. The book serves as a resource for healthcare professionals, and scholars who need a detailed understanding of these infectious diseases.

Readership
Scholars (medical microbiology, epidemiology), healthcare professionals (nursing and family medicine) and public health administrators.

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Veröffentlichungsjahr: 2024

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Table of Contents
BENTHAM SCIENCE PUBLISHERS LTD.
End User License Agreement (for non-institutional, personal use)
Usage Rules:
Disclaimer:
Limitation of Liability:
General:
PREFACE
List of Contributors
Neglected Tropical Diseases
Abstract
1. INTRODUCTION
2. Epidemiology and risk factors
2.1. Buruli Ulcer
2.2. Chikungunya
2.3. Chagas Disease
2.4. Dengue Fever
2.5. Human African Trypanosomiasis
2.6. Leishmaniasis
2.7. Lymphatic Filariasis
2.8. Soil-Transmitted Helminthiasis
2.9. Onchocerciasis
2.10. Scabies
2.11. Schistosomiasis
2.12. Trachoma
2.13. Rabies
2.14. Dracunculiasis (or Guinea Worm Disease)
2.15. Leprosy
3. Recommendations
Conclusion
References
Strategies to Overcome the Impact of Neglected Diseases on the World
Abstract
1. Introduction
2. Impact of NDTs
2.1. To Defeat the Impact of NDTs on World’s Health and Economy
2.1.1. Mass Drug Administration (MDA)
2.1.2. Improved Sanitation and Hygiene
2.1.3. Vector Control
2.1.4. Vaccination Programs
2.1.5. Health Education and Community Engagement
2.2. The Global Plan Focused on Four Main Pillars
2.2.1. Preventive Chemotherapy
2.2.2. Innovative and Intensified Disease Management
2.2.3. Vector Control and Vector-borne Diseases
2.2.4. Water, Sanitation, and Hygiene (WASH)
3. Global Goals
3.1. WHO-2012:Implementation of Roadmap
3.2. London Declaration on the Neglected Tropical Diseases
3.3. SDG 3: End of Ntds Epidemic
3.4. U.S. Government Efforts
3.5. Multidimensional and Other Efforts
3.6. Funding
4. COVID 19 and impact on NTDs
Conclusion
References
Current Therapeutic Strategies for the Management of Leprosy
Abstract
1. INTRODUCTION
2. Epidemiology
2.1. Etiologic Agent, the Mycobacterium leprae (M. leprae)
2.2. Genetic Determinants of Host Response
2.3. Transmission of Leprosy
2.4. Risk Factors
2.5. Interaction of M. leprae with Schwann Cells and Macrophages
2.6. Clinical Signs and Classifications
2.6.1. Tuberculoid Leprosy
2.6.2. Lepromatous Leprosy
2.6.3. Borderline Leprosy
2.7. Diagnosis of Leprosy
2.8. Leprosy Treatment Approaches
2.9. Issues and Challenges of Leprosy Treatment
Conclusion
References
Emerging Therapy for Dengue
Abstract
1. Introduction
1.1. Classification
2. Etiopathogenesis
2.1. Symptoms and Signs
2.2. Bioanalysis Methods for Anti-dengue Activity
2.2.1. Pre-clinical
2.2.2. Clinical
2.3. Treatment
2.3.1. Symptomatic Management
2.3.2. Management of the Critical Phase
2.3.3. Fluid Resuscitation
2.3.4. Blood Products
2.3.5. Immunomodulation
2.3.6. Corticosteroids
2.3.7. Intravenous Immunoglobulins
2.3.8. Other Supportive
2.3.9. Nucleoside Analogues
2.3.10. RNA Dependant RNA Polymerase(NS5) Inhibitor
2.3.11. Protease(NS2b-NS3) Inhibitors
2.3.12. Quinoline Containing Compounds
2.3.13. NS4b Inhibitor
2.3.14. Host Modulators
3. RIBAVIRIN
3.1. Mycophenolic Acid
3.2. Α Glycosidase Inhibitors
3.3. Lovastatin
3.4. Host Kinase Inhibitors
3.5. Heparin and Heparan Sulfate
3.6. Interferon
3.7. D4 Dopamine Receptor Antagonists
3.8. Pentoxifylline
3.9. Ivermectin
4. CHLOROQUINE
4.1. RNAi
4.2. Medicinal Plant Derivatives
CONCLUSION
References
Lymphatic Filariasis and Dracunculiasis
Abstract
1. INTRODUCTION
2. CAUSES AND TRANSMISSION
3. LIFECYCLE
4. CLINICAL MANIFESTATIONS OF LYMPHATIC FILARIASIS
4.1. Acute Disease
4.2. Chronic Disease
5. PATHOGENESIS
6. DIAGNOSIS
7. APPROACHES TO CONTROL AND ELIMINATE THROUGH MDA
8. WHO RECOMMENDATIONS FOR MDA TO ELIMINATE LYMPHATIC FILARIASIS
9. FUTURE CONSIDERATIONS
10. RISK FACTORS
11. INTRODUCTION TO DRACUNCULIASIS
11.1. Genus Dracunculus
11.2. Species of Dracunculus
11.3. Dracunculus Insignis
11.4. Dracunculus Lutrae
11.5. Dracunculus Fuelleborn
12. TRANSMISSION
13. CURRENT STATUS IN INDIA
14. GLOBAL SITUATION
15. ERADICATION OF GUINEA WORMS IN INDIA
16. LIFE CYCLE AND CLINICAL IMPACT
17. AREAS OF ERUPTION
18. DIAGNOSTIC FEATURE
19. TREATMENT
20. ECONOMIC IMPACT
21. THE ROAD TO ERADICATION
CONCLUDING REMARKS
REFERENCES
Current Therapeutic Strategies for Soil-Transmitted Helminthiasis
Abstract
1. INTRODUCTION
2. Clinical Features of Helminthiasis
2.1. Mode of Transmission of Helminth Infection
2.2. Nutritional Effects of Helminthiasis
2.3. Diagnosis of STH
2.4. Pathophysiology of STH
2.5. Therapeutic Strategies for Soil-transmitted Helminthiasis
2.6. Different Drug Administration Strategies
2.7. Drugs Recommended by WHO for the Treatment of Soil-transmitted Helminthiases
2.8. Risk Groups for Infection
2.9. The Intervention of Soil-transmitted Helminthiasis
2.10. Ayurvedic Strategies for Soil-transmitted Helminthiases
2.11. Prevention of Helminth Infection
2.11.1. Health Education
2.11.2. Regular Treatment
2.11.3. Sanitation
3. Future Aspects
CONCLUSION
REFERENCES
Current Therapeutic Strategies for Neurocysticercosis and Leshmaniasis
Abstract
1. Introduction
2. The parasite
3. Clinical Manifestation
4. Diagnosis and Treatment of NCC
4.1. Conventional Diagnosis
4.1.1. Excision Biopsy
4.1.2. Neuroimaging
4.1.3. Methods for Immunological Diagnosis Based on Blood or Serum
4.1.4. Antigen Detection Tests
4.2. Novel Methods of Diagnosis
4.2.1. Fast Imaging Utilizing Consistent State Securing
4.2.2. Microscopic Assessment of Defecation for Taenia Eggs
4.2.3. DNA-based Methods
4.3. Management of NCC
4.3.1. Surgery
5. Current medications for NCC treatment
5.1. Corticosteroids
5.2. Antiepileptic Drugs
5.3. Praziquantel (biltricide, cysticide, prazisan)
5.4. Albendazole
5.5. Combination Regimen
6. Limitations/drawbacks of currently used drugs
7. Future problems and their answers
7.1. Leishmaniasis
7.1.1. Introduction
7.1.2. Epidemiology
7.1.3. Causative Agent
7.1.4. Diagnosis
7.1.5. Pathophysiology/Life Cycle of Leishmania
7.1.6. Types and Clinical Manifestations
7.1.7. Cutaneous Leishmaniasis (CL)
7.1.8. Mucocutaneous leishmaniasis (MCL)
7.1.9. Visceral leishmaniasis (VL)
7.1.10. Treatment Goals
8. Traditional antileishmanial treatment
8.1. Pentavalent Antimonial
8.2. Amphotericin B
8.3. Pentamidine
8.4. Miltefosine
8.5. Paromomycin
8.6. Azoles
8.7. Allopurinol
8.8. Sitamaquine
8.9. Other Drugs
9. New Strategies for Leishmaniasis
9.1. Modern Strategies for CL and MCL
9.1.1. Local and Physical Therapies
9.1.1.1. Cryotherapy
9.1.1.2. Electrotherapy
9.1.1.3. Thermotherapy and CO2 Laser Administration
9.1.1.4. Wound Care
9.1.2. Topical Drug Treatment Options
9.1.2.1. Nitric Oxide Derivates
9.1.2.2. Intralesional Drug Administration
9.2. Modern Strategies for Visceral leishmaniasis
9.2.1. Combination/Multi-drug Therapy
9.2.2. Immunity Boosters
9.2.3. Microspheres
9.2.4. Nanotechnology
9.2.4.1. Liposomes
9.2.4.2. Polymeric Nanoparticles
9.2.4.3. Metal Oxide-based Nanoparticles
9.2.4.4. Nano Emulsions
9.2.4.5. Solid Lipid Nanoparticles (SLN)
9.2.4.6. Nano Disks
9.2.4.7. Gels
9.2.5. Drug Repurposing
9.2.6. Phytochemicals/Plants Used
9.2.7. Photodynamic Therapy
9.2.8. Vaccines
Conclusion
Abbreviations
References
Current Therapeutic Strategies for Buruli Ulcer
Abstract
1. INTRODUCTION
2. Ulcers
2.1. Types of Ulcers
2.1.1. Decubitus Ulcers
2.1.2. Venous Ulceration
2.1.3. Arterial Ulcers
2.1.4. Neuropathic Ulcers
2.1.5. Vasculitis Ulcer
3. Buruli Ulcer
3.1. Causative Organism
3.2. Epidemiology
3.3. Progression of the Disease
3.4. Pathogenesis
4. Current Control Strategy
5. Treatment Regimen
6. Challenges
7. Prevention
Conclusion
REFERENCES
Current Therapeutic Strategies for Trachoma
Abstract
1. INTRODUCTION
2. Chlamydia Trachomatis
2.1. Symptoms and Signs
2.2. Stages of Trachoma
2.2.1. Follicular Inflammation
2.2.2. Severe Inflammation
2.2.2.1. Scarring on the Eyelids
2.2.3. Twisted Eyelashes (trichiasis)
2.2.4. Cloudy Cornea (Opacity)
2.3. Causes
2.4. Risk Elements
2.4.1. Congested Housing Situations
2.4.2. Deficient Sanitation
2.4.3. Age
2.4.4. Sex
2.4.5. Flies
3. Cycle of Chlamydial Development
3.1. Affiliation and Invasion
3.2. Modification of the Intracellular Environment
3.2.1. Included Organelles and Size
3.2.2. Inclusion and Lipids
3.2.3. Alteration of the Metabolic Pathway
3.3. Host Evasion
3.4. Host Exit
4. Complications
5. Prevention
5.1. Washing your Hands and your Face
5.2. Fly Management
6. SURGERY
7. ANTIBIOTICS
8. FACE CLEANING
9. ECOLOGICAL FACTORS
CONCLUSION
REFERENCES
Current Therapeutic Strategies for Food Borne Trematodiases
Abstract
1. INTRODUCTION
2. THE LIFE CYCLE OF FOOD-BORNE TREMATODES
3. GEOGRAPHIC DISTRIBUTION
4. SYMPTOMS
4.1. Clonorchis Sinensis
4.2. Fasciola Hepatica and Fasciola Gigantica
4.3. Opisthorchis Viverrini
4.4. Paragonimus spp.
5. DIAGNOSIS
5.1. Parasitological Diagnosis
5.2. Immunodiagnosis
5.3. Molecular Techniques
6. CURRENT THERAPEUTIC STRATEGIES USED IN THE TREATMENT OF FOOD-BORNE TREMATODIASES
6.1. Prevention, Treatment and Control
6.2. Chemotherapy
6.3. In vitro Activity of Natural Plant Extracts
CONCLUSION
ACKNOWLEDGEMENT
REFERENCES
Emerging Approaches to Tackle Neglected Diseases: From Molecule to End Product
Edited by
Prerna Sharma
Guru Gobind Singh College of Pharmacy
Yamunanagar, India
Sumeet Gupta
MM College of Pharmacy
MMU, Mullana, Haryana
India
Hitesh Malhotra
Guru Gobind Singh College of Pharmacy
Yamunanagar, India
Bhawna Chopra
Guru Gobind Singh College of Pharmacy
Yamunanagar, India
&
Sunil Sharma
Guru Jambheshwar University of Science and Technology
Hisar, India

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PREFACE

This work will lead to an extensive debate as it covers an interesting topic. I feel compelled to share my knowledge, analyses, and conclusions after working for numerous years in the field of pharmacy. I have written many papers and book chapters on various aspects. Perhaps this description will increase the knowledge of the issue and initiate a discussion that could result in significant ideological transformations. There are two reading categories for this book. First off, it can be read by individuals with little to no prior knowledge of science. Professionals from academia and government organizations are the second set of readers. It is hard to believe that all members of the scientific community will comply with the concepts and ideas presented in this work. But I do hope that the knowledge and information provided will serve as a guide for all the sections of society.

Neglected tropical diseases (NTDs) are a diverse collection of 20 illnesses that are primarily found in tropical regions and impact more than 1 billion people who reside in underdeveloped communities. Numerous pathogens, such as viruses, bacteria, parasites, fungi, and toxins, are responsible for their development. More than one billion people suffer from terrible health, along with social, and fiscal effects of these diseases. There are 12 chapters in the book. The introduction to neglected diseases is broadly introduced in Chapter 1 of this book. The strategies to overcome the impact of neglected diseases on the world are discussed in Chapter 2, which also provides a step-by-step process to handle such conditions. The current therapeutic strategy for leprosy, dengue, lymphatic filariasis and dracunculiasis, helminthiasis, Chagas disease, neurocysticercosis and leishmaniasis, rabies, trematodiasis, Buruli ulcer and trachoma is introduced in Chapter 3 to 10, respectively, along with an account of the possible disease mechanism, transmission and management protocols.

I wish a lot of people read this book. In order to escape the mistakes of the past, we must alter course and begin utilising knowledge built up by scientists.

Prerna Sharma Guru Gobind Singh College of Pharmacy Yamunanagar, IndiaSumeet Gupta MM College of Pharmacy MMU, Mullana, Haryana IndiaHitesh Malhotra Guru Gobind Singh College of Pharmacy Yamunanagar, IndiaBhawna Chopra Guru Gobind Singh College of Pharmacy Yamunanagar, India &Sunil Sharma Guru Jambheshwar University of Science and Technology Hisar, India

List of Contributors

Anjali SharmaGuru Gobind Singh College of Pharmacy, Yamunanagar, IndiaArti SainiM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaAkash KambojGuru Gobind Singh College of Pharmacy, Yamunanagar, IndiaAshwani AryaDepartment of Pharmaceutical Education and Research, BPS Women University, Sonepat, Haryana, IndiaArvinder KaurG.H.G. Khalsa College of Pharmacy, Gurusar Sadhar, Ludhiana, IndiaAkash JainM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaAshwani DhingraGuru Gobind Singh College of Pharmacy, Yamunanagar, Haryana, IndiaDhirender SinghM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaDevkant SharmaCH. Devi Lal College of Pharmacy, Jagadhari, IndiaGarima MalikM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaHimani BajajAVIPS, Shobhit University, Gangoh, Saharanpur, UP, IndiaHasandeep SinghDepartment of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab-143005, IndiaInderjeet VermaM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaJasmine ChaudharyM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaKashish WilsonM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaLalit GuptaG.H.G. Khalsa College of Pharmacy, Gurusar Sadhar, Ludhiana, IndiaMeenakshi DhanawatAmity Institute of Pharmacy, Amity University Haryana, Gurugram, Haryana, IndiaManish DhallCollege of Pharmacy, PGIMS (SDPGIPS), Pt. B. D. Sharma University of Health Sciences, Rohtak-124001, Haryana, IndiaManisha BhatiaM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaMayank YadavAVIPS, Shobhit University, Gangoh, Saharanpur, UP, IndiaMd. Arif NaseerAVIPS, Shobhit University, Gangoh, Saharanpur, UP, IndiaNamratha MPJSS Academy of Higher Education and Research, Mysore, IndiaNitin GoelG.H.G. Khalsa College of Pharmacy, Gurusar Sadhar, Ludhiana, IndiaNidhi GuptaM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaPooja MittalChitakara College of Pharmacy, Chitkara University, Rajpura, Punjab, IndiaPoonam BhartiDepartment of Psychology, MMIMSR, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaPrerna SharmaGuru Gobind Singh College of Pharmacy, Yamunanagar, IndiaRenu KadianRam Gopal College of Pharmacy, Sultanpur, Farrukhnagar, Gurgaon-122507, Haryana, IndiaRajiv SharmaUniversity Institute of Pharma Science Chandigarh University, Gharuan, Mohali, IndiaSumeet GuptaM.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana, IndiaSrishti VatsGuru Gobind Singh College of Pharmacy, Yamunanagar, IndiaSuchitra NishalCollege of Pharmacy, PGIMS (SDPGIPS), Pt. B. D. Sharma University of Health Sciences, Rohtak-124001, Haryana, IndiaSatvinder KaurUniversity Institute of Pharma Science Chandigarh University, Gharuan, Mohali, IndiaSindhu AgarwalAVIPS, Shobhit University, Gangoh, Saharanpur, UP, IndiaVishnu MittalGuru Gobind Singh College of Pharmacy, Yamunannagar, Haryana, IndiaVani DawarGuru Gobind Singh College of Pharmacy, Yamunannagar, Haryana, India

Neglected Tropical Diseases

Garima Malik1,*,Meenakshi Dhanawat2,Kashish Wilson1
1 M.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, 133207, India
2 Amity Institute of Pharmacy, Amity University Haryana, Gurugram, Haryana, India

Abstract

Neglected tropical diseases (NTDs) are a widespread category of communicable illnesses that thrive in tropical and subtropical environments. More than a billion people are affected by these illnesses, which annually drain billions of dollars from developing nations' economies. The most severely impacted populations are those who lack access to basic sanitation, live in poverty, and are in close proximity to disease vectors, domestic animals, and livestock. The World Health Organization (WHO) is a United Nations department focusing on public health issues. NTDs pose a significant threat to public health both globally and in India. Lymphatic filariasis (LF), Visceral Leishmaniasis (VL), Rabies, Soil-Transmitted Helminthic Infections (STH), and Dengue are the principal parasitic and associated infections that the World Health Organization (WHO) has designated as neglected tropical diseases (NTDs). These neglected diseases represent a concern to millions of underprivileged Indians who live in deplorable conditions. The current chapter examines the common NTDs in India, their prevalence, the state of control strategies, and obstacles and prospects for NTD eradication.

Keywords: Communicable diseases, Diseases of poverty, Epidemiology, Global burden, Integrated control, Mass drug administration, Neglected Tropical Diseases, Poverty, Risk factors, World Health Organization.
*Corresponding author Garima Malik: M.M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, 133207, India; E-mail: [email protected]

1. INTRODUCTION

Neglected tropical illnesses are a serious issue for public health since they affect almost one billion people worldwide [1]. Regardless of the fact that these illnesses have been known for centuries, many nations, especially low- and middle-income ones (LMIC), are still working to eradicate NTDs [2]. The WHO classified seventeen significant parasite infections and associated disorders as neglected tropical diseases. These illnesses disproportionately affect the underprivileged and

poor populations of countries in Africa, Southeast Asia, and South America [3-5]. A massive campaign aimed at public health control and elimination of these diseases is closely related to neglected tropical diseases (NTDs), a group of tropical infections [6-8].

The three main types of diseases in India are communicable diseases, maternity and child health issues (which collectively account for around half the burden), and non-communicable disorders [9]. Thus, both the diseases of the industrialized world (such as diabetes mellitus and cardiovascular diseases) and the ailments of the underdeveloped world (such as infectious and neglected diseases) have been observed in India [10]. The recurrence of previously curable illnesses like leishmaniasis, malaria, and other vector-borne diseases has a major impact on underprivileged and rural populations. However, these diseases have received little attention globally because they primarily affect the poorer sections of the population. Thus, it will be appropriate to state that neglected diseases are a category of infectious and parasitic illnesses that often receive little attention from the pharmaceutical industry and mainly afflict the poorest members of society [11].

Upon the introduction of the Millennium Development Goals (MDGs) in the early 2000s, the NTD framework was initially put forth. HIV/AIDS, TB, and malaria were expressly included in the MDG's list of global infectious diseases, leaving out numerous tropical diseases with significant worldwide recurrence and disease burden. In response, 13 bacterial, protozoal, and helminthic “neglected” infectious disorders were grouped as NTDs. Later, WHO divided the NTDs into two groups: (1) individuals treated with preventative chemotherapy and transmission control (PCT) and (2) those demanding novel and rigorous disease management (IDM). The seven PCT-related illnesses were grouped based on the idea that they may all be treated at the same time with a “rapid-impact package” of drugs by mass drug administration (MDA; also known as preventative chemotherapy), as shown in Fig. (1) [12].

Schistosomiasis, lymphatic filariasis (LF), onchocerciasis, and trachoma were among the PCT disorders, as were the three major soil-transmitted helminth (STH) diseases (ascariasis, trichuriasis, and hookworm) [7]. As worldwide control and elimination operations gained significance internationally, the WHO formed a Department of NTDs and eventually added 18 major tropical illnesses to the NTD list. WHO has recently increased this figure to 20. In this book chapter, we review the public health initiatives for the control and eradication of NTDs, discuss current worldwide developments, and map a course for the future.

Fig. (1)) A compendium of Neglected Tropical Diseases. Much attention is given to previously neglected diseases such as malaria, HIV/AIDS, and TB. In contrast, schistosomiasis and soil-transmitted helminthiasis continue to be overlooked; this also includes zoonosis diseases from the interactions of humans and their animals.

2. Epidemiology and risk factors

To end the neglected tropical diseases for the achievement of goals incorporated in sustainable evolution, a protocol, namely 2021-2030 Neglected Tropical Diseases, has been adopted by the WHO Director-General and the Director of the Department of Control of Neglected Tropical Diseases.

The primary objectives of the year 2030 for neglected tropical disease awareness are listed below:

● Individuals needing therapy for NTDs decreased to 80-90% in particular areas.

● Approximately ten nations are in the process of eliminating NTDs.

● The most defined diseases, such as yaws and dracunculiasis, must be eliminated.

● All the matters related to NTDs, such as Disability-Adjusted Life Years, need to produce a 70-75% decline [13].

A ground plan helps in monitoring various distinct infections as well as setting standard targets for multiple factors, which includes decreased vector-instilled NTDs mortality within the limit of 70-75% along with the promotion of maximum ingress in supplying water as well as cleaning and sanitation procedure in various areas where NTDs is in the native range. The high expense of developing novel treatments has demoralized multinational pharmaceutical companies to make investments in these underfunded fields. Therefore, the populations of underdeveloped countries continue to experience major health concerns due to these neglected diseases [14]. Compared to established market economies or industrialized countries, the productive load in terms of contagious diseases, in particular individuals is sustained through disability-adjusted life years (DALYs), which are double in amount compared to market competition with advanced nations. Additionally, communicable, maternal, and perinatal diseases account for nearly 40% of the healthy years lost in underdeveloped nations; many of these conditions never existed or have been almost eliminated in developed market wealth [15].

The basic interpretation of brief description hygiene and hazardous factors associated with frequent NTDs.

2.1. Buruli Ulcer

Buruli ulcer (BU) is a fatal epidermis infection due to Mycobacterium ulcerans. This Mycobacterium initially develops slowly on the epidermis and tissues, which further causes infection, producing idle ulcers on the skin's surface [16]. More than 30 nations have reported occurrences of the sickness. Still, West Africa has seen the majority of them in various regions, Gulf of Guinea, Gold Coast, Niger, and Senegal accounting for 70- 80% descriptive in every arena. Up until 2010, there were over 5000 suspected Buruli ulcer cases reported per year in the world. From 2010 to 2016, there were just 61 instances documented, which was the lowest number ever. Since then, it signifies an absolute drift in the tally of victim causalities, reaching 2713 cases in 2018. The decrease in 2020 might be related to how COVID-19 affects active detection efforts [17, 18].

2.2. Chikungunya

The United States National Institute of Allergy and Infectious Diseases has recently designated chikungunya virus (CHIKV), which is generally transferred to people by Aedes (Ae.) aegypti insects and causes Group C infectious diseases since it is found in more than forty different nations. Ae. albopictus has recently migrated through other Asiatic regions and distributed itself among various parts of America, Europe, and Africa [19]. Public health issues are brought up by the ongoing spread of this disease in the Capital of Colombia and various Roman Latin United States nations. Treatment typically focuses on symptoms and includes getting enough rest, consuming extra fluids and food, and taking painkillers (paracetamol, for example). Avoid using aspirin. Pre-protecting oneself from mosquito bites is regarded as the most important way of preventing mosquito bites and the chikungunya virus. To do this, adopting an air conditioner along with closed windows as well as doors with slit and provision of the well protective net from mosquito along with a clothing with full sleeves and full jeans. Lastly, the use of different insect repellents requiring fogging treatment and disinfection with Diethyl-3methyl benzamide and linseed oil is mandatory [20, 21].

2.3. Chagas Disease

Triatoma infestans, also referred to as the kissing bug, is the primary vector of the sickness caused by the parasite Trypanosoma cruzi, which results in the development of Chagas disease. South America, Central America, and North America are all affected by the illness. The most severe adverse effect of this sponge is cardiomyopathy, which affects 20-30% of patients at risk for illness [22]. The vectors infect people repeatedly by placing them in the small spaces of clay shelves along with thatched roofs in simple rural homes. Trypanosoma cruzi, the sponge that leads to Chagas disease, is present to spread in about 6-7 people worldwide, primarily in Latin America. The majority of these victims in the United States Nation are brought from Latin parts of America, where three lakh people are living with this sickness. Increased frequency of myocarditis along with extremely fatal scenario compared to carrier-formed disease appears to be related to the formation of initiation of orally transferred T. cruzi infection. These contaminations mainly occur through eatables as well as drinks, which are adulterated with food or drink contaminated among carrier feces [23].

2.4. Dengue Fever

The four serotypes of the DENV virus, which causes dengue fever (DF), spread due to insects, chiefly Stegomyia aegypti and Stegomyia albopictus. The WHO estimates that 500,000 people annually suffer from this severe illness, and 1250 (or 2.5%) of them pass away. In Bangladesh, the monsoon season of 2000 witnessed a primary outbreak of dengue fever (DF) along with breakbone fever, which led to 5521 officially documented cases and 93 fatalities [24]. Dengue fever has no known effective treatment. Analgesics, fluid replacement, and bed rest are typically enough as supportive care. Fever and other symptoms can be treated with acetaminophen. Corticosteroids, aspirin, and nonsteroidal anti-inflammatory medications (NSAIDs) ought to be avoided. The treatment that cures acute dengue pyrexia requires mandatory management of electrolytes and water in the body and dynamic bleeding control measures such as platelet or whole blood transfusions [25].

2.5. Human African Trypanosomiasis

Trypanosoma brucei gambiense and T. brucei rhodesiense are two main parasites that cause Human African Trypanosomiasis (HAT), better known as sleeping sickness. Tsetse flies are the insect vectors that spread the disease. The WHO started a program in 2001 for the provision of good strength along with inspection to witness the decline of HAT in the upcoming years. Not more than a thousand instances of HATs are prone to be discovered in 2019. Generally, this decrease is produced because of no provision of practical supremacy measures, as mobile and submissive testing is mandatory [26]. For T. b. gambiense infection in the early stages, pentamidine is advised. Suramin, melarsoprol, eflornithine, and nifurtimox are additional medications used to treat African trypanosomiasis. The National Sleeping Sickness Control Program and the World Health Organization have collaborated on proof collection, and management, and risk analysis for HAT in the Democratic Republic of Congo. According to current estimates, the DRC's population of 36.6 million people and its 715 thousand km2 of geographical area are both at varying levels of risk from HAT. One of the pillars of HAT control is the quick identification and appropriate treatment of newly discovered HAT patients [27].

2.6. Leishmaniasis

Leishmania donovani, which causes Visceral Leishmaniasis (VL) or kala-azar, is a parasite that spreads from person to person through the sand fly Phlebotomus argentipes. More than 90% of the 200,000-400,000 latest victims of VL that are declared annually around the world are found in six countries: Brazil, India, Sudan, Bangladesh, South Sudan, and Ethiopia. Depending on the disease's kind, leishmaniasis is treated differently. Even without therapy, cutaneous leishmaniasis skin lesions typically heal independently [28]. The best strategy to avoid mucus leishmaniasis is the assurance of effective treatment of dermal inflammation. Severe (advanced) cases of visceral leishmaniasis generally result in death. Oral therapy of ketoconazole (Xolegel, Ketodan Kit) and arterial pentam with liposomes of AmBisome are possible therapies for some patients. Nepal has constantly achieved the status for a couple of ages after eradicating this disease at the district level. Ninety (90%) of the endemic sub-districts in Bangladesh have reached the eradication goal. More than two-thirds of endemic areas in India have shown progress toward the goal [29].

2.7. Lymphatic Filariasis

Lymphatic filariasis (LF) is a chronic, severe, and frequently disfiguring infection caused by lymphatic interference that produces substantial swelling in the genitalia and lower extremities. The filarial worm parasitic infection causes the sickness. Wuchereria bancrofti is the leading cause of sickness worldwide. Brugia timori and Brugia malayi can also spread the disease throughout Asia. Depending on the environment, a variety of mosquitoes might carry the parasite. Culex quinquefasciatus is the most common vector in Africa, and Anopheles is the most predominant vector in the Americas [30]. Aedes and Mansonia can spread the virus across Asia and the Pacific. According to international estimates, more than 1.3 billion people are at risk, with 120 million affected in 80 nations across the tropics and subtropics. Only in the sub-Saharan regions do 46-51 million persons get LF. The medication of preference is diethylcarbamazine (DEC). However, since DEC can exacerbate onchocercal eye illness, it should not be given to patients who also may have onchocerciasis. Ivermectin does not kill the mature worm; it only kills the microfilariae. According to some research, doxycycline treatment at 200 mg/day can kill adult worms [31].

2.8. Soil-Transmitted Helminthiasis

Soil-transmitted helminth infections, which are among the most ubiquitous diseases in the world, disproportionately affect the poorest and most vulnerable communities. They spread through eggs found in human feces, which pollute the soil in filthy areas. The most common species that infect humans are roundworms, whipworms, and hookworms [32]. Roughly, 1.5 billion inhabitants, or 24% of the world's population, are infected with soil-borne helminths. Tropical and subtropical regions are widely infected, with sub-Saharan Africa, China, and East Asia having the highest infection rates. S. stercoralis is thought to infect about 600 million people worldwide; however, because it is also spread in unsanitary environments, its geographic range overlaps with that of another helminthiase that is spread through the soil [33]. Albendazole (400 mg) and mebendazole (500 mg), the medications the WHO recommends, are efficient, affordable, and simple for non-medical persons. Generally, PC has diminished the number of persons with lethal STH infections by 85%. Data indicates that STH-related morbidity can be eradicated following ten years of annual PC therapies [34].

2.9. Onchocerciasis

Onchocerciasis is a parasitic condition brought on by the worm Onchocerca volvulus and spread by black flies. Scratching, skin rashes, and eyesight loss, including blindness, are all symptoms of the illness. Even though onchocerciasis is common in Egypt, Latin America, and Africa, Sub-Saharan Africa accounts for more than 99% of all recent episodes. One of the NTDs aimed at eradicating is onchocerciasis (river blindness) [35]. According to studies conducted in Mali and Senegal, Ivermectin (Stromectol) administration can be used to eliminate an infestation. However, in some “hot zones” where ivermectin treatment raises the risk of major adverse outcomes in people with high parasitemia, the eradication of the diseases remains a struggle. The Republic of Cameroon faces difficulties in limiting and eliminating the disease because of noncompliance with MDA, limited availability of yearly preventative chemotherapy, and healthcare personnel's inability to identify the illness [36] correctly.

2.10. Scabies

The mite Sarcoptes scabiei is the common parasite responsible for scabies. An estimate of 300 million cases per year has been made for global prevalence. Poor personal hygiene and unhygienic housing conditions facilitate the spread of scabies. Personal cleanliness and antiparasitic cream application on a large scale can significantly lower the occurrence. Based on a controlled study, scabies were evident in more than 60% of young students in religious institutions in Dhaka, Bangladesh [37]. Following intervention with the topical application of 5% permethrin cream to all students, teachers, and staff in the study areas, weekly health education classes, and daily monitoring of students for five critical personal hygiene practices over a four-month period, the ubiquity of scabies in the sub-districts fell to 5%, compared to 50% in the control areas. Ivermectin has been used in MDA programmes to try to reduce scabies in endemic regions all over the world. The effectiveness of such programs in comparison to alternative topical treatments is debatable, though, due to the following factors: (1) Pregnant ladies must be eliminated; (2) it is challenging to administer ivermectin in community-based programs on an empty stomach; and (3) its use is not advised in children under the age of five [38].

2.11. Schistosomiasis

Schistosomiasis or bilharzia is a rapacious disease transmitted through any of the ectoparasites worms (flukes) in the Schistosoma genus. Snails serve as intermediary parasites. People have been invaded by five species: S. mansoni, S. intercalatum, S. haematobium, S. japonicum, and S. mekongi. Schistosomiasis is thought to affect at least 230 million individuals worldwide, the bulk of whom reside in Africa. Rising temperatures, proximity to bodies of water, irrigation and dam building, agricultural and fishing professions, and poverty are all factors that contribute to the disease's continuous transmission in Sub-Saharan Africa [39]. Praziquantel is the standard management for schistosomiasis because it successfully rids the body of worms. Still, reinfection is frequently a problem because of how the parasites spread and how people behave. Despite significant efforts to control it using integrated approaches such as repeated mass chemotherapy with praziquantel, public health education focusing on lifestyle modifications toward risk factors, improved sanitation/hygiene, and snail habitat treatment, schistosomiasis remains a significant public health issue in Sub-Saharan Africa [40].

2.12. Trachoma

Chlamydia trachomatis is the source of the bacterial eye infection known as trachoma. It is transmitted from person to person by eye-seeking insects and through contact with the infected eye and nasal secretions, most commonly through hands and clothing. Repeated infections can produce trichiasis, a condition in which the eyelids roll inward and scar, causing the eyelashes to brush against the eye's cornea [41]. There are 1.2 billion people living in endemic areas worldwide, 40.6 million people with active trachoma, and five countries—Ethiopia, India, Nigeria, Sudan, and Guinea—represent 48.5% of the total burden of active trachoma. Africa is the continent most seriously impacted, accounting for 27.8 million (68.5% of the 40.6 million active trachoma cases). Trachoma is frequently observed in regions with inadequate access to clean water, sanitary facilities, and basic hygiene (WASH). The 1998 target of trachoma eradication looks to be a feasible and attainable objective with an MDA campaign using azithromycin [42].

2.13. Rabies

Rabies is one of the world's most lethal, persisting zoonotic diseases. The virus is usually transmitted through the bite of a wild animal. About half of the world's rabies burden is carried by South Asian countries. India is a significant contributor to the worldwide burden of rabies, accounting for 20,000 of the 70,000 annual deaths worldwide. About 10-100 cases of rabies-related human mortality are reported in Nepal each year [43]. Pre-exposure prophylaxis is advised for people who are more likely to come into contact with the rabies virus, such as animal handlers, lab workers, and veterinarians in endemic nations. The post-exposure prophylaxis prescribed by the WHO entails administering rabies immunoglobulins for high-risk exposures, prompt and appropriate wound care, and a course of antirabies vaccination [44].

2.14. Dracunculiasis (or Guinea Worm Disease)

Dracunculus medinensis is an approximately two- to three-foot-long worm that causes dracunculiasis, sometimes known as guinea worm disease. Drinking contaminated water from public sources, such as stagnant ponds with young worms and tiny water fleas, makes people sick. In the middle of the 1980s, an estimated 3.5 million cases of dracunculiasis were registered in 20 countries, 17 of which were in Africa and the remaining three in Asia. For the first time in 2007, there were fewer than 10,000 recorded cases, which further decreased to 542 instances (2012) [45]. Over the last eight years, most individual infections have been in the double digits. The mainstay of the treatment is to remove the adult worm from the patient by wrapping or winding it a few centimeters per day while using a stick to do so at the skin's surface. After cleaning the area, the worm is slowly pulled out using mild traction. Complete elimination can take days to weeks since the worm is so lengthy. In adults, metronidazole or thiabendazole is frequently used in conjunction with stick therapy. People are suggested to avoid the disease by promoting health awareness and psychosocial modifications such as consuming clean water and avoiding getting wet. The Gates Foundation awarded the Carter Center a $40 million grant for its work in eradicating guinea worms [46].

2.15. Leprosy

The bacillus Mycobacterium leprae causes the incurable infectious disease leprosy. M. leprae reproduces gradually, and the sickness develops typically over 5 years. The principal parts of the body affected by leprosy are the skin, peripheral nerves, upper airway mucosa, and eyes. Multidrug therapy can cure the condition [47]. When people come into close and repeated contact with untreated cases, it probably spreads by droplets from the mouth and nose. Leprosy, if left untreated, can harm the skin, nerves, limbs, eyes, and skin permanently. In 2020, there were 127558 new leprosy cases worldwide, according to official numbers from 139 countries in six WHO regions, including youngsters under 15. Concerning the child population, the new case detection rate was 4.4 per million. Dapsone is now combined with rifampicin and clofazimine to treat multibacillary leprosy. Single lesion paucibacillary leprosy has been treated with a single dosage of rifampicin (600 mg), ofloxacin (400 mg), and minocycline combination therapy (100 mg). The three medications are given to the child with a solitary injury at half the grownup dosage [48].

3. Recommendations

For successful NTD control, more extended investigation is needed to be processed to achieve the 2030 NTD domination. This covers the demand for better, safer medications, vector control, personal cleanliness, and vaccine development. We recommend the following considering this analysis:

1. In rural parts of West and Central Africa, it has been discovered that raising community awareness and detecting Buruli ulcers early on can reduce complications [26], but more research is required to determine how M. ulcerans is transferred among the surroundings to the different majority of people.

2. Chikungunya, dengue fever, and HAT epidemics can all be prevented through integrated vector management, which involves eradicating breeding grounds using mature larval techniques and individual safety precautions.

3. Initial investigation as well as therapy for significant spread of disease proves to be more effective than therapy at a later stage as the Early treatment of the acute phase of infection would be more effective than the management of the chronic stage of the disease because the potency of medical treatment in case of Chagas infection declines due to the increased effect of this infection. For both phases of Chagas disease, there is a need for medications that are more efficient, secure, and simple to use.

4. The guinea worm illness, also known as dracunculiasis, has been deemed extinct in more than 200 nations. Health education and behavioral modification are robust illness prevention measures.

5. The control of HAT depends on the early identification and treatment of new patients and vector control.

6. Due to reaction along with little compatibility with medication during these circumstances, treating onchocerciasis patients with ivermectin remains challenging, especially in those with high parasitemia rates. Ivermectin is not always advised for the treatment of scabies. Future research should focus on developing new, safer medications.

Regarding DALY, lymphatic filariasis, schistosomiasis, and dengue fever continue to carry the heaviest burden of NTDs. In reality, dengue fever epidemics have recently wreaked devastation in several underdeveloped nations [49]. There is a clear need for a dengue vaccination. For diseases that lead to the maximum causalities, and consequently, for the biggest lost years of productivity in different NTDs, significant attention to various domains of fitness in health sector protocols must be given.

Conclusion

More innovative public health strategies and research are required for the worldwide battle towards the management of NTDs to develop potent medications and vaccines. To confront NTDs along with provision of treatment to the maximum population worldwide, partnerships including vital supporter parties’ organization, philanthropic representatives, Red Cross organization, ministry officials, and therapeutic corporations, along with mandatory collaborator are essential. To promote and coordinate these efforts to stop NTDs from occurring and identify novel therapies, several partners have already pledged fresh funding. Although there has been advancement in the active participation, integrity, and positive approach to confronting NTDs, it still depends on supportive policy, solid political backing, and teamwork from all parties. It is also expected that when the London Declaration pledge is renewed, enough resources will be recruited to take this global effort to its ultimate demise in 2030.

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