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Abstract: Background: In today's world around 36 million deaths are due non communicable diseases (NCD) of which around 17 million are due to cardiovascular diseases (CVD). More significantly nearly one third of deaths occurs in middle aged groups. This study tries to find out risk factors leading to CVD. Aims and objectives :(1) To study the socio demographic profile of patients and life style related risk factors that causes CVD among patients admitted in cardiology department, RIMS. Methodology: Study design: Hospital based cross sectional study. Place of study:Cardiology inpatient department, RIMS. Duration of study: July-August, 2017. Sample size: 147.Sampling technique:Consecutive sampling. Data collection: pretested questionnaire. Results: Around 2/3rd of the patients were males......
Keywords: Cardiovascular disease, NCD, Diabetes, Hypertension, Sleep pattern
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[5]. Sugathan T N, Sankarnarayan K,Behavioural risk factors for non-communicable disease among adults in Kerela, India,Indian J Med Res, 127 June 2008, 555-563..
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Paper Type | : | Research Paper |
Title | : | Stem Cell Theraphy in Dentistry- Review |
Country | : | India |
Authors | : | Dr.Tharani.P || Dr.Vijay Ebenezer || Dr.Balakrishnana |
: | 10.9790/0853-1910020916 |
Abstract: Background: Stem cells are unspecialized cells in the human body that are capable of becoming specialized cells, each with new specialized cell functions. The best example of a stem cell is the bone marrow stem cell that is unspecialized and able to specialize into blood cells, such as white blood cells and red blood cells, and these new cell types have special functions, such as being able to produce antibodies, act as scavengers to combat infection and transport gases. Thus one cell type stems from the other and hence them term "stem cell". Basically, a stem cell remains uncommitted until it receives a signal to develop into a specialized cell. Stem cells have the remarkable properties.....
Keywords: stem cell, fetal,adult stem cell,,multipontent,pluripotent
[1]. Abbas A, Diakonov I, Sharpe P. Neural Crest Origin of Dental Stem Cells (0917). Pan European Federation of the International Association for Dental Research (PEF IADR). Accessed on 06.03.2010.
[2]. http://iadr.confex.com/iadr/pef08/techprogram/abstract_111214.htm.
[3]. Alastair J. Sloan & Rachel J. Waddingon. Dental pulp stem cells: what, where, how? International journal of paediatric dentistry 2009; 19: Pp. 61-70.
[4]. Alhadlaq A, Mao JJ. Mesenchymal stem cells: Isolation and therapeutics. Stem Cells Dev. 2004; 13: Pp. 436-48.
[5]. Alison MR. Stem cells in pathobiology and regenerative medicine. J Pathol 2009; 217: Pp. 141-143.
[6]. Alison MR and Islam S. Attributes of adult stem cells. J pathol 2009; 217: Pp. 144-160..
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Paper Type | : | Research Paper |
Title | : | Bone Graft in Dentistry- review |
Country | : | India |
Authors | : | Dr.Tharani.P || Dr.Vijay Ebenezer || Dr.Balakrishnana |
: | 10.9790/0853-1910021724 |
Abstract: Background: The bone graft serving as a scaffolds for the in-growth of vessels, perivascular tissue and mesenchymal cells forms the host bed exhibits the characteristic of osteoinduction. This scaffold allows gradual replacement of bone graft over time by resorption of old bone trebecule and formation of new bone. Each grafts type has its own healing and incopration mechanism. Replacement of bone is a complex and demanding undertaking. Bone formation occurs when osteoblasts secrete collagen molecules and ground substances. The collagen molecules polymerize to form collagen fibers. Calcium salts precipitate in the ground substance along the collagen fibers to form osteoid. Osteoblast become trapped in the osteoid and then are called osteocyes. Mature compact bone is composed of approximately 30% organic matrix and 70% calcium salts. 90% to 95% of the organic matrix is collagen fibers and.....
Keywords: bone graft,corticalbone ,cancellous bone, bone regeneration
[1]. Netter, Frank H. (1987), Musculoskeletal system : anatomy, physiology and metabolic disorders. Summit, New Jersey : Ciba-Geigy Corporation ISBN 0-914168-14-2.
[2]. Gomez, Santiago (Feb. 2002), "Crisotomo Martinez, 1638-1694: the discoverer of tabecular bone". Endocrine (United States). 17(1) : 3-4. Doi : 10.1385/ENDO:17:1:03. ISSN 1355-008X. PMID 12014701.
[3]. Netter, Frank H. (1987), Musculoskeletal system : anatomy, physiology and metabolic disorders. Summit, New Jersey : Ciba-Geigy Corporation ISBN 0-914168-88-6.
[4]. Nicklin MJ, Weith A, Duff GW (Jun 1994). "A physical map of the region encompassing the human interleukin-1 alpha, interleukin-1 beta, and interleukin-1 receptor antagonist genes". Genomics. 19(2): 382-4, doi : 10.1006/geno.1994.1076. PMID 8188271.
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Abstract: In this article we will deal with two developmental anamolies that usually coexist in 20 to 49% [1] of cases. One of the entities is Transverse Testicular Ectopy, also known as Crossed Testicular Ectopy, as the name suggests, is a condition in which both the testes descend through the same inguinal canal into the same hemi-scrotum. TTE is a rare case that occurs only 1 in 4 million patients [2]. The other entity is Persistent Mullerian Duct Syndrome, which is a rare form of male pseudo-hermaphroditism in which there are remnants of the Mullerian structures in an otherwise genotypically (46XY) and phenotypically normal male.....
Keywords:tte; transverse testicular ectopy; cte; crossed testicular ectopy; PMDS; PMD; persistantmullerain duct syndrome
[1]. Deshpande AV, La Hei ER. Impact of laparoscopy on the management of transverse testicular ectopia. J Laparoendosc Adv Surg Tech A 19 (2009): 443-446
[2]. Mohamed Abdelmalak, Saber Waheeb et al. Two Cases of Transverse TesticularEctopia inConsanguineous Boys. Eur J Pediatr Surg Rep 2018;6:e90–e93
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[4]. Hammoudi S: Transverse testicular ectopia.J Pediatr Surg 1989; 24: 223–224
[5]. Nilson O. Hernia uteri inguinalisbeim Manne. Acta ChirScand1939;83:231.
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Abstract: Background: Halitosis, a common reason for dental consultation raises a lot of concern among sufferers, as it negatively impacts on daily life style like communication with others, self-esteem, self-confidence, social and intimate relationship etc. There has been established association between inadequate oral hygiene practices and halitosis. Aim: The objective of this study was to assess whether the concerns about halitosis influences lifestyle, attitude and practices among Vikarabad population. Materials and methods: A survey has been conducted in a questionnaire format regarding halitosis, oral hygiene practices, lifestyle and attitude by selecting 100 subjects randomly from outpatient department of Sri Sai College of Dental Surgery, Vikarabad.....
[1]. Mubayrik AB, Al Hamdan R, Al Hadlaq EM, AlBagieh H, AlAhmed D, Jaddoh H, Demyati M, Shryei RA. Self-perception, knowledge, and awareness of halitosis among female university students. Clin, Cosmetic Invest Dent. 2017;9:45.
[2]. Hammad MM, Darwazeh AM, Al-Waeli H, Tarakji B, Alhadithy TT. Prevalence and awareness of halitosis in a sample of Jordanian population. J Int Soc Pre & Comm Dent. 2014;4(Suppl 3):S178.
[3]. Ashwath B, Vijayalakshmi R, Malini S. Self-perceived halitosis and oral hygiene habits among undergraduate dental students. J Indian Soc Periodontol.2014;18:357-60.
[4]. Azodo CC, Onyeagba MI, Odai CD. Does concern about halitosis influence individual's oral hygiene practices?. Niger Med J. 2011;52:254-9.
[5]. McNamara TF, Alexander JF, Lee M. The role of microorganisms in the production of oral malodor. Oral Surg Oral Med Oral Pathol.1972;34:41-8.
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Paper Type | : | Research Paper |
Title | : | Congenital Corneal Opacities |
Country | : | India |
Authors | : | Dr. Ashish Joshi || Dr. Rajat Jain |
: | 10.9790/0853-1910023646 |
Abstract: Congenital corneal opacity (CCO), by definition, is present in the newborn. The prevalence of CCO is approximately 3 per 1 lac newborns. However, this increases to 6 per 1 lac if congenital glaucoma is also included1. CCO is either unilateral or bilateral and the cause could be hereditary, developmental, metabolic or infectious. Accurate and early diagnosis is required for correct prediction of the natural history of the disorder, to look for associated ocular and systemic disorders, appropriate genetic counseling and for establishing a proper management plan. Congenital corneal opacities (CCO) have been classified traditionally by a pneumonic "STUMPED‟2 (Figure 1). However another classification system has been recently proposed which may be better considered from a perspective of pathogenesis, surgical.....
[1]. Nischal KK1, Naor J, Jay V, MacKeen LD, Rootman DS. Clinicopathological correlation of congenital corneal opacification using ultrasound biomicroscopy. Br J Ophthalmol. 2002 Jan;86(1):62- 9.
[2]. Waring GO, Rodrigues MM. Congenital and neonatal corneal abnormalities. In: TasmanW, Jaeger E, eds. Duane‟s Ophthalmology, CD-Rom. Philadelphia: Lippincott Williams & Wilkins; 2002.
[3]. Petroutsos G, Patey A, Savoldelli M, Pouliquen Y. Sclerocornea and Ultrastructural and morphologic study. J Fr Ophtalmol 1983; 6(10): 769–775
[4]. Waizenegger UR, Kohnen T, Weidle EG, Schutte E. Congenital familial cornea plana with ptosis, peripheral sclerocornea and conjunctival xerosis. Klin Monatsbl Augenheilkd 1995; 207(2): 111– 116.
[5]. Threlkeld AB, Green WR, Quigley HA, de la Cruz Z, Stark WJ. A clinicopathologic study of posterior polymorphous dystrophy:implications for pathogenetic mechanism of the associated glaucoma. Trans Am Ophthalmol Soc 1994; 92:133–165.
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Paper Type | : | Research Paper |
Title | : | End Stage Stevens Johnson Syndrome: Can We Do Something ??? |
Country | : | India |
Authors | : | Dr. Ashish Joshi || Dr. Rajat Jain |
: | 10.9790/0853-1910024752 |
Abstract: End stage ocular sequelae of Stevens Johnson Syndrome (SJS) is characterised by corneal scaring and opacity in a setting of a very severe dry eye. The options of visual rehabilitation in such a clinical setting are limited. We present a novel technique of management of such a case. To the best of our knowledge, this is the first such case performed in this region.....
[1]. French LE. Toxic epidermal necrolysis and Stevens Johnson syndrome: our current understanding. Allergol Int 2006;55:9-16.
[2]. Bastuji-Garin S, Rzany B, Stern RS et al. Clinical classification of cases of toxic epidermal necrolysis, Stevens-Johnson syndrome, and erythema multiforme. Arch Dermatol 1993;129:92-6.
[3]. Borrelli M, Schroder C, Dart JK et al. Long-term follow-up after submandibular gland transplantation in severe dry eyes secondary to cicatrizing conjunctivitis. Am J Ophthalmol 2010;150:894-904.
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Paper Type | : | Research Paper |
Title | : | Simple Hepatic Cyst: A Case Report |
Country | : | India |
Authors | : | Dr. Murugadasan P || Dr. Kalaranjani V |
: | 10.9790/0853-1910025356 |
Abstract: The term hepatic cyst usually refers to solitary non-parasitic cysts of the liver also known as simple cysts.The most common benign lesion found in the liver is the congenital or simple cyst. They are believed to be congenital in origin.Asymptomatic simple cysts are best managed conservatively. The preferred treatment for symptomatic cysts is ultrasound or CT-guided percutaneous cyst aspiration followed by sclerotherapy. If percutaneous treatment is unavailable or ineffective, treatment may include either laparoscopic or open surgical cyst fenestration. Unroofing of the extrahepatic portion of the cyst may be done.We report a case of simple hepatic cyst that presented with abdominal pain and its management.
Keyword: hepatic cyst, congenital, laparoscopic deroofing.
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[5]. Qiu JG, Wu H, Jiang H, et al: Laparoscopic fenestration vs open fenestration in patients with congenital hepatic cysts: A meta-analysis. World J Gastroenterol 17:3359–3365, 2003..
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Paper Type | : | Research Paper |
Title | : | Study of Maternal and Fetal Outcome in COVID-19 Pregnancies |
Country | : | India |
Authors | : | Dr Pushpa C || Dr Tushar T Palve |
: | 10.9790/0853-1910025763 |
Abstract: On 31st Dec 2019, Wuhan Municipal Commission,China,reported a cluster of 27 pneumonia cases of unknown etiology.[1]Samples tested positive for novel coronavirus. On 30th January, 2020,WHO declared this outbreak of novel coronavirus as "A Public Health EmergencyOf International Concern"[2,3]. Alarge number of cases have been diagnosed Globally. On 11th March 2020-WHO declared COVID-19 as a Global Pandemic.[4] Despite extensive studies on the epidemiology of COVID-19 infection, studies on pregnant women with COVID-19 diseases remain relatively less. The physiological changes occurring during pregnancy make pregnant women more vulnerable to corona infection......
[1]. CDC.2019 Novel Coronavirus, Wuhan, China.
https://www.cdc.gov/coronavirus/2019-ncov/about/in.dex.html.
[2]. Ramzy A, McNeil DG. WHO Declares Global Emergency as Wuhan CoronavirusSpreads. The New York Times.
https://nyti.ms/2RER70M
[3]. Gallegons A. WHO Declares Public Health Emergency For Novel Coronavirus.
https://www.medscape.com/viewarticle/924596.
[4]. The New York Times. WHO Declares Coronavirus as Pandemic.
http://www.nytimes.com/2020/03/11/world/coronavirus-news.html#link-682e5b06.
[5]. Maternal mortality among women with coronavirus disease 2019 by MJ Blitz
www.ajog.org.