Tuesday, March 22, 2016

MIDDLE EAST RESPIRATORY SYNDROME (MERS)

MIDDLE EAST RESPIRATORY SYNDROME (MERS)

·         Abstract: Middle East respiratory syndrome (MERS) is a viral respiratory disease caused by a novel coronavirus (MERSCoV) that was first identified in Saudi Arabia in 2012. Coronaviruses are a large family of viruses that can cause diseases ranging from the common cold to Severe Acute Respiratory Syndrome (SARS). Typical MERS symptoms include fever, cough and shortness of breath. Pneumonia is common, but not always present. Gastrointestinal symptoms, including diarrhoea, have also been reported. Approximately 36% of reported patients with MERS have died. Although the majority of human cases of MERS have been attributed to human-to-human infections, camels are likely to be a major reservoir host for MERS-CoV and an animal source of MERS infection in humans. However, the exact role of camels in transmission of the virus and the exact route(s) of transmission are unknown. The virus does not seem to pass easily from person to person unless there is close contact, such as occurs when providing unprotected care to a patient.
Key words: MERS Cov, viruses, pneumonia, respiratory distress, Darwinism and transmission
Introduction:
The Middle East respiratory syndrome coronavirus (MERS-CoV), is a novel positive-sense, single-stranded RNA virus of the genus Betacoronavirus.  It was first reported in 2012 after genome sequencing of a virus isolated from sputum samples from a person who fell ill in a 2012 outbreak of a new flu. MERS-CoV genomes are phylogenetically classified into two clades, clade A and B. The earliest cases of MERS were of clade A clusters (EMC/2012 and Jordan-N3/2012), and new cases are genetically distinct (clade B). As of July 2015, MERS-CoV cases have been reported in over 21 countries, including Saudi Arabia, Jordan, Qatar, Egypt, the United Arab Emirates, Kuwait, Turkey, Oman, Algeria, Bangladesh, Indonesia (none were confirmed), Austria, the United Kingdom, South Korea the United States,[5][6] Mainland China, Thailand, and the Philippines.
Outset:
The first confirmed case was reported in Saudi Arabia 2012. A second case was found in September 2012, a 49-year-old male living in Qatar presented with similar flu symptoms, and a sequence of the virus was nearly identical to that of the first case.
Dispatch:
On 13 February 2013, the World Health Organization stated "the risk of sustained person-to-person transmission appears to be very low. The Centers for Disease Control and Prevention (CDC) list MERS as transmissible from human-to-human.
1.      Non-human to human transmission: The route of transmission from animals to humans is not fully understood, but camels are likely to be a major reservoir host for MERS-CoV and an animal source of infection in humans. Strains of MERS-CoV that are identical to human strains have been isolated from camels in several countries, including Egypt, Oman, Qatar, and Saudi Arabia.
2.      Human-to-human transmission: The virus does not appear to pass easily from person to person unless there is close contact, such as providing unprotected care to an infected patient. There have been clusters of cases in healthcare facilities, where human-to-human transmission appears to be more probable, especially when infection prevention and control practices are inadequate. Thus far, no sustained community transmission has been documented.
Darwinism:
The evidence available to date suggests that the viruses have been present in bats for some time and had spread to camels by the mid 1990s. The viruses appear to have spread from camels to humans in the early 2010s. The original bat host species and the time of initial infection in this species have yet to be determined.
People at increased Risk:
1.      People with co-morbid condition included diabetes; cancer; and chronic lung, heart, and kidney disease and weakened immune systems.  

2.      Recent Travellers from the Arabian Peninsula

3.      Close Contacts of an Ill Traveller from the Arabian Peninsula

4.      Close Contacts of a Confirmed Case of MERS

5.      Healthcare Personnel Not Using Recommended Infection-Control Precautions

6.      People with Exposure to Camels

The incubation period for MERS: Are usually about 5 or 6 days, but can range from 2-14 days.
Symptoms:
Common symptoms are severe acute respiratory illness with symptoms of: fever, cough and shortness of breath.  Some people also had gastrointestinal symptoms including diarrhea and nausea/vomiting.
Treatment and Prevention:
·         There is no vaccine or specific treatment is available at present. Only supportive treatment is available based on the clinical symptoms. 
·         As a general precaution, anyone visiting farms, markets, barns, or other places where camels and other animals are present should practice general hygiene measures, including regular hand washing before and after touching animals, and should avoid contact with sick animals.
·         The consumption of raw or undercooked animal products, including milk and meat, carries a high risk of infection from a variety of organisms that might cause disease in humans. Animal products that are processed appropriately through cooking or pasteurization are safe for consumption, but should also be handled with care to avoid cross contamination with uncooked foods. Camel meat and camel milk are nutritious products that can continue to be consumed after pasteurization, cooking, or other heat treatments.
·         People at increase risk should avoid contact with camels, drinking raw camel milk or camel urine, or eating meat that has not been properly cooked.
·         Appropriate measures to decrease the risk of transmission of the virus from an infected patient to other patients, healthcare workers, or visitors. Healthcare workers should be educated and trained in infection prevention and control and should refresh these skills regularly.
Complication:
Pneumonia and kidney failure.  
Prognosis:
About 3-4 out of every 10 people reported with MERS have died.
Most of the people who died had an underlying medical condition. Some infected people had mild symptoms (such as cold-like symptoms) or no symptoms at all; they recovered.
Pneumonia due to MERS CoV is associated with a high rate of mortality that reached 76%.
Role of CDC in controlling MERS CoV:
1.      continued to collaborate with international partners on epidemiologic and laboratory studies to better understand MERS
2.      Improved the way to  collect data about MERS cases
3.      Increased lab testing capacity in states to detect cases
4.      Developed guidance and tools for health departments to conduct public health investigations when MERS cases are suspected or confirmed
5.      Provided recommendations for healthcare infection control and other measures to prevent disease spread
6.      Provided guidance for flight crews, Emergency Medical Service (EMS) units at airports, and U.S. Customs and Border Protection (CPB) officers about reporting ill travellers to CDC
7.      Disseminated up-to-date information to the general public, international travellers, and public health partners
8.      Used Advanced Molecular Detection (AMD) methods to sequence the complete virus genome on specimens from cases to help evaluate and further describe the characteristics of MERS-CoV.

Role of WHO in controlling MERS CoV:

1.      WHO is working with clinicians and scientists in affected countries and internationally to gather and share scientific evidence to better understand of the disease?.
2.      Working with countries to develop public health prevention strategies to combat the virus.
3.      WHO is coordinating the global health response to MERS, including: the provision of updated information on the situation; conducting risk assessments and joint investigations with national authorities; convening scientific meetings; and developing guidance and training for health authorities and technical health agencies on interim surveillance recommendations, laboratory testing of cases, infection prevention and control, and clinical management
4.      . WHO continues to request that Member States report to WHO all confirmed and probable cases of infection with MERS-CoV together with information about their exposure, testing, and clinical course to inform the most effective international preparedness and response.
Discussion:
Transmission of MERS CoV between patients to health care worker also reposted. It is not easy to diagnose this condition as early as possible as the symptoms are life flu and non specific. Prevention and spread control measure are only effective method to prevent the possible spread of MERS CoV in general public as well as in health care facility. Positive case of MERS CoV is not reported .in India yet, but the symptoms of swine flu and MERS Cov looks similar.  HINI virus which causes swine flu also derived form same group of virus. It is expected to follow prevention and control measure that we follow for influenza A (H1N1) to be free from MERS CoV in India even in the feature.
Reference:

1.      M. AlGhamdi; F. Mushtaq; N. Awn; S. Shalhoub “MERS CoV Infection in Two Renal Transplant Recipients: Case Report” American Journal of Transplantation. 2015;15(4):1101-1104.

2.      Memish Z, Cotton M, Meyer B, Watson S, Alsahafi A, Al Rabeeah A, et al. Human infection with MERS coronavirus after exposure to infected camels, Saudi Arabia, 2013. Emerg Infect Dis 2014; 20: 1012–15.

 3.  Raj VS, Farag E, Reusken CB, Lamers MM, Pas SD, Voermans J, et al. Isolation of MERS coronavirus from a dromedary camel, Qatar, 2014. Emerg Infect Dis 2014; 20: 1339–42.

4. Alagaili AN, Briese T, Mishra N, Kapoor V, Sameroff SC, de Wit E, et al. Middle East respiratory syndrome coronavirus infection in dromedary camels in Saudi Arabia. MBio 2014; 5: e00884–14.

5.  Reusken CBEM, Farag EABA, Haagmans BL, Mohran KA, Godeke G-J, Raj VS, et al. Occupational exposure to dromedaries and risk for MERS-CoV infection, Qatar, 2013–2014. Emerg Infect Dis 2015; 21.

Thursday, March 10, 2016

stress reduction techniques

STRESS REDUCTION TECHNIQUES
AUTHOR: S.K. Mohana sundhari
KEY:  stress, structured-teaching programme, stress-reduction techniques, and hostel.
TITLE:
         “A study to assess the effectiveness of structured-teaching programme on stress-reduction techniques among adolescent girls aged 15-18 years staying in a selected hostel at Chidambaram”
OBJECTIVES OF THE STUDY:
      To assess the pre-test knowledge regarding stress-reduction techniques among adolescent girls aged 15-18 years staying in a selected hostel at Chidambaram.
  To evaluate the effectiveness of structured-teaching programme regarding stress-reduction techniques among adolescent girls aged 15-18 years staying in a selected hostel at Chidambaram.
      To associate the selected demographic variables such as age, religion, educational status, occupation of the parents, educational status of the parents  and number of siblings with the knowledge regarding stress-reduction techniques.
RESEARCH DESIGN AND METHODOLOGY:
The one group pre-test and post-test design was adopted to assess the effectiveness of structured-teaching programme on stress reduction techniques among adolescent girls aged 15 - 18 years. The General System Theory was adopted for conceptual frame work.
A total of 60 adolescent girls staying in the Nandhanar girl’s hostel were selected by using simple random sampling techniques.
The instrument used for the study was a structured-questionnaire which consists of two sections. The first section consists of the demographic variables of the adolescent girls and the second section consists of 50 closed-ended questions to assess the knowledge regarding stress-reduction techniques.
The structured-teaching programme on stress-reduction techniques was provided through Lap top for a period of 30 minutes. A post-test was given after 7 days. The data were analyzed using the descriptive and   inferential statistics.
RESULT:                    
      The knowledge score of the adolescent girls was inadequate before STP. After the LCD teaching programme 18.33% had moderately adequate knowledge and 81.67% had adequate knowledge.
      The effectiveness of LCD teaching programme was statistically tested by paired‘t’ value and the result found to be significant at p<0.001 level.
      There was no significant relationship between demographic variables and pre-test knowledge of subjects on stress-reduction techniques.
CONCLUSION:
 These result demonstrated that STP was effective in improving the knowledge on stress-reduction techniques among adolescent girls who are staying in the hostel
BIBLIOGRAPHY:
      Ahuja. (1999). A Short Text Book Of Psychiatry. New Delhi: Jaypee Brothers Medical Publication.
      Bhatia, M.S. (2004). Short Text Book OF Psychiatric.  CBS Publisher & Distribution.
      Bunker. (2008). Text Book of Basic Nursing. Lippincott Williams & Wilkins Publishers.
           Barbara, P. (2007). Starting School Creates Stress New Research Shows Signs of Stress Up to 6 Months in Advance. American journal of health promotion, 17 (3), 638.
         Badger, M.J. (1995). Tips on managing stress on job. American journal of nursing. September, 31-33.
           Julie, T. (2007).   Starting School Creates Stress. New Research Shows Signs of Stress Up To 6 Months in Advance    Barbara Pytel. All Rights Reserved. August 31.
           LaurieHYPERLINK "http://ezinearticles.com/?expert=Laurie_Maddalena",HYPERLINK "http://ezinearticles.com/?expert=Laurie_Maddalena" M. (1997). Sixteen Strategies for Managing Stress. Principle And Practice Of Stress Management, London, Guildford press. 



protein supplimentation

PROTEIN SUPPLEMENTATION
AUTHOR: S.K.Mohanasundhari
KEY: Protein supplementation, Protein energy malnutrition and pre-school children.
INTRODUCTION:
          Nutrition is an input and foundation of growth and development. Better nutrition provides strong immune system, less illness and better health. In developing and under developed countries childhood malnutrition is a multi-dimensional problem. An increase in household income is not sufficient to reduce childhood malnutrition if children are deprived of food security, education, access to water, sanitation and health services. The highest prevalence of protein-energy under-nutrition is observed during early childhood, being also a time in which the presence of dental caries can be unusually aggressive. All systems in an organism are affected by protein-energy malnutrition (PEM), but one of the worst affected is the hematopoietic system. Globally 10-11 million under five deaths occur each year out of which around 60% are due to malnutrition In India 2.5 million under fives die each year. Prevalence of under five malnutrition in various states of India reveals that Orissa as the highest prevalence (55%) of fives in Orissa are under nourished out of which 25% are severely under nourished.
TITLE
          “A experimental study to evaluate the effectiveness of protein supplementation among pre-school children with various degree of protein energy malnutrition at selected community in kozhikode.”
OBJECTIVES OF THE STUDY 
   To assess the degrees of protein energy malnutrition among pre-school children with protein energy malnutrition at selected community in Kozhikode.
   To evaluate the effectiveness of protein supplementation among pre-school children with various degree of protein energy malnutrition at selected community in Kozhikode.
   To associate the degree of protein energy malnutrition among pre-school children with selected demographic variables at selected community in Kozhikode.
METHODOLOGY:
The true experimental study design was adopted to evaluate the effectiveness of protein supplementation in difference of anthropometric measurement among pre-school children with PEM. The General System Theory was adopted for conceptual frame work.
A total of 10 pre-school children with PEM were selected by using non probability purposive sampling techniques in the village of Kozhikode.
          The instrument used for the study was a standard scale for measuring anthropometry. Instrument consists of two sections. The first section consists of the demographic variables of the pre-school child with PEM and the second section consists of standard scale for assessing weight, height, mid-arm circumference, head and chest circumference. Gomez classification was used to classify degree of malnutrition. Data collection method adopted was Bio-physiological method (in-vitro). Height, weight, head circumference, mid-arm circumference, and chest circumference was obtained 1st day of data collection and 200 ml of milk, 2 boiled eggs and  50 gm of boiled ground nut was supplemented daily for 15 days and 16th day anthropometrics was obtained from the same group.  The data were analyzed using the descriptive and inferential statistics.
RESULT:
          According to Gomez criteria of degree of malnutrition it was found that in pre-test 2 child were belongs to 1st degree PEM, 3 child were 2nd degree PEM and 5 child were in 3rd degree PEM. In post test 4 child belongs to 1st degree PEM, 4 child were 2nd degree PEM and remaining children were in 3rd degree PEM.  
          There was significant difference exit between pre test and post test score of anthropometric measurements of preschool children with various degrees of PEM. It was statistically tested by paired ‘t’ value and the result found to be significant at p<0.001 level.
          There was significant association exit between sex of the child, economic status of the family and past history of diarrhoeal disease with degrees of protein energy malnutrition.
CONCLUSION:
          The study concluded that there is improvement in anthropometric measurement of pre-school children with PEM after protein supplementation as well as this study concludes that daily protein supplementations are having positive impact in improving the child from various degree of protein energy malnutrition.  
BIBLIOGRAPHY:
1. UNICEF. The state of the world’s children; Early childhood.
New Delhi: UNICEF; 2003.
2. Chandra RK. Nutrition and the immune system: an introduction. Am J Clin Nutr 1997; 66 : 460s-3s. 202 INDIAN J MED RES, SEPTEMBER 2007
3. Chevalier P, Sevila R, Sejas E, Zalles L, Belmonte G, Parent
G. Immune recovery of malnourished children takes longer
than nutritional recovery: implications for treatment and
discharge. J Trop Pediatr 1998; 44 :304-7.
4. Agarwal K N, Bhasin S K. Feasibility studies to control acute
diarrhea in children by feeding fermented milk preparations
Actimel and Indian Dahi. Eur J Clin Nutr 2002; 56 (Suppl 4) :
556-9.
5. Nagy S Telek L, Hall N T Berry R E. Potential food uses for
protein from tropical & subtropical plant leaves. J Agric Food
Chem 1978; 26 : 1016-8.
6. Ejot R, Mbiapo T, Fokou E. Nutrient composition of the leaves
and flowers of Colocasia esculenta and fruits of Solanum
melongera. Plant Foods Hum Nutr 1996; 49 : 107-12.
7. Oluwasola A J. Characterization of the leaf meals, protein
concentrates and residues from some leguminous plants. J Sci
Agr 2006; 86 : 1292-7.
8. World Health Organization. Manual of Severe Malnutrition:
A Manual for Physicians and Other Senior Health Workers.
Geneva: WHO; 1999.
9. Reid M, Badaloo A, Forrester T, Morlese JF, Heird WC, Jahoor
F. The acute-phase protein response to infection in edematous
and nonedematous protein-energy malnutrition. Am J Clin Nutr
2002; 76 : 1409-15.
10. Devi S, Devi PY, Siva Prakash M. Effect of Lactobacillus
supplementation on immune status of malnourished pre-school
children. Indian J Pediatr 1999; 66 : 663-8.


nephrotic syndrome case report



CASE REPORT ON NEPHRITIC SYNDROME.
Introduction
Nephrotic syndrome is a nonspecific kidney disorder characterized by three signs of disease: large proteinuria, hypoalbuminemia, and edema.[1] Essentially, loss of protein through the kidneys (proteinuria) leads to low protein levels in the blood (hypoalbuminemia), which causes water to be drawn into soft tissues (edema). Very low hypoalbuminemia can also cause a variety of secondary problems, such as water in the abdominal cavity (ascites), around the heart or lung (pericardial effusion, pleural effusion), high cholesterol (hence hyperlipidemia), loss of molecules regulating coagulation (hence increased risk of thrombosis). Nephrotic syndrome has many causes and may either be the result of a glomerular disease that can be either limited to the kidney, called primary nephrotic syndrome (primary glomerulonephritis), or a condition that affects the kidney and other parts of the body, called secondary nephrotic syndrome. Along with obtaining a complete medical history, a series of biochemical tests are required in order to arrive at an accurate diagnosis that verifies the presence of the illness.
The treatment of primary nephrotic syndrome such as minimal change nephropathy, membranous nephropathy, and focal segmental glomerulosclerosis nephropathy remains challenging. Whilst most cases of idiopathic nephrotic syndrome respond to steroid therapy and experience a limited number of relapses prior to complete remission, some cases suffer from frequent relapses and become steroid dependent or are primarily steroid resistant. Treatment options are limited to immunosuppressive drugs with significant side effect profiles. This present case study discusses the disease process and prognosis of the 3 children with various type of nephritic syndrome.
For the comparative study, 3 patients are selected randomly from the paediatric ward AIIMS Rishikesh, who were diagnosed with Nephritic syndrome.
The details of the patients are followed:-
Bio demographic data
Patient I
Patient II
Patient III
Name
Age
Sex
Address
IPD No.
Education
Religion
Date of admission
Varsh
6 years
Male
Jwalapur, haridwar
456054/01/16
1st class
Hindu
29/01/16
Divya
6 years
Female
Tehri garhwal
37746/09/15
Kinduganden
Hindu
9/10/15
Aayan
6 years
Male
Lalpur balawala bijnor
134578/1015
play school
Muslim
8/10/15

 Definition
Nephritic syndrome is a syndrome characterized by edema and Lange amounts of proteins in the urine and usually increased blood cholesterol, usually associated with glomemlonephritis or within a complication of systemic disease.
Incidence
Incidence of the condition is 2-7 per 1000 children most common in male. Mean age of occurrence is about 2-5 years.
Classification
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)

TYPE I- Idiopathic nephritic syndrome/Primary glomerulonephrosis


·         Approximately 90% of children with nephritic syndrome have idiopathic nephritic syndrome, idiopathic nephritic syndrome is anointed with primary glomeular disease without evidence of a specific systemic cause.
·         Idiopathic nephritic syndrome includes multiple histological types: minimal change disease, mesangial proliferation, focal segmental glomerulosclerosis, and membranous nephropathy. 
Type- II secondary nephritic syndrome
·         Nephritic syndrome can occur as a secondary feature of many form of glomerular disease.
·         This may be associated with membranous nephropathy, membranous proliferative glomerulo nephrites, lupus nephritis, malaria, schistoso-miaris, malignancy and therapies with numerous drugs and chemicals  
Type III. Congenital nephritic syndrome
·         Congenital nephritic syndrome is defined as nephritic syndrome manifesting at birth or within first 3 month of life congenital nephritic syndrome may be primary or secondary


Idiopathic nephritic syndrome

Secondary nephritic syndrome
Patient Divya was diagnosed previously to have septicaemia 

Idiopathic nephritic syndrome.
Minimal changes disease

Etiology
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)
the etiological or risk factor are divided into 2 types:-
a.      Primary glomerulo nephritis
b.      Secondary glomerulo nephritis
Primary glomerulonephrities- caused by any glomerulor disease limited to kidney only
            i.            Minimal change disease- cause due to minimal changes in glomerulus
          ii.            Focal segmental glomerulosis- caused by tissue scanning in glomeruli
        iii.            Membranous glomerulonephritis-inflammation of glomeular membrane
        iv.            Membranoproliferative glomerulo nephritis- inflammation of glomeruli along t antibodies deposition in membrane
          v.            Rapidly progressive glomerulo nephritis-glomeruli are in moon shaped.
-          GFR decreased by 30%
Secondary glomerulonephritis- caused by any glomeruloe disease that affect the whole kidney as well as other parts of body
         i.            Diabetic nephropathy- complication of diabetes
       ii.            Systemic lupus erythematosis- it is an autoimmune disease that can affect many organs.
     iii.            Sarcoidosis – accumulation of inflammatory granules in kidney.
    iv.            Syphilis
      v.            Hepatitis
    vi.            Sjoguevis syndrome
 vii.            HIV/AIDS
 viii.            Amyloidosis- Deposition of amyloidal substance in glomeruli modifying thin shape and function
     ix.            Multiple myeloma- cancerous cell in kidney
      x.            Genetic disease
     xi.            Drugs- penicillin gold salt, captopril etc.
The etiologic in patient Vansu was minimal change disease which results in the abnormal kidney function
(primary glomerulo nephrities)

 The etiologic in patient Divya was minimal change disease which results in the abnormal kidney function
(primary glomerulo nephrities)

The etiologic in patient Aayan was minimal change disease which results in the abnormal kidney function
(primary glomerulo nephrities)

Clinical manifestation
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)
The onset of the disease is usually gradual or may be acute.
        I.            The child may present with periorbital puffiness
      II.            Edema may be minimal or masive
   III.            Profound weight gain within a short period of days or week is found
    IV.            Dependent edema develops in the ankle, feet genetalia (scotum) and hands.
      V.            Striae may appear on the skin due to overstretching by edema
    VI.            Fluid accumulation in body spaces
a.       Ascites
b.       Plemal effurion
 VII.            Generalized edema (anasarca)
VIII.            Urine output reduced
    IX.            Concentrated & frothy appearance of urine.
      X.            GT disturbances usually found as vomiting, loss of appetite & diarrhoea
    XI.            Other features includes like:- fatigue, lethargy, pallor, irritability.
 XII.            Hypertension, hematuria, hepatomegaly and wasting of muscle may found in some cases   
·         Periorbital puffiness
·         Oedema
·         Wt gain (28.5kg)
·         Ascetics present
·         Generalized edema
·         Urine output reduced
·         Fatigue
·         lethargy
·         Irritability
·         Wasting of muscle
·         Proteinuria

·         Periorbital puffiness
·         Oedema
·         Plural effusion present
·         Generalized Oedema
·         Fatigue
·         Lethargic
·         Irritable
·         Hematuria
·         Proteinuria
·         Oedema
·         Ascetic
·         Wt gain
·         Proteinunia
·         Fatigue
·         Lethargic
·         Irritability



Etiological factor
 
Pathophysiology
 

 


Diagnostic Measure
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)
·         History of illness and physical examination to exclude clinical features help to diagnose the condition clinically.
·         Laboratory investigations to confirm the diagnosis may includes the followings:-
·         Urine examination shows gross proteinuria (2 to 20 g 1 day), presence of cast, slight hematuria and increased specific gravity. 
·         Blood examination demonstrates reduced total protein, albumin less than 2.5 gl/dl and cholesterol more than 200 mg/dl.
·         Lipoproteins and BUN (blood urea nitrogen) are increased.
·         Serum albumin and globulin ratio is reversed
·         Hypogammaglobulinemia, hypomagnesemia and low-ceatinine level  
·         Renal biopsy is indicated in case of poor response to steroid therapy
·         Other investigation show low ASO titer and IgM, raised IgC & IgE, serum complements is normal
·         Serum total protein =3.9 gm/dl
·         Serum albumin=1.2 gm/dl
·         Serum globulin= 2.7 gm/dl
·         A.G ratio =0.4
Ø  Urine examination
·         Protein =+ve appro. 500mg/dl
·         Leucoogtis= tve
·         Casts = granulan cast present
Ø  Hematological report
·         TLC = 13400 cells/cumm.
Ø  Other investigation are normal
Ø  Renal biopsy is not indicated
Ø  Biochemisty examination
·         serum total protein = 3.5 gm/dl
·         serum albumin=1.5 gm/dl
·         serum globulin= 2.9 gm/dl
·         A.G ratio = 0.5
Ø  Urine examination
·         Protein =+ve  appro. 400 mg/dl
·         Costs= present
Ø  Haematological report
·         Neutrophitis =31.8%
·         Eosinophilis = 6.8%
·         MCH= 24.9 pg
Ø  Lipid profile
·         Total cholesterol 446.0 mg/dl
·         Serum triglycerides 229 mg/dl
Ø  Other investigation are normal  
Ø  Renal biopsy is not done

Ø  Biochemistry examination
·         Serum total protein = 3.0 gm/ldl
·         Serum albumin= 1.0 gm/dl
·         Serum globulin= 2.0 gm/dl
·         A. G ration = 0.5
Ø  Urine examination
·         Protein= +ve
·         Appro. 500 mg/dl
·         Blood = present
·         Leukucyte= present
Ø  Haematological report
·         Hb= 9.6 gm/dl
·         RBC = 3.92 million cells cumm
·         Lymphocytes =47%
·         Hematocrit = 28.6%
Ø  Lipid profile
Total cholesterol= 320.0 mg/dl
Medical & nursing management
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)
Ø  Bed rest and high protein diet with restriction of fluid intake are important aspects of management
Ø  Steroid therapy with oral predni solone is the most significant aspect of management of nephritic syndrome. It is given 2 mg 1 kg iday in 2to 3 divided doses for at teat 4 to 6 weeks and then gradually tapered off or abruptly stopped, after another 4 to 6 weeks.
Ø  Antacid is given along with prednisolone to prevent gastic complication
Ø  antibiotic therapy is indicated in the presence of any infection
Ø  Diuretics are prescribed in the presence ascites frusemide 1 to 3 mg 1kg 1 day in 2 divided doses in given
Ø  Rapid fluid loses should not be attempted in 8 to 12 hours
Ø  Potassium supplementation to be given along with diuretics
Ø  Albumin infusion (1g 1 kg 1 day) may be given in case of masive edema & ascetics. It helps to shift the fluid from interstitial space into the vascular system.
Ø  Blood transfusion or plasma may be given is some cases to treat hypoalbuminemia.
Ø  Immunasuppresive drugs (leuamisole, methotrexate, cyclophosphamide, cyclosporine, chlorambucil) may be administered along with prednisolone in case of frequent (4 or more per year) relapse and in steroid dependent cases.
Ø  Renal transplantation is indicated in end stage failure
·         Bed rest & high protein diet is recommender   to client
·         Antibiotic therapy i e. Cefexime & augmentine is prescribed to the patient
·         Lasix (furosemide) is prescribed to patient
·         Low sodium diet is  recomemded.
·         Bed rest & high protein diet is recommended to client
·         Antibiotic therapy  IV metrogyl 15mg  TDS, oral is prescribed to the patient 
·         Wysolone (prednidolone) 10mg, BD, oral is prescribed to patient
·         Syp gelusil (magnesium hydrochloride) 10 ml OD, oral is prescribed
·         Furosemide (lasix) 21mg 18 hourly 1 oral is prescribed to patient
·         Fluid intake restriction
·         low sodium diet  
·         Bed rest & high protein diet i.e. 1.2g ml /kg /day is recommended to patient
·         Antibiotic therapy i.e. cetixine 200gm/orally/TDS and augmentin 375mg/ orally/ BD is prescribed by doctor
·         Lasix (furose mide) is prescribed 20mg/orally/BD.
·         Input/ output chart should be maintain
·         Albumin 600gm/IU/ TDS is administered to patient

Prognosis:
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)
Ø   Generally good although this depends on the underlying cause, the age of the patient and their response to treatment.
·         The child is 6 years old. Enema was reduced, child showed adequate urine output. Childs
·         Child was referred to other hospital with reference note.
·          Urine out put was moderaqtely adequate, weight was reducing little. Periorbital Oedema reduced.

Complications
Book picture
Patient picture
Patient I (Vansh)
Patient II (Divya)
Patient III (Aayan)
·         Thromboembolic disorders
·         Infections:
·         Acute kidney failure .
·         Pulmonary edema:
·         Hypothyroidism
·         Hypocalcaemia:
·         Iron deficiency  anaemia
·         Protein malnutrition:
·         Growth retardation:
·         Vitamin D deficiency 
·         Cushing's Syndrome
·         Iron deficiency anaemia
·         Protein energy malnutrition
·         Growth restriction
·         Iron deficiency anaemia.
·         Growth retardation
·          Growth retardation
·         Iron deficiency anaemia.

Discussion: the nephritic syndrome becomes common renal disease among children now days. The causes are idiopathic for most of the children. And this leads to secondary nephritic syndrome. The children with nephritic syndrome admit in the paediatric ward very often with recurrence. In the above 3 cases baby Divya admitted 3rd time in the paedia ward with recurrence. The treatment of choice is depended upon age and type of nephritic syndrome. Steroid therapy is proved to be affective management in treating nephritic syndrome. Baby Divya was treated with hydrocortisone because of the recurrent attract of the same disease but not other two babies were not received steroids. Master Varsh and Divya discharged form hospital once they started to show progress were as master Aayan got discharged against medical advice. 
Reference:
1.       Ghai. Eesntial pediatric nursing. 8th edition. CBS publishers. 477-482.
2.       Gupta P. Essential pediatric nursing. 3rd edition. CBS publishers. 508-510          
3.       Gupte S. The short textbook of paediatrics. 11th edition. Jaypee brothers medical publishers (P) LTD. 517.
4.       Wongs. Essentials of p[ediatric nursing. 8th edition. Elsveier publication.  958-962.
5.       Beevi A. Testbook of pediatric nursing. Elsevier publication. 306-307
6.       Panda Un. Handbook of pediatric nursing. AITBS publishers. 258-259
7.       Kyle T& Carman S. Essentials of pediatric nursing. 2nd edition. Lippincot Williams & Wilkins. 773-775