PANEL DISCUSSION ON ASTHMA IN CHILDREN WITH OR WITHOUT COVID 19,by Experts,moderated by Dr.Dev,M.D,Pediatric Pulmonologist and Respiratory intensivist ,Delhi ncr

PANEL DISCUSSION ON ASTHMA IN CHILDREN WITH OR WITHOUT COVID 19,by Experts,moderated by Dr.Dev,M.D,Pediatric Pulmonologist and Respiratory intensivist ,Delhi ncr

https://m.facebook.com/story.php?story_fbid=1406721312822521&id=412160705929917?sfnsn=wiwspwa&extid=jHdMecjhkGPw6XDM&d=w&vh=eAsthma is the most common chronic respiratory disease in children worldwide.
It is being discussed by international experts.Please click below

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This is being published here to update the knowledge of doctors treating asthmatic child.
It should be translated into the better care of asthmatic children all over the world.

NEWER TESTS TO DETECT INFECTION WITH Mycobacterium Tuberculosis,Dr.Dev,M.D.,Pediatrician and Pediatric Pulmonologist,Mohan Nagar,Ghaziabad,Delhi NCR

The oldest and time tested test to detect Tuberculosis infection in an individual is TST(Tuberculin skin test),also known as Mantoux test.It is being done with PPD RT -23.The standard strength for its use is 2TU(tuberculin unit).

But this strength is not available in the market and pathologists are compelled to use 5TU,the cut off value of induration for which is not standarized.

Moreover ,there may be false positive results, due to cross reactivity with Mycobacteria other than Mycobacterium tuberculosis (NTM)and BCG Vaccination particularly if the vaccination has been done after the infantile period.

The latest test which will be available in market very shortly is C-Tb skin test.

C-Tb skin test

C-Tb test- This test is done in a similar manner as Mantoux test.Instead of PPD-RT23,in this test, antigens either ESAT6 or CFP 10 are used ,which are also used in Quaniferon Gold test.

This is the reason,it does not cross react with non tuberculous Myobacterium(NTM) as well as with BCG.At the same time, the test is not as complicated as Quantiferon Gold as it does not require sophisticated laboratory.

In the same way as in Mantoux test,0.1 ml of antigen is inoculated intradermally and the induration is meassured after 48-72 hours with ball pen and scale method. The cut off point has been established at 5mm for all age groups,irrespective of HIV status,irrespective of BCG Vaccine status.

The positive result indicates only the infection specifically to Mycobacterium tuberculosis but not the active disease

IGRA TEST

IGRA TEST:This test is interferon gamma release assay test.This is based on the principle that when T lymphocytes infected with Mycobacterium tuberculosis is exposed to specific antigen of M.Tb, in the form of either ESAT6 or CFP10 ,they release interferon gamma which is then measured.There are two tests,

QUANTIFERON  TB GOLD ;In this test total interferon gamma which are released is measured

and

T spot TB. -It is a variant of Ellispot .In this test the number of effector T cells are measured which release interferon gamma upon exposure to specific antigens.

So ,this test is specific for Mycobacterium tuberculosis and it is not positive in cases of NTM(non tuberculosis mycobacteria) or in cases of BCG vaccination.

There is no need of a technique of intradermal inoculation and the measurement of induration as this test uses blood withrawn from patients.

There is no need of different cut off point of induration for HIV and non HIV patients

This test indicates only the infection,not the active disease

But ,this is not reliable below the age of 5 years.

REFERENCES:

1. World Health Organization. Guidelines on the management of latent tuberculosis infection. 2015. Report No.: WHO/HTM/TB/2015.01

2. Aggerbeck H, Giemza R, Joshi P, Tingskov PN, Hoff ST, Boyle J, et al. Randomised Clinical Trial Investigating the Specificity of a Novel Skin Test (C-Tb) for Diagnosis of M. tuberculosis Infection. PLoS ONE 2013;8(5):e64215 10.1371/journal.pone.0064215 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

3.Hoff ST, Peter JG, Theron G, Pascoe M, Tingskov PN, Aggerbeck H, et al. Sensitivity of C-Tb: a novel RD-1-specific skin test for the diagnosis of tuberculosis infection. Eur Respir J 2015. December 17;47(3):919–28. 10.1183/13993003.01464-2015 [PubMed] [CrossRef] [Google Scholar]

4.Ruhwald M, Aggerbeck H, Gallardo RV, Hoff ST, Villate JI, Borregaard B, et al. Safety and efficacy of the C-Tb skin test to diagnose Mycobacterium tuberculosis infection, compared with an interferon gamma release assay and the tuberculin skin test: a phase 3, double-blind, randomised, controlled trial. Lancet Respir Med 2017. January 31;5(4):259–68. 10.1016/S2213-2600(16)30436-2 [PubMed] [CrossRef] [Google Scholar]

5. World Health Organization. Guidance for national tuberculosis programmes on the management of tuberculosis in children – 2nd ed. 2014. Report No.: WHO/HTM/TB/2014.03.

6.C-Tb skin test to diagnose Mycobacterium tuberculosis infection in children and HIV-infected adults: A phase 3 trial
PLoS ONE. 2018; 13(9)

7. Mori T, Sakatani M, Yamagishi F, Takashima T, Kawabe Y, Nagao K, et al. Specific detection of tuberculosis infection: an interferon-gamma-based assay using new antigens. Am J Respir Crit Care Med 2004. July 1;170(1):59–64. 10.1164/rccm.200402-179OC [PubMed] [CrossRef] [Google Scholar]

8.Sollai S, Galli L, de MM, Chiappini E. Systematic review and meta-analysis on the utility of Interferon-gamma release assays for the diagnosis of Mycobacterium tuberculosis infection in children: a 2013 update. BMC Infect Dis 2014;14 Suppl 1:S6. [PMC free article] [PubMed] [Google Scholar

9.Sensitivity of C-Tb: a novel RD-1-specific skin test for the diagnosis of tuberculosis infection.
[Eur Respir J. 2016]
10.Safety and efficacy of the C-Tb skin test to diagnose Mycobacterium tuberculosis infection, compared with an interferon γ release assay and the tuberculin skin test: a phase 3, double-blind, randomised, controlled trial.
[Lancet Respir Med. 2017]
11.Review Gamma interferon release assays for detection of Mycobacterium tuberculosis infection.
[Clin Microbiol Rev. 2014]
12.Specific detection of tuberculosis infection: an interferon-gamma-based assay using new antigens.

TERMS USED TO DESCRIBE RESISTANT TUBERCULOSIS,Dr.Dev,M.D.,Pediatrician and Pediatric Pulmonologist,Mohan Nagar,Ghaziabad,Delhi NCR

The burden of resistant tuberculosis is on the rise which is a threat to WHO END Tuberculosis programme .

Children are also becoming victim but data are not sufficient yet

Primary resistance:When an individual is infected with resistant strain of Mycobacterium tuberculosis

Secondary resistance:When an individual is infected with drug sensitive strain of Mycobacterium tuberculosis but during the course of treatment the organism acquire resistance due to suboptimal treatment,incomplete treatment with high bacterial load.It is also known as acquired resistance.

MONORESISTANCE:When the organism is resistant to only one drug

POLYRESISTANCE;When the organism is resistant to  2 drugs but not to both Rifampicin and Isoniazid

MULTI DRUG RESISTANCE(MDR): When there is resistance to both Rifampicin and Isoniazid

PRE EXTENSIVELY RESISTANCE(PRE-XDR):When there is resistance to Rifampicin,Isoniazid with resistance to either Fluoroquinolones or Second line injectables(SLI) but not to both.

EXTENSIVELY DRUG RESISTANCE:When there is resistance to Rfampicin ,Isoniazid and both Fluoroquinolones and SLI

RR Tb: When there is resistance to Rifampicin with or without resistance to other anti tuberculosis drug

SLI(second line injectables): Amikacin,Kanamycin and Capreomycin

REFERENCES:Indian Journal of Pediatrics,volume 87/number 10/October 2020

 

 

 

USUAL SYMPTOMS,UNUSUAL DIAGNOSIS,A CASE REPORT,Dr.Dev,M.D.,Pediatrician and Pediatric Pulmonologist,Mohan Nagar,Sahibabad,Ghaziabad,Delhi NCR

11 years old female child presented to our clinic with complaints of

Fever for 24 days,

cough for 15 days

less appetite for 10 days

pain abdomen for 7 days

headache for 5 days

swelling of both lower limbs for 3-4 days

On examination;

Temperature 103 dF,pallor +,icterus+

Pulse rate 56/m regular(relative bradycardia)

Respiratory rate 26/minute ,regular

Generalised lymphadenopathy

bilateral pedal edema

Abdomen-not distended,no tenderness,hepatosplenomegaly+

Chest-bilateral equal breath sound,bilateral vesicular breath sound,bilateral crackles

CVS-NAD

CNS-NAD

Following diagnoses were suspected

Malaria

Typhoid

Viral hepatitis with secondary bacterial infection

Disseminated tuberculosis

Leptospirosis

Scrub typhus

Investigations were planned and done accordingly.

Hb 9 gm/dl

TLC 6800/cmm,P56,L34,E03,M07,B00,Platelet 90000/cmm

SGPT-102,SGOT146,ALP 200,S.BIL 3.8mg/dl

Serum Sodium 130mE/L,Serum potassium 4.4mE/dl

Serum widal-negative

Malaria antigen-negative

Chest X-Ray -bilateral reticulonodular opacities with bilateral pleural effusion

Mantoux test-negative

GA for CBNAAT -negative

The child was emperically treated as enteric fever with cefixime but there was no response.Then the child was treated emperically for malaria and again there was no response.

At this point of time,it was suspected that the child may be suffering from scrub typhus as the child travelled to Uttrakhand during last month.

IgM ELISA for scrub typhus was sent and it came to be positive and the child responded well to doxycycline.

DISCUSSION

:Rickettsia is intracellular ,gram negative proteobacteria with coccobacillar shapes.The disease caused by it is called Rickettsiosis.It is a zoonosis ,transmitted into human by mites(chiggers),ticks or fleas and rodents. Humen are the incidental host.No human to human transmission has been observed.

This disease is frequently seen in Uttrakhand,Rajsthan,assam.West Bengal ,Jammu and Kashmir,Maharashtra Tamil Nadu and Kerala region of India and many countries out of India.

pathogens causing disease in human have been broadly classified into three groups

1.Spotted fever group

2.Typhus group

3.Scrub typhus group

Scrub typhus is causing a health impact in Asia

Pathogenesis;The principle pathogenetic mechanism is vasculitis involving medium and small vessels.It causes increased vascular permeability by disrupting the endothelial tight junctions due to the bacterial load and tumour necrosis factor.Main cause of mortality is pulmonary edema and cerebral edema.

CLINICAL FEATURES OF SCRUB TYPHUS WHICH IS COMMON IN INDIA:

The usual incubation period is 10-12 days with a variability of 6-21 days.Symptoms varies from mild self limiting to severe causing death.

After the period of approximately 5-6 days of bite by mites,there occurs the formation of ESCHAR(shown in the figure) at the site of inoculation of the mite.It is a painless necrotic lesion over skin resembling a cigarette burnt skin surface.The usual sites are groin,axilla,back,neck and other exposed parts of the body.Eschar, if visibl,e makes a clear cut diagnosis of scrub typhus without any investigation.But it is not ususally seen in children.Its prevalence varies from 7-80%.

After about 5-7 days flu like symptoms occurs.In most of the cases fever has been observed with  severe headache.

There may be myalgia,weakness,pain abdomen,vomiting,diarrhoea,cough.

O/E There may be relative bradycardia,generalised lymphadenopathy,generalised body rashes and pedal edema

On systemic examination:there may be hepatosplenomegaly

On investigation:

BLOOD-there may be anemia,thrombocytopenia,raised liver enzymes,raised serum bilirubin,hyponatremia,raised blood urea and serum creatinine

Chest X-Ray may show reticulonodular opacities,features of pulmonary edema,bilateral pleural effusion

ECG may shows features of myocarditis with nonspecific ST-T  changes,features of heart block

LUMBAR PUNCTURES :CSF pictures are indicative of meningoencephalitis.The CSF picture is similar to Tuberculous meningitis with lymphocytic pleocytosis and raised protein.

DIAGNOSIS; The gold standard is INDIRECT IMMUNOFLUORECENT ANTIBODY TEST(IFA), but it is not available everywhere.The next best is IgM ELISA which is widely available and should be done as the sensitivity of Weil-Felix test is very poor.

TREATMENT.The drug of choice is doxycycline,oral or i.v. in the dose of 2.2 mg/kg 12 hourly below 40 kg of weight and 100 mg b.d. above 40 kg of weight,for a period of 7 days of 3 days after the fever subsides.Now it has been recommended for children of any age to treat Rickettsial diseases as it has not caused enamel hypoplasia or teeth staining even after multiple courses.

Alternative medicine is Azithromycin in the dose of 10 mg/kg/day

Other drugs which may be used in special cases are -clarithromycin.chloramphanicol and Rifampicin

Mortality is above 50% if not recognised and treated timely

COMPLICATIONS.HLH(hemophagocytic lymphohistiocytosis and it is very serious complication.

REFERENCES:

AbdadMY,Abou AbdallahR,FoumierP-E,StenosJ,Vasoo S.Aconcise review of the epidemiology and diagnostics of rickettsioses:Rickettsia and Orientia spp.J clin Microbiol.2018;56:eo1728-17

IssacR,VargheseGM,MathaiE,et al.Scrub typhus:prevalence and diagnostic issue in rural southern India.Clin infect dis.;2004:39;1395-6

Rathi N ,Kulkarni A ,Yewale V;Indian Academy of Pediatrics Guidelines on Rickettsial diseases in children committee.IAP Guideline on Rickettsial disesase in children.Indian Pediatr.2017;54:223-9

Elisabeth BN,Cristina S,DidIer R,Phillipe P.Treatment of Ricketssial spp.infections:a review.Exp rev anti infect Ther.2012;10:1425-37

 

 

NASAL POLYP,WORKING KNOWLEDGE,Dr.DEV,M.D,Pediatrician and Pediatric Pulmonologist,Mohan Nagar,Sahibabad,Ghaziabad,Delhi NCR

Nasal polyp is not uncommon in children and parents often get afraid of it when it is visible.

It is rare below the age of 10 yeras.

It is an abnormal growth which is semitransparent and may arise from any portion of nasal mucosa or epithelium of paranasal sinuses usually at its outflow.

Contrary to the common belief,it is associated more commonly with non allergic than allergic conditions.

It is seen more commonly in children with non allergic asthma than allergic asthma

It may be single or multiple depending on etiology.

CLINICAL FEATURES:

Small polyps are asymptomatic which are usually discovered during nasal examination for other causes,when they are located anterior to the anterior edge of middle turbinate

Symptoms depend on size and location of the polyp.

Small polyp arising from middle meatus may produce symptoms by blocking the outflow tract,causing chronic and recurrent sinusitis.

common symptoms are

Rhinorrhoea,

post nasal drip

facial pain

headache

toothache

hyposmia,

anosmia,

loss of taste,

blocked nose,

snoring.

When the size becomes large,it may  cause obstructive sleep apnea

DIAGNOSIS;

Clinical examination is sufficient for the idendification of this lesion.Anterior rhinoscopy wll defines it.

Non contrast CT scan of nasal and paranasal sinuses are required to see the extent of lesions as in rare circumstances there may be malignant lesions.SO the imaging investigation of choice is non contrst CT scan.

CAUSES:

It arises due to chronic inflammation of nasal or paranasal mucosa,so it is commonly seen in children with allargic or non allergic rhinitis or sinusitis.

Multiple polyps are seen in children with cystic fibrosis,primary ciliary dyskinesia ,asthma and  allergic fungal sinusitis.

TRATMENT:

Treatment is medical in most of the cases.Surgery is required only rarely when medical treatment fails.

In most of the cases ,short term oral corticosteroid and or intranasal steroid is needed.

REFERENCES:

 

Bernstein JM, Gorfien J, Noble B. Role of allergy in nasal polyposis: a review. Otolaryngol Head Neck Surg. 1995 Dec. 113 (6):724-32. [Medline].

Tos M, Sasaki Y, Ohnishi M, Larsen P, Drake-Lee AB. Fireside conference 2. Pathogenesis of nasal polyps. Rhinol Suppl. 1992. 14:181-5. [Medline

Rudmik L, Schlosser RJ, Smith TL, Soler ZM. Impact of topical nasal steroid therapy on symptoms of nasal polyposis: a meta-analysis. Laryngoscope. 2012 Jul. 122 (7):1431-7. [Medline].

Lund VJ, Flood J, Sykes AP, Richards DH. Effect of fluticasone in severe polyposis. Arch Otolaryngol Head Neck Surg. 1998 May. 124 (5):513-8. [Medline

Rudmik L, Schlosser RJ, Smith TL, Soler ZM. Impact of topical nasal steroid therapy on symptoms of nasal polyposis: a meta-analysis. Laryngoscope. 2012 Jul. 122 (7):1431-7. [Medline].

 

 

 

OIL MASSAGE TO BABY-KNOW THE FACT,DR.DEV,M.D.,PEDIATRICIAN AND PEDIATRIC PULMONOLOGIST,SAHIBABAD,GHAZIABAD,DELHI NCR

OIL massage is an important part of giving health to babies.

Oil maasage should be given to all babies starting at the period of newborn.

The best time to start oil massage to baby is ,approximately 10 days after birth when the umbilical stump falls off automatically.

The best time to give massage is before giving bath and it should be 90 minutes before or after the feed.

If the massage is given in close proximity to feed,there is more chance of vomiting.

The massage should be given preferably by mother so that there occurs a good bonding between mother and child.

The best oil for massaging a baby is pure coconut oil and the next best is olive oil.

If possible the massage should be given in open sun light provided there is no cold wind.

Baby should be unclothed fully during massage in warm ambience.

Massage can be given starting from top to bottom or in reverse order.

Lie the baby on his or her back and start massaging with oil from head.oil the scalp hair and massage gently,then start from mid point of forehead and go towards both sides gently.Massage the nose gently because the bone of baby’s nose is soft.DO NOT INSTIL OIL INTO NOSTRILS  OR EARS.

Massage the back of ears then cheeks then armpits.Chest massage should be started from the midline moving toward both sides(periphery)

Massage the tummy in a clockwise movements of your hands very gently.

Arms should be massaged from low to high for 5-6 times.Then both the palms should be massaged.Legs should be massaged from low to high again 5-6 times ,then soles should be massaged.Oil should always be applied in the area of groin .

Now, the baby should lie on the tummy and back massage should be done starting from centre towards both sides.

Oil massage stimulates the different nerves of the baby,increases blood circulation in different parts of body, thereby helps in promoting growth of the baby.It can also detect some hidden injury when baby starts crying in pain which is easily recognised by mother.By increasing bonding with mother, when the baby enjoy the massage,it also helps in overall development of the baby.

Oil massage should preferably be done two times per day and during winter season, it also protects the baby from cold environment.

 

Five signs of disturbed sleep in children,Dr.Dev,M.D.,Pediatrician and Pediatric Pulmonologist,Sahibabad,Ghaziabad,Delhi NCR

Sleep is very important state of health.

Sleep is a state in which body and mind repares itself.

Adequate sleep is related to time and quality of sleep.

Either less time of sleep or poor quality of sleep ,may affect the body and mind adversely.

Children require more hours of sleep in comparision to adults.

A newborn,less than 4 weeks of age,require 16-18 hours of sleep per day.

A school going children,6-12 years of age require 9-10 hours of sleep per day.

Sleep is essential for the smooth functioning of body and mind.

Following are the 5 signs of disturbed sleep.

1.MORNING HEADACHE:

This is a very important sign of inadequate sleep.It is caused by CO2 retention due to sleep apnea(stoppage of breathing for more than 20 seconds)

2.HYPERACTIVITY:

This is a separate disease entity in children due to many causes,but sleep disturbances is an important cause.

3.ATTENTION DEFICIT:

Excessive sleepiness during day time and poor academic performances is an important sign of inadequate sleep but the child may become inattentive with less capacity to concentrate on anything due to less and bad quality of sleep.

4.RESTLESSNESS AND FRAGMENTED SLEEP:

Frequent arousal during sleep and excessive movement of any part of body is an important sign of disturbed sleep.

5.SOUND DURING SLEEP:

Sleep should ideally be soundless.Any audible sound during sleep is a sign of sleep disordered breathing.

Noisy breathing in the form of snoring is an important sign of upper airway obstruction,which leads to poor growth of body and mind of child and in long term ,it may cause heart disease in children.

 

FFP- an option to treat Hereditary Angioedema,Dr.Dev,M.D.,Pediatrician and Pediatric Pulmonologist,Sahibabad,Ghaziabad,Delhi NCR

Hereditary angioedema(HAE) is a   rare disorder caused by deficiecny of C1 –inhibitor(C1- INH) since birth.

There are two types of HAE,TYPE 1 and TYPE 2

In type 1 HAE ,there is hereditary deficiency of C1- INH ,whereas in type 2,the level of C1- INH in serum may be normal or elevated but the C 1-INH function is impaired.

C 1- INH interact with approximately 60 other proteins in the body to protect the body from infections.

In its absence,there is failure of degradation of bradykinin, the level of which rises in blood.

Bradykinin,increases the permeability of blood vessels by causing inflammation and dilatation of the vessels.

In effect,the intravascular fluids leak from the blood vessels and accumulate between layers of skin and epithelium.

There occurs swelling all over the body including tongue and lips causing disfigurement.

 

When the swelling occurs in the respiratory airways ,particularly involving larynx,it may be life threatening,unless treated on emergency basis.

These swellings,usually do not respond to antihistamine,adrenaline,and corticosteroids.

The specific treatment is Berinert , HAEGARDA , or Bradykinin receptor antagonist FIRAZYR(ICATIBANT)which is difficult to get in resource poor countries including India.

There is one case report from Pakistan,a 30 year patient was admitted in emergency after a fall. In the hospital,it was found from the medical record that the patient was a known case of HAE.

The patient got swelling including laryngeal edema which did not respond to antihisamine,adrenaline and corticosterois.The patient developed respiratory distress and went into pulseless cardiac arrest ,revived after CPR and had to be intubated.

Treating doctors decided to give FFP, in view of non availability of specific treatment of HAE.

FFP(Fresh frozen plasma) was given 6 hourly and the patient responded after 18 hours,extubated after 3 days and stepped down from ICU to the ward.He was discharged on danazol prophylaxis and did well on follow up.

There was no adverse effect noted due to FFP.

This is first case report ,published in CUREUS.

FFP contains so many substances apart from C1-INH,which may cause harm to an individual.

If more ,multcentric studies prove its efficacy and safety profile ,,it will be a boon to the patients in resource poor countries.

REFERENCES;OCTOBER 12,2020,In News,By FOREST RAY

Forest Ray received his PhD in systems biology from Columbia University, where he developed tools to match drug side effects to other diseases. He has since worked as a journalist and science writer, covering topics from rare diseases to the intersection between environmental science and social justice. He currently lives in Long Beach, California.
Fact Checked By:
Ines Martins, PhD
Inês holds a PhD in Biomedical Sciences from the University of Lisbon, Portugal, where she specialized in blood vessel biology, blood stem cells, and cancer. Before that, she studied Cell and Molecular Biology at Universidade Nova de Lisboa and worked as a research fellow at Faculdade de Ciências e Tecnologias and Instituto Gulbenkian de Ciência. Inês currently works as a Managing Science Editor, striving to deliver the latest scientific advances to patient communities in a clear and accurate manner.

Corona virus on human skin,Dr.Dev,Pediatrician and Pediatric Pulmonologist,Sahibabad,Ghaziabad,Delhi NCR

It is very difficult to study the virus on human skin due to fear of spread of infection among volunteers.

This is the reason,researchers have chosen to study on the skin of cadaver,which is used for the graft purposes.

Research has proven that the novel corona virus survives on human skin for more than 9 hours.

Influenza A virus survives on human skin for less than 2 hours.

Both viruses are killed when hands are rubbed for 15 seconds using 80% alcohol .

Viruses are also killed when hands are washed with soap water for at least 20 seconds.

Inspite of the fact that novel corona virus spreads mainly by droplets or aerosoles,CDC has recommended sanitizing hands with 60-95% alcohlo based hand sanitizers or washing hands with soap water for at least 20 seconds to check the spread of corona virus.

REFERENCES:https://bit.ly/34vrdlm Clinical Infectious Diseases, online October 3, 2020.

BREATH HOLDING ATTACKS,DR.DEV,M.D.,Pediatrician and Pediatric Pulmonologist,Sahibabad,Ghaziabad,Delhi NCR

Breath holding spells is not uncommon in children.

The phenomenon is very much frightening to the parents.

It is usually seen in children after the age of 6 months.

It usually starts between the age of 6-18 months and mostly observed in the age group of 1-3 years.

It abolishes automatically after 4-6 years of age.

There is no difference between male and female.

There are two types of attacks-1.Pallid spells and 2. cyanotic spells

In pallid spells, the heart rate of the child becomes slow,the child looks pale(more white) and there is loss of consciousness for few seconds ,but definitely ,less than 60 seconds(1 minute).

The pallid spell is usually triggered by pain ,like fall from the bed ,fall on the ground while playing,or minor impact on head of child by gently slapping.

In CYANOTIC SPELLS-

The colour of child becomes blue or purple specially around the lips.It is triggered by aggression,frustation,emotional distrubances and crying in fear or frightening environment to the child.There occurs a short burst of cry or single cry in which at the end of cry the child exhales for a slightly long period and holds the breath in exhalaltion ,not followed immediately by inhalation.There is loss of consciousness for a brief period ,not more than a minute.The muscels of the body may becomes stiff and there may be arching of the body in backward direction.Sometimes,there may be abnormal body movement and rarely there may be seizure.

This phenomena is typically described by parents as the child sometimes forget to take breath.

WHAT TO DO IN THESE SITUATIONS:This condition is harmless to the child with no long term effect on the brain and growth of the child.

The parent should not panic and should be very calm and comfortable.Those objects which may cause injury to the child and particularly sharp objects should be taken away from near of the child.

Make the child lie on the lap.

Do not through water on the face of the child as is usually practiced.It may be dangerous.

The child regain consciousness within a minute.If not,take the child to a doctor/clinic/hospital nearby.

If this episode is the first time,certainly go to the doctor/clinic/hospital.This is because, there may be some serious problems in heart and or brain of the child leading to these symptoms.There may be seizure disorder presenting like this.There may be congenital prolonged QT syndrome presenting like this.

If by proper clinical examination and if required proper investigations,it becomes clear that it is not due to any pathology in the brain and or heart,nothing to be worried.

It has been observed that ,these attacks are more common in children suffering from iron deficiency anemia

It should be investigated and treated ,the child becomes normal.

In some children,the episodes happens many times a day and in others only after few days or months.

It has been seen that ,it happens more frequently in circumstances where parents are more apprehensives.

So,parents should take care of themselves,not to show apprehensions in front of children and not to allow secondary gain to children.

Sometimes ,the episode becomes life threatening,and parents should learn ,how to resuscitate babies by giving mouth to mouth breath and chest compressin if required.

Sometimes ,medications in the form of atropine may be required,which should strictly be used by a qualified medical doctor.