Saturday, May 26, 2018

Awareness needs to be created to dispel fears about Nipah virus




Another aspect of the Nipah outbreak is coming to light, and a rather unfortunate one at that.

Yesterday, the TOI Kozhikode edition reported that health workers are facing social ostracism with reports of nurses being ostracized and staff at a crematorium allegedly showing reluctance to cremate the body of a victim who fell prey to the deadly virus.

Doctors and nurses work tirelessly and with devotion for their patients, whose interests and welfare are above all for doctors and nurses.  

Doctors and nurses are doing their duty to care for the affected patients without concern for their own personal safety. Nipah is a potentially life-threatening illness. A nurse passed away days after she acquired the infection as she was part of the team that treated the first victim of the Nipah virus.

Such dedicated service should be recognized, respected and accorded a national honor. This would have surely merited an honor if it were the military personnel.

This social ostracism indicates the extent of fear and panic amongst the public and also highlights the need to create awareness about the disease in question. The public should not react in such a manner. More importantly, the media should not overplay such stories. They should instead run awareness campaigns to dispel various fears and doubts among the public.

Dr KK Aggarwal
Padma Shri Awardee
Vice President CMAAO
Group Editor-in-Chief IJCP Publications
President Heart Care Foundation of India
Immediate Past National President IMA


Friday, May 25, 2018

On this World Malaria Day, let us pledge to “Test. Treat. Track” every malaria case


India is a malaria endemic country. The reported malaria cases in the country last year have declined by 23% compared to 2016, yet India still accounts for 87% of malaria cases in the South Asia region. Also, as per the World Malaria Report, India has among the weakest malaria surveillance systems globally, with only 8% of cases detected by the surveillance system.

The World Health Organization (WHO) Global Technical Strategy for Malaria has set a target of reducing malaria case incidence by at least 90%, reducing malaria mortality rates by at least 90%, eliminating malaria in at least 35 countries and preventing a resurgence of malaria in all countries that are malaria-free.

There is still a long road ahead before the goal of elimination of malaria throughout the country by 2030 is achieved.

Malaria is entirely a preventable disease. It is also a treatable disease provided it is diagnosed and treated in time. The symptoms of malaria are non specific and can be variable. So it may be mistaken for other diseases such as viral infections, typhoid and the diagnosis of malaria may be missed as a result.

It is important to remember here that malaria is not a clinical diagnosis; the diagnosis has to be confirmed by microscopy or a rapid diagnostic test (RDT).

The ‘T3’ initiative of the WHO Global Malaria Program supports malaria-endemic countries in their efforts to achieve universal coverage with diagnostic testing and antimalarial treatment, as well as in strengthening their malaria surveillance systems

T3 stands for Test. Treat. Track., which means:

  • Every suspected malaria case should be tested
  • Every confirmed case should be treated with a quality-assured antimalarial medicine
  • The disease should be tracked through a timely and accurate surveillance system.

Adopting and implementing this initiative will be a step in the right direction in the efforts to control and eliminate malaria.


Every patient of fever must be investigated for malaria to either confirm the diagnosis or exclude it as a cause of fever.

Thursday, May 24, 2018

Investigate your patients for iron deficiency




Many patients present to us with complaints of exertional dyspnea or tachycardia. Such patients may undergo extensive cardiovascular assessment, indicating an underlying sinister pathology for their symptoms. While this evaluation is justified, sometimes the underlying cause may not be so dangerous.

Iron deficiency, even before a full-fledged anemia develops may be the cause of such symptoms, which have been shown to improve on iron supplementation.

Iron deficiency (depleted iron stores in the body) and anemia are often perceived as interchangeable terms. While iron deficiency is the most common cause of anemia, but the two are different.

Deficiency of iron without anemia is much more prevalent than is detected. A person may have iron deficiency even if the hemoglobin is normal. The majority are unaware of their iron deficient state

Iron has a crucial role in oxidative metabolism within the mitochondria and production of hemoglobin and myoglobin (BMJ Open. 2018 Apr 5;8(4):e019240). Anemia due to iron deficiency impairs oxygen-carrying and tissue oxidative capacity, resulting in a diminished peak oxygen consumption (pVo2) and ability to endure submaximal exertion. Even in the absence of anemia, iron deficiency can attenuate exercise performance (J Am Coll Cardiol. 2008;51(2):103-12).

The FERRIC-HF trial, published in the Journal of the American College of Cardiology in 2008, which examined the effect of intravenous iron sucrose on exercise tolerance in anemic and nonanemic patients with symptomatic chronic heart failure and iron deficiency showed that IV iron supplementation improved exercise capacity and symptoms in patients with CHF and evidence of abnormal iron metabolism. Benefits were more evident in anemic patients.

If the patient has exertional breathlessness or symptoms such as fatigue, palpitations, headache or has a history of frequent absenteeism, also look for iron deficiency as a cause. Iron study, which measures serum iron, ferritin, transferrin, transferrin saturation, total iron-binding capacity should be done. Low serum ferritin is indicative of iron deficiency. Ferritin levels can be elevated by inflammatory processes and can mask iron deficiency (BMJ. 2017;357:j3175).

Iron supplementation, if iron deficiency found, improves functional capacity in these iron-deficient individuals even before anemia is corrected.

Dr KK Aggarwal
Padma Shri Awardee
Vice President CMAAO
Group Editor-in-Chief IJCP Publications
President Heart Care Foundation of India
Immediate Past National President IMA





Wednesday, May 23, 2018

Lipid management: Individualize treatment



Atherosclerotic cardiovascular disease (ASCVD) is a major cause of morbidity and mortality. An acute cardiac event can be prevented by effective management of risk factors including dyslipidemia, which is a major risk factor for initiation and progression of the atherosclerotic process and thereby to cardiovascular events. Hence, managing the dyslipidemia-related cardiovascular risk in these patients is important for secondary prevention of CAD.

Major professional cardiology and endocrinology associations have issued guidelines on management of dyslipidemia, which differ in their approaches in managing lipids in these patients regarding assessment of risk, lipid goals and targets and pharmacological treatment.

Latest in this list of guidelines on management of dyslipidemia are recommendations from the American Association of Clinical Endocrinologists and American College of Endocrinology (AACE/ACE) released in 2017. These guidelines have for the first time defined an “extreme” cardiovascular risk category and also bring back the concept of ‘target’-based lipid management.

The AHA/ACC guidelines issued in 2013 had recommended “appropriate intensity” of statin therapy for the four groups of primary- and secondary-prevention patients instead of treating dyslipidemia to specific ‘targets’. Hence, these guidelines removed specific targets or goals for LDL- or non-HDL-cholesterol … a change from the ATP III recommendations in 2001, which advised determination of risk category and set goals according to the risk category.

The 2017 AACE/ACE guidelines have categorized patients into five atherosclerotic cardiovascular disease (ASCVD) risk categories – low risk, moderate risk, high risk, very high and extreme risk - and now recommend lipid goals for all the five categories.

·         Low risk: Individuals with no risk factors: LDL < 130 mg/dL, non-HDL < 160 mg/dL, apoB not relevant is recommended.

·         Moderate risk: Individuals with 2 or fewer risk factors and a calculated 10-year risk < 10%: LDL < 100 mg/dL, non-HDL < 130 mg/dL, apoB < 90 mg/dL is recommended.

·         High risk: Individuals with an ASCVD equivalent including diabetes or stage 3/4 CKD with no other risk factors, or individuals with ≥2 risk factors and a 10-year risk of 10%- 20%: LDL < 100 mg/dL, non-HDL < 130 mg/dL, apoB < 90 mg/dL is recommended.

·         Very high risk: Individuals with established or recent hospitalization for acute coronary syndrome (ACS); coronary, carotid or peripheral vascular disease; diabetes or stage 3/4 CKD with ≥1 risk factors; a calculated 10-year risk > 20%; or heterozygous familial hypercholesterolemia [HeFH]): LDL < 70 mg/dL, non-HDL < 80 mg/dL, apoB < 80 mg/dL is recommended.

·         Extreme risk: Individuals with progressive ASCVD, including unstable angina that persists after achieving an LDL <70 or established clinical ASCVD in individuals with diabetes, stage 3/4 CKD, and/or HeFH, or in individuals with a history of premature ASCVD (males <55 years; females <65 years): LDL < 55 mg/dL, non-HDL < 80 mg/dL, apolipoprotein B (apoB) < 70 mg/dL is recommended.

Lowering cholesterol is important for all age groups, both men and women, regardless of the presence of absence of heart disease. A 1% rise in cholesterol level can raise the chances of heart attack by 2%. 1% reduction of “good” HDL cholesterol increases the chances of suffering from a heart attack by 3%.

However, it is important to keep in mind that every patient is different; hence, treatment, including lipid goals should be individualized according to that particular patient. 

Dr KK Aggarwal
Padma Shri Awardee
Vice President CMAAO
Group Editor-in-Chief IJCP Publications
President Heart Care Foundation of India
Immediate Past National President IMA

Tuesday, May 22, 2018

Nipah virus encephalitis: A newly emerging disease



The cause of death of three people, who were suffering from acute viral encephalitis, in Kozhikode has been confirmed to be due to the Nipah virus by the National Virology Institute in Pune.

Nipah and Hendra viruses are two related zoonotic pathogens that have emerged in the Asia-Pacific region. Both are RNA viruses that belong to the Paramyxoviridae family. The viruses jump the species barrier and infect a secondary animal host (e.g., pigs or horses), and transmit infections to humans

Here are some key facts about Nipah virus infection.

  • Nipah virus infection is a newly emerging zoonosis, which causes severe disease in both humans and animals. The associated mortality is high.

  • The natural hosts for the Nipah virus are the fruit bats of the Pteropus genus, which are symptomless carriers. Mainly four species have been demonstrated to have serologic evidence of infection with this virus. The virus is shed in the saliva, urine, semen and excreta of the infected bats.

  • Nipah virus spreads to humans through direct contact with infected bats, infected pigs, or other people who are infected with the virus. People have been also cautioned to avoid eating fruits that have fallen to the ground.

  • Nipah virus was first identified in 1998 as the cause of an outbreak of viral encephalitis among pig farmers in Malaysia, where pigs were the intermediate hosts. The virus derives its name from Sungai Nipah, a village in the Malaysian Peninsula where the pig farmers became ill with encephalitis.  Since then, several outbreaks of acute Nipah encephalitis have been reported from Bangladesh, West Bengal (Siliguri), India with reports of person-to-person transmission in hospital settings and in the Southern Philippines. Raw date palm sap that had been contaminated by infected fruit bats was identified as the source of infection in an outbreak that occurred in Bangladesh in 2004.

  • The incubation period is 5 to 14 days.

  • Clinically, the main presentation of Nipah virus infection is as an encephalitic syndrome characterized by onset of non specific symptoms - sudden onset of fever, headache, myalgia, nausea and vomiting followed by drowsiness, disorientation and mental confusion. The infected person can become comatose within 24 to 48 hours.

  • The case fatality rate of Nipah encephalitis ranges from 9 to 75%

  • Meningismus is seen in approximately one-third of patients although marked nuchal rigidity and photophobia are uncommon.

  • Patients infected with Hendra virus have presented with fever and influenza like illnesses, or with meningoencephalitis

  • Nipah virus infection can be diagnosed by ELISA test.

  • On MRI, typically multiple, small (less than 5 mm), asymmetric focal lesions in the subcortical and deep white matter without surrounding edema are seen.

  • There is no effective treatment for Nipah virus infection. The mainstay of treatment is supportive care focusing on managing fever and the neurological symptoms. Infection control practices and barrier nursing are important as person-to-person transmission may occur. Severely ill patients need intensive care.

  • Ribavirin, a nucleoside analog, can be given empirically as it has a broad spectrum of antiviral activity against both RNA and DNA viruses. In the Malaysian outbreak, 140 treated patients were compared to 54 control patients who did not receive ribavirin. Fewer treated patients died (32% vs 54%). However, treated patients were identified later in the outbreak so it is possible that they were given better general medical care compared to untreated patients seen earlier. Subsequent animal models found that ribavirin, as well as chloroquine, were ineffective.

  • Anti-thrombotic agents, aspirin and pentoxyfylline, were administered in some patients based upon the recognition that arterial thrombosis may play an important role in the CNS disease. 

  • Nipah virus is classified internationally as a biosecurity level (BSL) 4 agent. Biosafety Level 4 is required for work with dangerous and exotic agents that pose a high individual risk of aerosol-transmitted laboratory infections and life-threatening disease that is frequently fatal, for which there are no vaccines or treatments, or a related agent with unknown risk of transmission (CDC).

Dr KK Aggarwal
Padma Shri Awardee
Vice President CMAAO
Group Editor-in-Chief IJCP Publications
President Heart Care Foundation of India
Immediate Past National President IMA


Monday, May 21, 2018

Notification of adverse drug reactions should be made mandatory




Adverse drug reaction (ADR) reporting or pharmacovigilance is an integral part of quality patient care as ADRs not only impair quality of life for the patient, they also increase treatment costs as they increase the likelihood of hospitalization. At times, they may be potentially life-threatening. The World Health Organisation (WHO) has defined pharmacovigilance as “the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug related problems”.

A database of ADRs will help the clinician to identify any clinical event occurring as a result of a drug being administered and manage it in time. This was the very objective of the Pharmacovigilance Programme of India (PvPI) i.e. to generate data about ADRs across the country by promoting ADR reporting. PvPI is run by the Indian Pharmacopoeia Commission (IPC) as its National Coordination Centre (NCC) under the aegis of the Health Ministry.
Like all programs, several challenges undermine its effectiveness. Under reporting is one such challenge.

PvPI encourages reporting of all types of suspected adverse reactions with all pharmaceutical products irrespective of whether they are known or unknown, serious or non-serious and frequent or rare.

ADRs should be reported without delay as a contribution to the safety profile of a drug, which is still evolving. If this information is given to the competent authorities, hitherto unknown risks can be identified and tackled.

At IJCP, we receive several case reports describing adverse effects of drugs, which are not mentioned in the PvPI database. In view of this, we propose that no case report linked to a drug side effect should be published or presented in a conference unless it is notified in PvPI. We have adopted this as part of our publishing policy.

The Heart Care Foundation of India (HCFI) has also written to IPC in this regard with the suggestion that notification of ADRs to PvPi should be made mandatory before a case report is published in any journal or is presented at a conference or any clinical meeting.

This will help in strengthening the PvPI program.



Dr KK Aggarwal
Padma Shri Awardee
Vice President CMAAO
Group Editor-in-Chief IJCP Publications
President Heart Care Foundation of India
Immediate Past National President IMA



Sunday, May 20, 2018

This has been an unusual summer so far in North




The early summer season or ‘grishma ritu’ is hot and dry, while the later part of summer, when rains are on the horizon is hot and moist.

Rains are not usual in early summer in North India. But, this year, early summer has been marked by an unusually increased frequency of dust storms, thunder storms and rains. In Vedas this is termed vikruti (vitiation) of ritu (season), when the weather forgets its dharma and behaves abnormally.

When this happens, all body circadian rhythms also behave abnormally and every function of the body is exaggerated.

In such weather conditions, wind-sensitive individuals with no evidence of target organ damage can have accelerated hypertension. Such individuals are sensitive to changes in atmospheric pressure.

Modern medicine has no answer for this phenomenon. But, the answer to this may lie in our ancient texts. Atharveda, the fourth Veda, includes the principles of medicine, based on which, Ayurveda has evolved. Ayurveda, which talks of vayu vikruti, has been also called as ‘Upa Veda’ of Atharveda.

“As is the microcosm, so is the macrocosm” is a common Vedic saying. The universe is made up of five elements: space, air, fire, water and earth. These five elements also make human body in the form of three characteristics, which are called Vata, Pitta and Kapha in Ayurveda. In modern medicine language, the Vata represents movement function, Pitta metabolism and Kapha represents structure.

As per Ayurveda, each dosha accumulates (kaya), aggravates (Prakopa) and becomes normal (Prasamana) in different Ritus. Vata (movement function) accumulates in summer, aggravates in rainy seasons and calms down in autumn. Pitta (metabolism) accumulates in rainy season, aggravates in autumn (Sharad Ritu) and calms down in early winter. Kapha (structure and secretions) accumulates in late winter, aggravates in spring (Vasant Ritu) and calms down in summer.

Vitiation of Vata (movement) leads to high blood pressure, arrhythmia; pitta (metabolism) increases metabolism and more acidity, while vitiated Kapha (structure) may disrupt sugar profile.

In the current wind storms in Delhi, we saw a large number of patients developing accelerated hypertension.

Any change in environment affects the functions of the body. This is well-known in Vedic sciences. Modern medicine should look into it and find answers to this phenomenon.

Dr KK Aggarwal
Padma Shri Awardee
Vice President CMAAO
Group Editor-in-Chief IJCP Publications
President Heart Care Foundation of India
Immediate Past National President IMA