Monday 30 April 2012

"Sustain Gains, Save Lives"


“Sustain Gains, Save Lives” was the theme for this year’s World Malaria Day which was on the 25th of April.

Global efforts to combat malaria have saved over one million lives worldwide and reduced malaria deaths in Africa by over 33% in 10 years according to the World Health Organisation. Despite this reported success there is a need to sustain this progress in the global campaign against malaria, and this can be done through increased investment and smarter inventions.

Tony Blair, the former UK Prime Minister, does not see any reason why malaria – an utterly preventable disease – cannot be eradicated in Africa and elsewhere.  Prevention and treatment of malaria is cheap. One insecticide-treated net plus distribution costs less than $10 while anti-malaria drug is less than $2 per person.


Rapid Diagnostic Tests (RDTs) help in the diagnosis of malaria by detecting evidence of malaria parasites in human blood. They allow the testing of people who cannot access diagnosis based on microscopy. Photo by Novartis AG

There is a challenge at present to raise around $3.2 billion to get to the point of a near-zero deaths by 2015. This additional funding would be used to purchase bed nets, which needs to be replaced every three years – this help control malaria as well as address the issue of drug resistance – and facilitate access to medicines and rapid diagnosis.

Children holding bed nets. Photo by Afrika Force

The African Leaders Malaria Alliance with Liberian President Ellen Johnson Sirleaf as its new chairman has agreed to close this resource gap through the following measures:

  • Using World Bank funding to protect the eradication campaign’s progress and prevent a resurgence of the disease

  • Increasing domestic financing for health services to achieve a previously agreed target allocation of 15% of public sector budgets to the health sector

  • Considering innovative financing approaches to further expand Africa’s resource pool for health


However several donors and organization are doing a lot to eradicate malaria.

  • Partnership for Transforming Health System 2 is working with the Clinton Health Access Initiative to help distribute artemisinin-based combination therapies in five Nigerian states through the Affordable Medicines Facility for malaria initiative, an innovative financing mechanism designed to expand countries access to ACT.
  • African Development Bank meanwhile is helping support the control of communicable diseases in the Southern African Development Community region with a $30 million grant.
  • The World Health Organization is also playing a part by launching a new initiative tagged T3: Test, Treat, Track. This initiative urges the global health community to scale up diagnostic testing, treatment and surveillance of malaria.


These new initiatives are a welcome addition to the many other program working to bring malaria deaths to a near-zero.

Monday 9 April 2012

Lassa Fever In Nigeria


At the beginning of 2012, the Federal Ministry of Health in Nigeria notified the World Health Organisation of an outbreak of Lassa Fever in the country. As of 22nd March 2012, 623 suspected cases have been recorded and this includes 70 deaths from 19 out of the 36 States since the beginning of the year. Among the fatalities are 3 doctors and 4 nurses. The presence of the Lassa virus has been confirmed in 108 patients by laboratory analysis at the Irrua Specialist Teaching Hospital, Irrua, Edo State.   (It must be noted that this information is provisional and subject to change as more laboratory results of suspected cases becomes available.)

The Federal and State government have responded to the outbreak by setting up an emergency response team for the purpose of enhancing the disease surveillance to enable early detection, reinforce treatment of patients and conduct awareness campaigns among the affected population.

WHO does not advise or recommend any restriction on travel or trade with Nigeria but travellers returning from affected areas are however advised to seek medical advice if they develop symptoms of fever, malaise, headache, sore throat, muscle pain, chest pain, nausea, vomiting, diarrhoea and abdominal pain.


From this report it can be seen that Lassa fever cases have continue to increase in Nigeria. A previous report dated 22nd February 2012 stated that in the first six weeks of 2012 there had been 392 cases of Lassa fever and 40 fatalities across the country. The Minister of Health reported that 2 doctors and 4 nurses were among the dead and cases were reported in 12 states: Edo, Nasarawa, Plateau, Ebonyi, Taraba, Yobe, Ondo, Rivers, Gombe, Anambra, Delta and Lagos. Currently the outbreak has spread to 19 states.

Map of Nigeria

Lassa fever is a zoonotic disease caused by the Lassa virus. The rodent of the genus Mastomys – commonly known as the “multimammate rat” – is the animal reservoir host for the Lassa virus. Mastomys rodents infected with the Lassa virus do not become ill and they shed the virus in their excreta.

Image from CDC: Special Pathogen Branch

The virus was first discovered in 1969 when two missionary nurses died in the town of Lassa, Borno State, Nigeria.

Humans become infected with the Lassa virus when they are exposed to the excreta of infected Mastomys rodents and the infection can spread further between humans through direct contact with the blood, urine, faeces or other bodily secretions of persons with Lassa fever. Person-to-person transmission occurs in both community and health care settings where the virus may spread through contaminated medical equipment such as re-used needles. The virus is present in semen for up three months after the disease begins, thus sexual transmission of Lassa virus can occur however there is no epidemiological evidence supporting airborne spread of the virus between humans.

In the absence of an effective vaccine, rodent control is the best option for the control of the current outbreak. Health care workers should also follow strict hygiene procedures during nursing of patients so as to prevent secondary cases.

Other preventive measures include:
  • Good personal hygiene
  • Good environmental hygiene
  • Blocking all rodent hideouts
  • Food items like grains, garri, yam powders etc which are used at homes should be stored in plastic sealed containers or rodent-proof containers and not in cartons or bags.
  • Do not spread or keep food where rats can have access to them
  • Clean the top of any can drink before mouthing or better still use a straw
  • Public awareness about the outbreak of Lassa fever is also vital

Friday 6 April 2012

Ongoing Investigation On The Outbreak Of Shigella flexneri Among MSM in UK


Shigellosis, also called bacillary dysentery, is caused by four species namely: Shigella dysenteriae, Shigella flexneri, Shigella boydii and Shigella sonnei. Shigella was discovered over 100 years ago by the Japanese microbiologist, Kiyosi Shiga for whom the genus is named.

Bacillary dysentery is primarily a human disease often transmitted by the consumption of food or drinking water contaminated with human faeces. Shigellosis can also be transmitted sexually. Sexual transmission of Shigella was first described in the United States during the 1970s. Since then, several outbreaks of sexually transmitted Shigella, predominantly in Men who have Sex with Men (MSM), have been reported. In 2006, an outbreak of Shigella among MSM in London coincided with a similar outbreak in Berlin suggesting that travel plays a role in introducing Shigella species to populations at risk. Man is the only significant reservoir of Shigella infection.

Other enteric illnesses, such as those caused by hepatitis A, Entamoeba histolytica, Giardia lamblia, Campylobacter, and Salmonella, also can be transmitted sexually. Because faeces can contain multiple pathogens, polymicrobial infections can result from a single sexual exposure. Outbreaks of sexually transmitted shigellosis might be observed more frequently than outbreaks of other sexually transmissible enteric organisms because the infectious dose is lower - as few as 10 to 100 organisms can cause disease - the illness produces symptoms that are more likely to bring patients to medical attention, and laboratory diagnosis is simpler.

The incubation period is between 12 and 96 hours. Illness is characterized by diarrhea, sometimes with blood and mucus and is common amongst young children although infection can occur in all ages after travel to areas where hygiene is poor. Invasive disease is rare but extra intestinal complications such as Haemolytic Uraemic Syndrome can occur. Cases maintain a low level of infectivity for as long as the organism is excreted in the stool. Shigella species may survive for up to 20 days in favorable environmental conditions and this may lead to transmission through contact with contaminated fomites.

In the Eurosurvelliance an article was published on an ongoing investigation by the Health Protection Agency (HPA) into the outbreak of Shigella flexneri serotype 3a in men who have sex with men in England and Wales using data from 2009 to 2011. An increase in UK-acquired cases of the infection was detected in London in November 2010 and Greater Manchester during the spring of 2011 and as a result a national outbreak control team (OCT) was established in September 2011 and an enhanced surveillance was set up to collect additional information for all laboratory-confirmed cases with sample dates between 1 September and 31 December 2011.

S. flexneri diagnoses reported by the national laboratories between 2001 and 2011 were also analysed to provide context to the current outbreak and to produce historical time trends.

One hundred and forty-five S. flexneri cases were diagnosed during the enhanced surveillance period between September and December 2011. Thirty-seven (25.5%) of these cases were non-travel related – a non-travel related case was defined as a laboratory confirmed case of S. flexneri with a specimen date between 1 September and 31 December 2011 with no recent travel.

Thirty-one of these cases were confirmed as being UK-acquired whereas six reported diagnoses were likely to be secondary cases linked to a symptomatic contact with recent travel to a high-risk country.

Eighty-six cases (59.3%) were associated with travel to high-risk countries - high-risk travel-associated diagnoses was defined as individuals who returned to the UK in the four days before onset of illness after travel to countries with high risk for Shigella infection (South America, Asia and Africa) - and the travel history was unknown for 22 individuals (15.2%). No low-risk travel-associated cases of S. flexneri were reported during the enhanced surveillance period - low-risk travel-associated individuals was defined as individuals who returned to the UK in the four days before onset of illness after travel to countries with low risk for Shigella infection (Europe, North America and Australia).

The UK-acquired cases were mainly males (n=26) with eleven of these male cases reporting MSM activity in the week before developing gastroenteritis. Interviews with seven MSM cases showed that they all had one long term partner and attended regular medical examinations. However, all cases reported having a casual sexual partner in the week preceding illness. These interviews revealed lack of awareness about Shigella and of the risks associated with unprotected oral and oral-anal sex. Ten of the thirty-one reported UK-acquired S. flexneri cases were serotype 3a.

From there investigations it was discovered that the historical time trends in diagnosed cases of shigellosis between 2001 and 2011 showed a gradual increase in the number of cases in both males and females with no or unknown history of travel up until 2008. However, from 2009 onwards, the number of diagnosed male cases increased rapidly compared to that of females.

Based on this study a strong association was observed between UK-acquired S.flexneri and transmission in MSM despite the fact that some individuals refused to disclose their sexual orientation. This outbreak will continued to be monitored, in the mean time some control measures aimed at effective management of cases and prevention of transmission have been put in place.

These include:
  • Awareness among clinicians and MSM
  • Prompt diagnosis and treatment
  • Increased testing of MSM with diarrhoea
  • Treatment of laboratory confirmed cases

As well as behavioural changes such as:
  • Wash hands after use of toilets, before preparing or eating food and after sexual activity;
  • Avoid anal sex, oral-anal, scat and rimming whilst symptomatic and until test for infection shows clearance;
  • Use of condoms, gloves, dental dams during sex;
  • Avoid sharing douching materials and sex toys;
  • Avoid swimming pools and spa centres whilst ill and for two weeks after recovery.
Work is still ongoing by the investigators into identifying other risk factors for infection and evaluating other possible control measures such as screening of asymptomatic contacts.