PERTUSSIS (also known as WHOOPING COUGH or 100-DAY COUGH) is a highly contagious bacterial disease . Initially, symptoms are usually similar to those of the common cold with a runny nose , fever , and mild cough . This is then followed by weeks of severe coughing fits. Following a fit of coughing, a high-pitched whoop sound or gasp may occur as the person breathes in. The coughing may last for 10 or more weeks, hence the phrase "100-day cough". A person may cough so hard that they vomit, break ribs , or become very tired from the effort. Children less than one year old may have little or no cough and instead have periods where they do not breathe . The time between infection and the onset of symptoms is usually seven to ten days. Disease may occur in those who have been vaccinated, but symptoms are typically milder.
Prevention is mainly by vaccination with the pertussis vaccine .
Initial immunization is recommended between six and eight weeks of
age, with four doses to be given in the first two years of life. The
vaccine becomes less effective over time, with additional doses often
recommended for older children and adults.
An estimated 16.3 million people worldwide were infected in 2015. Most cases occur in the developing world , and people of all ages may be affected. In 2015, it resulted in 58,700 deaths – down from 138,000 deaths in 1990. Nearly 0.5% of infected children less than one year of age die. Outbreaks of the disease were first described in the 16th century. The bacterium that causes the infection was discovered in 1906. The pertussis vaccine became available in the 1940s.
* 1 Signs and symptoms
* 1.1 Incubation period
* 2 Cause
* 2.1 Spread from other animals
* 3 Mechanism * 4 Diagnosis
* 5 Prevention
* 5.1 Vaccine
* 6 Treatment * 7 Prognosis
* 8 Epidemiology
* 8.1 US outbreaks
* 9 History
* 9.1 Discovery * 9.2 Vaccine * 9.3 Controversy
* 10 References * 11 External links
SIGNS AND SYMPTOMS
Play media A boy with pertussis
The classic symptoms of pertussis are a paroxysmal cough, inspiratory
whoop, and fainting , or vomiting after coughing. The cough from
pertussis has been documented to cause subconjunctival hemorrhages ,
rib fractures , urinary incontinence , hernias , and vertebral artery
dissection . Violent coughing can cause the pleura to rupture,
leading to a pneumothorax .
The illness usually starts with mild respiratory symptoms, mild coughing, sneezing, or a runny nose . This is known as the catarrhal stage. After one to two weeks, the coughing classically develops into uncontrollable fits, each with five to ten forceful coughs, followed by a high-pitched "whoop" sound in younger children, or a gasping sound in older children, as the person tries to inhale (paroxysmal stage).
Coughing fits can occur on their own or can be triggered by yawning, stretching, laughing, eating, or yelling; they usually occur in groups, with multiple episodes on an hourly basis throughout the day. This stage usually lasts two to eight weeks, or sometimes longer. A gradual transition then occurs to the convalescent stage, which usually lasts one to four weeks. This stage is marked by a decrease in paroxysms of coughing, both in frequency and severity, and a cessation of vomiting. A tendency to produce the "whooping" sound after coughing may remain for a considerable period after the disease itself has cleared up.
The time between exposure and the development of symptoms is on average 7–14 days (range 6–20 days), rarely as long as 42 days.
SPREAD FROM OTHER ANIMALS
Uncertainties have existed of B. pertussis and whooping cough as a zoonotic disease since around 1910 but in the 1930s, knowledge was gained that the bacteria lost their virulent power when repeatedly spread on agar media. This explained the difficulties to reproduce results from different studies as the pre-inoculating handlings of the bacteria were not standardized among scientists.
Today it is established that at least some primate species are highly susceptible to B. pertussis and develop clinical whooping cough in high incidence when exposed to low inoculation doses. The bacteria may be present in wild animal populations, but this is not confirmed by laboratory diagnosis, although whooping cough is known among wild gorillas . Several zoos also have a long-standing custom of vaccinating their primates against whooping cough.
It acts primarily via its pertussis toxin but also via invasion of tissues and alveolar macrophages. B. pertussis attaches to the cilia of respiratory epithelial cells, where it produces cilia-paralyzing toxins, and causes inflammation of the respiratory tract, thereby interfering with the "mucociliary escalator" by which pulmonary secretions (i.e., mucus) are cleared.
Gram stain of
A physician's overall impression is most effective in initially making the diagnosis. Single factors are much less useful.
Methods used in laboratory diagnosis include culturing of nasopharyngeal swabs on a nutrient medium (Bordet-Gengou medium ), polymerase chain reaction (PCR), direct fluorescent antibody (DFA), and serological methods (e.g. complement fixation test ). The bacteria can be recovered from the person only during the first three weeks of illness, rendering culturing and DFA useless after this period, although PCR may have some limited usefulness for an additional three weeks.
Serology may be used for adults and adolescents who have already been infected for several weeks to determine whether antibody against pertussis toxin or another virulence factor of B. pertussis is present at high levels in the blood of the person. By this stage, they have been contagious for some weeks and may have spread the infection to many people. Because of this, adults, who are not in great danger from pertussis, are increasingly being encouraged to be vaccinated.
A similar, milder disease is caused by B. parapertussis .
The primary method of prevention for pertussis is vaccination . Evidence is insufficient to determine the effectiveness of antibiotics in those who have been exposed, but are without symptoms. Preventive antibiotics, however, are still frequently used in those who have been exposed and are at high risk of severe disease (such as infants).
The multicomponent acellular pertussis vaccine is 71–85% effective, with greater effectiveness for more severe strains. Despite widespread vaccination, however, pertussis has persisted in vaccinated populations and is today "one of the most common vaccine-preventable diseases in Western countries". The 21st-century resurgences in pertussis infections are attributed to a combination of waning immunity and bacterial mutations that elude vaccines.
Immunization does not confer lifelong immunity; a 2011 CDC study indicated that protection may only last three to six years. This covers childhood, which is the time of greatest exposure and greatest risk of death from pertussis.
An effect of widespread immunization on society has been the shift of reported infections from children aged 1–9 years to infants, adolescents, and adults, with adolescents and adults acting as reservoirs for B. pertussis and infecting infants with fewer than three doses of vaccine.
Both WHO and the CDC found that the acellular pertussis vaccines were effective at prevention of the disease, but had a limited impact on infection and transmission, meaning that vaccinated people could act as asymptomatic reservoirs of infection.
The antibiotics erythromycin , clarithromycin , or azithromycin are typically the recommended treatment. Newer macrolides are frequently recommended due to lower rates of side effects. Trimethoprim-sulfamethoxazole (TMP/SMX) may be used in those with allergies to first-line agents or in infants who have a risk of pyloric stenosis from macrolides.
A reasonable guideline is to treat people age >1 year within 3 weeks of cough on