Rubella: A Comprehensive Review

Nikita Girnare , Sameera Kara , Krishnarati Patil* , Rajeshree Padvi

Ali Allana College Of Pharmacy Akklkuwa. Nandurbar  (MH) India

*Correspondence: patilkrishnarati@gmail.com;

INTRODUCTION

Rubella, or German measles, is a mild viral infection that typically occurs in children and non-immune young adults. It typically begins with low-grade fever, malaise, and lymphadenopathy, followed by a brief generalized erythematous maculopapular rash. [1][2]

In nonpregnant individuals, rubella is generally a self-limited and benign infection. However, maternal rubella infection, especially during the first 10 weeks of gestation, can result in miscarriage, fetal death, or severe birth defects collectively known as congenital rubella syndrome (CRS). [3]

After the introduction of the live attenuated rubella vaccine in 1969, the incidence of rubella infection has decreased dramatically in many countries and was effectively eradicated from the United States; however, rubella remains a public health concern and a significant source of disability around the world. [2]

ETIOLOGY

Rubella virus is the sole member of the genus Rubivirus within the newly classified Matonaviridae family. [4] It is a single-stranded, positive sense enveloped RNA virus. Rubella virus encodes two non-structural proteins (p90 and p150) and three structural proteins; glycoprotein (E1 and E2) and the capsid protein (CP). The E1 protein is responsible for receptor-mediated endocytosis and induces the immune response through hemagglutination-neutralizing epitopes. [5][6] The virus is sensitive to heat (temperature >56°C), ultraviolet light, and extremes of pH (pH <6.8 or >8.1). [1]

EPIDEMIOLOGY

In the pre-vaccine era, the peak incidence of rubella was in children aged 5 to 9 years, and the peak rates usually occur in late winter and early spring, with sporadic cases appearing year-round in temperate climates. [1][2][5] After the implementation of widespread vaccination in the United States, rubella has become increasingly rare, with only occasionally imported cases from those countries where rubella is endemic. [1]

Rubella affects both sexes equally in children, whereas in adults, rubella affects more women than men. [1] After the introduction of the live-virus vaccine, outbreaks occurred more commonly among older adolescents and young adults. [4][5] Risk factors for rubella include under-vaccinated or unvaccinated individuals, traveling to endemic areas, exposure to household members with rubella, and immunodeficiency. [1]

In countries where rubella is endemic, it is estimated to occur at a rate of 1.30/100,000 in the general population. [2]

PATHOPHYSIOLOGY

Humans are the only known reservoir for rubella. The virus is contracted through person-to-person contact via aerosolized particles from the respiratory tract secretions of affected individuals. [1][2][5] After infecting the cells of the susceptible host through receptor-mediated endocytosis, the virus replicates in the nasopharyngeal cells and then spreads to the regional lymphoid tissue of the nasopharynx and upper respiratory tract. This process is followed by a viremic phase, which is characterized by hematogenous dissemination of the virus to multiple organs, and it usually occurs 5 to 7 days after inoculation. The exanthem appears approximately 2 to 8 days after the onset of viremia and resolves 3 days later as the humoral immune response develops. [1] An infected individual is contagious from 8 days before to 8 days after the onset of the rash. [2] Immunity acquired after recovering from natural infection or through vaccination is life-long; however, reinfection has been reported after both wild type rubella infection and after receiving one dose of rubella vaccine. [2]

In congenital rubella syndrome (CRS), fetal infection occurs transplacentally during the maternal viremic phase. [1] The risk of transmission to the fetus depends on the time of maternal infection; when infection with rubella occurs before 10 weeks of gestation, it may cause multiple fetal defects in up to 90% of cases. The risk of congenital defects declines with infection later in gestation. The pathogenesis of CRS is multifactorial and not well understood. [2] In CRS, damage to the fetus may result from several mechanisms including epithelial necrosis of chorionic villi, apoptosis of infected cells by direct viral damage, inhibition of mitosis, and restricted development of precursor cells by the virus, and cytopathic damage to endothelial cells of blood vessels resulting in ischemia of developing organs. [1]

HISTORY AND PHYSICAL

Postnatal infection with rubella can be asymptomatic in approximately 25% to 50% of the patients, especially in young children. The incubation period ranges from 14 to 21 days and is followed by a prodromal illness characterized by low-grade fever, malaise, anorexia, headaches, sore throat, and adenopathy. The lymphadenopathy typically involves postauricular, suboccipital, and anterior cervical lymph nodes. The exanthem could be the first manifestation in children and consists of pinpoint pink macules and papules that classically begin on the face and rapidly spreads to involve the trunk and extremities. Occasionally, the rash is scarlatiniform or purpuric. The rash typically lasts for 3 days and fades in the same directional pattern as it appears. [1] Petechiae on the soft palate (Forchheimer spots) can also be observed in approximately 20% of the patients. 

Rubella infection during embryogenesis leads to the classic triad of cataracts, congenital heart defects, and sensorineural deafness; however, many other defects might be observed. During the neonatal period, CRS has been associated with low birth weight, thrombocytopenic purpura, hemolyticanemia, hepatosplenomegaly, and meningoencephalitis. These manifestations are usually transient. Other clinical manifestations of CRS include ophthalmopathies (retinopathy, glaucoma, chorioretinitis, iris hypoplasia, and microphthalmia), cardiac abnormalities (patent ductus arteriosus, pulmonary artery hypoplasia), psychomotor retardation, and microcephaly.

Of all the manifestations, deafness is the most common finding and could be the only defect observed. Individuals that survive the neonatal period may face severe disabilities (e.g., visual and hearing impairments) and have an increased risk for developmental disorders, including autism. In addition, a variety of late-onset endocrine, cardiovascular and neurological abnormalities have been described. [1][2]

TREATMENT / MANAGEMENT

Treatment of postnatally acquired rubella in non-gravid individuals is mainly supportive and consists of the use of non-steroidal anti-inflammatory drugs for fever, arthralgia and/or arthritis. [1] In pregnant women, the management depends on the gestation age at the onset of infection. [2] If the infection occurs before 18 weeks of gestation, the fetus is at high risk for infection and subsequent malformation, and management should include the consideration of pregnancy termination according to local ethical and legislative regulations. If the infection occurs after 18 weeks of gestation, the pregnancy could be continued with ultrasound monitoring and specific neonatal management. [2]  Treatment of children with congenital rubella syndrome should be symptomatic and organ-specific. It usually involves a multidisciplinary approach and requires pediatric, ophthalmologic, cardiac, audiological, and neurodevelopmental evaluation. Long-term follow up is needed to monitor for delayed manifestations. [1]

DIFFERENTIAL DIAGNOSIS

Rubella needs to be distinguished from other infections with similar maculopapular rashes, including measles, human herpesvirus 6 and 7, infectious mononucleosis, cytomegalovirus, arboviruses (Zika virus, West Nile fever, Ross River fever, and Chikungunya virus), enteroviruses, scarlet fever, and mycoplasma infection. Other conditions to be considered in the differential diagnosis for rubella are non-infectious causes like Kawasaki disease, drug eruption, and contact dermatitis. [1]

PROGNOSIS

Rubella infection of children and adults is usually mild, self-limiting and often asymptomatic. However, the prognosis of children with congenital rubella syndrome is less favorable and varies depending on the severity and number of organs affected. The risk of mortality risk is high in infants with thrombocytopenia, interstitial pneumonia, and pulmonary hypertension. Also, individuals with congenital rubella syndrome are at risk of long-term complications, including blindness, cardiac failure, developmental delays, and reduced life expectancy. [1]

COMPLICATIONS

The development of polyarthritis and polyarthralgia is the most common complication of rubella infection, affecting up to 70% of adolescents and adult women. It is usually symmetric and involves the wrists, fingers, knees, and ankles. Other manifestations, although rare, include thrombocytopenia, hemolyticanemia, myocarditis, pericarditis, hepatitis, orchitis, retinopathy, uveitis, Guillain-Barré syndrome, and post-infection encephalitis. Rubella infection during pregnancy may lead to miscarriage, intrauterine fetal demise, premature labor, intrauterine growth retardation, and congenital rubella syndrome.  The risk of developing complications is highest if the infection is contracted within the first 12 weeks of gestation. [1]

PATIENT EDUCATION

Parents should be educated and counseled on the importance of routine immunization in infants and young children. It is also essential to identify and immunize all susceptible women of childbearing age prior to conception. 

ENHANCING HEALTHCARE TEAM

Suspected cases of rubella should be notified immediately to the Centers for Disease Control and Prevention (CDC). Once the diagnosis of rubella is confirmed, the patient should be promptly isolated for at least 7 days after onset of the rash. Because rubella is transmitted primarily by inhalation of virus-laden airborne droplets, standard and droplet precautions are recommended for hospitalized patients. The management of congenital rubella syndrome should include a multidisciplinary team, as previously discussed. Children with congenital Srubella syndrome can shed the virus in saliva and urine for several months and therefore are contagious. These individuals should be isolated until two pharyngeal or urine cultures have negative results. [1]

CONCLUSION

Congenital Rubella Syndrome is a constellation of abnormalities found in individuals who were infected with the rubella virus before birth, Manifestation may be transient and limited to the newborn period or permanent be present at birth or develop over the lifespan of an involved individual. Almost every body system can be involved brain, eyes, ears, heart, lungs, liver, endocrine glands, gastrointestinal tract. No cure is available but therapy is aimed at improved quality of life and may include corrective surgery, hearing aids, OT, PT, and SLP therapy and others. CRS can be prevented by immunization with MMR or Rubella vaccine.

ACKNOWLEDGMENTS

I would like to express my special thanks of gratitude to subject teacher Dr. Qazi Majaz for their able guidance and support completing our project.

I would also like to extend my gratitude to principal sir Dr. G J Khan for providing me with all the facility that was required.                             

REFERENCE

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4.      Woyessa AB, Ali MS, Korkpor TK, Tuopileyi R, Kohar HT, Dogba J, Baller A, Monday J, Abdullahi S, Nagbe T, Mulbah G, Kromah M, Sesay J, Yealue K, Nyenswah T, Gebrekidan MZ. Rubella transmission and the risk of congenital rubella syndrome in Liberia: a need to introduce rubella-containing vaccine in the routine immunization program. BMC Infect Dis. 2019 Sep 18;19(1):813. 

5.      Pukuta E, Waku-Kouomou D, Abernathy E, Illunga BK, Obama R, Mondonge V, Dahl BA, Maresha BG, Icenogle J, Muyembe JJ. Genotypes of rubella virus and the epidemiology of rubella infections in the Democratic Republic of the Congo, 2004-2013. J Med Virol. 2016 Oct;88(10):1677-84.

6.      https://pubmed.ncbi.nim.nih.gov/16022642/