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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="research-article"><?properties manuscript?><front><journal-meta><journal-id journal-id-type="nlm-journal-id">101155475</journal-id><journal-id journal-id-type="pubmed-jr-id">30416</journal-id><journal-id journal-id-type="nlm-ta">Expert Rev Vaccines</journal-id><journal-id journal-id-type="iso-abbrev">Expert Rev Vaccines</journal-id><journal-title-group><journal-title>Expert review of vaccines</journal-title></journal-title-group><issn pub-type="ppub">1476-0584</issn><issn pub-type="epub">1744-8395</issn></journal-meta><article-meta><article-id pub-id-type="pmid">28276305</article-id><article-id pub-id-type="pmc">5544348</article-id><article-id pub-id-type="doi">10.1080/14760584.2017.1294069</article-id><article-id pub-id-type="manuscript">HHSPA882217</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Severe varicella in persons vaccinated with varicella vaccine (breakthrough
varicella): a systematic literature review</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Leung</surname><given-names>Jessica</given-names></name><degrees>MPH</degrees><xref ref-type="aff" rid="A1">1</xref><xref rid="FN1" ref-type="author-notes">*</xref></contrib><contrib contrib-type="author"><name><surname>Broder</surname><given-names>Karen R.</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="A2">2</xref></contrib><contrib contrib-type="author"><name><surname>Marin</surname><given-names>Mona</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="A1">1</xref></contrib></contrib-group><aff id="A1">
<label>1</label>Epidemiology Branch, Division of Viral Diseases, National Center for
Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta,
GA, USA</aff><aff id="A2">
<label>2</label>Immunization Safety Office, Division of Healthcare Quality Promotion,
National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control
and Prevention, Atlanta, GA, USA</aff><author-notes><corresp id="FN1"><label>*</label>Corresponding author: Jessica Leung, MPH, Centers for Disease
Control and Prevention, 1600 Clifton Rd NE, MS A-34, Atlanta, GA 30333, Tel: 404-639-6067,
Fax: 404-315-2486, <email>JLeung@cdc.gov</email></corresp></author-notes><pub-date pub-type="nihms-submitted"><day>7</day><month>6</month><year>2017</year></pub-date><pub-date pub-type="epub"><day>28</day><month>2</month><year>2017</year></pub-date><pub-date pub-type="ppub"><month>4</month><year>2017</year></pub-date><pub-date pub-type="pmc-release"><day>04</day><month>8</month><year>2017</year></pub-date><volume>16</volume><issue>4</issue><fpage>391</fpage><lpage>400</lpage><!--elocation-id from pubmed: 10.1080/14760584.2017.1294069--><abstract><sec id="S1"><title>INTRODUCTION</title><p id="P1">Varicella vaccines are highly effective at preventing disease, but varicella
may occur among vaccinated persons (termed breakthrough varicella). Breakthrough
varicella is generally mild, but severe cases have been reported. The objective of this
review is to describe severe breakthrough varicella.</p></sec><sec id="S2"><title>AREAS COVERED</title><p id="P2">We conducted a systematic review of articles published during
1974&#x02013;2016. A total of 34 articles were included in our review: 21 described
breakthrough varicella with disseminated varicella-zoster virus (VZV) infection with
other organ involvement in addition to skin (none among two-dose vaccinees); 9 described
hospitalized breakthrough varicella without mention of other organ involvement in
addition to skin (of which 2 reported 4 two-dose vaccinees); and 4 described both. A
total of 52&#x02013;60 unique breakthrough varicella cases with disseminated VZV
infection with other organ involvement in addition to skin reported with the following
complications, not mutually exclusive: pneumonia (n=8&#x02013;9 cases),
neurologic (n=18&#x02013;24 cases), hematologic (n=10&#x02013;11 cases),
ocular (n=5 cases), renal (n=2 cases), hepatic (n=3 cases),
secondary infection with bacteremia or sepsis (n=8 cases), and other
complication (n=4 cases). There were 6 cases of fatal breakthrough
varicella.</p></sec><sec id="S3"><title>EXPERT COMMENTARY</title><p id="P3">With &#x0003e;31 million doses distributed annually worldwide since 2007, severe
breakthrough varicella can occur but they appear to be uncommon.</p></sec></abstract><kwd-group><kwd>Varicella</kwd><kwd>vaccine</kwd><kwd>varicella-zoster virus (VZV)</kwd><kwd>chickenpox</kwd><kwd>breakthrough</kwd><kwd>modified varicella</kwd><kwd>literature review</kwd><kwd>varicella vaccine failure</kwd></kwd-group></article-meta></front><body><sec id="S4"><title>1. Introduction</title><p id="P4">Varicella (chickenpox) is a highly contagious disease caused by infection with
varicella-zoster virus (VZV). It presents as a generalized maculopapulovesicular rash with
~250&#x02013;500 lesions. Varicella is usually a self-limited disease<sup><xref rid="R1" ref-type="bibr">1</xref></sup> but can cause significant morbidity and can lead to
death, more commonly in immunocompromised patients, with skin and soft tissue infections,
pneumonia, and encephalitis being the most frequent complications<sup><xref rid="R2" ref-type="bibr">2</xref>, <xref rid="R3" ref-type="bibr">3</xref></sup>. A varicella
vaccine containing live-attenuated VZV (named Oka strain) was developed in Japan in the
early 1970s<sup><xref rid="R4" ref-type="bibr">4</xref></sup>. Several licensed varicella
vaccines are available, all using live-attenuated VZV and all based on the Oka strain except
the vaccine developed in South Korea<sup><xref rid="R5" ref-type="bibr">5</xref></sup>. The
vaccine is available as a single-antigen vaccine or in combination with measles, mumps, and
rubella (MMRV). While the varicella vaccines are licensed worldwide, varicella vaccination
is routinely recommended in a limited number of countries, either as a one or two-dose
program<sup><xref rid="R6" ref-type="bibr">6</xref>&#x02013;<xref rid="R8" ref-type="bibr">8</xref></sup>. Varicella vaccine is not recommended for most
immunocompromised persons<sup><xref rid="R3" ref-type="bibr">3</xref></sup>. The United
States was the first country to recommend a routine one-dose program in 1996, then updated
its recommendations to a routine two-dose program in 2006<sup><xref rid="R3" ref-type="bibr">3</xref></sup>.</p><p id="P5">Varicella vaccine is safe and effective at preventing varicella<sup><xref rid="R9" ref-type="bibr">9</xref>&#x02013;<xref rid="R12" ref-type="bibr">12</xref></sup>. One
dose is approximately 81% effective against any clinical disease and &#x0003e;95%
effective against combined moderate and severe varicella; the second dose provides
additional protection against any varicella<sup><xref rid="R9" ref-type="bibr">9</xref>,
<xref rid="R13" ref-type="bibr">13</xref>, <xref rid="R14" ref-type="bibr">14</xref></sup>. Varicella due to wild-type (WT)-VZV may occur in some persons vaccinated
with varicella vaccine after exposure to WT-VZV and is termed breakthrough varicella (i.e.,
vaccine failure). Breakthrough varicella is generally milder in severity and duration than
varicella in unvaccinated persons<sup><xref rid="R1" ref-type="bibr">1</xref></sup>;
clinical symptoms usually consist of a rash with &#x0003c;50 lesions, predominately maculopapular
although sometimes also with vesicular lesions<sup><xref rid="R15" ref-type="bibr">15</xref></sup>. However, there have been cases of breakthrough varicella that resulted
in extensive rash, complications, and even death<sup><xref rid="R1" ref-type="bibr">1</xref>, <xref rid="R16" ref-type="bibr">16</xref></sup>. A systematic review of severe
breakthrough varicella has not been performed to date. Understanding the range of severe
complications of varicella among vaccinated persons is an important component of evaluating
the varicella vaccination program. The objective of this literature review is to summarize
and describe severe breakthrough varicella.</p></sec><sec id="S5"><title>2. Methods</title><sec id="S6" sec-type="background"><title>2.1 Literature search</title><p id="P6">We searched the PubMed Database for articles published from November 30, 1974,
when information on varicella vaccine was first published, through August 1, 2016 using
the following search terms: &#x0201c;(varicella or VZV or varicella-zoster virus or
chickenpox) and (&#x0201c;breakthrough&#x0201d; or &#x0201c;vaccine failure&#x0201d; or
&#x0201c;adverse event&#x0201d; or &#x0201c;vaccine effectiveness&#x0201d; or
&#x0201c;vaccine safety&#x0201d; or &#x0201c;vaccinated&#x0201d; or
&#x0201c;immunized&#x0201d;)&#x0201d;.</p><p id="P7">We reviewed each title and abstract to determine if the article might include
data on breakthrough varicella cases. For articles that passed this initial screen, we
reviewed the full text if the article was available in English; if the full text was not
available in English, we used the information from the abstract. We also reviewed any
additional references that described breakthrough varicella that were identified from the
reference section of the articles reviewed and were not retrieved by the PubMed
search.</p></sec><sec id="S7"><title>2.2 Definitions</title><p id="P8">Breakthrough varicella is defined as varicella in a person who received at least
one dose of varicella vaccine (single-antigen or MMRV vaccines) &#x02265;42 days before
occurrence of symptoms, without other apparent cause<sup><xref rid="R17" ref-type="bibr">17</xref></sup>. Forty-two days, which equals two incubation periods for
varicella<sup><xref rid="R1" ref-type="bibr">1</xref></sup>, is used to differentiate
breakthrough cases from potential vaccine-strain varicella-like rashes. Post-licensure
experience showed that vaccine-strain rashes occurred typically 21 days post-vaccination
with a range of 5&#x02013;42 days post-vaccination<sup><xref rid="R18" ref-type="bibr">18</xref></sup>.</p><p id="P9">For the purpose of our review, we defined severe breakthrough varicella as
breakthrough varicella that resulted in 1) disseminated VZV infection with other organ
involvement in addition to skin: pneumonia, complications related to nervous, hematologic,
ocular, renal, and hepatic systems, sepsis and secondary infection resulting in
bacteremia, and other complications, 2) any hospitalizations in addition to cases that met
the first criterion, or 3) death. For articles that described severe breakthrough
varicella, we abstracted, when available, data on number of breakthrough varicella cases
reported, vaccine type, number of vaccine doses, age of vaccination, immune status or
medication of case-patients, interval between vaccination and breakthrough varicella
onset, complications, laboratory test results, and if hospitalized.</p><p id="P10">We excluded cases of 1) varicella due to vaccine-strain VZV, 2) re-activation
(due to either vaccine-strain or WT-VZV) that were diagnosed as herpes zoster (shingles)
or had a rash suggestive of herpes zoster, and 3) varicella-like illness in persons who
had received herpes zoster vaccine, which is recommended for persons aged &#x02265;60
years in the United States<sup><xref rid="R19" ref-type="bibr">19</xref></sup>.</p><p id="P11">Two co-authors reviewed each article and classified severe breakthrough
varicella according to our case definition (including classification by organ system
category). When questions arose about the case classification, the articles were reviewed
by and discussed with the third co-author (physician). A breakthrough case may have had
multiple complications and be described in more than one organ system category. We present
the number of articles that described severe breakthrough varicella and the number of
unique cases. Due to the use of the same surveillance systems in some publications it is
likely that some of the cases were presented more than once; thus, it was difficult to
determine the total number of unique cases. Therefore, we included a range based on our
determination of the information presented in the articles.</p></sec></sec><sec id="S8"><title>3. Results</title><p id="P12">We identified and screened 915 articles published between 1974 and 2016 (<xref rid="F1" ref-type="fig">Figure 1</xref>). Of the 215 articles that described potential
breakthrough varicella cases (publication years: 1977 to 2016), <bold>34</bold> met
inclusion criteria for our review (publication years: 1980 to 2016): <bold>21</bold>
articles described breakthrough varicella cases with disseminated VZV infection with other
organ involvement in addition to skin; <bold>9</bold> articles described hospitalized
breakthrough varicella cases without mention of other organ involvement in addition to skin;
<bold>4</bold> articles described both [<xref rid="F1" ref-type="fig">Figure
1</xref>, <xref rid="T1" ref-type="table">Table 1</xref>], for a total of
52&#x02013;60 unique breakthrough varicella cases with disseminated VZV infection with other
organ involvement in addition to skin and 266 hospitalized breakthrough cases without
mention of other organ involvement in addition to skin. Varicella cases with disseminated
VZV infection are described below; range accounts for cases we identified that potentially
were reported in multiple publications (<xref rid="T2" ref-type="table">Table 2</xref>).
Most (20) of the articles described severe breakthrough varicella after receipt of Merck
varicella vaccine products licensed in the United States [<xref rid="T1" ref-type="table">Table 1</xref>]; this is likely due to the United States being
the country with the longest duration of a routine varicella vaccination program, and with
the majority of the post-licensure varicella vaccine safety articles<sup><xref rid="R20" ref-type="bibr">20</xref></sup>.</p><p id="P13">No articles indicated severe breakthrough varicella cases with disseminated VZV
infection with other organ involvement in addition to skin in a person who received 2 doses
of varicella vaccine. There were 2 articles that indicated hospitalized breakthrough
varicella cases without mention of other organ involvement in addition to skin in 4 patients
who received 2 doses of varicella vaccine<sup><xref rid="R21" ref-type="bibr">21</xref>,
<xref rid="R22" ref-type="bibr">22</xref></sup>, although in 1 paper<sup><xref rid="R21" ref-type="bibr">21</xref></sup> it was unclear whether 2 of these patients were
breakthrough cases or the vaccine was received &#x0003c;42 days before rash onset.</p><sec id="S9"><title>3.1 Pneumonia</title><p id="P14">We identified 5 articles that described breakthrough varicella cases with
<bold>pneumonia</bold>. Most pneumonia cases were identified in articles describing
results of post-licensure vaccine surveillance. Using data from an active surveillance
project, Chaves et al<sup><xref rid="R15" ref-type="bibr">15</xref></sup>, reported 1 case
of pneumonia among 1,661 breakthrough cases in children aged 1&#x02013;14 years during
1997&#x02013;2005 in the United States. Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> reported 4 cases of pneumonia among a total of 36
hospitalized breakthrough cases in children from 29 health care centers in Turkey; these
cases were identified as part of a national prospective study on pediatric varicella
hospitalizations during 2008&#x02013;2013.</p><p id="P15">Galea<sup><xref rid="R24" ref-type="bibr">24</xref></sup> et al reported 2 cases
of pneumonia in immunocompetent persons out of 5,054 cases of breakthrough varicella based
on Merck&#x02019;s post-marketing worldwide surveillance data 1995&#x02013;2005. Quian et
al<sup><xref rid="R25" ref-type="bibr">25</xref></sup> reported 1 pneumonia case in a
hospitalized 5 year-old with varicella who had been vaccinated at age 3 years among 462
varicella-related hospitalizations, of which 6 were breakthrough varicella, during
1997&#x02013;2005 in Uruguay. Pileggi et al<sup><xref rid="R26" ref-type="bibr">26</xref></sup> reported a breakthrough varicella case with pneumonia and probable
macrophage activation syndrome in a patient with juvenile rheumatic disease who was on
methotrexate (and possibly other immunosuppressive drugs) at the time of vaccination. The
patient was a nonresponder to varicella vaccine based on serology testing using commercial
assays. The patient developed severe breakthrough varicella after a known exposure to
WT-VZV 2&#x02013;3 years after vaccination; the patient was receiving antitumor necrosis
factor therapy at the time of exposure.</p></sec><sec id="S10"><title>3.2 Neurologic complications</title><p id="P16">We identified 11 articles that described breakthrough cases with
<bold>neurologic</bold> complications; diagnoses included meningitis, encephalitis,
acute cerebellar ataxia, transverse myelitis, and cerebellitis. Seven articles described
meningitis cases. Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup>
reported 9 breakthrough cases with meningitis/encephalitis in their study of pediatric
varicella hospitalizations; no additional information was provided on these cases. In the
review of national safety data of varicella vaccine in the United States
1995&#x02013;2005, Chaves et al<sup><xref rid="R10" ref-type="bibr">10</xref></sup>,
described 4 cases of meningitis associated with breakthrough varicella in children aged
&#x02264;12 years, 2 of whom had a CSF specimen positive for VZV by PCR, strain type not
indicated. One of the laboratory confirmed cases was also described in a case report by
Schwab et al<sup><xref rid="R27" ref-type="bibr">27</xref></sup>. This was a healthy 5
year-old who developed meningitis without ataxia who presented with fever, headache and
rash. The patient had received varicella vaccine at age 3 years and developed varicella 18
months after vaccination. Upon treatment with acyclovir the patient made an uneventful
recovery but at the 6 week follow-up visit, demonstrated mild to moderate sensorineural
hearing loss on the right side. Two years later, the patient&#x02019;s hearing was normal.
In their review of the safety of varicella vaccine using Merck&#x02019;s post-marketing
worldwide surveillance database for 1995&#x02013;2005, Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> reported 1 aseptic meningitis case in an
immunocompetent patient with breakthrough varicella; no other details provided. Sharrar et
al<sup><xref rid="R18" ref-type="bibr">18</xref></sup> reported 1 hospitalized
breakthrough varicella case with meningitis. The database used by these two publications
was the same, with the Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup>
article covering the period analyzed by Sharrar et al<sup><xref rid="R18" ref-type="bibr">18</xref></sup>; it is likely that these were the same cases. Reynolds et
al<sup><xref rid="R28" ref-type="bibr">28</xref></sup> reported breakthrough varicella
with meningitis in a 5 year-old with asthma. The child was admitted to the intensive care
unit for 1 day for meningitis, and discharged with a diagnosis of altered mental
status/post-varicella syndrome; by 6 weeks the child&#x02019;s mental status had returned
to normal.</p><p id="P17">Naruse et al<sup><xref rid="R29" ref-type="bibr">29</xref></sup> described a
45-month old boy in Japan hospitalized with breakthrough varicella and meningitis
vaccinated 21 months earlier with the Biken vaccine. After exposure to a child with
varicella, the patient developed a rash (97 lesions), and headache and frequent vomiting 2
days after rash onset. The patient responded to intravenous (IV) acyclovir with resolution
of symptoms within 2 days of treatment initiation and had no recurrent symptoms. His
cerebrospinal fluid (CSF) specimen was positive for VZV DNA by PCR; type information not
provided.</p><p id="P18">Breakthrough cases with encephalitis were described in 3 articles. One is the
publication by Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> that
reported 9 breakthrough cases with encephalitis/meningitis. Chaves et al<sup><xref rid="R15" ref-type="bibr">15</xref></sup>, reported 1 case of breakthrough varicella
with encephalitis in a healthy 4 year-old in the study from the varicella active
surveillance project. Ibraheem et al<sup><xref rid="R30" ref-type="bibr">30</xref></sup>
described a 4 year-old girl without a known immunocompromising condition, who died from
VZV encephalitis. Her past medical history included a nasal septum perforation with
recurrent sinusitis, and hypocalcemia-related seizures at 1 year of age. She was
vaccinated with 1 dose at age 13 months. The patient was admitted with sudden severe
headache and right eye pain. She did not have a rash. The patient&#x02019;s condition
worsened during hospitalization and she died on day 6 of hospitalization. PCR of
post-mortem brain specimens were positive for WT-VZV DNA and VZV encephalitis was the
likely cause of death<sup><xref rid="R30" ref-type="bibr">30</xref></sup>. Of note, the
authors mentioned that in the absence of the rash they were unable to determine whether
the patient&#x02019;s encephalitis was because of breakthrough infection or herpes
zoster.</p><p id="P19">Acute cerebellar ataxia was described in 2 articles. Sharrar et al<sup><xref rid="R18" ref-type="bibr">18</xref></sup> and Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> reported 2 hospitalized breakthrough varicella cases
with ataxia and 2 immunocompetent case-patients with breakthrough varicella and ataxia,
respectively. As above there is the possibility of overlap due to the use of the same
database.</p><p id="P20">Two case-reports described breakthrough varicella with transverse myelitis
diagnosed after the rash had resolved. LaRovere et al<sup><xref rid="R31" ref-type="bibr">31</xref></sup> described a case in an immunocompetent 14 year-old boy, vaccinated at
6 years of age. He developed fever and a generalized papulovesicular rash that lasted 6
days. Six days after his rash resolved, the patient reported a sharp &#x0201c;mid-scapular
pain that radiated to his chest&#x0201d;, and 2 days later, he developed bilateral leg
paresthesias and weakness, unsteady gait, and urinary retention. VZV antibody was detected
in CSF. After 15 days of hospitalization, his neurologic examination was normal although
he still had weakness in his extremities. Two months after presentation, he was
asymptomatic and his neurologic exam was normal. Aslan et al<sup><xref rid="R32" ref-type="bibr">32</xref></sup> described a case in a 10 year-old girl without
identified immunosuppressive conditions or medications who was vaccinated at age 12
months. She was hospitalized with lower extremity paralysis and urinary retention. She had
developed a mild rash (20&#x02013;25 lesions) without fever, 16 days before
hospitalization that lasted approximately 2 days. Fourteen days after the rash resolved,
she developed bilateral leg paralysis, weakness, and unsteady gait. Her blood was positive
for VZV IgG and IgM antibodies and the serum/CSF ratio of VZV antibody was reduced
compared with ratios for total IgG and albumin, consistent with intrathecal synthesis of
VZV antibody<sup><xref rid="R33" ref-type="bibr">33</xref></sup>. One month after
hospitalization, the patient was asymptomatic and MRI showed normal findings of spinal
cord.</p><p id="P21">Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> reported 1
breakthrough case with cerebellitis based on hospital surveillance data from Turkey,
without additional details.</p></sec><sec id="S11"><title>3.3 Hematologic complications</title><p id="P22">There were 9 articles describing <bold>hematologic complications</bold> in 11
patients; diagnoses included neutropenia, thrombocytopenia, pancytopenia, possible
macrophage activation syndrome, hemorrhagia, and disseminated intravascular coagulation
(DIC). Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> reported 4
breakthrough cases with hematologic complications: 2 with neutropenia (of which one was
febrile neutropenia) and 2 with thrombocytopenia. The previously mentioned case described
by Pillegi et al<sup><xref rid="R26" ref-type="bibr">26</xref></sup> with pneumonia, also
developed probable macrophage activation. Kakish et al<sup><xref rid="R34" ref-type="bibr">34</xref></sup> described a breakthrough case in a previously healthy 4 year-old
child who developed varicella 12 weeks after varicella vaccination. He had a 2-day history
of fever and maculopapulovesicular rash, when he presented with ecchymotic patches on the
elbows and multiple purpuric skin lesions around the eyes with bilateral subconjunctival
hemorrhages. His 3 year-old sibling had recovered from varicella 10 days previously. He
was diagnosed with pancytopenia which was not responsive to multiple treatments (IV immune
globulin, platelet transfusion, pulse dose corticosteroids, granulocyte colony stimulating
factor). Bone marrow aspirate showed scarcity of all cell lines. Bone marrow transplant
was recommended. Follow up information was not reported.</p><p id="P23">Hemorrhagia was described in 2 articles. Chaves et al<sup><xref rid="R15" ref-type="bibr">15</xref></sup> reported 1 breakthrough varicella case with
hemorrhagia in a study using active surveillance data; no other details were provided.
Reynolds et al<sup><xref rid="R28" ref-type="bibr">28</xref></sup> reported 1 breakthrough
varicella case in a previously healthy 2 year-old who developed bleeding diathesis. These
2 papers used the same data source with overlapping years of data analyzed; it is possible
that both describe the same case.</p><p id="P24">DIC was reported in 2 cases<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R35" ref-type="bibr">35</xref>, <xref rid="R36" ref-type="bibr">36</xref></sup>.
These cases are described under the complication we considered initiated the chain of
events that led to DIC (hepatic complications and sepsis, respectively). Lastly, Leung et
al<sup><xref rid="R16" ref-type="bibr">16</xref></sup> described a fatal breakthrough
case in a 7 year-old with malignant ependymoma and on dexamethasone (2 mg/day) who
developed thrombocytopenia during the course of her illness; this case was also reported
by Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup>. Limited clinical
information was available on this case.</p></sec><sec id="S12"><title>3.4 Ocular complications</title><p id="P25">There were 5 articles that described 5 breakthrough varicella patients with
<bold>ocular complications</bold>, which included keratitis, conjunctivitis,
subconjunctival hemorrhage, retinitis, blurred vision, and hemorrhagic retinitis. Galea et
al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> reported 1 patient with
breakthrough varicella and keratitis. Kurugol et al<sup><xref rid="R37" ref-type="bibr">37</xref></sup> reported conjunctivitis in a 10 year-old healthy child from Turkey
who developed breakthrough 9 years after receipt of 1-dose of varicella vaccine. The child
was hospitalized for disseminated rash and fever and received oral and topical acyclovir
for conjunctivitis; the patient fully recovered. The patient described above by Kakish et
al<sup><xref rid="R34" ref-type="bibr">34</xref></sup> with hematologic complications,
also developed ocular complications (bilateral subconjunctival hemorrhages).</p><p id="P26">Ross et al<sup><xref rid="R38" ref-type="bibr">38</xref></sup> described 1
breakthrough case in a 7 year-old child with T-cell acute lymphoblastic leukemia (ALL) in
remission who developed varicella retinitis, blurred vision, and hemorrhagic retinitis. He
was vaccinated with 1 dose at age 4, 27 months before he was diagnosed with ALL at age 6
years. He was VZV IgG positive at the time of his ALL diagnosis. He presented to the
oncology clinic with high fever (104&#x000b0; F) and generalized vesicular rash and was
clinically diagnosed with varicella. His last course of chemotherapy was 3 weeks before
rash onset. He was exposed to a child with varicella in his school. After IV and oral
acyclovir the rash resolved and the patient was discharged with all skin lesions crusted.
Two weeks following varicella, he presented with blurred vision in the right eye, without
new skin lesions. He developed a right afferent pupillary defect and superior temporal
defect, and subsequently hemorrhagic retinitis in the inferotemporal quadrant. He was
re-admitted, and received prolonged therapy with acyclovir and prednisolone ophthalmic
drops that prevented progression of the retinitis. A residual scar remained in the area of
previous retinitis.</p><p id="P27">Additionally, Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> identified 1 hospitalized breakthrough varicella case with severe eye
involvement; details of the ocular complications were not included.</p></sec><sec id="S13"><title>3.5 Renal complications</title><p id="P28">There were 2 articles that described <bold>renal complications</bold> in 2
patients. Pillai et al<sup><xref rid="R39" ref-type="bibr">39</xref></sup> described a
breakthrough case in a 24 year-old male with no history of renal disease or varicella who
was vaccinated almost 2 years prior. He presented to the hospital with rash, gross
hematuria, shaking chills, fever, and mild hypertension (130/94). Urinalysis revealed
4+ protein, 4+ blood, many red blood cells (RBC), and granular casts.
Blood pressure and urinary abnormalities resolved in approximately 3 weeks; urinalysis 7
months later revealed 3&#x02013;5 RBCs. WT-VZV was cultured from skin lesion specimens.
Goulleret et al<sup><xref rid="R11" ref-type="bibr">11</xref></sup> reported 1 case with
renal complications out of 261 cases of breakthrough varicella based on Merck&#x02019;s
post-licensure surveillance data from Europe during 2003&#x02013;2008. The case occurred
in a 3 year-old who was vaccinated at age 12 months, and 2 years later developed
breakthrough varicella with nephrotic syndrome that required hospitalization. The child
recovered completely. No specimens were collected for VZV laboratory testing.</p></sec><sec id="S14"><title>3.6 Hepatic complications</title><p id="P29">There were 4 articles that described 3 cases of breakthrough varicella with
<bold>hepatic complications</bold> including hepatomegaly, hepatitis, and hepatic
necrosis. Nunoue et al<sup><xref rid="R40" ref-type="bibr">40</xref></sup> described 1
case with hepatomegaly. This was a child with acute leukemia treated with
immunosuppressive therapy at the time of vaccination and after vaccination. She was
vaccinated at age 3 years and developed varicella 11 months after vaccination. Her
symptoms included fever, generalized rash (&#x0003e;100 lesions) that lasted 10 days,
hepatomegaly, and elevated amino transferase levels. VZV culture was negative.</p><p id="P30">Kelley et al<sup><xref rid="R41" ref-type="bibr">41</xref></sup> described 1
case with hepatitis that resulted in multi-organ failure and death; this death was also
included in the summary of breakthrough varicella deaths in the paper by Leung et
al<sup><xref rid="R16" ref-type="bibr">16</xref></sup>. This was a breakthrough case
in a 15 year-old boy with T-cell precursor ALL who was undergoing reinduction chemotherapy
and on Decadron (20 mg/day). He had received 1-dose of varicella vaccine at age 2 years
(based on our earlier article<sup><xref rid="R16" ref-type="bibr">16</xref></sup>; Kelley
et al<sup><xref rid="R41" ref-type="bibr">41</xref></sup> reported he was vaccinated at
age 5), and was up-to-date on other vaccinations. He presented with fever and a sharp
stabbing back pain and 3 days later developed a rash described as nonvesiculated acne-like
believed to be related to medication; on day 7 the rash started to vesiculate and PCR
identified WT-VZV DNA in the vesicular fluid. On day 9 of illness, the patient developed
hepatitis, and subsequently multi-organ failure and died. Wise et al<sup><xref rid="R36" ref-type="bibr">36</xref></sup> and Sharrar et al<sup><xref rid="R18" ref-type="bibr">18</xref></sup> each describe the same fatal breakthrough varicella case in a 9
year-old girl with chronic severe asthma, on high-dose inhaled corticosteroids (60 mg/day,
steroid not specified). This patient had received the 1<sup>st</sup> dose of varicella
vaccine shortly before her 8<sup>th</sup> birthday. No rash had been recognized before
death, but at autopsy, 2 of several scattered papules showed &#x0201c;intraepidermal
vesicles with viral inclusions and multinucleated cells&#x0201d;. Autopsy disclosed
fulminant hepatitis, esophagitis and epiglottitis, DIC and positive VZV cultures from
pharynx, lung, blood, and urine; PCR identified WT-VZV. Her liver was diffusely necrotic,
and few surviving hepatocytes showed viral cytopathic changes.</p></sec><sec id="S15"><title>3.7 Sepsis and Secondary Infection resulting in bacteremia</title><p id="P31">There were 7 articles that described <bold>sepsis</bold> (bacterial or viral) as
a complication in 8 breakthrough varicella cases. The specific organism that caused sepsis
was reported in 3 cases (Staph aureus or Group A streptococcus)<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R35" ref-type="bibr">35</xref>, <xref rid="R36" ref-type="bibr">36</xref>, <xref rid="R42" ref-type="bibr">42</xref></sup>. The first
case was a fatal case of breakthrough varicella described by Sharrar et al<sup><xref rid="R18" ref-type="bibr">18</xref></sup> and Wise et al<sup><xref rid="R36" ref-type="bibr">36</xref></sup>, mentioned above with hepatic complications that also
developed <italic>Staph aureus</italic> sepsis. The second case, described by Kwak et
al<sup><xref rid="R35" ref-type="bibr">35</xref></sup>, was in a previously healthy 38
month-old girl with necrotizing fasciitis on the left abdominal wall and streptococcal
toxic shock syndrome; she was vaccinated at 12 months. Three days after onset of rash, she
was seen in the emergency department for increased pain and swelling in the left flank.
She had several ruptured blisters, macular rash, and painful purplish swelling surrounding
some of the skin lesions on her left flank. Computerized tomography scan showed extensive
soft tissue swelling of the left anterior abdominal wall, both flanks, and inguinal area
and magnetic resonance imaging identified necrotizing fasciitis on the same sites. Group A
Streptococcus was isolated by tissue culture. Laboratory investigation revealed
disseminated intravascular coagulation. The patient recovered and was discharged after 5
weeks of hospitalization. The third case, described by Laskey et al<sup><xref rid="R42" ref-type="bibr">42</xref></sup>, was in a previously healthy 3 year-old boy who
developed varicella 6 months after vaccination with no apparent skin infection, but the
patient developed group A &#x003b2;-hemolytic streptococcus (GABHS) bacteremia, resulting
in endocarditis. Ten days after rash onset, the patient was admitted with a 3-day history
of nausea, vomiting, fever along with increased irritability, decreased urine output and
right foot pain with difficulty walking. Examination revealed crusted skin lesions without
erythema, an I/VI systolic ejection murmur and worsening joint pain. On hospital day 2
blood cultures were positive for GABHS. The hospital course was complicated by bilateral
pulmonary infiltrates, hypoalbuminemia, elevated liver function tests. On hospital day 8,
the patient developed a diastolic murmur consistent with aortic regurgitation and subungal
hemorrhages were noted. Echocardiography revealed thickening of the aortic valve with
moderate aortic insufficiency. The patient was started on a 6-week treatment with IV
penicillin G. However, after 2 weeks, the diastolic murmur was harsher and
echocardiography revealed a large vegetation on the posterior leaflet of the aortic valve
with severe aortic insufficiency and a dilated left ventricle. He was treated for
congestive heart failure. A month after the initial echocardiography, the patient
continued to have worsening aortic regurgitation and mitral regurgitation. The patient
received an additional 4 weeks of antibiotic followed by aortic valve replacement. He had
an unremarkable postoperative course and was doing well on follow-up examination.</p><p id="P32">There were 5 additional cases of sepsis reported, without information on the
specific organism leading to sepsis, 3 alleged to be cases of bacterial sepsis. Dinleyici
et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> identified 1 breakthrough
varicella case in a child with leukemia who developed a secondary bacterial infection and
sepsis, who ultimately died. Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> reported 2 breakthrough cases in immunocompetent persons who developed
sepsis from secondary infection. The 7 year-old patient with malignant ependymoma,
described earlier with thrombocytopenia and reported by Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> and Leung et al<sup><xref rid="R16" ref-type="bibr">16</xref></sup>, also developed sepsis. This case had no evidence of bacterial
infection (unpublished surveillance data). Sharrar et al<sup><xref rid="R18" ref-type="bibr">18</xref></sup> reported an additional hospitalized breakthrough
varicella case with dehydration and possible sepsis.</p></sec><sec id="S16"><title>3.8 Other complications</title><p id="P33"><bold>Other complications</bold> included hypotension and transient hearing
loss, which were described in the 2 cases mentioned above, reported by Kwak et
al<sup><xref rid="R35" ref-type="bibr">35</xref></sup> (described under sepsis) and
Schwab et al<sup><xref rid="R27" ref-type="bibr">27</xref></sup> (described under
neurologic complications), respectively. Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> reported 1 patient with breakthrough varicella who developed
myocarditis; no other details were provided on this case. Kriner et al<sup><xref rid="R43" ref-type="bibr">43</xref></sup> described 1 fatal breakthrough case in a patient with
ALL who developed multi-organ failure; she was on maintenance therapy
(Vincristine/dexamethasone).</p></sec><sec id="S17"><title>3.9 Other Hospitalizations</title><p id="P34">Thirteen articles described a <bold>hospitalized breakthrough varicella case
without mention of other organ involvement in addition to skin</bold> for a total
estimated number of 266 cases<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R21" ref-type="bibr">21</xref>&#x02013;<xref rid="R23" ref-type="bibr">23</xref>,
<xref rid="R25" ref-type="bibr">25</xref>, <xref rid="R28" ref-type="bibr">28</xref>,
<xref rid="R44" ref-type="bibr">44</xref>&#x02013;<xref rid="R50" ref-type="bibr">50</xref></sup>. Eleven of these articles described data from various surveillance
systems in different countries <sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R21" ref-type="bibr">21</xref>&#x02013;<xref rid="R23" ref-type="bibr">23</xref>,
<xref rid="R25" ref-type="bibr">25</xref>, <xref rid="R28" ref-type="bibr">28</xref>,
<xref rid="R44" ref-type="bibr">44</xref>, <xref rid="R45" ref-type="bibr">45</xref>,
<xref rid="R47" ref-type="bibr">47</xref>, <xref rid="R49" ref-type="bibr">49</xref>,
<xref rid="R50" ref-type="bibr">50</xref></sup>. Among 8 with information on total
number of hospitalized varicella cases, in 7 the proportion of breakthrough
hospitalizations among all varicella hospitalizations was 0&#x02013;4%; in 1 the
proportion was 12%<sup><xref rid="R45" ref-type="bibr">45</xref></sup>. From 7
papers with information on the interval between varicella vaccination and hospitalization,
the median interval was 0.8&#x02013;4.7 years (range, 0.1&#x02013;14 years)<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R22" ref-type="bibr">22</xref>, <xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R25" ref-type="bibr">25</xref>, <xref rid="R28" ref-type="bibr">28</xref>, <xref rid="R45" ref-type="bibr">45</xref>, <xref rid="R50" ref-type="bibr">50</xref></sup>. Where information was provided, majority of
these hospitalized cases occurred in immunocompromised children or adolescents and reasons
for hospitalization included cellulitis, secondary bacterial infection limited to the
skin, dehydration, or for precautionary reasons due to their immune status. Additionally,
Yamada et al<sup><xref rid="R46" ref-type="bibr">46</xref></sup> described 1 breakthrough
varicella case in a 12 year-old cancer patient who was vaccinated at age 1. The patient
was hospitalized for a prolonged rash for at least 14 days, with a maximum of 12 lesions
at the peak of illness. Haddad et al<sup><xref rid="R48" ref-type="bibr">48</xref></sup>,
described a varicella outbreak in a school, which involved one student with severe rash
with &#x0003e;500 lesions who was hospitalized for 3 days and treated with IV antibiotics for
Group A streptococcal secondary skin infection. Hospitalized breakthrough varicella with
febrile seizure was reported by Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup> in Turkey (2 cases), Streng et al<sup><xref rid="R49" ref-type="bibr">49</xref></sup> in Germany (2 cases) and Quian et al<sup><xref rid="R25" ref-type="bibr">25</xref></sup> in Uruguay (1 case in a 2 year-old vaccinated 4 months
previously).</p></sec><sec id="S18"><title>3.10 Death</title><p id="P35">There have been 6 cases of <bold>fatal</bold> breakthrough varicella reported in
8 articles, all described above<sup><xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R30" ref-type="bibr">30</xref>, <xref rid="R36" ref-type="bibr">36</xref>, <xref rid="R41" ref-type="bibr">41</xref>, <xref rid="R43" ref-type="bibr">43</xref></sup>. Five of these deaths were reported from the
United States and summarized in the article by Leung et al<sup><xref rid="R16" ref-type="bibr">16</xref></sup>, the 6<sup>th</sup> death was reported from Turkey by
Dinleyici et al<sup><xref rid="R23" ref-type="bibr">23</xref></sup>. The deaths occurred
in 1-dose vaccinees (interval between vaccination and death was 1&#x02013;13 years;
information available for 5 cases), in children aged &#x0003c;18 years (ages 4, 4, 7, 9, 15 and
&#x0003c;18 years) and 5 of the 6 occurred in immunocompromised persons due to either medical
conditions or medications; the year of death was 1997, 2004, 2011, 2012, 2013, and
2008&#x02013;2013 for the death reported from Turkey (specific year of death not indicated
in the publication). Reported complications included: hepatitis, hemorrhagia, and
sepsis<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R36" ref-type="bibr">36</xref></sup>; sepsis and thrombocytopenia<sup><xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R24" ref-type="bibr">24</xref></sup>; hepatitis and multi-organ
failure<sup><xref rid="R41" ref-type="bibr">41</xref></sup>; sepsis<sup><xref rid="R23" ref-type="bibr">23</xref></sup>; encephalitis<sup><xref rid="R30" ref-type="bibr">30</xref></sup>; and multi-organ failure<sup><xref rid="R43" ref-type="bibr">43</xref></sup>.</p></sec></sec><sec id="S19"><title>4. Expert Commentary and five-year view</title><p id="P36">Varicella vaccines have led to substantial declines in varicella disease<sup><xref rid="R3" ref-type="bibr">3</xref>, <xref rid="R9" ref-type="bibr">9</xref>, <xref rid="R10" ref-type="bibr">10</xref>, <xref rid="R12" ref-type="bibr">12</xref>, <xref rid="R51" ref-type="bibr">51</xref></sup>. The World Health Organization estimated an
annual average of 31 million varicella vaccine doses distributed worldwide between 2007 and
2011<sup><xref rid="R52" ref-type="bibr">52</xref></sup>; in the US &#x0003e;145 million
doses of varicella vaccine have been distributed since program implementation through 2013.
No vaccine is 100% safe or effective and adverse events following vaccination, and
cases of vaccine failure, including breakthrough varicella, have been reported. A review of
the epidemiological and mechanistic (clinical and biological) evidence of selected adverse
events after varicella vaccination associated with Oka VZV (i.e., vaccine-strain) was
performed by the Institute of Medicine (IOM) in 2011<sup><xref rid="R20" ref-type="bibr">20</xref></sup>. We focused our review on the occurrence of varicella due to wild-type
VZV in previously vaccinated persons (i.e., vaccine failure), which was not reviewed by the
IOM report.</p><p id="P37">This is the first systematic review to describe clinical characteristics and
complications of severe varicella presentations among vaccinated children and summarize the
information reported in the literature. Considering primarily the number of skin lesions,
previous studies of varicella among vaccinated children described cases of breakthrough as
mostly mild but indicate that ~25% of cases had clinical presentation more similar
to unvaccinated children<sup><xref rid="R15" ref-type="bibr">15</xref></sup>. Most of these
studies were not large enough to detect uncommon, serious complications of breakthrough
varicella. Chaves et al<sup><xref rid="R53" ref-type="bibr">53</xref></sup>, reported that
vaccinated children with &#x02265;50 lesions were twice as likely to have complications,
such as pneumonia, ataxia and skin superinfections, than vaccinated children with &#x0003c;50
lesions. Our review documented that severe complications with disseminated VZV infection
with other organ involvement in addition to skin among breakthrough cases do occur but they
appear uncommon. We found a similar pattern of complications in breakthrough varicella as
compared to varicella in unvaccinated children with pneumonia, neurologic complications, and
bacterial superinfection being most common<sup><xref rid="R2" ref-type="bibr">2</xref></sup>. Based on the number of published case-reports and cases identified by the
post-marketing surveillance, severe complications of breakthrough varicella are likely less
common than severe complications among unvaccinated patients. Ecologically, this statement
is supported by evidence from studies that documented substantial declines in severe
outcomes of varicella (i.e., hospitalizations and deaths) in countries with a varicella
vaccination program<sup><xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R22" ref-type="bibr">22</xref>, <xref rid="R49" ref-type="bibr">49</xref>, <xref rid="R51" ref-type="bibr">51</xref>, <xref rid="R54" ref-type="bibr">54</xref>, <xref rid="R55" ref-type="bibr">55</xref></sup>. Even in the presence of a decline, when information on
vaccination status was known, studies documented that the majority of hospitalizations which
continue to occur are among unvaccinated patients.</p><p id="P38">Besides describing the types of complications and likely rarity of severe
breakthrough varicella, our review allows for several other conclusions. First, although
more frequent among immunocompromised children, severe breakthrough varicella-related
outcomes can occur among healthy children too. Second, the data do not suggest that severe
breakthrough varicella are more likely to occur with increased time since vaccination as
most published cases occurred in children, rather than in young adults. Although we were not
able to formally evaluate this question because of the lack of information on all cases, we
found that majority of severe breakthrough cases that resulted in disseminated VZV infection
with other organ involvement in addition to skin occurred within 5 years of varicella
vaccination with 4 cases that occurred 8&#x02013;13 years post-vaccination<sup><xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R31" ref-type="bibr">31</xref>, <xref rid="R32" ref-type="bibr">32</xref>, <xref rid="R37" ref-type="bibr">37</xref>, <xref rid="R41" ref-type="bibr">41</xref></sup>; hospitalizations of breakthrough varicella
without mention of other organ involvement in addition to skin occurred at a median of
0.8&#x02013;4.7 years post-vaccination<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R22" ref-type="bibr">22</xref>, <xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R25" ref-type="bibr">25</xref>, <xref rid="R28" ref-type="bibr">28</xref>, <xref rid="R45" ref-type="bibr">45</xref>, <xref rid="R50" ref-type="bibr">50</xref></sup>.
The question of whether severe breakthrough varicella is related to time since vaccination
will be important to continue monitoring. Third, we did not identify any severe
complications with disseminated VZV infection with other organ involvement in addition to
skin among 2 dose vaccine recipients; there were 4 hospitalized breakthrough cases with skin
infection who received 2 doses of varicella vaccine. Nonetheless, physicians should consider
in the differential diagnosis possible varicella-related complications when biologically
plausible, even when varicella vaccine was received. Additionally, given the atypical
presentations of breakthrough varicella, a diagnosis of varicella in vaccinated persons may
not be readily made or a mild rash with few lesions may be missed altogether. Continued
surveillance for varicella disease among vaccinated persons is important to evaluate the
varicella vaccination program, detect any changes in the epidemiology of varicella in the
context of a routine one- or two-dose varicella vaccination program, and understand the
differences in disease presentation between persons who had received 1 or 2 doses of
varicella vaccine.</p><p id="P39">Our review has several limitations. We were unable to calculate rates of
complications for severe breakthrough varicella. It was challenging to determine the number
of cases in each symptom category group since a case may have been reported in multiple
articles. We indicated the potential overlap in reporting of the same breakthrough cases
among different articles when information in the articles allowed us to make that
determination. There was limited information on clinical course, medical history, and
vaccination history for some of the cases with information often presented as aggregate data
instead of case-level data. We may have missed severe breakthrough cases because of
under-reporting; however, we believe that these cases would be more likely to be reported.
Our literature review does not include data on all hospitalized breakthrough cases and
therefore the number of hospitalizations we report should be interpreted with this caveat.
The 12 articles included in our review described postlicensure surveillance from 9 countries
and may have only included data on select populations or surveillance sites. Additionally,
data from national datasets in the United States are not included because information on
vaccination status is not available in these datasets. Nonetheless, in the articles included
in our review, the proportion of breakthrough varicella cases among all varicella-related
hospitalizations is small, ranging from 0 to 4%.</p><p id="P40">The majority of cases were clinically diagnosed. Confirmation as WT-VZV infection
was limited (5 cases, with additional 3 cases with VZV DNA detected but not typed). Even for
cases with laboratory-confirmed WT-VZV infection, we are unable to definitively link the
complications to WT-VZV infection. Some of the complications could have also been caused by
vaccine-strain VZV during primary infection or re-activation since the vaccine-strain is a
live virus. However, we minimized these possibilities by 1) excluding varicella-like cases
that occurred &#x0003c;42 days post-vaccination, which are more likely to represent
vaccine-strain varicella cases, and 2) excluding cases diagnosed as herpes zoster or with
localized rash suggestive of herpes zoster. Lastly, we excluded cases from one article that
analyzed data from postlicensure surveillance systems in which severe outcomes were reported
at varying intervals (6&#x02013;128 days) after vaccination among persons who received
varicella vaccine and that occurred in the absence of rash, a diagnosis of breakthrough
varicella, or laboratory confirmation of VZV infection<sup><xref rid="R36" ref-type="bibr">36</xref></sup>; it is unlikely that these cases were associated with breakthrough
varicella.</p></sec></body><back><ack id="S21"><p><bold>Funding Details:</bold> None</p></ack><fn-group><fn fn-type="COI-statement" id="FN2"><p><bold>Disclosure Statement:</bold> The authors have no potential conflicts of interest to
report.</p></fn><fn id="FN3"><p><bold>Disclaimer:</bold> The findings and conclusions in this report are those of the
authors and do not necessarily represent the official position of the Centers for Disease
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did not indicate varicella complications or hospitalizations (15 articles) or reported
cases were classified as herpes zoster (2 articles)</p></caption><graphic xlink:href="nihms882217f1"/></fig><table-wrap id="T1" position="float" orientation="portrait"><label>Table 1</label><caption><p>Overview of 34 References Describing Severe Breakthrough Varicella</p></caption><table frame="box" rules="all"><thead><tr><th valign="top" align="left" rowspan="1" colspan="1">Variable Category</th><th valign="top" align="center" rowspan="1" colspan="1"># Articles (%)</th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold>Article Publication Year</bold></td><td align="center" valign="top" rowspan="1" colspan="1"/></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">1980&#x02013;1994<xref rid="TFN1" ref-type="table-fn">a</xref></td><td align="center" valign="top" rowspan="1" colspan="1">3 (9%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">1995&#x02013;2009</td><td align="center" valign="top" rowspan="1" colspan="1">14 (41%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">2010&#x02013;2016</td><td align="center" valign="top" rowspan="1" colspan="1">17 (50%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold>Country</bold></td><td align="center" valign="top" rowspan="1" colspan="1"/></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">United States</td><td align="center" valign="top" rowspan="1" colspan="1">18 (53%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Turkey</td><td align="center" valign="top" rowspan="1" colspan="1">3 (9%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Australia</td><td align="center" valign="top" rowspan="1" colspan="1">2 (6%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Japan</td><td align="center" valign="top" rowspan="1" colspan="1">2 (6%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Europe<xref rid="TFN2" ref-type="table-fn">b</xref></td><td align="center" valign="top" rowspan="1" colspan="1">2 (6%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Brazil</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Canada</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Israel</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Korea</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Taiwan</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">United Arab Emirates</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Uruguay</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold>Article Type</bold></td><td align="center" valign="top" rowspan="1" colspan="1"/></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Post-licensure disease surveillance</td><td align="center" valign="top" rowspan="1" colspan="1">13 (38%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Case-report</td><td align="center" valign="top" rowspan="1" colspan="1">13 (38%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Post-licensure safety and/or immunogenicity report</td><td align="center" valign="top" rowspan="1" colspan="1">6 (18%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Pre-licensure safety and efficacy</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Outbreak investigation report</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold>Number of vaccine doses among patients
described</bold></td><td align="center" valign="top" rowspan="1" colspan="1"/></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">1 Dose</td><td align="center" valign="top" rowspan="1" colspan="1">22 (65%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">&#x02265;1 Doses<xref rid="TFN3" ref-type="table-fn">c</xref></td><td align="center" valign="top" rowspan="1" colspan="1">2 (6%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Unknown</td><td align="center" valign="top" rowspan="1" colspan="1">10 (29%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold>Vaccine Type</bold></td><td align="center" valign="top" rowspan="1" colspan="1"/></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Biken</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">GSK VZV Vaccines</td><td align="center" valign="top" rowspan="1" colspan="1">2 (6%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Merck VZV Vaccines</td><td align="center" valign="top" rowspan="1" colspan="1">20 (59%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Oka, unspecified</td><td align="center" valign="top" rowspan="1" colspan="1">3 (9%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Okavax</td><td align="center" valign="top" rowspan="1" colspan="1">1 (3%)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Multiple VZV Vaccine Types</td><td align="center" valign="top" rowspan="1" colspan="1">7 (21%)</td></tr></tbody></table><table-wrap-foot><fn id="TFN1"><label>a</label><p>Two were published prior to vaccine licensure, one from Japan and other from the United
States.</p></fn><fn id="TFN2"><label>b</label><p>Data are from Merck&#x02019;s Varicella Zoster Virus Identification post-marketing
safety surveillance program in European countries; report by country not available.</p></fn><fn id="TFN3"><label>c</label><p>These 2 articles described reports of hospitalized breakthrough varicella in persons
who had received one or two doses of varicella vaccine.</p></fn></table-wrap-foot></table-wrap><table-wrap id="T2" position="float" orientation="portrait"><label>Table 2</label><caption><p>Breakthrough Varicella with Disseminated Varicella-Zoster Virus (VZV) Infection with
Organ Involvement in Addition to Skin</p></caption><table frame="box" rules="all"><thead><tr><th valign="top" align="left" rowspan="1" colspan="1">Complication Category</th><th valign="top" align="center" rowspan="1" colspan="1"># Articles</th><th valign="top" align="center" rowspan="1" colspan="1"># Breakthrough Varicella Cases<xref rid="TFN4" ref-type="table-fn">a</xref></th><th valign="top" align="center" rowspan="1" colspan="1">Diagnoses</th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">Pneumonia</td><td align="center" valign="top" rowspan="1" colspan="1">5<sup><xref rid="R15" ref-type="bibr">15</xref>, <xref rid="R23" ref-type="bibr">23</xref>&#x02013;<xref rid="R26" ref-type="bibr">26</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">8&#x02013;9<xref rid="TFN5" ref-type="table-fn">b</xref>,<xref rid="TFN6" ref-type="table-fn">c</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Pneumonia</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Neurologic</td><td align="center" valign="top" rowspan="1" colspan="1">11<sup><xref rid="R10" ref-type="bibr">10</xref>, <xref rid="R15" ref-type="bibr">15</xref>, <xref rid="R18" ref-type="bibr">18</xref>,
<xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R27" ref-type="bibr">27</xref>&#x02013;<xref rid="R32" ref-type="bibr">32</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">18&#x02013;24<xref rid="TFN5" ref-type="table-fn">b</xref>,<xref rid="TFN9" ref-type="table-fn">f</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Meningitis, Encephalitis, Acute cerebellar ataxia,
Transverse myelitis, Cerebellitis</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Hematologic</td><td align="center" valign="top" rowspan="1" colspan="1">9<sup><xref rid="R15" ref-type="bibr">15</xref>, <xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R18" ref-type="bibr">18</xref>,
<xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R26" ref-type="bibr">26</xref>, <xref rid="R28" ref-type="bibr">28</xref>, <xref rid="R34" ref-type="bibr">34</xref>&#x02013;<xref rid="R36" ref-type="bibr">36</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">10&#x02013;11<xref rid="TFN5" ref-type="table-fn">b</xref>,<xref rid="TFN6" ref-type="table-fn">c</xref>,<xref rid="TFN7" ref-type="table-fn">d</xref>,<xref rid="TFN8" ref-type="table-fn">e</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Neutropenia, Thrombocytopenia, Pancytopenia, possible
Macrophage activation syndrome, Hemorrhagia, Disseminated intravascular
coagulation</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Ocular</td><td align="center" valign="top" rowspan="1" colspan="1">5<sup><xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R34" ref-type="bibr">34</xref>,
<xref rid="R37" ref-type="bibr">37</xref>, <xref rid="R38" ref-type="bibr">38</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">5<xref rid="TFN7" ref-type="table-fn">d</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Keratitis, Conjunctivitis, Subconjunctival hemorrhage,
Retinitis, Blurred vision, Hemorrhagic retinitis</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Renal</td><td align="center" valign="top" rowspan="1" colspan="1">2<sup><xref rid="R11" ref-type="bibr">11</xref>, <xref rid="R39" ref-type="bibr">39</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">2</td><td align="center" valign="top" rowspan="1" colspan="1">Gross hematuria, Nephrotic syndrome</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Hepatic</td><td align="center" valign="top" rowspan="1" colspan="1">4<sup><xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R36" ref-type="bibr">36</xref>, <xref rid="R40" ref-type="bibr">40</xref>,
<xref rid="R41" ref-type="bibr">41</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">3<xref rid="TFN8" ref-type="table-fn">e</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Hepatomegaly, Hepatitis, Hepatic necrosis</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Secondary infections and Sepsis</td><td align="center" valign="top" rowspan="1" colspan="1">7<sup><xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R23" ref-type="bibr">23</xref>,
<xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R35" ref-type="bibr">35</xref>, <xref rid="R36" ref-type="bibr">36</xref>, <xref rid="R42" ref-type="bibr">42</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">8<xref rid="TFN8" ref-type="table-fn">e</xref>,<xref rid="TFN9" ref-type="table-fn">f</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Specific organism that caused sepsis was reported in 3
cases (Staph aureus in 1 case and Group A streptococcus in 2 cases)</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Other</td><td align="center" valign="top" rowspan="1" colspan="1">4<sup><xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R27" ref-type="bibr">27</xref>, <xref rid="R35" ref-type="bibr">35</xref>,
<xref rid="R43" ref-type="bibr">43</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">4<xref rid="TFN9" ref-type="table-fn">f</xref></td><td align="center" valign="top" rowspan="1" colspan="1">Hypotension, Transient hearing loss, Myocarditis,
Multi-organ failure</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Deaths</td><td align="center" valign="top" rowspan="1" colspan="1">8<sup><xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R23" ref-type="bibr">23</xref>,
<xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R30" ref-type="bibr">30</xref>, <xref rid="R36" ref-type="bibr">36</xref>, <xref rid="R41" ref-type="bibr">41</xref>, <xref rid="R43" ref-type="bibr">43</xref></sup></td><td align="center" valign="top" rowspan="1" colspan="1">6<xref rid="TFN8" ref-type="table-fn">e</xref>,<xref rid="TFN10" ref-type="table-fn">g</xref></td><td align="center" valign="top" rowspan="1" colspan="1"/></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Total unique case-patients with any of the complications
above</td><td align="center" valign="top" rowspan="1" colspan="1">25</td><td align="center" valign="top" rowspan="1" colspan="1">52&#x02013;60</td><td align="center" valign="top" rowspan="1" colspan="1"/></tr></tbody></table><table-wrap-foot><fn id="TFN4"><label>a</label><p>A breakthrough case may have had multiple clinical features and is included in more
than one organ system category.</p></fn><fn id="TFN5"><label>b</label><p>It is likely that some of the cases were included in multiple articles. This is why we
have included a range of total number of unique breakthrough cases in each of the
respective complication categories, which is based on our determination of the
information presented in the articles.</p></fn><fn id="TFN6"><label>c</label><p>The case described by Pillegi et al<sup><xref rid="R26" ref-type="bibr">26</xref></sup>
developed pneumonia and hematologic complications and was included in both complication
categories.</p></fn><fn id="TFN7"><label>d</label><p>The case described by Kakish et al<sup><xref rid="R34" ref-type="bibr">34</xref></sup>
developed ocular and hematologic complications and was included in both complication
categories.</p></fn><fn id="TFN8"><label>e</label><p>The case described by Sharrar et al<sup><xref rid="R18" ref-type="bibr">18</xref></sup>
and Wise et al<sup><xref rid="R36" ref-type="bibr">36</xref></sup> developed hepatic
complications and sepsis, and ultimately died; this case was included under all 3
complication categories. The case described by Galea et al<sup><xref rid="R24" ref-type="bibr">24</xref></sup> and Leung et al<sup><xref rid="R16" ref-type="bibr">16</xref></sup> developed hematologic complications and sepsis, and ultimately
died; she was included in all 3 complication categories.</p></fn><fn id="TFN9"><label>f</label><p>The case described by Kwak et al<sup><xref rid="R35" ref-type="bibr">35</xref></sup>
who developed sepsis also developed hypotension. The case described by Schwab et
al<sup><xref rid="R27" ref-type="bibr">27</xref></sup> with neurologic complications
also developed transient hearing loss.</p></fn><fn id="TFN10"><label>g</label><p>All deaths were previously included in at least one of the other complication
categories.</p></fn></table-wrap-foot></table-wrap><boxed-text id="BX1" position="float" orientation="portrait"><caption><title>5. Key Issues</title></caption><sec id="S20"><title>Main messages</title><list list-type="bullet" id="L1"><list-item><p id="P42">Severe varicella in vaccinated persons (breakthrough varicella) involving
disseminated VZV infection with other organ involvement in addition to skin, other
hospitalizations, or death can occur but they appear to be uncommon. Providers should
consider varicella as part of the differential diagnosis of severe clinical
presentations when biologically plausible, even if a person had received varicella
vaccine; rapid antiviral treatment is important in these situations<sup><xref rid="R56" ref-type="bibr">56</xref></sup>.</p></list-item><list-item><p id="P43">With &#x0003e;31 million varicella vaccine doses distributed annually worldwide
since 2007, 34 published articles described severe breakthrough varicella; of them 25
described ~60 cases with disseminated VZV infection with other organ involvement in
addition to skin. Complications of varicella are likely less common in persons who
were vaccinated than those who were not vaccinated.</p></list-item><list-item><p id="P44">Complications involving disseminated VZV infection with other organ
involvement in addition to skin in persons with breakthrough varicella are similar to
those seen in varicella among unvaccinated persons. These complications were reported
among one-dose vaccine recipients only; none were reported among two-dose vaccine
recipients.</p></list-item><list-item><p id="P45">Of hospitalized breakthrough varicella cases without mention of other organ
involvement in addition to skin, a few (4) were reported in two-dose vaccine
recipients, but the majority were reported among one-dose vaccine recipients.</p></list-item><list-item><p id="P46">Severe breakthrough varicella can occur among healthy persons, but appear to
be more common among immunocompromised persons, who are usually not recommended to
receive varicella vaccination.</p></list-item><list-item><p id="P47">Varicella vaccines are safe and effective, and had a significant impact on
reducing varicella morbidity and mortality.</p></list-item><list-item><p id="P48">Continued surveillance for varicella disease among vaccinated persons is
important to determine changes in the varicella epidemiology and whether changes in
disease presentation with time since vaccination occur.</p></list-item></list></sec></boxed-text></floats-group></article>