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Burden of herpes zoster-associated chronic pain in Italian patients aged 50 years and over (2009–2010): a GP-based prospective cohort study
BMC Infectious Diseasesvolume 14, Article number: 637 (2014)
Post-herpetic neuralgia (PHN) is the most common complication in herpes zoster (HZ) patients.
We performed a longitudinal, prospective study in 108 general practices throughout Italy to assess how many immunocompetent patients aged ≥50 years with newly diagnosed HZ develop HZ-associated pain, its duration and management over 6-months. HZ-associated pain was assessed by a direct question to the patient and by self-assessment of the worst pain felt in the previous two weeks on a visual analogue scale (VAS), a score ≥3 was taken as pain. PHN was defined as pain reported during the study period persisting for ≥3 months. Quality of life (QoL) was measured using the SF-12 questionnaire.
At enrolment, 370 of the 413 patients (89.6%) reported HZ-associated pain which was still present in 20.6% and 9.2% of patients after three and six months, respectively, despite many patients receiving recommended anti-viral therapy. The overall QoL scores were lower than those in healthy Italians of similar age; scores for patients with HZ-associated pain were lower. The presence of >50 vesicles and VAS score ≥3 at enrolment, and being male were significantly associated with PHN at three months.
These results suggest that HZ and PHN represent an important burden of disease in the elderly. There is a need for interventions that can prevent and reduce the burden of HZ to help improve the quality of life of the elderly. These data may be useful as baseline epidemiology data for the assessment of the impact of the VZV vaccine in Italy, after its implementation.
Varicella zoster virus (VZV) is a herpes virus that infects nearly all humans in temperate regions resulting in a highly contagious primary infection of varicella, usually in childhood . After this infection, the virus remains latent in sensory ganglia until it is reactivated to cause herpes zoster (HZ) . In Europe, almost all adults (>95%) are healthy carriers of VZV following childhood varicella and are, therefore, at risk of developing HZ .
The immune system declines with age (immunosenescence); the decline of VZV-specific T-cell-mediated immunity is thought to be involved in this reactivation . The incidence and severity (number of vesicles, and pain intensity and duration) of HZ increase with age, but it is difficult to predict who will develop HZ ,. Although patients with treatment- or disease-associated immunosuppression are at higher risk for HZ, 90% of patients with HZ are immunocompetent. Other risk factors include sex, ethnicity, genetic susceptibility, familial history of HZ, mechanical trauma, psychological stress, depression and diabetes -.
Herpes zoster is characterized by a, usually painful, unilateral vesicular rash, generally limited to a single dermatome, corresponding to the sensory ganglion from which the latent VZV was reactivated . The most frequent localization (>50%) is thoracic, followed by cranial, including the ophthalmic division of the trigeminal nerve; the incidence of this latter localization increases with age .
Pain may occur during three distinct phases of the disease:
prodromal pain: often occurs prior to rash onset;
acute pain or neuritis: begins with the rash and usually disappears within 2 to 4 weeks;
chronic pain i.e. post-herpetic neuralgia (PHN): most commonly defined as pain occurring or persisting for ≥3 months after rash onset.
HZ-associated pain is debilitating and often has a substantial, negative impact on patients’ normal life and health, particularly among the elderly whose activities and basic tasks of daily living can be impaired and anxiety and depression can occur ,. In addition, when PHN occurs, pain management is difficult and patients suffer from important side effects . Treatment with antiviral agents within 72 hours of rash onset for seven days is recommended in some patient groups to accelerate rash healing and to limit the severity and duration of pain . However, observational studies in France, Italy, the Netherlands and the UK and a meta-analysis gave heterogeneous results -.
The annual HZ incidence is similar throughout Europe, increasing with age from around 1–4/1 000 in adults aged <50 years to about 7–8/1 000 in those ≥50 years, up to 10/1 000 at >80 years . After the introduction of antivirals drugs, about 10% to 30% of patients aged ≥50 years with HZ develop PHN in Europe . Most studies estimating the percentage of patients with HZ who develop PHN are retrospective. In addition, there is no consensus for the definition of PHN making comparisons between studies difficult .
In Italy, there are insufficient data on the burden of HZ and PHN because there is no HZ-specific national surveillance system. In one nationwide study the annual incidence of general practitioner (GP) visits for HZ was 4.1/1 000 persons aged ≥15 years; 19.6% presented with PHN and 26.1% presented ≥1 complications . One study in 2004 in the Piedmont region reported an overall HZ incidence rate of 1.59/1 000 inhabitants and a hospitalization incidence rate of 0.12/1 000 . In another study that analysed data from four regions in Italy, the HZ incidence in adults aged ≥50 years was 6.6/1 000, and 9.4% and 7.2% of the patients had PHN at 1 month and 3 month, respectively . Another study that analysed data from 1999 to 2005 reported a mean annual number of 4 503 HZ hospitalisations and 543 day-hospitalisations; 62% of patients were >65 years .
In the perspective of a VZV vaccine to prevent and reduce the severity of HZ becoming available in Europe, it was decided to obtain baseline data on the occurrence of PHN in a multicenter, longitudinal, prospective, observational study involving general practitioners (GPs) throughout Italy, the HER.O.E.S. Study – HERpes zoster Outcome: Epidemiological Study. The primary objective was to assess the percentage of patients with HZ that have HZ-associated chronic pain and its duration.
This study was conducted in compliance with the Declaration of Helsinki (Seoul revision; 2008), Good Epidemiological Practice Guidelines and Italian national regulations ,. The protocol and study documentation were approved by Ethics Committee for each local health unit (See Table 1).
The co-primary objectives of the six-month study were:
to assess the percentage of patients with HZ who developed HZ-associated chronic pain and how long the pain lasted.
to collect disease management data from diagnosis to resolution of the acute symptoms, and data on the management of HZ-related pain.
The secondary objectives were to assess quality of life (QoL) in the patients with HZ/PHN using the SF-12 instrument and to assess HZ-related pain intensity using a visual analogue scale (VAS). We also recorded the presence of clinical variables that have been identified as risk factors for HZ and assessed the patients’ care pathway and their disease progression during the study period.
Patients aged >50 years old with a new clinical diagnosis of HZ, who were immunocompetent and who signed an informed consent form were enrolled in the study. Each patient was expected to attend four visits at 0, 1 (± 15 days), 3 (± 21 days) and 6 (± 30 days) months. Patients could be excluded from the analysis for one visit for non-respect of the time window, but included in the analysis for a subsequent visit, if it occurred within the time window.
At the initial visit (V0), descriptive information was collected: socio demographic data, clinical description, medical history. The patients were asked if they had HZ-associated pain at the visit and their quality of life was assessed using the physical component summary (PCS-12) and the mental component summary (MCS-12) scores from the SF-12 questionnaire. The scores ranged from 0 (lowest level of health) to 100 (highest level of health) . A score of <50 indicates a below-average health status. The level of pain was assessed using a visual analogue scale (VAS) for the worst pain felt during the previous two weeks, with scores ranging from 0 (‘no pain’) to 10 (‘worst pain imaginable’). A VAS score of ≥3 was considered to be correlated with pain interfering with activities of daily living . At each follow-up visit the presence of HZ-associated pain, the level of pain using the VAS and quality of life (QoL) scales were assessed. In addition, data on the clinical evolution and the health care resources used were collected.
The presence of allodynia, itching, paresthesia and malaise were all assessed by the physicians during the clinical examination at corresponding study visit. Data were collected using an electronic case report form (eCRF) which enabled a real-time quality control of the data at entry. In addition, a clinical research assistant telephoned the GPs monthly and also performed ad hoc monitoring visits during the study.
Assessment of HZ-associated pain
In HEROES, PHN (primary outcome) was defined as pain that persisted for more than three months after rash onset assessed by the patient replying ‘yes’ at a study visit when asked by the GP about the presence of HZ-associated pain. This assessment mode was chosen to be pragmatic, since physicians do not use tools to measure pain systematically. For the secondary outcome, HZ-associated pain was assessed with a score ≥3 on the VAS, reflecting the worst pain the patient had felt during the two-weeks prior to the visit.
Sample size calculation
Based on information obtained from a questionnaire survey conducted on 317 GPs throughout Italy in 2008 that collected data on the number of patients with HZ they treated annually and how many had PHN, and other published data, - we assumed that between 15% and 40% of patients with HZ would have HZ-associated pain. Thus, with a threshold of p = 0.05 and a pain incidence of 40%, it was estimated that we needed to enrol 400 patients to guarantee a precision of ±4.8%. We decided to enrol 500 patients to allow for 20% erroneously-enrolled patients.
The descriptive analyses were performed with SAS (Statistical Analysis System), V9.2. The recorded or derived variables were summarized as frequencies (absolute or relative) or means or medians with their associated distribution (number of observations, mean, standard deviation, median, minimum, maximum). For all clinically-relevant variables, 95% confidence intervals (CIs) were calculated. Analyses were stratified on gender, age group (50–59, 60–69 and ≥70), and presence of pain at the respective visit.
Variables present at the initial visit associated (p = 0.25) with PHN at 3-months in univariate analyses were included in a multivariate regression model to identify PHN predictive factors (p ≤ 0.05). The fit of the final model was assessed using the Hosmer and Lemeshow goodness-of-fit test. The estimated β coefficients and the corresponding 95% CIs were calculated. Odds ratios and the corresponding 95% CIs were also calculated.
A total of 108 of the 147 GPs who accepted to participate in the study included at least one patient. These 108 GPs were from 21 local health units localized in 12 Italian regions. Their regional distribution was similar to the national distribution (data not shown). They enrolled 435 patients with a new diagnosis of HZ from 27 March 2009 to 5 July 2010 of whom 413 were included in the study (Figure 1).The majority of the GPs (72.2%) respected the time windows for all their patients’ follow-up visits.
The patients were aged 67.9 ± 10.7 years old and 64.2% were women (Table 2). Almost half (46.7%) of the study population were aged ≥70 years. The majority (81.4%) lived with their family; about 25% were working. Most patients (90.3%) had been followed by their GP for >5 years with a mean of 8.2 visits during the previous 12 months. More than 60% of the patients presented ≥1 chronic condition (diabetes, chronic cardiovascular disease or chronic respiratory diseases); the percentage increased with age.
Clinical characteristics and treatment of HZ
The mean delay from HZ prodrome and rash onset to consultation was 4.5 days and 3 days, respectively. This delay was longer in older patients; delay since prodrome: 3.7 days for those aged 50–59; 4.3 days for those aged 60–69 and 5.1 days for those aged ≥70 and since rash onset: 2.3 days for those aged 50–59; 2.7 days for those aged 60–69 and 3.2 for those aged ≥70. All patients (100%) presented with a rash and 77% had <50 vesicles. The rash was mainly localized in the thoracic dermatome area (59.1%) followed by cervical (15.0%), lumbar (13.8%), cranial (12.6%) and sacral segment (11.1%) dermatome areas, respectively (Table 2).
Among the patients presenting with pain at the initial visit, 59.7% had allodynia, 74.3% itching and 58.9% paresthesiae (Table 3). Many patients who reported pain during the study follow-up visits still had allodynia (49.2%, 56.2% and 52.9% at the 1-month, 3-month and 6-month visits, respectively) whereas there was a decrease in the percentage of patients with paresthesiae and itching.
Most of the patients (91.5%) received an oral antiviral (acyclovir: n = 149; brivudin: n = 103; valacyclovir: n = 86; famciclovir: n = 42) for a median duration of 6.0 days. Oral antiviral treatment was initiated a median of two days after rash onset (mean = 3.4 days); 70% of the patients initiated oral antiviral treatment within three days after rash onset. Topical antiviral treatment was administered to 9.4% of patients (acyclovir: n = 37; tromantadine hydrochloride: n = 2).
Only 23% of the patients received pain therapy for a median duration of 12.5 days (mean = 3 days); analgesics (codeine-paracetamol, oxycodone, paracetamol, tramadol, tramadol-paracetamol) (n = 48), nonsteroidal anti-inflammatory drugs (NSAID)s (n = 36), anti-epileptics (n = 29) or psycho-analeptics (n = 12).
Among the 104 patients who worked at the initial visit, 36 took sick-leave due to their HZ episode for: 1 to 5 days (53%); 6 to 10 (33%); and more than 10 days (14%). At the 1-month visit, 33 patients reported that they had taken sick-leave, 2 at the 3-month visit and 1 at the 6-month visit.
About 12% of the patients (n = 52) consulted ≥1 specialist during the study (mainly a dermatologist, neurologist or ophthalmologist). None of the patients were hospitalised due to HZ.
Herpes zoster-associated pain
Overall, 370/413 (89.6% [86.2-92.3]) patients reported HZ-associated pain at the initial visit with a mean score of 5.8 ± 2.4 (Table 3). Among the 353 patients who completed the three-month visit 73 (20.6% [16.5-25.2]) still reported pain, satisfying our definition for PHN; the percentage increased with age (14.3% of those aged 50–59 years, 20.2% of those aged 60–69 years and 24.5% of those aged ≥70 years) (Figure 2A). PHN was still present in 34 of the 368 patients at the six-month visit (9.2% [6.5-12.7]). The prevalence of pain at the month 3 and 6 visits was higher among patients who reported pain at the one-month visit (Figure 3). There was a non-statistically significant trend for more men than women to report pain at the one- and three-month visits (all p values >0.05).
The mean VAS score for patients who reported pain at each visit decreased from 5.8 (median 6) at enrolment to 3.7 (median 3) at the six-month visit. The percentage of patients with a VAS score ≥3 was 81.7% [77.6% - 85.4%] at the initial visit; 49.7% [44.5% - 54.9%] at the 1-month visit; 22.4% [18.1% - 27.2%] at the 3-month visit and 15.2% [12.0% - 20.0%] at the 6-month visit (Figure 2B).
Predictive factors for persistent HZ-associated pain
The results from the univariate analyses showed that the presence at the initial visit of >50 vesicles, allodynia, a VAS score ≥3, the PCS-12 score, the presence of diabetes or chronic cardiovascular disease or respiratory disease, age, a rash localized on the lumbar dermatome, being male and the MCS-12 score were potential predictive factors for the persistence of pain at three months (PHN). Multivariate analysis, including these variables, showed that the presence of >50 vesicles (OR = 2.595 [1.267-5.314]), a VAS score ≥3 (OR = 4.599 [1.181-17.907]) and being male (OR = 2.017 [1.006-4.042]) were significantly associated with PHN (p < 0.05) (Table 4).
Quality of life assessment
At the initial visit, the patients’ mean SF-12 scores were below the mean value of 50 (PCS-12 score = 40.1 ± 8.7, MCS-12 score = 41.7 ± 10.6 – Table 2). Both scores were lower in women and in older patients, particularly the PCS-12 score; patients without pain present at the visit had higher scores than those with pain. The mean PCS-12 and MCS scores in the study were lower than those in the healthy Italian population (Table 2) . During the study, the PCS-12 and MCS-12 scores in patients presenting with pain at the respective visit did not vary, except for a small decrease in the MCS-12 score (Table 3).
The results from this prospective study, performed in a large network of GPs in Italy, show that patients aged ≥50 years report that HZ is painful, it has a negative impact on their QoL, working patients need to take sick leave and increasing age is a risk factor for severity. The incidence of PHN was high (20.6% at three-months and 9.2% at 6-months), although the majority of patients received antiviral treatment.
All the patients included had a rash even if the presence of rash was not an inclusion criterion, suggesting that the GPs diagnosed HZ based on the presence of the typical rash. We cannot exclude erroneous diagnosis since there was no laboratory confirmation. In the pivotal HZ vaccine clinical trial in adults, 5–6% of the clinical diagnoses were not confirmed in the laboratory . Similarly, a prospective study of HZ diagnoses by GPs found 17% of diagnoses to be incorrect .
In HEROES, the patients enrolled do not seem to have suffered from severe disease as none were hospitalised. In Italy, the HZ hospitalization rate has been reported to be 5.6 per 100,000 patients and 10.3 per 100,000 for those with PHN . The study was designed to have sufficient power to estimate the percentage of patients with HZ-associated pain, but was insufficient to detect HZ hospitalization. It is possible that patients with more severe disease may have consulted a specialist or were hospitalized directly. In addition, the low rate of consultations with specialists (12.3% during the six-month study) and the delay of about three days between rash onset and the GP visit suggest that the patients included in this study were suffering from non- severe to moderately-severe disease.
We observed a higher incidence of HZ-associated pain than that observed in the placebo group of the pivotal study (12% for PHN 3 months); however, the percentage of men was higher in the pivotal study and the subjects were older (≥60 years) so the age distribution was different . In a French study, 11.6% of patients with HZ suffered from HZ-associated pain at 3-months, as declared by the patients whereas in a UK study there were about 27% of patients who suffered from PHN ,. These differences could be due to different access to healthcare and pain management or the method used to assess the HZ-associated pain. This last point is highlighted by the slightly different estimates for HZ-associated pain for the primary and secondary outcomes we observed in our study. Additionally, the VAS score was missing for 10.2% and 13.6% of patients at the 3- and 6-month visits, respectively; we cannot exclude that patients who suffered more from pain were more likely to complete the VAS score.
The percentage of patients with PHN reported in retrospective database studies ranged from 6.9% to 32% ,,,-. Retrospective studies using International Classification of Disease (ICD) codes to extract data from databases do not always provide a reliable estimate of HZ and PHN incidences because of possible miscoding and under-coding. Additionally, the absence of a specific ICD code for PHN makes database extraction less reliable for this endpoint. The prospective design of our study, including three follow-up visits, enabled a better diagnosis of PHN than retrospective studies. Nevertheless, even if the actual estimates were different, the studies also generally reported an age-related increase in the percentage of patients with HZ-associated pain. The percentage of patients with PHN observed in HEROES was lower than the 40% assumed for the sample size estimation. Although we recruited fewer than the original target of 500 patients, we had data for the planned 400 patients needed to estimate the percentages of patients with PHN at 3 and 6 months with good precision. PHN can last for several months to several years but in this study we followed the patients for six months. This may have led to an underestimation of the true clinical burden of PHN. In this study, general practitioners recruited the participants. In Italy patients need to be referred for specialist care by their general practitioner, and even when they use private healthcare to consult a specialist directly, they have to report to their general practitioner for reimbursement of prescriptions via the national health system. Hence are results are likely to be generalizable in healthcare systems requiring referral for specialist appointments.
The presence of >50 vesicles, a VAS score ≥3 and being male were identified as variables that were associated with PHN at three months. The first two variables have been reported previously to be associated with a higher risk of developing PHN at three months suggesting that PHN is probably linked to more severe acute episodes of HZ . However, other studies have either not reported any gender differences or have reported an increased risk in women, unlike our study. This may be due to differences in study methodology or, perhaps, in our study, women underestimated the level of their pain. It is also conceivable that there are more women in the older-age groups, so that there is confounding with age .
Most of the patients (91.5%) in HEROES received antivirals as recommended, which is similar to that reported in other studies ,,. In contrast, only 23% of our patients were reported as receiving pain therapy. This could be due to the low disease severity or because in Italy the most frequent pain therapies, i.e. paracetamol and NSAIDs are available without prescription and were, therefore, not reported by the physicians.
With the predicted ageing of the European population in the coming decades, the number of people affected by HZ and its related complications, including PHN, can also be expected to increase . Preventive strategies, including vaccines, are thought to play an important role in the promotion of healthy ageing. Immunosenescence is reported to increase the risk of developing HZ due to an impaired T -cell-mediated immunity. In the Shingles Prevention Study, a live-attenuated Oka/Merck strain VZV vaccine was shown to reduce the incidences of HZ and PHN significantly, compared with placebo . This vaccine is indicated in the EU for adults aged ≥50 years; in 2013, the UK started a shingles vaccination program targeting those aged between 70 and 79 years.
These data suggest that there is an important burden of disease in the elderly due to HZ. There is a need for interventions that can prevent and reduce the burden of HZ to help improve the quality of life of the elderly. These data may be useful as baseline epidemiology data for the assessment of the impact of the VZV vaccine in Italy, after its implementation.
Electronic case report form
HERpes zoster Outcome: Epidemiological Study
International Classification of Disease
Mental component score
Physical component score
Quality of life
Statistical Analysis System
Short form-12 (quality of life questionnaire)
Visual analogue scale
Varicella zoster virus
Johnson RW: Herpes zoster and postherpetic neuralgia. Expert Rev Vaccines. 2010, 9 (3 Suppl): 21-26. 10.1586/erv.10.30.
Kimberlin DW, Whitley RJ: Varicella-zoster vaccine for the prevention of herpes zoster. N Engl J Med. 2007, 356 (13): 1338-1343. 10.1056/NEJMct066061.
Johnson RW, Wasner G, Saddier P, Baron R: Postherpetic neuralgia: epidemiology, pathophysiology and management. Expert Rev Neurother. 2007, 7 (11): 1581-1595. 10.1586/1473718.104.22.1681.
Arvin A: Aging, immunity, and the varicella-zoster virus. N Engl J Med. 2005, 352 (22): 2266-2267. 10.1056/NEJMp058091.
Johnson RW: Herpes Zoster and Postherpetic Neuralgia: a review of the effects of vaccination. Aging Clin Exp Res. 2009, 21 (3): 236-243. 10.1007/BF03324909.
Schmader K: Herpes zoster in older adults. Clin Infect Dis. 2001, 32 (10): 1481-1486. 10.1086/320169.
Hicks LD, Cook-Norris RH, Mendoza N, Madkan V, Arora A, Tyring SK: Family history as a risk factor for herpes zoster: a case–control study. Arch Dermatol. 2008, 144 (5): 603-608. 10.1001/archderm.144.5.603.
Thomas SL, Hall AJ: What does epidemiology tell us about risk factors for herpes zoster?. Lancet Infect Dis. 2004, 4 (1): 26-33. 10.1016/S1473-3099(03)00857-0.
Prevention of herpes zoster. Recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. 2008, 57: 1-30.
Arvin AM: Varicella-zoster virus. Clin Microbiol Rev. 1996, 9 (3): 361-381.
Meister W, Neiss A, Gross G, Doerr H, Hobel W, Malin J, von Essen J, Reimann B, Witke C, Wutzler P: Demography, symptomatology, and course of disease in ambulatory zoster patients. A physician-based survey in Germany. Intervirology. 1998, 41 (6): 272-277. 10.1159/000024949.
Drolet M, Brisson M, Schmader KE, Levin MJ, Johnson R, Oxman MN, Patrick D, Blanchette C, Mansi JA: The impact of herpes zoster and postherpetic neuralgia on health-related quality of life: a prospective study. CMAJ. 2010, 182 (16): 1731-1736. 10.1503/cmaj.091711.
Volpi A, Gatti A, Pica F, Bellino S, Marsella LT, Sabato AF: Clinical and psychosocial correlates of post-herpetic neuralgia. J Med Virol. 2008, 80 (9): 1646-1652. 10.1002/jmv.21254.
Hempenstall K, Nurmikko TJ, Johnson RW, A’Hern RP, Rice AS: Analgesic therapy in postherpetic neuralgia: a quantitative systematic review. PLoS Med. 2005, 2 (7): e164-10.1371/journal.pmed.0020164.
Dworkin RH, Johnson RW, Breuer J, Gnann JW, Levin MJ, Backonja M, Betts RF, Gershon AA, Haanpaa ML, McKendrick MW, Nurmikko TJ, Oaklander AL, Oxman MN, Pavan-Langston D, Petersen KL, Rowbotham MC, Schmader KE, Stacey BR, Tyring SK, Van Wijck AJ, Wallace MS, Wassilew SW, Whitley RJ: Recommendations for the management of herpes zoster. Clin Infect Dis. 2007, 44 (Suppl 1): S1-S26. 10.1086/510206.
Bouhassira D, Chassany O, Gaillat J, Hanslik T, Launay O, Mann C, Rabaud C, Rogeaux O, Strady C: Patient perspective on herpes zoster and its complications: an observational prospective study in patients aged over 50 years in general practice. Pain. 2012, 153 (2): 342-349. 10.1016/j.pain.2011.10.026.
Forbes HJ, Thomas SL, Smeeth L, Langan SM: Prescription of antiviral therapy after herpes zoster in general practice: who receives therapy?. Br J Gen Pract. 2012, 62 (605): e808-e814. 10.3399/bjgp12X659277.
Opstelten W, van Essen GA, Moons KG, van Wijck AJ, Schellevis FG, Kalkman CJ, Verheij TJ: Do herpes zoster patients receive antivirals? A Dutch National Survey in General Practice. Fam Pract. 2005, 22 (5): 523-528. 10.1093/fampra/cmi055.
Parruti G, Tontodonati M, Rebuzzi C, Polilli E, Sozio F, Consorte A, Agostinone A, Di Masi F, Congedo G, D’Antonio D, Granchelli C, D'Amario C, Carunchio C, Pippa L, Manzoli L, Volpi A: Predictors of pain intensity and persistence in a prospective Italian cohort of patients with herpes zoster: relevance of smoking, trauma and antiviral therapy. BMC Med. 2010, 8: 58-10.1186/1741-7015-8-58.
Li Q, Chen N, Yang J, Zhou M, Zhou D, Zhang Q, He L: Antiviral treatment for preventing postherpetic neuralgia. Cochrane Database Syst Rev 2009, (2):Cd00686.,
Pinchinat S, Cebrian-Cuenca AM, Bricout H, Johnson RW: Similar herpes zoster incidence across Europe: results from a systematic literature review. BMC Infect Dis. 2013, 13: 170-10.1186/1471-2334-13-170.
Mick G, Hans G: Postherpetic neuralgia in Europe: the scale of the problem and Outlook for the future. J Clin Gerontol Geriat. 2013, 4 (4): 102-108. 10.1016/j.jcgg.2013.03.001.
di Luzio PU, Arpinelli F, Visona G: Herpes zoster and its complications in Italy: an observational survey. J Infect. 1999, 38 (2): 116-120. 10.1016/S0163-4453(99)90079-8.
Di Legami V, Gianino MM, Ciofi degli Atti M, Massari M, Migliardi A, Tomba GS, Zotti C: Epidemiology and costs of herpes zoster: background data to estimate the impact of vaccination. Vaccine. 2007, 25 (43): 7598-7604. 10.1016/j.vaccine.2007.07.049.
Gialloreti LE, Merito M, Pezzotti P, Naldi L, Gatti A, Beillat M, Serradell L, di Marzo R, Volpi A: Epidemiology and economic burden of herpes zoster and post-herpetic neuralgia in Italy: a retrospective, population-based study. BMC Infect Dis. 2010, 10: 230-10.1186/1471-2334-10-230.
Gabutti G, Serenelli C, Cavallaro A, Ragni P: Herpes zoster associated hospital admissions in Italy: review of the hospital discharge forms. Int J Environ Res Public Health. 2009, 6 (9): 2344-2353. 10.3390/ijerph6092344.
Guidelines for the classification and conduct of pharmaceutical observation studies [Linee guida per la classificazione e conduzione degli studi osservazionali sui farmaci] , [http://www.agenziafarmaco.gov.it/allegati/det_20marzo2008.pdf]
Good Epidemiological Practice (GEP) , [http://ieaweb.org/good-epidemiological-practice-gep/]
Ware J, Kosinski M, Keller SD: A 12-item short-form health survey: construction of scales and preliminary tests of reliability and validity. Med Care. 1996, 34 (3): 220-233. 10.1097/00005650-199603000-00003.
Coplan PM, Schmader K, Nikas A, Chan IS, Choo P, Levin MJ, Johnson G, Bauer M, Williams HM, Kaplan KM, Guess HA, Oxman MN: Development of a measure of the burden of pain due to herpes zoster and postherpetic neuralgia for prevention trials: adaptation of the brief pain inventory. J Pain. 2004, 5 (6): 344-356. 10.1016/j.jpain.2004.06.001.
Cebrian-Cuenca AM, Diez-Domingo J, San-Martin-Rodriguez M, Puig-Barbera J, Navarro-Perez J: Epidemiology and cost of herpes zoster and postherpetic neuralgia among patients treated in primary care centres in the Valencian community of Spain. BMC Infect Dis. 2011, 11: 302-10.1186/1471-2334-11-302.
Scott FT, Leedham-Green ME, Barrett-Muir WY, Hawrami K, Gallagher WJ, Johnson R, Breuer J: A study of shingles and the development of postherpetic neuralgia in East London. J Med Virol. 2003, 70 (Suppl 1): S24-S30. 10.1002/jmv.10316.
Mick G, Gallais JL, Simon F, Pinchinat S, Bloch K, Beillat M, Serradell L, Derrough T: Burden of herpes zoster and postherpetic neuralgia: incidence, proportion, and associated costs in the french population aged 50 or over. Rev Epidemiol Sante Publique. 2010, 58 (6): 393-401. 10.1016/j.respe.2010.06.166.
SF-12 health survey: Italian version [Questionario sullo stato di salute SF-12 Versione italiana) , [http://crc.marionegri.it/qdv/downloads/SF12%20Manuale.pdf]
Oxman MN, Levin MJ, Johnson GR, Schmader KE, Straus SE, Gelb LD, Arbeit RD, Simberkoff MS, Gershon AA, Davis LE, Weinberg A, Boardman KD, Williams HM, Zhang JH, Peduzzi PN, Beisel CE, Morrison VA, Guatelli JC, Brooks PA, Kauffman CA, Pachucki CT, Neuzil KM, Betts RF, Wright PF, Griffin MR, Brunell P, Soto NE, Marques AR, Keay SK, Goodman RP: A vaccine to prevent herpes zoster and postherpetic neuralgia in older adults. N Engl J Med. 2005, 352 (22): 2271-2284. 10.1056/NEJMoa051016.
Whitley RJ, Volpi A, McKendrick M, Wijck A, Oaklander AL: Management of herpes zoster and post-herpetic neuralgia now and in the future. J Clin Virol. 2010, 48 (Suppl 1): S20-S28. 10.1016/S1386-6532(10)70005-6.
Cebrian-Cuenca AM, Diez-Domingo J, Rodriguez MS, Puig-Barbera J, Navarro-Perez J: Epidemiology of herpes zoster infection among patients treated in primary care centres in the Valencian community (Spain). BMC Fam Pract. 2010, 11: 33-10.1186/1471-2296-11-33.
Gauthier A, Breuer J, Carrington D, Martin M, Remy V: Epidemiology and cost of herpes zoster and post-herpetic neuralgia in the United Kingdom. Epidemiol Infect. 2009, 137 (1): 38-47. 10.1017/S0950268808000678.
Schiffner-Rohe J, Jow S, Lilie HM, Koster I, Schubert I: Herpes zoster in Germany. A retrospective analyse of SHI data [Herpes zoster in Deutschland. Eine retrospektive Analyse von GKV-Daten]. MMW Fortschr Med. 2009, 151 (Suppl 4): 193-197.
Johnson RW, Dworkin RH: Treatment of herpes zoster and postherpetic neuralgia. BMJ. 2003, 326 (7392): 748-750. 10.1136/bmj.326.7392.748.
Eurostat: Active Ageing and Solidarity Between Generations. A Statistical Portrait of the European Union 2012. In 12th edition. Luxembourg: Publications Office of the European Union; 2012.
The authors take full responsibility for the contents of this manuscript but would like to thank Margaret Haugh, MediCom Consult (supported by Sanofi Pasteur MSD) for her assistance in the preparation of the manuscript.
The authors would like to thank all the study investigators: local health unit (LHU) of Asti: G. De Maria, C. Torello, C. Nuti; LHU of Bologna: A. Guerra, L. Gaggioli, M. Casadei, A.L. Lalli, A. Matrà; LHU of Brindisi: G.A. D’Urso, P. Caliandro, F. Siliberto, G. Gatti, G. Mastro, B. Giordano, A. Suma; LHU of Bussolengo (VR): S. Mantovani, A. Severi, A.M. Oliva, A. Panzino, C. Zanotto; LHU of Carbonia (CI): E. Piras, L. Lisci, S. Massa, R.Rovere, B. Putzolu; LHU of Catanzaro: G.G. Arturi, C.L. Rossi, A. De Felice, F. Bellini, V. Capilupi, A. Battaglia, F. Vasta, F. Moniaci; LHU of Ferrara: S. Gamberoni, C. Roveggio, M. Gennari, B. Fabbri; LHU of Grosseto: G. Guidoni, A. Salvetti, T. Iocca, M. Zuccarello, G. Bellumori, L. Steri; LHU of Lecce: S. Miglietta, V. Ferrari, A. Chiriatti, I. Colona, A. Andrani; LHU of Milano: M.B. Pagani, V. Bova, D. Ciaci, C. Pirovano, S. Croci, G. Grandinetti, F. Marrali, I. Mussi, E. Noia, R. Palmieri, P. Rodriguez, N. Santoro, G. Scavone, U. Binda; LHU of Napoli/5: A. Apicella, G. Perasole, D. De Riso, A. Frunzio, A. Varone, G. Arpaia; LHU of Pescara: W. Del Ponte, S. Di Marco, M. Palombo, C. Carunchio, O. Di Domizio, M. Buffone; LHU of Ragusa: B. La TerraBella, G. Dezio, S. Dipasquale, R. Zelante, G. DiGiacomo, M. Iudice, S. Bennardo, G. Ferro; LHU of Roma/C: A. Nobile, G. Piccolelli, C. Prono, M. Pitrolo, P. LeVoci, P. Marchetti, C. Di Mauro, G. Salvi; LHU of Roma/H: A. Nigro, M. Mazzilli, G. Riggio, C. Villari, F. LaManna, G. Cerroni, V. Gatti, E. Grimaldi, F. De Ligio, A. Ottaviani; LHU of Teramo: G. De Berardinis, G. D’Isidoro, M. Di Paolantonio, U. Scardecchia, O. Di Andrea; LHU of Torino/1: E. Bianco, S. Panèro, P. Fracchia, M. M. Di Sario, P. Lapi, M. Grasso, A. Pugliese, A. Lambarelli; LHU of Treviso: A.Moro, G. Simeone, P. Tullio; LHU of Varese: L. Felloni, G. Ronzi, F. Blesi, F. Colombo, M. Passamonti, W. Colombo, M.E. Perego, T. Dell’Arciprete, F. Baranzini; LHU of Verona: A.Tosi, H. Mehrabi, L. Menegazzi, A. Guido, E. Mascalzoni, R. Trespidi; LHUof Vibo Valentia: A. D’Amico, A. Burello, C. Zavettieri, G. Spanarello, A. Teramo, N.B. Arena.
The authors would also like to thank Pierrel Research (Milano, Italy) for project management, study monitoring, data management and statistical analyses, and the following Sanofi Pasteur MSD employees for their contributions to the study: Raffaele Di Marzo (study design), Laurence Serradell-Vallejo (study management) and Perrine Bertet (data management).
Helene Bricout and Emilia Perinetti: work for Sanofi Pasteur MSD who commercialise the vaccine Zostavax®, produce by MSD, in Europe.
Paolo Marchettini: has been an advisor for Sanofi Pasteur MSD.
Pietro Ragni: has received grants from Sanofi Pasteur MSD for being a member of advisory boards over the last five years.
Carla Maria Zotti: declared no conflicts of interest.
Giovanni Gabutti: over the last five years, has received grants from Sanofi Pasteur MSD, GlaxoSmithKline Biologicals SA, Novartis, Crucell/Janssen and Pfizer for taking part in advisory boards, expert meetings, being a speaker or an organiser of congresses / conferences, and acting as investigator in clinical trials; is a member of an Independent Data Monitoring Committee of a phase 3 clinical trial on an herpes zoster vaccine.
Antonio Volpi: over the last five years, has received grants from Sanofi Pasteur MSD and GlaxoSmithKline for advisory boards, expert meetings, and acting as an investigator in clinical trials is as a member of an Independent Data Monitoring Committee of a phase 3 clinical trial on a varicella vaccine.
Elisabetta Franco: has received research grants paid by Sanofi Pasteur MSD and Pfizer to her institution; has received payments from GlaxoSmithKline Biologicals SA, Pfizer, Janssen and Sanofi Pasteur MSD for travel and accommodation for meeting attendance.
All authors contributed to the drafting and review of the manuscript and validated the final version. HB: Study follow-up, data management and data analysis, study report, interpretation of the results, writing of the manuscript outline. EP: Study coordination and review of all study documents. PM: Protocol development, critical review and interpretation of the data. PR: Conception, design and planning of the study. CMZ: Recruitment of investigators in Turin LHUs and assistance to the MMG during the study. AV: Conception, design and planning of the study, critical review and interpretation of the data. EF: Conception, design and planning of the study, critical review and interpretation of the data. GG: Conception, design and planning of the study, critical review and interpretation of the data. All authors read and approved the final manuscript.