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BMJ Open logoLink to BMJ Open
. 2021 Dec 17;11(12):e057225. doi: 10.1136/bmjopen-2021-057225

Influenza and morbidity and mortality risk in patients in Mexico with systemic arterial hypertension alone or with comorbidities: a retrospective, observational, cross-sectional study from 2014 to 2020

Alejandrina Malacara-Villaseñor 1, Hermes Ilaraza-Lomeli 2, Roberto Tapia-Conyer 3, Elsa Sarti 1,
PMCID: PMC8685964  PMID: 34921092

Abstract

Objectives

In Mexico, patients with systemic arterial hypertension (SAH) are excluded from the influenza vaccination programme despite their risk of cardiovascular events as influenza-related complications. We investigated the impact of influenza on morbidity and mortality in patients with SAH.

Design

This was a retrospective cross-sectional study that analysed data from early 2014 to mid-2020.

Setting

Data were obtained from the Influenza Epidemiological Surveillance System in Mexico database.

Participants

32 663 cases of influenza in people aged ≥20 years with a confirmed case of influenza-like illness, severe respiratory infection and/or influenza death were investigated.

Primary and secondary outcome measures

Influenza deaths, hospitalisation frequency and the impact on hospitalisation and/or death due to influenza by the SAH variate alone and in combination with diabetes, obesity, chronic obstructive pulmonary disease, cardiovascular disease and/or smoking, and by vaccination status were assessed.

Results

The hospitalisation frequency increased with age. Notably, 46.0% (15 033/32 663) of confirmed influenza cases had at least one comorbidity, with SAH (19.2%; 6260/32 663) and obesity (18.7%; 6106/32 663) being the most prevalent. Most confirmed SAH cases (80.8%; 5057/6260) were in those who had not been vaccinated against influenza. There were 3496 deaths due to influenza (mortality rate, 0.69×1 00 000 inhabitants), with the highest rates seen in those aged ≥80 years (80–89 years, 2.0%; ≥90 years, 3.6%). The case fatality rate due to influenza and SAH was significantly higher than those due to influenza without SAH in those aged <50 years, but not in the other age groups (20–29 years, 9.8%, p<0.0005; 30–39 years, 8.2%, p<0.035; 40–49 years, 17.8%, p<0.0005; vs 15.1%–20.0%, p=0.31–0.99 for those aged ≥50 years).

Conclusions

Our findings support the need to include SAH in public policies of influenza vaccination as a secondary prevention measure to avoid fatal outcomes.

Keywords: epidemiology, hypertension, public health


Strengths and limitations of this study.

  • Our study helped clarify the risk–benefit balance of excluding patients with systemic arterial hypertension (SAH) from the influenza vaccination programme in Mexico.

  • This large-scale retrospective study included data of over 30 000 influenza patients.

  • We assessed the impact of SAH (among other comorbidities) on various outcomes related to influenza infection, such as death and hospitalisation frequency.

  • The study was limited in that the database from which influenza morbidity data were obtained covers <10% of the health units throughout Mexico.

  • A further limitation was that vaccination history was obtained by questioning the patient, which is likely to be less reliable than official paper or electronic documentation.

Introduction

Influenza, which is caused by an RNA virus, is a public health problem affecting approximately 5%–10% of adults and 20%–30% of children worldwide, with 3–6 million cases reported each year and more than 640 000 deaths per year.1 2 Additionally, influenza has a great potential to cause respiratory disease pandemics.3 4

Vaccination is one of the most cost-effective strategies for the prevention and control of many diseases. In the case of influenza, the implementation of vaccination campaigns worldwide has decreased mortality and morbidity.5 Currently, the vaccination policy offered in Mexico covers children <5 years old; adults >60 years of age; those aged 5–60 years with risk factors such as asthma, heart diseases, immunodeficiencies, haemoglobinopathies, asplenia, chronic kidney disease, diabetes, obesity and arthritis; and pregnant women and healthcare workers.6 7 However, it excludes people diagnosed with systemic arterial hypertension (SAH), leaving patients with this chronic disease unprotected and at risk of having a cardiovascular disease (CVD) episode as a complication of influenza infection.8 9

During the last 20 years, SAH has been identified as one of the most important risk factors for morbidity and mortality globally.10 According to the 2018 Mexican National Health and Nutrition Survey (ENSANUT), the prevalence of SAH in the population aged 20 years and older is 18.4% (women, 20.9%; men, 15.3%), representing at least 15.2 million Mexican people.11 12 Although few studies focused on SAH and the impact of influenza vaccination are published,13–16 the WHO recently recommended including patients with only SAH as a risk group to be vaccinated.17

Given that the prevalence of SAH in Mexico is steadily increasing, mainly in adults older than 20 years,11 12 and that SAH by itself is not considered a risk factor for access to influenza vaccination in accordance with the public health policy of Mexico, this study was designed to determine the risk for each of the usual influenza outcomes (outpatient illness, hospitalisation and/or death) in patients with SAH in Mexico.

Methods and analysis

Study design and patients

The present study was a retrospective cross-sectional study using data from the Influenza Epidemiological Surveillance System in Mexico (SISVER). As this was an observational study with a secondary data source, it was not considered research with risk per article 17 of the Regulations of the General Health Law in the Field of Health Research.18

The SISVER sentinel surveillance system uses an influenza case definition as follows: (a) suspected cases include a clinical diagnosis of influenza-like illness (ILI) and/or an epidemiological association and (b) confirmed cases are diagnosed by real-time quantitative RT-PCR (qRT-PCR). The system collects biological samples and exhaustive clinical and epidemiological information on 10% of ILI cases and 100% of severe acute respiratory infection (SARI) cases and deaths due to influenza that occur in Mexico.6 19 The sampling strategy for deciding which of the 10% of ILI cases were collected and analysed is as follows: in each health unit from SISVER, samples were to be taken from the first suspected case and sent to the laboratory for confirmation. Samples were not collected for the following nine cases and the process was repeated for every 10 cases.6 19 Regarding the information collected, if the case was ambulatory, the clinical information was collected through patient interview, but if it was an in-hospital case, it was collected from medical chart review. A case was considered an in-hospital case if the patient spent at least 24 hours in hospital. In cases where the patient died, the information was also collected from the death certificate.

In this retrospective cross-sectional study, the SISVER database (Oficio de transparencia DGE-DGAE de la Secretaría de Salud con número 005533 referente a la Solicitud 0001200189920 del 4 de junio de 2020; the database was provided via a disk for the purpose of analysis and is not publicly available) entries from 1 January 2014 to 15 May 2020 were included. The analysis included all records of patients ≥20 years old who were diagnosed with a laboratory confirmed influenza infection of ILI or SARI by qRT-PCR and who requested medical attention. A case of death by influenza included any deceased patient with ILI or SARI, who had a positive laboratory result for influenza, and whose death certificate contained a diagnosis of influenza or pneumonia as the basic cause of death. If something other than influenza or pneumonia was listed as the basic cause of death on the death certificate, that individual was not considered to be a case of death by influenza and was excluded from the present study. All influenza deaths were rectified or ratified by an influenza-specific governmental scientific committee. Deaths ratified by this committee were included in the present study.19

Outcomes and statistical analysis

A descriptive analysis of the variables studied was performed, as well as bivariate and stratified (by age group) analyses considering the impact on hospitalisation and/or death due to influenza by the SAH variate alone and/or combined with diabetes, obesity, chronic obstructive pulmonary disease (COPD), CVD and/or smoking, and by influenza vaccination status. ORs were calculated considering the comparison between confirmed influenza cases with SAH alone or with other comorbidities, versus confirmed influenza cases without SAH, diabetes, obesity, COPD, CVD or a smoking habit. However, they could have diseases or lesions other than those listed. Statistical significance was determined using the χ2 test or Fisher’s exact test. Incidence rates were estimated considering the total number of new confirmed influenza cases per 100 000 inhabitants of each specific age group and totalled for persons-years of observation. Similarly, case fatality rates were determined by calculating the cases with influenza-related death over the confirmed cases per 100 inhabitants. Although the incidence rate calculations did not take into account the sampling scheme, the mortality and hospitalisation calculations took into account 100% of influenza cases reported in Mexico. For statistical analyses, Microsoft Excel (Microsoft Corp, Redmond, Washington, DC, USA), SPSS-PC (IBM, Armonk, New York, USA) and Epi Info software (Centers for Disease Control and Prevention, Atlanta, Georgia, USA) were used.

Patient and public involvement

Patients or the public were not involved in the design, conduct, or reporting or dissemination plans of our research.

Results

Cases

A total of 32 663 confirmed cases of influenza were analysed; most of them were women (56.0% (18 284/32 663) vs 44.0% (14 379/32 663) men), the mean and median ages for women were 46 and 44 years, and for men, 47 and 46 years, respectively. The years 2014 (21.1%, 6892/32 663), 2016 (21.9%, 7149/32 663) and 2017 (15.8%, 5147/32 663) had the highest number of confirmed influenza cases, which corresponded to the seasons that also had the highest rates.20

The highest proportion of cumulative cases was in the group aged 30–39 years (21.3%, 6952/32 663), followed by the group aged 40–49 years (20.8%, 6806/32 663); however, the highest incidence rate per 100 000 inhabitants corresponded to elderly patients, especially those aged ≥80 years. Among all confirmed influenza cases, 19 948/32 663 (61.1%) were inpatient cases, and 12 715/32 663 (38.9%) were outpatient cases. The highest proportion of hospitalised influenza cases was in patients aged ≥80 years, with the frequency of hospitalisation increasing with age. For each outpatient case of influenza, 1.56 persons were hospitalised (online supplemental table S1).

Supplementary data

bmjopen-2021-057225supp001.pdf (249.2KB, pdf)

Among all confirmed influenza cases, 46.0% (15 033/32 663) of patients had at least one comorbidity. SAH and obesity were the most prevalent, at 19.2% (6260/32 663) and 18.7% (6106/32 663), respectively, followed by type 2 diabetes (17.7%, 5794/32 663), smoking (11.4%, 3711/32 663), COPD (6.5%, 2136/32 663) and CVD (4.9%, 1607/32 663). When comorbidities were broken down by age group, the burden of influenza disease and obesity was notable mainly in those <50 years of age, and among those aged ≥50 years, SAH and diabetes were more prevalent (figure 1). The combination of SAH with another comorbidity of interest was more frequent for diabetes (8.8%, 2884/32 663) and obesity (6.6%, 2143/32 663) and less frequent for COPD (2.8%, 925/32 663), smoking (2.7%, 881/32 663) and CVD (2.4%, 772/32 663).

Figure 1.

Figure 1

Cumulative influenza cases by age and comorbidity groups. COPD, chronic obstructive pulmonary disease; CVD, cardiovascular disease; SAH, systemic arterial hypertension.

Regarding the vaccination history against influenza, 80.8% of those with a confirmed case of SAH (5057/6260) had not been vaccinated, and only 15.1% (944/6260) had been vaccinated. The percentages do not add up to 100% because the vaccination status was unknown for some patients.

Deaths

In total, 3496 deaths due to influenza (overall mortality rate of 0.69×100 000 inhabitants) were reported, with the group aged ≥80 years presenting the highest rates, followed by the group aged 60–69 years. Regarding case fatality rates, the overall rate was 10.7% (3496/32 663), with the group aged 60–69 years presenting the highest rate (19.4%, 690/3562), even when compared with the group aged ≥90 years (17.1%, 72/421).

Similar trends were observed with the mortality rates of influenza and SAH, where the higher the age group, the higher the mortality rate; however, in the case of fatality due to influenza and SAH, the groups aged <50 years had significantly higher rates in comparison with the same age groups but without SAH, showing that having influenza with SAH leads to worse outcomes in specific age groups (table 1).

Table 1.

Overall mortality and case fatality rates by influenza alone and combined with systemic arterial hypertension (SAH), by age group

Age group, years Confirmed influenza cases Deaths from confirmed influenza cases (n) Overall mortality rate* Fatality rate of confirmed influenza cases† Confirmed cases of influenza and SAH Deaths from confirmed influenza and SAH (n) Confirmed influenza and SAH mortality rate* Fatality rate of confirmed influenza and SAH cases† P value‡
20–29 5782 150 0.1 2.6 153 15 0.01 9.8 <0.0005
30–39 6952 380 0.3 5.5 380 31 0.03 8.2 <0.035
40–49 6806 784 0.8 11.5 984 175 0.2 17.8 <0.0005
50–59 5630 889 1.2 15.8 1553 247 0.3 15.9 0.92
60–69 3562 690 1.5 19.4 1412 273 0.6 19.3 0.99
70–79 2175 338 1.4 15.5 984 149 0.6 15.1 0.73
80–89 1335 193 2.0 14.5 614 94 1.0 15.3 0.52
≥90 421 72 3.6 17.1 180 36 1.8 20.0 0.31
Total 32 663 3496 0.7 10.7 6260 1020 0.2 16.3

*Per 100 000 person-years.

†Per 100.

‡χ2 test.

The influenza case fatality rates found in patients with SAH (16.3%; 1020/6260) increased when data were analysed by pairs of SAH plus other comorbidities such as diabetes (19.5%; 534/2741), obesity (18.6%; 385/2068), CVD (19.1%; 138/721), COPD (16.8%; 146/871) and smoking (21.8%; 185/849) (online supplemental table S2).

When observing the influenza case fatality rates with the presence of SAH alone (figure 2A) compared with those who died without a history of SAH, a clear impact of this morbid condition was observed in those aged <50 years (mainly in those aged 20–29 years), but not in those aged ≥50 years, where it seems that the effect of age itself contributed to death.

Figure 2.

Figure 2

(A) ORs and CIs of case fatality rates by age group when compared between patients with and without SAH and (B) influenza case fatality rates in patients with SAH according to their age group and vaccination status. Error bars show 95% CIs in (A). SAH, systemic arterial hypertension.

When the analysis was performed considering the different SAH pairs, a greater risk effect was observed in the group of patients aged 30–39 years when combined with diabetes, obesity, COPD, CVD and smoking. Notably, in the combination of SAH with obesity, the greatest risk was found in the group aged 20–29 years (table 2).

Table 2.

Case fatality rates of influenza and systemic arterial hypertension (SAH) combined with other comorbidities and ORs of these rates when compared with patients who died without comorbidities

Influenza+SAH and diabetes Influenza +SAH and obesity
Age group, years Influenza deaths (n)/influenza cases (n) (with SAH and diabetes) CFR with SAH and diabetes, % Influenza deaths (n)/influenza cases (n) (without SAH and diabetes) CFR without SAH and diabetes, % OR CI P value Influenza deaths (n)/influenza cases (n) (with SAH and obesity) CFR with SAH and obesity, % Influenza deaths (n)/ influenza cases (n) (without SAH and obesity) CFR without SAH and obesity, % OR CI P value
20–29 0/23 0.0 150/5759 2.6 0 to 6.6 0.43 3/49 6.1 147/5733 2.6 2.4 0.7 to 7.7 0.29
30–39 10/91 11.0 370/6861 5.4 2.0 1.1 to 3.9 0.053 18/172 10.5 362/6780 5.3 2.0 1.2 to 3.2 0.01
40–49 86/389 22.1 698/6417 10.9 2.0 1.6 to 2.6 0.0000001 92/422 21.8 692/6384 10.8 2.0 1.6 to 2.6 0.00006
50–59 141/770 18.3 748/4860 15.4 0.9 0.7 to 1.1 0.4 112/605 18.5 777/5025 15.5 1.2 1.0 to 1.5 0.11
60–69 159/776 20.5 531/2786 19.1 1.1 0.9 to 1.3 0.49 99/494 20.0 591/3068 19.3 1.0 0.8 to 1.3 0.78
70–79 88/529 16.6 250/1646 15.2 1.1 0.8 to 1.4 0.53 37/261 14.2 301/1914 15.7 0.9 0.6 to 1.3 0.64
80–89 35/241 14.5 158/1094 14.4 1.0 0.7 to 1.5 0.97 21/121 17.4 172/1214 14.2 1.2 0.7 to 2.0 0.49
≥90 15/65 23.1 57/356 16.0 1.4 0.8 to 2.7 0.32 3/19 15.8 69/402 17.2 0.9 0.3 to 3.2 0.89
Total 534/2884 18.5 2962/29 779 10.0 2.0 1.8 to 2.2 0.003 385/2143 18.0 3111/30 520 10.2 1.7 1.6 to 2.0 0.001
Influenza+SAH and CVD Influenza+SAH and COPD
Age group, years Influenza deaths (n)/influenza cases (n) (with SAH and CVD) CFR with SAH and CVD, % Influenza deaths (n)/influenza cases (n) (without SAH and CVD) CFR without SAH and CVD, % OR CI P value Influenza deaths (n)/influenza cases (n)(with SAH and COPD) CFR with SAH and COPD, % Influenza deaths (n)/influenza cases (n) (without SAH and COPD) CFR without SAH and COPD, % OR CI P value
20–29 0/12 0.0 150/5770 2.6 0 to 19.9 0.57 0/4 0.0 150/5778 2.6 0 to 58.7 0.74
30–39 5/35 14.3 375/6917 5.4 2.6 1.0 to 6.8 0.036 4/22 18.2 376/6930 5.4 3.4 1.1 to 9.8 0.018
40–49 13/71 18.3 771/6735 11.5 1.6 0.9 to 2.9 0.11 13/57 22.8 771/6749 11.4 2.0 1.1 to 3.7 0.02
50–59 29/144 20.1 860/5486 15.7 1.3 0.9 to 1.9 0.27 14/115 12.2 875/5515 15.9 0.8 0.4 to 1.3 0.42
60–69 42/195 21.5 648/3367 19.3 1.1 0.8 to 1.6 0.52 30/220 13.6 660/3342 19.8 0.9 0.5 to 1.5 0.68
70–79 25/171 14.6 313/2004 15.6 0.9 0.6 to 1.4 0.76 36/237 15.2 302/1938 15.6 0.9 0.6 to 1.5 0.83
80–89 18/109 16.5 175/1226 14.3 1.2 0.7 to 2.0 0.58 34/205 16.6 159/1130 14.1 1.2 0.8 to 1.8 0.48
≥90 6/35 17.1 66/386 17.1 1.0 0.4 to 2.5 0.99 15/65 23.1 57/356 16.0 1.4 0.8 to 2.7 0.32
Total 138/772 17.9 3358/31 891 10.5 1.2 1.0 to 1.4 0.09 146/925 15.8 3350/31 738 10.5 1.1 0.9 to 1.4 0.35
Influenza+SAH and smoking Influenza+SAH, diabetes and obesity
Age group, years Influenza deaths (n)/ influenza cases (n) (with SAH and smoking) CFR with SAH and smoking, % Influenza deaths (n)/influenza cases (n) (without SAH and smoking) CFR without SAH and smoking, % OR CI P value Influenza deaths (n)/ influenza cases (n) (with SAH, diabetes and obesity) CFR with SAH, diabetes and obesity, % Influenza deaths (n)/ influenza cases (n) (without SAH, diabetes and obesity) CFR without SAH, diabetes and obesity, % OR CI P value
20–29 0/19 0.0 150/5763 2.6 0 0 to 8.3 0.48 0/12 0 136/5592 2.4 0 to 15.0 0.58
30–39 10/62 16.1 370/6890 5.4 3.0 1.5 to 5.9 0.002 7/50 14.0 314/6426 4.9 2.9 1.3 to 6.4 0.006
40–49 28/143 19.6 756/6663 11.4 1.7 1.1 to 2.6 0.012 38/186 20.4 530/5525 9.6 2.1 1.5 to 3.1 0.00001
50–59 40/201 19.9 849/5429 15.6 1.3 0.9 to 1.8 0.2 62/319 19.4 498/3693 13.5 1.4 1.1 to 1.9 0.015
60–69 50/209 23.9 640/3353 19.1 1.3 0.9 to 1.7 0.19 62/289 21.5 361/1995 18.1 1.2 0.9 to 1.6 0.25
70–79 26/128 20.3 312/2047 15.2 1.3 0.9 to 2.1 0.24 20/145 13.8 169/1184 14.3 1.0 0.6 to 1.6 0.99
80–89 22/93 23.7 171/1242 13.8 1.7 1.1 to 2.8 0.04 7/62 11.3 115/856 13.4 0.8 0.4 to 1.9 0.81
≥90 9/26 34.6 63/395 16.0 2.2 1.0 to 4.8 0.09 1/5 20.0 51/306 16.7 1.2 0.0 to 11.0 0.86
Total 185/881 21.0 3311/31 782 10.4 2.0 1.7 to 2.4 0.000001 197/1068 18.5 2174/25 577 8.5 2.2 1.9 to 2.5 0.0001

CFR, case fatality rate; COPD, chronic obstructive pulmonary disease; CVD, cardiovascular disease.

Concerning vaccination history, age groups and the presence or absence of SAH, influenza-related deaths were notably lower among patients who were vaccinated (<2%) compared with unvaccinated patients (range 7%–17%) (figure 2B). Similar trends were observed in patients with SAH and other comorbidities.

The risk of hospitalisation (OR 3.3; 95% CI 3.1 to 3.5; p<0.0001) and death due to influenza (OR 1.9; 95% CI 1.8 to 2.1; p<0.0001) was shown in patients with SAH, and these risks increased more in the presence of other comorbidities (online supplemental table S2). The risks of hospitalisation and death due to influenza were also high among unvaccinated patients, and these risks further increased in the presence of other comorbidities (online supplemental table S3).

Discussion

Several studies have investigated the impact of influenza and vaccination against influenza on morbidity and mortality in patients with comorbidities such as CVDs, diabetes, obesity, COPD and cerebrovascular disease, among others.6–9 However, few studies have been published regarding patients with only SAH and the impact of influenza vaccination. One Danish study showed that vaccination against influenza is associated with a reduction in the risk of all-cause mortality, cardiovascular mortality and myocardial infarction or stroke mortality in hypertensive patients without CVD.13 14 Nevertheless, this study did not compare this population with non-hypertensive patients, as all patients studied had SAH. Others have reported alterations in circulation in patients with influenza and patients with hypertension,8 15 and there is a high prevalence of hypertension (63%) and mortality due to myocardial infarction and influenza.8 16 The present study is among the few in which an association was found that explains the impact of influenza on morbidity and mortality in patients having SAH only.

Regarding the cases of influenza and its epidemiological pattern, the present results are consistent with those reported by other authors: the greater the number of comorbidities, the greater the risk of hospitalisation and death from influenza, and the older the patient, the higher the incidence and hospitalisation rates.21–23 Notably, the absolute number of cases was higher in the group aged 30–50 years (working-age population) who become a source of contagion in their work environment; the negative economic impact that this can have has been previously reported.24 Regarding comorbidities, obesity and diabetes were the second and third most prevalent comorbidities in this study, after SAH. While a link between risk factors such as obesity, hypertension, diabetes and black/Hispanic ethnicity and the severity of influenza infection has been previously reported,25 26 the presence of obesity has been suggested to be a possible confounding factor for these associations.27 The mechanism through which these four risk factors are associated with the severity of influenza infection is not yet fully understood.

In the present study, most of the patients with confirmed cases of influenza presented associated comorbidities, and 19.2% of the entire population evaluated, including patients >20 years of age, had SAH. This percentage is very similar to that published by the ENSANUT,11 which was 18.4% among a population >20 years of age. Therefore, despite the limitations of our study, we can infer that the results adequately reflect the situation in the country.

Regarding influenza fatality, most publications report that the older the age, the higher the death rate.28–31 However, in our study, the group with the highest case fatality rate was the group aged 60–69 years, even when compared with the case fatality rate in the groups aged ≥70 years. This supports the vaccination programme in Mexico where vaccination is offered free of charge to the whole population aged >60 years.

However, it is worth reflecting on other age groups. For instance, in the group aged 50–59 years, the case fatality rate was similar to that of the group aged 70–79 years and was even higher than that of the group aged 80–89 years. This has already been recognised by the Mexican health authorities, and even though the recommendation by the collegiate bodies on vaccination includes this group (in those >50 years old),7 the immunisation policy has yet to include this age group. A similar result was recently reported in a cross-sectional epidemiological study, in which the case fatality and mortality rate in this age group (50–59 years) was similar to that of patients >60 years old,24 equivalent to an estimated range of 0.3–2.9 million cases per year. The same study also reported that vaccination of this population is cost-effective; thus, implementing vaccination in this age group would be a necessary step.

People with a diagnosis of SAH alone are not considered as a vulnerable or at-risk population in the official guidelines. In the present study, the highest ORs were found in groups <50 years of age, mainly in the group aged 20–39 years, and these are groups that are not considered in the vaccination recommendations either because of their age or because of a comorbidity with hypertension. In the last national health survey of the country,12 it was reported that among adults aged 20–29 years, 5.6% had a previous diagnosis of SAH, in addition to 6.5% who were detected as hypertensive during the survey; in the group aged 30–39 years, these frequencies were 8.4% and 7.7%, respectively, and in the group aged 40–49 years, the frequencies increased to 16.8% for previous diagnosis and 12.1% by survey finding. Combining these results with our present findings, we found that 12.1% of those aged 20–29 years, 16.1% of the group aged 30–39 years and 28.9% of the group aged 40–49 years had a mortality risk from influenza that was 1.7 to 4 times higher than that in the population without a comorbidity with SAH. The population with SAH is not recommended for vaccination in the current policy in Mexico, which would lead to an increase in the risk of hospitalisation and death from influenza in unvaccinated patients with SAH especially when other comorbidities are present.

Conversely, the effect of SAH in younger age groups was not observed in those aged 60–79 years where the highest overall fatality was observed. A possible explanation is that because this group of patients is known to be hypertensive, they were hospitalised earlier and received a more careful medical supervision, thus avoiding a fatal outcome. Of note, the official recommendations include this group among those recommended for vaccination.

It is essential to point out that hypertension alone is not the direct cause of death, but rather that influenza can lead to a cardiovascular event in a hypertensive patient.32–34 In this regard, there is evidence indicating that in patients with coronary artery disease, it is advisable to vaccinate against influenza since it is associated with a decrease in all-cause mortality.35 The same occurs with heart failure patients in whom this decrease in all-cause mortality is also shown.

Overall, findings from this study support the need to apply the vaccine recommendation to those >50 years of age and to include populations with SAH17 in the influenza vaccination programme as a secondary prevention measure to avoid fatal outcomes. Specifically, we recommend the current guidelines be changed to replace ‘Cardiovascular disease excluding SAH’ with ‘Cardiovascular disease including SAH’.36 We expect that this new recommendation will benefit around 15 million people.

The present study has some limitations. Data for this study were obtained from a government database, and there are generally several limitations that must be considered for a correct interpretation of the results. For example, even though the results presented here give an epidemiological overview of the country, they do not represent the burden of disease (morbidity) because SISVER in Mexico operates under a sentinel model that covers less than 10% of the total number of health units in the country. This is not the case for deaths because according to official guidelines, 100% of influenza deaths should be reported to SISVER. Other possible reporting biases are related to vaccination history and comorbidities. Regarding the vaccination history, this is obtained by questioning the patient instead of via the submission of documents, so having an electronic vaccination system would objectively substantiate the vaccination status of any patient. As for the presence of comorbidities, this can be substantiated in inpatients, as opposed to outpatients, where it is only based on the information given by the patient. Additionally, we were not able to adjust for unknown potential risk factors because either the information was not requested from patients or may not have been listed in the clinical record and, as such, could not be reported in the database.

Conclusions

The present analysis of data from confirmed influenza cases collected by a sentinel system and 100% of deaths from influenza in Mexico during 2014 to week 20 of the year 2020 clearly shows the impact and risk that influenza has on morbidity, hospitalisation and death in patients with SAH (as the only comorbidity) as well as in those with SAH and other comorbidities. This publication adds value to the current literature in that the data show that having SAH might represent an additional risk for complications in patients infected with influenza, highlighting the need for this group of patients to be vaccinated to reduce the morbidity and mortality risks. Therefore, we recommend that patients with SAH be included in the national recommendations for vaccination against influenza, per 2020 WHO recommendations.

Supplementary Material

Reviewer comments
Author's manuscript

Acknowledgments

The authors wish to thank Michelle Belanger, MD, of Edanz (www.edanz.com), for providing editorial assistance, which was funded by Sanofi Pasteur México; Salma Pacheco, MD, for assisting with the first draft of the protocol and Rodrigo Saucedo, MD, for supporting us with the editorial reviews.

Footnotes

Contributors: Conceptualisation, ES and AM-V; methodology, ES; validation, ES and AM-V; formal analysis, ES; writing—original draft preparation, ES; reviewing and correcting the draft manuscript, ES, AM-V, RT-C and HI-L; writing—review and final editing, ES, AM-V, RT-C and HI-L; supervision, ES; funding acquisition, AM-V.ES is responsible for the overall content as a guarantor. All authors have read and agreed to the published version of the manuscript.

Funding: This research was funded by Sanofi Pasteur México (award/grant number is not applicable). The authors ES and AM-V are employees of Sanofi Pasteur México and had roles in conceptualisation of the study design, analysis and interpretation of the data, drafting the manuscript and reviewing the content for publication.

Competing interests: ES and AM-V are employees of Sanofi Pasteur México. RT-C and HI-L have no relevant conflicts of interest to report.

Provenance and peer review: Not commissioned; externally peer reviewed.

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Data availability statement

Data may be obtained from a third party and are not publicly available. All data relevant to the study are included in the article or uploaded as supplementary information. The data used in this study were obtained from the Mexican Ministry of Health and can be obtained from this source following a formal request: 'Oficio de transparencia DGE-DGAE de la Secretaría de Salud con número 005533 referente a la Solicitud 0001200189920 del 4 de junio de 2020'.

Ethics statements

Patient consent for publication

Not applicable.

References

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary data

bmjopen-2021-057225supp001.pdf (249.2KB, pdf)

Reviewer comments
Author's manuscript

Data Availability Statement

Data may be obtained from a third party and are not publicly available. All data relevant to the study are included in the article or uploaded as supplementary information. The data used in this study were obtained from the Mexican Ministry of Health and can be obtained from this source following a formal request: 'Oficio de transparencia DGE-DGAE de la Secretaría de Salud con número 005533 referente a la Solicitud 0001200189920 del 4 de junio de 2020'.


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