Skip to main content
Journal of Epidemiology logoLink to Journal of Epidemiology
. 2022 Sep 5;32(9):401–407. doi: 10.2188/jea.JE20200505

Association of Pneumococcal and Influenza Vaccination With Patient–Physician Communication in Older Adults: A Nationwide Cross-sectional Study From the JAGES 2016

Koryu Sato 1,2, Naoki Kondo 1,2, Chiyoe Murata 3, Yugo Shobugawa 4, Kousuke Saito 4, Katsunori Kondo 5,6
PMCID: PMC9359899  PMID: 33551389

Abstract

Background

Increasing the coverage of vaccinations recommended by the World Health Organization in the older adult population is an urgent issue, especially in the context of avoiding co-epidemics during the current coronavirus disease 2019 crisis. The aim of this study was to examine factors associated with the quality of perceived patient–physician communication and whether this variable was associated with increased odds of vaccination.

Methods

We used cross-sectional data from the Japan Gerontological Evaluation Study conducted from October 2016 to January 2017. The participants were 22,253 physically and cognitively independent individuals aged 65 or older living in 39 municipalities in Japan. Multilevel logit models were used to estimate the odds of vaccination.

Results

Among the participants, 40.0% and 58.8% had received pneumococcal and influenza vaccinations as per the recommended schedule, respectively. People with low educational levels were more likely to have a family physician but rate their experience in asking questions lower than those with higher educational levels. Having a family physician and high rating for physicians’ listening attitude were positively associated with increased odds of pneumococcal and influenza vaccinations. High rating for patients’ questioning attitude and shared decision-making, compared to an ambiguous attitude toward medical decision-making, were positively associated with increased odds of pneumococcal vaccination.

Conclusion

The results suggest that promotion of having a family physician, better patient–physician communication, and shared decision-making may encourage older adults to undergo recommended vaccinations.

Key words: patient–physician communication, shared decision-making, pneumococcal vaccine, influenza vaccine, older adults

INTRODUCTION

Pneumococcal diseases and influenza pose a substantial health burden, especially among older adults.1,2 Vaccination for these diseases may reduce the risk of morbidity in this population.3,4 A routine single dose of a 23-valent polysaccharide vaccine and an annual influenza vaccination are, therefore, recommended for all persons aged 65 or older in the international guidelines developed by the World Health Organization and Centers for Disease Control and Prevention.5,6

In the present scenario of the coronavirus disease 2019 (COVID-19) pandemic, undergoing influenza vaccination is more crucial than ever for several reasons,7,8 and the same reasoning can apply to pneumococcal vaccination. First, COVID-19, pneumococcal diseases, and influenza are contagious respiratory illnesses that present with similar symptoms, making diagnosis difficult. Moreover, as older adults are vulnerable to these illnesses,9,10 medical and long-term care facilities have to be more careful of mass infections. Second, studies suggest that co-infection of COVID-19 with pneumococcal diseases or influenza may result in a more severe disease course, increased number of complications, and even death.1113 Third, hospitalization for vaccine-preventable diseases could overwhelm the already limited medical resources available for patients with COVID-19. However, there is a gap between target rates and actual vaccine coverage for older adults in many developed countries.14 In Japan, the Immunization Act mandated municipalities to subsidize routine 23-valent polysaccharide vaccinations every 5 years and annual influenza vaccinations for persons aged 65 or older in 2014 and 2001, respectively. Nevertheless, vaccine coverage is suboptimal: 35.0% for pneumococcal vaccination and 48.2% for influenza vaccination.15

Physicians play an essential role in decision-making regarding preventive medical services. Systematic reviews point out that recommendation from physicians is a significant factor in the vaccination decision.16,17 Among adults aged 50–64 years, having a family physician (defined as a usual source of healthcare and advice) has been shown to be associated with higher odds of receiving preventive care, including influenza vaccination.18 The quality of patient–physician communication may also be influential. For example, high-quality patient–physician communication was positively associated with the receipt of meningococcal and human papillomavirus vaccination among adolescents aged 13–17,19 mammograms among women aged 40 or older,20 and colorectal cancer screening among persons aged 50 or older.21 However, few studies have examined the relationship between patient–physician communication and vaccination among older adults. Older patients need careful consultation because of the considerable heterogeneity in this population in terms of comorbidity, medical history, treatment options, and risks of adverse events.22,23 Nevertheless, some studies suggest that the quality of patient–physician communication in the context of older adults is not satisfactory.24,25 Hence, studying patient–physician communication with a focus on the older population is important to fill the knowledge gap.

In this study, we examined factors associated with the quality of perceived patient–physician communication and whether this variable was associated with increased odds of receiving pneumococcal and influenza vaccines using nationwide data of Japanese older adults aged 65 or older.

METHODS

Study participants

We analyzed cross-sectional data from the Japan Gerontological Evaluation Study (JAGES) in 2016. The JAGES is a large population-based study of Japanese people aged 65 or older who were physically and cognitively independent (ie, not needing public long-term care). Self-reported questionnaires were mailed to older adults in 39 municipalities from October 2016 to January 2017. Random sampling was employed in 22 large municipalities, while a census of all residents aged 65 or older was conducted in 17 smaller municipalities. Of 34,566 people invited to participate, 24,260 returned the questionnaires (response rate: 70.2%). Among the respondents, 2,002 were not eligible because they were certified as needing public long-term care. We also excluded five respondents who did not report their gender. Thus, our analytical sample comprised 22,253 individuals (10,180 men and 12,073 women; mean age, 74.2 years). All study participants provided informed consent, and the study protocol was reviewed and approved by ethics committees at the University of Tokyo (2019238NI), the National Center for Geriatrics and Gerontology (992), and Chiba University (2493).

Outcome and explanatory variables

To identify whether a participant had undergone the recommended vaccinations, we asked, “Did you receive pneumococcal vaccination in the past 5 years?” and “Did you receive flu vaccination in the past year?”. If a participant answered “no,” they had to select all the following options that applied: “I will not get sick even without vaccination,” “I do not like injections;” “Vaccination is too expensive,” and “I did not know about the vaccination.”

The survey studied patient–physician communication in the following four domains. First, “having a family physician” corresponded to the question, “Do you have a family physician?”. In Japan, a family physician is not institutionalized like a general practitioner in the United Kingdom, and we defined it in the questionnaire as “the physician you go to when you have a health problem, and it does not matter what the physician’s specialty is.” Second, “physicians’ listening attitude” was evaluated by the question, “How would you rate how well your physician listened to you?”.26 We asked participants to recall their last visit to a physician and answer the question (the same applied to the following questions). Responses were recorded on a five-point Likert scale (1 = poor, 2 = fair, 3 = good, 4 = very good, 5 = excellent). Third, “patients’ questioning attitude” was assessed using the question, “How would you rate how well you were able to ask your physician about something you did not understand?”. Responses were recorded on a four-point Likert scale (1 = poor, 2 = fair, 3 = good, 4 = excellent). Fourth, “style of decision-making” was determined by the question, “How did you make a decision on your medical care?”. Based on the literature, we identified three communication styles19,27: (a) physician-driven decision making, called the “paternalistic” style, corresponding to the option “my physician decided everything”; (b) patient-driven decision making, called the “informed” style, corresponding to the option “I listened to my physician’s explanation and then made my own decision”; and (c) a mid-point on the continuum called the “shared” style, corresponding to the option “I listened to my physician’s explanation and then made a decision in consultation with him/her.” We also offered the option of “not sure.”

Covariates

We adjusted for potential confounders, namely gender, age, education (low: ≤9 years, middle: 10–12 years, high: ≥13 years), marital status (married, other), engagement in paid work, annual equivalized household income (low: ≤1.9 million Japanese Yen [JPY], middle: 2–3.9 million JPY, high: ≥4 million JPY), receipt of public assistance based on the Public Assistance Act, self-reported diagnosis of diseases (heart disease, diabetes, respiratory disease, kidney or prostate gland disease, others), the copayment amount in the past month (did not visit a physician, 0 JPY, 1–4,999 JPY, 5,000–9,999 JPY, 10,000–19,999 JPY, 20,000 JPY or more), instrumental activities of daily living measured with the Tokyo Metropolitan Institute of Gerontology Index of Competence (fully capable: 5 points, less capable: ≤4 points),28 depressive symptoms assessed with the short form of the Geriatric Depression Scale (not depressed: ≤4 points, depressive tendency: 5–9 points, depression: ≥10 points),29 self-rated health measured with a four-point Likert scale (1 = poor, 2 = fair, 3 = good, 4 = excellent), smoking status, and perceived social capital at the individual level consisting of civic participation, social cohesion, and reciprocity.30 Civic participation was measured as the number of the following groups participants were involved in per month: volunteer groups, sports groups, hobby activities, study or cultural groups, and activities for teaching specific skills (none, one, two, over three). Social cohesion was determined using the number of participants who answered “strongly/moderately agree” on three questions about community trust, norms of reciprocity, and community attachment. Reciprocity was determined using the number of participants who answered “any one or more” on three questions about receiving and providing emotional support and receiving instrumental support. Total scores for each social capital variable ranged from 0 to 3.

Statistical analysis

First, we explored socioeconomic and health-related factors associated with patient–physician communication using generalized linear models. A logit model was adopted for “having a family physician”; an ordinal logit model was adopted for “physicians’ listening attitude” and “patients’ questioning attitude”; and a multinomial logit model was adopted for “style of decision-making.” Second, we examined the associations between each domain of patient–physician communication and vaccination. To consider regional variations in vaccine coverage rates, we applied a multilevel logit model with random intercepts; individuals at level 1 were nested within municipalities at level 2. We show unadjusted and adjusted models with adjustment for the covariates shown above. Models for physicians’ listening attitude, patients’ questioning attitude, and style of decision making were also adjusted for based on whether one had a family physician. To address potential bias caused by missing values, we adopted multiple imputation under the missing at random assumption (ie, a missing mechanism is related to other variables measured in the same survey for that subject). Incomplete variables were imputed with a chained equation using all variables as explanatory variables. We created 10 datasets, and the estimates were combined. All analyses were performed using Stata version 16.1 (Stata Corp., College Station, TX, USA).

RESULTS

Of the sample, 77.7% reported having a family physician (Table 1). The greatest number of participants rated their physicians’ listening attitude as “very good” (39.0%), followed by a large number of participants who rated it as “good” (28.7%). Most participants rated their experience in asking questions of their physician as “excellent” (31.8%) or “good” (45.5%). More than half of the participants (50.4%) made a decision on medical care in consultation with their physician, that is, in a “shared” style.

Table 1. Characteristics of participants (N = 22,253).

Variables n % Mean (SD)
Men 10,180 45.8  
Age, years 22,253 100.0 74.2 (6.3)
Education      
 Low 7,351 33.0  
 Middle 8,922 40.1  
 High 5,629 25.3  
 Missing or others 351 1.6  
Marital status      
 Married 15,689 70.5  
 Others 6,235 28.0  
 Missing 329 1.5  
Engagement in paid work      
 Yes 5,294 23.8  
 No 12,954 58.2  
 Missing 4,005 18.0  
Household income      
 Low 8,495 38.2  
 Middle 6,728 30.2  
 High 1,979 8.9  
 Missing 5,051 22.7  
Receipt of public assistancea      
 Yes 410 1.8  
 No 21,528 96.7  
 Missing 315 1.4  
Disease diagnosis      
 Heart disease 2,148 9.7  
 Diabetes 2,881 12.9  
 Respiratory disease 1,152 5.2  
 Kidney or prostate gland disease 1,548 7.0  
 Others 10,675 48.0  
 Missing 1,147 5.2  
Copayment      
 No visit 1,932 8.7  
 0 JPY 907 4.1  
 1–4,999 JPY 9,431 42.4  
 5,000–9,999 JPY 4,846 21.8  
 10,000–19,999 JPY 1,916 8.6  
 20,000 JPY or more 1,007 4.5  
 Missing 2,214 9.9  
Instrumental activities of daily living      
 Fully capable 19,351 87.0  
 Less capable 2,192 9.9  
 Missing 710 3.2  
Depressive symptoms      
 Not depressed 14,115 63.4  
 Depressive tendency 3,154 14.2  
 Depression 938 4.2  
 Missing 4,046 18.2  
Self-rated health 21,596 97.0 3.0 (0.6)
Smoking      
 Yes 2,335 10.5  
 No 19,391 87.1  
 Missing 527 2.4  
Social capital      
 Civic participation 16,401 73.7 0.8 (1.1)
 Social cohesion 21,298 95.7 2.0 (1.1)
 Reciprocity 21,080 94.7 2.8 (0.5)
Having a family physician      
 Yes 17,280 77.7  
 No 3,471 15.6  
 Missing 1,502 6.7  
Physicians’ listening attitude      
 Excellent 3,797 17.1  
 Very good 8,676 39.0  
 Good 6,391 28.7  
 Fair 643 2.9  
 Poor 165 0.7  
 Missing 2,581 11.6  
Patients’ questioning attitude      
 Excellent 7,081 31.8  
 Good 10,118 45.5  
 Fair 2,081 9.4  
 Poor 161 0.7  
 Missing 2,812 12.6  
Style of decision making      
 Paternalistic 2,841 12.8  
 Shared 11,224 50.4  
 Informed 2,105 9.5  
 Not sure 573 2.6  
 Missing 5,510 24.8  

a“Receipt of public assistance” indicates those receiving public assistance based on the Public Assistance Act.

Coverage was 40.0% for pneumococcal vaccination and 58.8% for influenza vaccination (Table 2). Many participants who did not undergo flu vaccination stated, “I will not get sick even without it” (68.1%). In comparison, the proportions of participants who cited the same reason (37.4%) and who stated “I did not know about the vaccination” (30.6%) in the context of why they did not undergo pneumococcal vaccination were similar.

Table 2. Vaccination and reasons of not receiving it.

Variables n %
Pneumococcal vaccination    
Yes 8,893 40.0
No 11,516 51.8
Missing 1,844 8.3
Reasons of not receiving the vaccination
(n = 11,516):
   
 I will not get sick even without it. 4,309 37.4
 I do not like injections. 899 7.8
 It is too expensive. 567 4.9
 I did not know the vaccination. 3,524 30.6

Influenza vaccination    
Yes 13,015 58.5
No 8,023 36.1
Missing 1,215 5.5
Reasons of not receiving the vaccination
(n = 8,023):
   
 I will not get sick even without it. 5,461 68.1
 I do not like injections. 1,194 14.9
 It is too expensive. 485 6.0
 I did not know the vaccination. 497 6.2

Table 3 presents socioeconomic and health-related factors associated with patient–physician communication. Age was positively associated with the odds of having a family physician, higher ratings for physicians’ listening attitude and patients’ questioning attitude. Further, older participants were less likely to experience shared and informed decision-making. People with low educational levels were more likely to have a family physician and rate their experience of asking questions lower compared to those with high education.

Table 3. Generalized linear models for socioeconomic and health-related determinants of patient–physician communicationa (N = 22,253).

Variables Having a family physician Physicians’ listening attitude Patients’ questioning attitude Style of decision making

Paternalistic Shared Informed
OR 95% CI OR 95% CI OR 95% CI RR 95% CI RR 95% CI RR 95% CI
Having a family physician     2.46 2.26 2.67 2.44 2.24 2.67 1.83 1.43 2.34 2.12 1.70 2.65 1.29 1.001 1.65
Men 0.65 0.59 0.71 0.95 0.89 1.02 0.97 0.91 1.04 1.81 1.46 2.24 1.50 1.22 1.85 1.33 1.06 1.66
Age 1.07 1.06 1.08 1.03 1.02 1.03 1.02 1.02 1.03 1.01 0.99 1.02 0.97 0.95 0.98 0.97 0.95 0.99
Educationb                                    
 Low 1.47 1.31 1.65 1.03 0.95 1.11 0.79 0.73 0.85 0.68 0.52 0.89 0.55 0.43 0.70 0.52 0.40 0.68
 Middle 1.13 1.02 1.25 0.97 0.91 1.04 0.89 0.82 0.95 0.90 0.70 1.15 0.78 0.61 0.99 0.77 0.59 0.99
Married 1.11 1.01 1.23 0.88 0.82 0.95 0.88 0.82 0.94 0.91 0.72 1.16 0.96 0.78 1.18 0.92 0.72 1.17
Paid work 1.14 1.03 1.25 1.07 0.996 1.15 1.03 0.95 1.11 0.94 0.72 1.23 0.85 0.65 1.12 0.92 0.72 1.18
Household incomeb                                    
 Low 0.97 0.84 1.11 1.02 0.92 1.14 0.89 0.81 0.98 1.22 0.84 1.79 0.89 0.62 1.26 1.01 0.66 1.54
 Middle 0.98 0.85 1.12 0.97 0.88 1.07 0.93 0.84 1.02 1.21 0.86 1.69 1.04 0.75 1.45 1.05 0.71 1.53
Receipt of public assistancec 1.81 1.31 2.49 1.57 1.24 1.98 1.41 1.13 1.77 1.35 0.70 2.60 0.90 0.49 1.62 0.71 0.38 1.32
Disease diagnosis                                    
 Heart disease 4.40 3.60 5.40 1.13 1.03 1.24 1.08 0.97 1.21 1.42 0.91 2.20 1.46 0.94 2.25 1.49 0.96 2.34
 Diabetes 4.19 3.47 5.06 1.12 1.02 1.22 1.04 0.93 1.15 1.45 0.97 2.17 1.33 0.93 1.90 1.20 0.78 1.85
 Respiratory disease 3.23 2.48 4.20 1.05 0.93 1.20 1.01 0.88 1.17 2.09 1.19 3.65 2.19 1.22 3.94 1.96 1.09 3.53
 Kidney disease 2.36 1.93 2.88 0.99 0.88 1.11 0.96 0.85 1.09 2.07 1.21 3.54 2.55 1.50 4.35 1.99 1.12 3.56
 Others 3.16 2.82 3.53 0.96 0.89 1.04 0.94 0.85 1.03 0.91 0.68 1.22 0.99 0.78 1.25 0.96 0.75 1.24
Copaymentb                                    
 0 JPY 1.82 1.49 2.22 1.41 1.19 1.67 1.49 1.25 1.77 1.70 1.13 2.56 1.42 0.97 2.07 1.37 0.89 2.13
 1–4,999 JPY 3.97 3.52 4.49 1.08 0.97 1.21 1.19 1.06 1.32 2.20 1.64 2.96 2.25 1.70 2.97 2.03 1.52 2.70
 5,000–9,999 JPY 4.60 3.95 5.36 1.17 1.03 1.32 1.23 1.08 1.39 2.07 1.47 2.93 2.12 1.56 2.89 1.80 1.29 2.49
 10,000–19,999 JPY 4.93 3.99 6.10 1.36 1.18 1.57 1.34 1.16 1.54 1.90 1.24 2.91 1.89 1.29 2.79 1.80 1.18 2.73
 20,000 JPY or more 4.54 3.58 5.76 1.58 1.35 1.84 1.43 1.21 1.70 2.46 1.46 4.15 2.24 1.38 3.63 2.17 1.26 3.73
Capable of IADLc 0.85 0.73 0.98 1.00 0.91 1.11 1.29 1.17 1.42 0.94 0.69 1.28 1.34 1.001 1.80 1.41 1.03 1.93
Depressive symptomsb                                    
 Depressive tendency 0.82 0.72 0.92 0.75 0.69 0.82 0.64 0.58 0.70 0.75 0.57 0.99 0.63 0.48 0.83 0.75 0.56 1.00
 Depression 0.65 0.53 0.80 0.61 0.52 0.71 0.48 0.41 0.57 0.65 0.44 0.95 0.46 0.32 0.65 0.57 0.38 0.87
Self-rated healthc 1.13 1.04 1.22 1.27 1.21 1.34 1.34 1.26 1.42 1.06 0.90 1.26 0.98 0.84 1.15 1.07 0.90 1.26
Smokingc 0.81 0.71 0.91 1.14 1.04 1.26 1.32 1.19 1.47 1.06 0.76 1.48 1.02 0.76 1.37 1.06 0.76 1.48
Social capitalc                                    
 Civic participation 1.04 0.99 1.08 0.92 0.90 0.95 0.94 0.91 0.98 0.99 0.88 1.10 1.16 1.04 1.29 1.18 1.05 1.32
 Social cohesion 1.16 1.12 1.21 1.21 1.18 1.25 1.14 1.11 1.17 1.20 1.09 1.32 1.26 1.15 1.38 1.15 1.05 1.26
 Reciprocity 1.20 1.11 1.30 1.15 1.08 1.22 1.20 1.13 1.27 1.42 1.26 1.61 1.73 1.53 1.96 1.60 1.40 1.84

CI, confidence interval; IADL, instrumental activities of daily living; JPY, Japanese Yen; OR, odds ratio; RR, risk ratio.

aA logit model is used for having a family physician, an ordinal logit model is used for physicians’ listening attitude and patients’ questioning attitude, and a multinomial logit model is used for style of decision making. The reference category for the multinomial logit model is “not sure.”

bThe reference category is “high” for education and household income, “no visit” for copayment, and “not depressed” for depressive symptoms.

c“Receipt of public assistance” indicates those receiving public assistance based on the Public Assistance Act; “Capable of IADL” indicates those who are fully capable of IADL; “Self-rated health” is measured with a four-point Likert scale; “Smoking” indicates those who are currently smoking; three sub-measures of “Social capital” represent scores ranged from 0 to 3.

Table 4 presents the associations between patient–physician communication and vaccination (for the other covariates, see eTable 1). We separately conducted regressions for each of the four domains in patient–physician communication. In the unadjusted models, only the variable of having a family physician was clearly associated with increased odds of pneumococcal vaccination. After adjusting for possible confounders, having a family physician (odds ratio [OR] 1.66; 95% confidence interval [CI], 1.51–1.82), physicians’ listening attitude (OR 1.44; 95% CI, 1.02–2.03; excellent vs poor), patients’ questioning attitude (OR 1.48; 95% CI, 1.04–2.12; excellent vs poor), and the shared decision-making style (OR 1.22; 95% CI, 1.01–1.47; compared to an ambiguous attitude) were associated with increased odds of pneumococcal vaccination. On the other hand, influenza vaccination was positively associated with all four domains in patient–physician communication in the unadjusted models. After adjusting for confounders, the associations attenuated, though the directions of point estimates were similar; having a family physician (OR 2.28; 95% CI, 2.09–2.49) and physicians’ listening attitude (OR 1.59; 95% CI, 1.13–2.25; excellent vs poor) were associated with increased odds of influenza vaccination. In addition, compared to an ambiguous attitude toward medical decision-making, the informed decision-making style was associated with decreased odds of influenza vaccination (OR 0.82; 95% CI, 0.67–0.999). To examine whether the status of having a family physician modifies the associations, we checked the interaction terms between having a family physician and the other patient–physician communication variables (ie, physicians’ listening attitude, patients’ questioning attitude, and style of decision making). These interaction terms did not appear to be associated with vaccination (see eTable 2), which suggests that the associations between patient–physician communication and vaccination were not different between the group that had a family physician and the group that did not.

Table 4. Multilevel logit models for associations between patient–physician communication and vaccination (N = 22,253).

  Pneumococcal vaccination Influenza vaccination
Unadjusted Adjusteda Unadjusted Adjusteda
OR 95% CI OR 95% CI OR 95% CI OR 95% CI
Having a family physician                        
 Yes 2.22 2.05 2.41 1.66 1.51 1.82 3.39 3.15 3.65 2.28 2.09 2.49
 No Ref.     Ref.     Ref.     Ref.    

Physicians’ listening attitude                        
 Excellent 0.95 0.87 1.05 1.44 1.02 2.03 2.22 1.98 2.47 1.59 1.13 2.25
 Very good 0.86 0.79 0.93 1.41 1.004 1.97 1.91 1.73 2.10 1.56 1.11 2.18
 Good 0.80 0.73 0.87 1.47 1.05 2.05 1.55 1.41 1.72 1.51 1.08 2.11
 Fair 0.68 0.57 0.80 1.40 0.97 2.02 1.27 1.06 1.53 1.44 0.99 2.08
 Poor Ref.     Ref.     Ref.     Ref.    

Patients’ questioning attitude                        
 Excellent 0.92 0.85 1.00 1.48 1.04 2.12 2.03 1.84 2.25 1.10 0.77 1.58
 Good 0.84 0.78 0.91 1.48 1.03 2.12 1.68 1.52 1.85 1.04 0.73 1.49
 Fair 0.68 0.61 0.76 1.37 0.95 2.00 1.28 1.13 1.44 0.93 0.65 1.33
 Poor Ref.     Ref.     Ref.     Ref.    

Style of decision making                        
 Paternalistic 0.86 0.76 0.97 1.03 0.84 1.26 1.60 1.43 1.78 0.98 0.81 1.18
 Shared 1.03 0.93 1.13 1.22 1.01 1.47 1.73 1.58 1.89 1.08 0.90 1.29
 Informed 0.75 0.66 0.87 0.97 0.78 1.19 1.20 1.06 1.35 0.82 0.67 0.999
 Not sure Ref.     Ref.     Ref.     Ref.    

CI confidence interval; OR, odds ratio.

aAdjusted for gender, age, education, marital status, paid work, household income, receipt of public assistance, self-reported diagnosis of diseases, the amount of copayment, instrumental activities of daily living, depressive symptoms, self-rated health, smoking status, and social capital. Models for physicians’ listening attitude, patients’ questioning attitude, and style of decision making are also adjusted for based on whether one has a family physician.

DISCUSSION

This study explored the association between patient–physician communication and vaccination in Japanese older adults. The results show that having a family physician, positive perceptions of physicians’ listening attitude and their own questioning ability, and shared decision-making were associated with increased odds of pneumococcal vaccination among people aged 65 or older. We found similar associations with influenza vaccination.

In a previous study, a conceptual model was used to describe how positive patient–physician communication can lead to receipt of preventive medical services.31 Patients may want their physician to listen to their descriptions of their symptoms or explain what they do not understand. Exchanging information in a way the patient understands promotes patient knowledge and understanding and leads to greater trust in the physician. It also fosters self-efficacy and feelings of empowerment, which lead to improved treatment adherence, health habits, and self-care. Thus, good patient–physician relationships encourage patients to follow through with recommended treatment, and in turn, induce timely receipt of preventive care. While this pathway has been observed in previous studies, they mostly pertained to younger patients.19,21,32 Although a previous study did not find a clear association between patient–physician communication and influenza vaccination for persons aged 50 or older,20 the present study suggests that the theory can, in fact, apply to vaccination in the older population (Table 4). Family physicians play an important role in the uptake of the recommended vaccination in the older population because they can build close relationships with their patients, and because older patients are more likely to have a family physician than younger patients.33 In line with another report,33 77.7% of our participants had a family physician (Table 1). In our participants, overconfidence that they could not be infected was the most common reason for not undergoing vaccination (Table 2). Appropriate communication would eliminate any such misconceptions and help patients understand the need for vaccination. Provision of information from a physician is also essential to increase the uptake of pneumococcal vaccination because many people are not aware of it.

We tested various decision-making styles and found that shared decision-making was most likely to be associated with increased odds of pneumococcal vaccination (Table 4). In previous studies, however, the paternalistic decision-making style was associated with increased odds of meningococcal and human papillomavirus vaccination among adolescents aged 13–1719 and of parents’ acceptance of vaccinations for their children34,35 rather than shared or informed decision-making. We found a negative association between informed decision-making and influenza vaccination, which may be in line with these previous findings. In contrast, the patients’ age may explain the positive association between shared decision-making and pneumococcal vaccination in this study. Prior research has reported that preference for shared decision-making increases with age.36 Shared decision-making promotes information exchange in a way that addresses patients’ needs,27 and being treated in the preferred way fosters trust in a physician and may increase vaccination acceptance. Involving older patients in the decision-making process may increase vaccination uptake especially for pneumococcal vaccination, which is not well known.

The present study also explored socioeconomic and health-related factors associated with patient–physician communication (Table 3). In accordance with previous studies, we found that age was positively associated with having a family physician and higher ratings for physicians’ listening attitude and patients’ questioning attitude.3739 This may be because older adults tend to visit physicians more frequently than other age groups, giving them more opportunities to build close relationships.37 The same logic can apply to more favorable perceptions among participants who had some diseases and who paid more copayments. Evidence regarding the association between educational attainment and quality of perceived patient–physician communication has been mixed.3739 Our results showed that people with higher education tended to rate their experience in asking questions higher but physicians’ listening attitude lower compared to those with low educational levels. This may be interpreted as indicating that education and increased knowledge enabled patients to ask questions of their physicians, but at the same time, their raised expectations of their physicians were not met.37 We also found that people with low educational levels were more likely to have a family physician. This suggests that family physicians play an essential role in helping them understand the need for vaccination and in reducing social disparity in vaccination rates across different levels of education.

This study has several limitations. First, we asked participants to recall their communication during their last visit to a physician. Hence, we could not evaluate the quality of communication when a participant decided to undergo vaccination. In addition, healthy participants may experience difficulty recalling their last communication with a physician because they seldom visit a physician and talk about their health problems. Further, we did not seek to understand physicians’ perspective, despite the fact that their confidence in and willingness to recommend vaccines affect patient acceptance.16 Further studies with close observations of communication on vaccination between physician and older patients are needed. Second, although our questions on patient–physician communication were similar to those used in studies such as the Community Tracking Study26 and Health Information National Trends Survey, the Japanese questionnaire has not been validated. A previous study reported that only 14.6% Japanese physicians adopted shared decision making, whereas 58% of American physicians decision making for lifestyle modification.40 More than half of our participants reported that they experienced shared decision making, which is similar to the American sample rather than the Japanese sample. There are possibilities of measurement errors and misclassification. Third, the culture of patient–physician communication, attitudes toward vaccination, and healthcare systems vary across countries. The generalizability of our findings, therefore, may be limited. Fourth, we could not obtain some important covariates, such as characteristics of the institutions the participants visited, disease severities, and the frequency of physician visits. Although we adjusted for self-reported disease diagnoses, the amount of copayment in the past month, instrumental activities of daily living, and self-rated health, which can partially surrogate the omitted variables, bias could remain if the adjustment was not sufficient.

In summary, this study found that pneumococcal vaccination for older adults aged 65 and above was positively associated with having a family physician, physicians’ listening attitude, patients’ questioning attitude, and shared decision-making. Influenza vaccination was also positively associated with having a family physician and the physicians’ listening attitude. The results suggest that promotion of having a family physician, better patient–physician communication, and shared decision-making may encourage older adults to undergo recommended vaccinations.

ACKNOWLEDGEMENTS

Contributors: Koryu Sato: Conceptualization, Methodology, Software, Validation, Formal analysis, Writing original draft, Funding acquisition. Naoki Kondo: Investigation, Resources, Data curation, Review and editing, Supervision, Funding acquisition. Chiyoe Murata and Yugo Shobugawa: Investigation, Review and editing. Kousuke Saito: Review and editing. Katsunori Kondo: Investigation, Data curation, Review and editing, Supervision, Project administration, Funding acquisition.

Funding: This study used data from the Japan Gerontological Evaluation Study (JAGES), which was supported by the Grants-in-Aid for Scientific Research (KAKENHI) Program from the Japan Society for the Promotion of Science (15H01972, 20K18931), Health Labour Sciences Research Grant from Ministry of Health, Labour and Welfare of Japan (H28-Choju-Ippan-002), Japan Agency for Medical Research and Development (JP17dk0110017, JP18dk0110027, JP18ls0110002, JP18le0110009), and the Research Funding for Longevity Sciences from National Center for Geriatrics and Gerontology (29-42). The funder of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the manuscript.

Conflicts of interest: KS was an employee of the Ministry of Health, Labour and Welfare of Japan but had no role in the funding. The views presented in this paper do not represent the views of the Ministry.

SUPPLEMENTARY MATERIAL

The following is the supplementary data related to this article:

eTable 1. Multilevel logit models for associations between patient-physician communication and vaccination

eTable 2. Multilevel logit models for the associations of vaccination with interaction terms between patient-physician communication and having a family physiciana

je-32-401-s001.pdf (251.5KB, pdf)

REFERENCES

  • 1.Li W, Ding C, Yin S. Severe pneumonia in the elderly: a multivariate analysis of risk factors. Int J Clin Exp Med. 2015;8(8):12463–12475. [PMC free article] [PubMed] [Google Scholar]
  • 2.Centers for Disease Control and Prevention. Flu & People 65 Years and Older. Published August 14, 2020. Accessed August 15, 2020. https://www.cdc.gov/flu/highrisk/65over.htm.
  • 3.Bonten MJM, Huijts SM, Bolkenbaas M, et al. Polysaccharide conjugate vaccine against pneumococcal pneumonia in adults. N Engl J Med. 2015;372(12):1114–1125. 10.1056/NEJMoa1408544 [DOI] [PubMed] [Google Scholar]
  • 4.Demicheli V, Jefferson T, Di Pietrantonj C, et al. Vaccines for preventing influenza in the elderly. Cochrane Database Syst Rev. 2018;2:CD004876. 10.1002/14651858.CD004876.pub4 [DOI] [PubMed] [Google Scholar]
  • 5.Matanock A, Lee G, Gierke R, Kobayashi M, Leidner A, Pilishvili T. Use of 13-valent pneumococcal conjugate vaccine and 23-valent pneumococcal polysaccharide vaccine among adults aged ≥65 years: updated recommendations of the Advisory Committee on Immunization Practices. MMWR Morb Mortal Wkly Rep. 2019;68(46):1069–1075. 10.15585/mmwr.mm6846a5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.World Health Organization . Vaccines against influenza WHO position paper – November 2012. Wkly Epidemiol Rec. 2012;87(47):461–476. [PubMed] [Google Scholar]
  • 7.Maltezou HC, Theodoridou K, Poland G. Influenza immunization and COVID-19. Vaccine. 2020;38(39):6078–6079. 10.1016/j.vaccine.2020.07.058 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Jaklevic MC. Flu vaccination urged during COVID-19 pandemic. JAMA. 2020;324(10):926–927. 10.1001/jama.2020.15444 [DOI] [PubMed] [Google Scholar]
  • 9.Petrilli CM, Jones SA, Yang J, et al. Factors associated with hospital admission and critical illness among 5279 people with coronavirus disease 2019 in New York City: prospective cohort study. BMJ. 2020;369:m1966. 10.1136/bmj.m1966 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.ECDC Public Health Emergency Team, Danis K, Fonteneau L, et al. High impact of COVID-19 in long-term care facilities, suggestion for monitoring in the EU/EEA, May 2020. Euro Surveill. 2020;25(22). 10.2807/1560-7917.ES.2020.25.22.2000956 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Hashemi SA, Safamanesh S, Ghafouri M, et al. Co-infection with COVID-19 and influenza A virus in two died patients with acute respiratory syndrome, Bojnurd, Iran. J Med Virol. 2020;92(11):2319–2321. 10.1002/jmv.26014 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Ma S, Lai X, Chen Z, Tu S, Qin K. Clinical characteristics of critically ill patients co-infected with SARS-CoV-2 and the influenza virus in Wuhan, China. Int J Infect Dis. 2020;96:683–687. 10.1016/j.ijid.2020.05.068 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Toombs JM, Van den Abbeele K, Democratis J, Mandal AKJ, Missouris CG. Pneumococcal coinfection in COVID-19 patients. J Med Virol. 2021;93(1):177–179. 10.1002/jmv.26278 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.de Gomensoro E, Del Giudice G, Doherty TM. Challenges in adult vaccination. Ann Med. 2018;50(3):181–192. 10.1080/07853890.2017.1417632 [DOI] [PubMed] [Google Scholar]
  • 15.Ministry of Health, Labour and Welfare. The number of people receiving routine vaccinations. Published January 29, 2020. Accessed August 16, 2020. https://www.mhlw.go.jp/topics/bcg/other/5.html.
  • 16.Paterson P, Meurice F, Stanberry LR, Glismann S, Rosenthal SL, Larson HJ. Vaccine hesitancy and healthcare providers. Vaccine. 2016;34(52):6700–6706. 10.1016/j.vaccine.2016.10.042 [DOI] [PubMed] [Google Scholar]
  • 17.Eilers R, Krabbe PFM, de Melker HE. Factors affecting the uptake of vaccination by the elderly in Western society. Prev Med. 2014;69:224–234. 10.1016/j.ypmed.2014.10.017 [DOI] [PubMed] [Google Scholar]
  • 18.Blewett LA, Johnson PJ, Lee B, Scal PB. When a usual source of care and usual provider matter: adult prevention and screening services. J Gen Intern Med. 2008;23(9):1354–1360. 10.1007/s11606-008-0659-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Moss JL, Reiter PL, Rimer BK, Brewer NT. Collaborative patient-provider communication and uptake of adolescent vaccines. Soc Sci Med. 2016;159:100–107. 10.1016/j.socscimed.2016.04.030 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Villani J, Mortensen K. Patient-provider communication and timely receipt of preventive services. Prev Med. 2013;57(5):658–663. 10.1016/j.ypmed.2013.08.034 [DOI] [PubMed] [Google Scholar]
  • 21.Carcaise-Edinboro P, Bradley CJ. Influence of patient-provider communication on colorectal cancer screening. Med Care. 2008;46(7):738–745. 10.1097/MLR.0b013e318178935a [DOI] [PubMed] [Google Scholar]
  • 22.Boyd CM, Fortin M. Future of multimorbidity research: how should understanding of multimorbidity inform health system design? Public Health Rev. 2010;32(2):451–474. 10.1007/BF03391611 [DOI] [Google Scholar]
  • 23.Boyd CM, Darer J, Boult C, Fried LP, Boult L, Wu AW. Clinical practice guidelines and quality of care for older patients with multiple comorbid diseases: implications for pay for performance. JAMA. 2005;294(6):716–724. 10.1001/jama.294.6.716 [DOI] [PubMed] [Google Scholar]
  • 24.Kaplan SH, Gandek B, Greenfield S, Rogers W, Ware JE. Patient and visit characteristics related to physicians’ participatory decision-making style: results from the Medical Outcomes Study. Med Care. 1995;33(12):1176–1187. 10.1097/00005650-199512000-00002 [DOI] [PubMed] [Google Scholar]
  • 25.Brown SJ. Patient-centered communication. Annu Rev Nurs Res. 1999;17(1):85–104. 10.1891/0739-6686.17.1.85 [DOI] [PubMed] [Google Scholar]
  • 26.Center for Studying Health System Change. Community Tracking Study Household Survey, 2003: [United States]. Published online 2007. doi:10.3886/ICPSR04216.v2. 10.3886/ICPSR04216.v2 [DOI]
  • 27.Charles C, Gafni A, Whelan T. Shared decision-making in the medical encounter: what does it mean? (or it takes at least two to tango). Soc Sci Med. 1997;44(5):681–692. 10.1016/S0277-9536(96)00221-3 [DOI] [PubMed] [Google Scholar]
  • 28.Koyano W, Shibata H, Nakazato K, Haga H, Suyama Y. Measurement of competence: reliability and validity of the TMIG Index of Competence. Arch Gerontol Geriatr. 1991;13(2):103–116. 10.1016/0167-4943(91)90053-S [DOI] [PubMed] [Google Scholar]
  • 29.Burke WJ, Roccaforte WH, Wengel SP. The short form of the geriatric depression scale: a comparison with the 30-item form. J Geriatr Psychiatry Neurol. 1991;4(3):173–178. 10.1177/089198879100400310 [DOI] [PubMed] [Google Scholar]
  • 30.Saito M, Kondo N, Aida J, et al. Development of an instrument for community-level health related social capital among Japanese older people: the JAGES Project. J Epidemiol. 2017;27(5):221–227. 10.1016/j.je.2016.06.005 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Epstein RM, Street RL. Patient-Centered Communication in Cancer Care: Promoting Healing and Reducing Suffering. NIH Publication No. 07-6225. U.S. Department of Health and Human Services, National Institutes of Health, National Cancer Institute; 2007.
  • 32.Flach SD, McCoy KD, Vaughn TE, Ward MM, Bootsmiller BJ, Doebbeling BN. Does patient-centered care improve provision of preventive services? J Gen Intern Med. 2004;19(10):1019–1026. 10.1111/j.1525-1497.2004.30395.x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Eguchi N, Deguchi M. The 7th Survey on Attitudes toward Medical Care in Japan. Japan Medical Association Research Institute; 2020. Accessed December 31, 2020. https://www.jmari.med.or.jp/download/WP448.pdf.
  • 34.Opel DJ, Mangione-Smith R, Robinson JD, et al. The influence of provider communication behaviors on parental vaccine acceptance and visit experience. Am J Public Health. 2015;105(10):1998–2004. 10.2105/AJPH.2014.302425 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Hofstetter AM, Robinson JD, Lepere K, Cunningham M, Etsekson N, Opel DJ. Clinician-parent discussions about influenza vaccination of children and their association with vaccine acceptance. Vaccine. 2017;35(20):2709–2715. 10.1016/j.vaccine.2017.03.077 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Cofield SS, Thomas N, Tyry T, Fox RJ, Salter A. Shared decision making and autonomy among US participants with multiple sclerosis in the NARCOMS Registry. Int J MS Care. 2017;19(6):303–312. 10.7224/1537-2073.2016-091 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Spooner KK, Salemi JL, Salihu HM, Zoorob RJ. Disparities in perceived patient-provider communication quality in the United States: trends and correlates. Patient Educ Couns. 2016;99(5):844–854. 10.1016/j.pec.2015.12.007 [DOI] [PubMed] [Google Scholar]
  • 38.DeVoe JE, Wallace LS, Fryer GE Jr. Measuring patients’ perceptions of communication with healthcare providers: do differences in demographic and socioeconomic characteristics matter? Health Expect. 2009;12(1):70–80. 10.1111/j.1369-7625.2008.00516.x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Ok H, Marks R, Allegrante JP. Perceptions of health care provider communication activity among American cancer survivors and Adults Without Cancer Histories: an analysis of the 2003 Health Information Trends Survey (HINTS) Data. J Health Commun. 2008;13(7):637–653. 10.1080/10810730802412172 [DOI] [PubMed] [Google Scholar]
  • 40.Kuga S, Kachi Y, Inoue M, Kawada T. Characteristics of general physicians who practice shared decision making: a mail survey of all clinics in 12 municipalities in Tokyo. J Japan Primary Care Assoc. 2016;39(4):209–213. 10.14442/generalist.39.209 [DOI] [Google Scholar]

Associated Data

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

Supplementary Materials

je-32-401-s001.pdf (251.5KB, pdf)

Articles from Journal of Epidemiology are provided here courtesy of Japan Epidemiological Association

RESOURCES