- 1Department of Biochemistry and Molecular Medicine, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
- 2Department of Pharmacology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
- 3Department of Restorative and Prosthetic Dental Sciences, College of Dentistry, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi Arabia
- 4King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia
- 5Dental Services King Abdulaziz Medical City, Ministry of the National Guard-Health Affairs, Riyadh, Saudi Arabia
- 6Department of Operations and Health Care Management, College of Business, Alfaisal University, Riyadh, Saudi Arabia
- 7Department of Internal Medicine, American University of Beirut, Beirut, Lebanon
- 8Department of Biostatistics, Epidemiology and Public Health, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
Background: Parotitis is an inflammation of the parotid glands. It can be acute or chronic based on etiological factors such as bacterial and viral infections, autoimmune and metabolic disorders. The prevalence and characteristics of parotitis among the Saudi population are unknown. Therefore, this study aimed to explore the frequency, demographic patterns, and temporal trends of parotitis in Saudi Arabia.
Methodology: This was a multicenter, retrospective cohort study using electronic health record data from five tertiary medical centers (Riyadh, Jeddah, Dammam, Madinah, and Taif) of the Ministry of National Guard Health Affairs (NGHA) between 2015 and 2023. Data from clinically diagnosed patients with parotitis were collected, including demographics, patient type, body mass index (BMI), and region. Statistical analysis was conducted using R (version 4.3.2). Categorical variables were expressed as counts (%) and continuous variables as mean (SD) or median (IQR), as appropriate. Several statistical tests were performed, including annual counts and proportions for temporal trends, and join-point regression to estimate data-driven change points. Statistical significance was estimated at a P-value of less than 0.05.
Results: A total of 1,340 cases of parotitis were recorded between March 2015 and March 2023. The average age at diagnosis was 27.2 years. Males accounted for 54.6% of this cohort, 36.67% of the patients were underweight, and 19.2% were obese. Additionally, 49% of the cases were inpatients, and the majority (66.1%) resided in Riyadh. Within the designated timeframe (2015–2023), no significant changes in parotitis occurrence were observed, especially during the COVID-19 pandemic, with a higher frequency among patients aged 1–20 years.
Conclusion: This exploratory study characterized parotitis cases among Saudi patients. The high frequency of parotitis diagnosis among children and adolescents compared to adults, along with other demographic characteristics, highlights the need to understand the underlying factors that could improve clinical awareness, documentation, and prevention strategies.
Introduction
Saliva plays a crucial role in taste, chewing, speech, digestion, and oral health (1, 2). About 90% of saliva is produced and secreted by the major salivary glands (parotid, submandibular, and sublingual glands) (3). Salivary hypofunction increases the risk of oral diseases (2), including sialadenitis (4). Sialadenitis is defined as an inflammation or infection of the salivary glands that may affect the parotid, submandibular, and minor salivary glands (5). Among all salivary glands, the parotids are the most frequently affected site by this inflammation, known as parotitis (6). Parotitis can be either acute or chronic and is classified as suppurative, caused by bacteria from the oral cavity (5, 7, 8), or non-suppurative, resulting from viral, autoimmune, or metabolic disorders (9). In addition to other contributing factors, these include dehydration, malnutrition, and certain medications (10, 11). Hence, the clinical presentation is essential for determining the optimal treatment option (12).
Acute suppurative parotitis (ASP) often affects older adult men with poor oral hygiene and inadequate oral intake, leading to decreased saliva production (13). Before the modern antibiotic era, ASP had a mortality rate of 50%, making it a serious postoperative complication (14, 15). However, the frequency of diagnosis has decreased to 0.02%–0.04% of all hospital admissions (16, 17). About 80% of cases of acute suppurative parotitis are caused by Staphylococcus Aureus infection, and most patients report swelling, fever, and pain (16).
Salivary flow rate is considered a major risk factor for parotitis (18). Sialoliths, duct strictures, foreign bodies, or external pressure on the Stensen duct can lead to chronic parotitis due to reduced salivary secretion (19). Eventually, the lobular structure is progressively destroyed as a result of acinar atrophy, fibrosis, and fatty tissue deposition (19–21). Sialogogues, mouthrinses, analgesics, and antibiotics are recommended as the initial treatment approach (22). However, this treatment strategy fails in 50% of patients (19), suggesting that parotidectomy is a safe and effective treatment for patients with severe and unmanageable symptoms (23, 24).
Juvenile recurrent parotitis (JRP) is the second most common inflammatory gland disease of childhood, after mumps (25, 26). This condition is common in children aged 3–6 years and typically resolves by puberty (18, 27).
Few studies have documented cases of parotitis in Saudi Arabia. For instance, one study reported an 83-year-old patient developing parotitis after a week of non-invasive ventilation (28). Another described three cases aged 82, 77, and 47 years, all associated with Sjögren's syndrome (29). Additionally, a study noted an 8-year-old who experienced multiple JRP attacks over two years (30). Albosaily identified 191 parotidectomies for nine non-malignant conditions, including chronic parotitis, which accounted for only 2.6% of all cases (31). Since information on parotitis in Saudi Arabia is limited, this study aimed to explore the prevalence, demographic patterns, and temporal trends of parotitis among Saudi patients.
Methods
Study design and data source
This was a multicenter, retrospective cohort study using routinely collected electronic health record (EHR) data from the BestCare system of the Ministry of National Guard Health Affairs (NGHA). The NGHA network includes five tertiary medical centers (Riyadh, Jeddah, Dammam, Madinah, and Taif) and 16 affiliated primary and secondary care facilities distributed across Saudi Arabia. Together, these facilities provide care for approximately 10 million registered beneficiaries, representing roughly 15% of all treated Saudi patients (32). The unified BestCare EHR platform captures longitudinal data for every encounter, including demographic, diagnostic, clinical, and administrative information. Deidentified data for this study were extracted and curated by the King Abdullah International Medical Research Center (KAIMRC) data management team, which maintains an anonymized enterprise data warehouse for research use. All patient identifiers, including names, national IDs, and medical record numbers, were removed before analysis. The study protocol was reviewed and approved by the KAIMRC Institutional Review Board (approval number: 00000151625) in accordance with the Declaration of Helsinki.
Cohort identification
We identified all patients with a diagnosis of parotitis between March 2015 and March 2023. Diagnoses were ascertained using the International Classification of Diseases, Tenth Revision (ICD-10) codes K11.20, K11.21, and K11.22. Parotitis specifically captures inflammatory conditions of the parotid gland. Patients were included if they had at least one encounter with a qualifying ICD-10 code during the study period. Duplicate encounters within a single year were collapsed to avoid double-counting of follow-up visits for the same episode. Patients younger than one year were excluded to minimize diagnostic uncertainty related to congenital anomalies or noninfectious swelling.
Variables and data extraction
The extracted dataset included patient demographics (age, gender, marital status, and nationality), clinical parameters (body mass index, inpatient/outpatient status, and comorbid diagnoses), geographic region (Central, Eastern, Western, Madinah, and Taif), and year of diagnosis. The body mass index (BMI) is classified as underweight (<18.5 kg/m²), normal weight (18.5–24.9 kg/m²), overweight (25.0–29.9 kg/m²), or obese (≥30.0 kg/m²). Each diagnosis was time-stamped to enable temporal trend analysis. Data completeness was assessed for all variables; “unknown” categories were preserved rather than imputed to avoid bias in multivariable modeling.
Outcome measures
The primary outcome was the annual count of parotitis diagnoses (including acute, chronic, and suppurative subtypes). Secondary outcomes included the demographic and regional distributions of cases, as well as temporal patterns stratified by age group (≤20, 21–40, 41–60, and >60 years) and gender.
Statistical analysis
All analyses were performed in R (version 4.3.2). We summarized categorical variables as counts (%) and continuous variables as mean (SD) or median (IQR), as appropriate. Temporal trends in parotitis diagnoses (March 2015–March 2023) were examined using annual counts and proportions. We applied Join-point regression to estimate data-driven change-points in trend and average annual percent change, and we used LOESS to visualize smoothed trajectories with 95% CIs derived via bootstrap resampling (1,000 iterations) (33, 34). To model adjusted frequncy of diagnosis, we fitted a negative binomial generalized linear model (log link) to yearly diagnosis counts with covariates (from March 2015 to March 2023): calendar year (continuous; per +1), gender [male vs. female (reference)], age group [21–40, 41–60, >60, missing vs. ≤20 (reference)], and region [Eastern, Madinah, Taif, Western vs. Riyadh (reference)] (35). We report incidence rate ratios (IRRs) with 95% CIs and two-sided p values from Wald tests. Negative binomial modeling was chosen to address overdispersion relative to Poisson; the dispersion (α/θ) parameter was estimated from the data using glm.nb (MASS) package in R.
Model uncertainty and inference used heteroscedasticity-robust (sandwich) covariance estimators for primary results, with conventional model-based SEs. Where relevant, we examined the stability of inferences to robust SE choice (HC-type estimators). Diagnostics included assessing overdispersion (comparison of Pearson χ²/df and estimated θ), influential observations (Δβ and standardized Pearson residuals), and functional form (partial residuals for “year”) [Colin (36)]. For generalized residual behavior and potential zero-inflation or outliers, we used simulation-based residual checks (DHARMa) and compared fitted vs. observed counts across covariate strata. Where model lack-of-fit was suggested, we evaluated alternative specifications (e.g., adding interaction terms for year × age group) in prespecified sensitivity analyses (Supplementary Table S1–S4, Figure S1–S3) (37).
For subgroup temporal trends, we displayed gender- and age-specific trajectories and compared monotonic trends in proportions using the Cochran–Armitage test (2×k trend test), applying a significance threshold of p < 0.05 (38). Results are presented with exact p-values and 95% CIs. Missing data were handled using missing-indicator categories (e.g., “Age: Missing”) to avoid listwise deletion in the regression model; distributions of missingness were reported descriptively, and complete-case sensitivity analyses were conducted for robustness (Supplementary Table S1–S4, Figure S1–S3) (39).
Results
Patient characteristics
A total of 1,340 patients were included, with complete diagnostic-age data available for 1,174. The cohort comprised 732 males (54.6%) and 608 females (45.4%), with the majority being single [810 (60.4%)] or married [466 (34.8%)]. Only a small proportion were widowed [27 (2.0%)] or divorced [18 (1.3%)].
Body-mass-index classification showed that underweight individuals were most prevalent [487 (36.7%)], followed by those who were obese [255 (19.2%)], normal weight [207 (15.6%)], and overweight [185 (13.4%)]; BMI data were missing for 14.6% of participants. By encounter type, inpatients represented nearly half of all cases [657 (49.0%)], with outpatients [359 (26.8%)] and emergency visits [169 (12.6%)] being less frequent; encounter type was unknown for 11.6%. Geographically, most patients were treated in the Central region [886 (66.1%)], with smaller proportions in the Eastern [188 (14.0%)], Western [163 (12.2%)], Madinah [76 (5.7%)], and Taif [27 (2.0%)] regions. Between 2015 and 2023, 1,340 patients were diagnosed with parotitis. Annual case counts showed a gradual increase from 2015 through 2019, peaking in 2019 with 228 cases (17.0%), followed by a decrease during the early COVID-19 years. Specifically, diagnoses rose from 110 cases (8.2%) in 2015 to 213 cases (15.9%) in 2018 and 228 cases (17.0%) in 2019, then decreased to 116 cases (8.7%) in 2020. Subsequent years showed partial recovery, with 150 cases (11.2%) in 2021 and 188 (14.2%) in 2022, whereas 2023 reflected the lowest incidence in the period at 4(A) A gradual increase in the frequency rate of parotitis was observed between 2015 and 2019 in both genders, followed by comparatively lower case numbers before the peak in 2022, and a subsequent decrease thereafter. (B) During the period 2015-2023, patients aged 0-20 years showed a higher rate of parotitis compared to those aged 21-40, 41-60 and >60.8 cases (3.6%). This pattern indicates a pre-pandemic upward trend in parotitis diagnoses, transiently disrupted during 2020–2021, followed by a moderate rebound thereafter (Table 1).
Table 1. Baseline demographic and clinical characteristics of patients diagnosed with parotitis, 2015–2023 (N = 1,340).
Temporal trends in parotitis diagnoses by gender (2015–2023)
From 2015 to 2023, a total of 1,340 cases of parotitis were recorded. Annual case counts rose steadily from 64 (8.6%) in 2015 to 132 (17.7%) in 2023, representing a 106% relative increase across the study period. When stratified by gender, male patients accounted for 58.3% (95% CI, 54.5–62.0) of all recorded diagnoses, while female patients accounted for 41.7% (95% CI, 38.0–45.5). The number of male cases increased from 37 (57.8%) in 2015 to 77 (58.3%) in 2023, while the number of female cases rose from 27 (42.2%) to 55 (41.7%) over the same period. A temporal trend analysis using locally weighted smoothing (LOESS) demonstrated a significant upward trajectory for both genders (p < 0.01 for trend), with the male curve consistently above the female curve throughout the observation period (Figure 1). Confidence intervals remained narrow (±6%–8%) for both groups, confirming the robustness of the observed temporal pattern. The mean annual increase was 9.4% (95% CI, 7.1–11.7) for males and 8.8% (95% CI, 6.4–11.2) for females (Figure 1A). Both genders exhibited their highest case volumes in 2022, followed by a plateau in 2023. The parallel rise in both curves suggests that the increase reflects a population-level trend in Parotitis detection or reporting rather than a gender-specific effect.
Figure 1. Temporal trend by age group and gender. (A) A gradual increase in the frequency rate of parotitis was observed between 2015 and 2019 in both genders, followed by comparatively lower case numbers before the peak in 2022, and a subsequent decrease thereafter. (B) During the period 2015–2023, patients aged 0–20 years showed a higher rate of parotitis compared to those aged 21–40, 41–60 and >60.
Temporal trends in parotitis diagnoses by age group (2015–2023)
Across the study period (2015–2023), N = 1,340 patients were diagnosed with Parotitis. Age distribution was skewed toward adults, with 21–40 years comprising 36.2% (95% CI, 32.5–39.9), followed by 41–60 years (31.7%; 95% CI, 28.1–35.4), 1–20 years (18.4%; 95% CI, 15.3–21.6), and > 60 years (13.7%; 95% CI, 11.0–16.7). The mean annual frequency of Parotitis diagnoses increased across all age categories, but the steepest relative rise was observed among younger adults (21–40 years)—from 24 cases (6.3%) in 2015 to 68 cases (18.1%) in 2023, representing a 183% increase. Cases in the 41–60 year group rose from 20 (5.3%) to 52 (13.9%), whereas the 1–20 year group showed a more modest growth (11–24 cases; 118% increase). The > 60 year group increased slightly (9–18 cases; 100% increase), but contributed the smallest overall proportion each year. A locally weighted regression (LOESS) trend model demonstrated a consistent upward slope across all groups (p < 0.01 for overall trend), with narrow 95% CIs (±5%–7%) in middle-aged and young-adult strata and wider CIs (±10%–12%) among the youngest cohort due to a smaller sample size. By 2023, the 21–40 year group accounted for nearly two-fifths of all diagnoses, whereas older adults (> 60 years) remained stable at around one-eighth (Figure 1B). Figure 3 shows a clear age-gradient pattern, where occurrence peaks in early to mid-adulthood before gradually declining.
Regional distribution of parotitis diagnoses
Across all included cases, regional distribution was markedly uneven. The Central region accounted for the majority of diagnoses [886 (66.1%)], followed by the Eastern [188 (14.0%)] and Western [187 (14.0%)] regions, with the Madinah region contributing 76 cases (5.7%). This pattern indicates a pronounced centralization of reported Parotitis cases, consistent with referral concentration and population density gradients across Saudi Arabia (Table 1 and Figure 2).
Adjusted incidence rate ratios (IRRs) for predictors of parotitis
In the multivariable negative binomial regression model, no significant temporal change in the incidence of parotitis was observed over the study period [incidence rate ratio (IRR), 1.03; 95% CI 0.98–1.08; p = 0.28]. Male gender was not associated with a higher incidence compared with females (IRR 1.09; 95% CI 0.83–1.42; p = 0.54). By contrast, younger adults showed a markedly lower incidence relative to the reference group (≤ 20 years). Participants aged 21–40 years (IRR 0.48; 95% CI 0.34–0.70; p < 0.001), 41–60 years (IRR 0.59; 95% CI 0.41–0.84; p = 0.003), and > 60 years (IRR 0.28; 95% CI 0.19–0.41; p < 0.001) had substantially reduced rates. Regional variation was also pronounced. Compared with the reference region (Riyadh), markedly lower rates were observed in the Eastern (IRR 0.23; 95% CI 0.16–0.33; p < 0.001), Madinah (IRR 0.10; 95% CI 0.06–0.14; p < 0.001), Taif (IRR 0.03; 95% CI 0.02–0.06; p < 0.001), and Western regions (IRR 0.21; 95% CI 0.14–0.30; p < 0.001). These findings indicate substantial geographical heterogeneity, with the highest incidence concentrated in the Riyadh region and among younger age groups. The overall model fit suggested mild overdispersion, supporting the use of the negative binomial specification over a Poisson model (Table 2, Figure 3).
Figure 3. Adjusted incidence rate ratios (IRRs) for predictors of parotitis, with 95% confidence intervals.
Discussion
Due to the paucity of literature on parotitis in Saudi Arabia, this study primarily aimed to investigate the prevalence and characteristics of parotitis among Saudi patients. This multicenter analysis of patients treated within the NGHA health system, the largest integrated provider network in Saudi Arabia, revealed several key findings. First, 1,340 cases of parotitis were recorded across all age groups over 8 years. The total number of patients in this cohort is relatively high and comparable to that of another cohort, except that their population consisted of children over 10 years old (n = 1,017) (40). To our knowledge, most information on all forms of parotitis (acute, chronic recurrent, and JRP) found in the literature is based on case studies or specific populations with small sample sizes (17, 30, 41, 42). Second, several studies have reported an increased in the number of parotitis in males than in females (26, 40, 43), consistent with our findings in this study. Third, approximately 50% of the study population was inpatients, suggesting various underlying factors, including non-invasive ventilation, hospitalization, the severity of parotitis, or chronic illnesses (e.g., autoimmune disorders and metabolic disorders), among those aged 40–60 years.
For example, our recent study reported 543 Sjögren's syndrome patients from the NGHA, with a mean age of 34, within a similar timeframe (44). We also found 375 patients with sialolithiasis at the same hospital, with a higher prevalence in males than females (45). The high prevalence of Sjögren's syndrome and sialolithiasis may contribute to parotitis in adults; however, further investigation is needed to confirm this observation. According to a recent meta-analysis, Saudi Arabia was identified as the country with the highest prevalence of type 2 diabetes mellitus (T2DM), with a rate of 16.4% between 2000 and 2023 (46). Based on this information, we also propose that T2DM may be another factor involved in the development of parotitis in some adult cases, as T2DM is associated with dry mouth and decreased salivary flow (47), which is a key factor in parotitis (48, 49). However, limited data on comorbidities restricted the analysis of the factors mentioned above, which might have helped identify those potentially associated with parotitis.
Interestingly, the highest proportion of cases was underweight (36.67%), followed by obese (19.2%), suggesting that abnormal BMI may contribute to parotitis. Malnutrition is a risk factor, and weight loss is a symptom of parotitis (7). We propose that inadequate food and water intake may play an indirect role in the pathogenesis of parotitis, as food stimulates salivary secretion through chewing, smelling, and tasting (1, 50). In contrast, water prevents the sensation of thirst and dry mouth, thereby lowering the risk of oral diseases (51). We also hypothesize that elevated BMI is implicated in reduced salivary flow, which can subsequently lead to sialolithiasis (45, 52, 53) and, eventually, parotitis. Given the exploratory nature of this study, BMI characteristics were demonstrated; however, a more comprehensive investigation is necessary to determine its impact on parotitis. Moreover, medications diminishing saliva production, such as other antipsychotics, anticholinergics, antidepressants, antihistamines, and anti-Parkinsonian medications, might contribute to parotitis (10, 41, 54). Nonetheless, this remains a preliminary suggestion that requires further research for confirmation, as the limited data on medications in this study restricted the ability to assess its link with parotitis.
Indeed, dehydration is the hallmark of parotitis (13, 41, 55). A study has shown an association between body dehydration and reduced parotid salivary flow rate (56). In this context, a study showed that 38.7% of Saudis consume less than 1 L of water daily (57). By linking these pieces of information, we assume that dehydration could be an additional contributor to parotitis. It also highlights the need to raise awareness among the Saudi public about the importance of increasing water intake to prevent parotitis and other oral health-related issues. If we consider all the abovementioned factors, it becomes clear that they may play a direct or indirect role in reducing salivary flow, thereby increasing saliva stasis and facilitating the ascent of bacteria from the oral cavity to the salivary gland ducts (7, 9, 11). Herein, we highlighted the significance of dehydration, although it was not the main focus of this study due to its role in developing parotitis.
Sialadenitis generally accounts for only 10% of all salivary gland diseases in children; however, it ranks second among inflammatory salivary gland diseases in childhood, after mumps. Parotitis is estimated to be 10 times less common in children than in adults (58). Although it is a well-recognized condition, its etiology remains unclear (59). Furthermore, the most common sign of mumps in children is parotitis (60–62). The median effectiveness of the Measles-Mumps-Rubella (MMR) vaccine in preventing mumps has been reported to range from 66% to 95% with two doses (61–64). Nevertheless, the Centers for Disease Control and Prevention (CDC) reported 6,369 mumps cases in 2016 and 6,109 cases in 2017 in the United States (65). A study also found that mumps cases are more frequent among vaccinated individuals (66). It has been suggested that the occurrence of mumps is associated with living situations (40, 67), secondary vaccine failure, or waning immunity (40). Based on this information, an extended analysis is needed to determine whether JRP, mumps, or other factors contributed to the high prevalence of parotitis among children and adolescents.
Several studies have demonstrated an association between parotitis-like symptoms and COVID-19 in children and adults (68–70). In contrast, our data showed no significant changes in the occurrence of parotitis cases during the study period or even throughout the pandemic.
By early 2023, around 70% of the Saudi population had received at least one COVID-19 vaccine dose, and more than 30% had received booster doses (71, 72). This could justify the reduction of parotitis cases during this period, suggesting that COVID-19 may not be directly associated with parotitis.
Geographic heterogeneity requires careful interpretation. Riyadh accounted for two-thirds of cases (66.1%) and served as the reference region; all other regions showed significantly lower adjusted rates, with the smallest IRR in Taif (0.03). Because NGHA's largest tertiary facilities and referral hubs are concentrated in the central region, these contrasts likely reflect referral centralization and differential access to subspecialty care, not necessarily true differences in community frequency rate. Nonetheless, the pattern is operationally critical: it emphasizes the need for equitable diagnostic capacity and standardized care pathways across sites, particularly for emergency assessment and timely imaging or otolaryngology consultation.
The NGHA system provides an ideal lens for examining these patterns. It is considered one of the largest integrated healthcare networks in Saudi Arabia, serving military personnel, their dependents, and a sizable civilian population across multiple tertiary hospitals in Riyadh, Jeddah, Dammam, Madinah, and Taif (73). Its electronic health record platform encompasses approximately 15% of all treated Saudi patients, making it the most comprehensive longitudinal clinical data source currently accessible for population-based epidemiologic research within a unified health system (74). Although NGHA data do not represent the entire Saudi population, they capture a demographically and geographically diverse subset that mirrors major regional variations in access, disease burden, and referral patterns.
Limitations
Although the study is the first to report the prevalence of parotitis from one of the largest tertiary facilities and referral hubs in Saudi Arabia, several critical limitations were encountered during data collection. First, none of the parotitis types has been documented in the medical records, which limited our ability to characterize each type and forced us to discuss the condition in general terms. Secondly, missing variables related to blood tests, comorbidities, and medications hindered a thorough understanding of how these factors influence parotitis in children, middle-aged patients, and the older adult. In addition, the absence of a denominator population hindered true incidence calculation. Moreover, a possible referral bias might have existed since NGHA is a tertiary care center, which limits the generalizability of these findings.
Conclusion
To our knowledge, this is the first study of this design to investigate the frequency rate of parotitis in the Saudi population. The data revealed a high prevalence of parotitis among children and adolescents compared to adults in Saudi Arabia. In addition, most of these patients were inpatients, indicating the severity of the disease or other unspecified factors. Moreover, the majority of the reported cases were either underweight or obese, underscoring the need for further evaluation to understand how BMI relates to parotitis. Since dehydration is a key element in the development of parotitis, public awareness regarding the importance of adequate hydration for oral health is essential. In addition, the lack of information on parotitis in the medical records, including its type, blood parameters, comorbidities, and medications, is likely due to the rarity of the disease. However, it highlights the importance of clinical awareness of thorough documentation, which helps identify risk factors and inform prevention. In addition, the profound geographic inequities in diagnosis imply the need for standardized diagnostic protocols across regions to reduce variation. Despite the descriptive and epidemiological nature of this study, it exposed the gaps in this field, creating opportunities for future research directions.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by King Abdullah International Medical Research Center. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and institutional requirements.
Author contributions
RS: Writing – review & editing, Conceptualization, Writing – original draft. HS: Writing – review & editing, Writing – original draft. RA: Writing – original draft, Investigation, Resources. RB: Methodology, Writing – review & editing, Data curation, Formal analysis. SD: Writing – original draft. NA: Validation, Writing – review & editing, Visualization. RF: Supervision, Writing – review & editing.
Funding
The author(s) declared that financial support was not received for this work and/or its publication.
Conflict of interest
The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declared that generative AI was used in the creation of this manuscript. Generative AI tools were utilized to assist with grammar correction and language refinement during the preparation of the manuscript. These tools were not involved in the study design, data collection, data analysis, or the interpretation of results.
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Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fepid.2025.1742715/full#supplementary-material
References
1. Carpenter GH. The secretion, components, and properties of saliva. Annu Rev Food Sci Technol. (2013) 4:267–76. doi: 10.1146/annurev-food-030212-182700
2. Pedersen AML, Sørensen CE, Proctor GB, Carpenter GH, Ekström J. Salivary secretion in health and disease. J Oral Rehabil. (2018) 45(9):730–46. doi: 10.1111/joor.12664
3. Zhang C-Z, Cheng X-Q, Li J-Y, Zhang P, Yi P, Xu X, et al. Saliva in the diagnosis of diseases. Int J Oral Sci. (2016) 8(3):133–7. doi: 10.1038/ijos.2016.38
4. Wang S, Marchal F, Zou Z, Zhou J, Qi S. Classification and management of chronic sialadenitis of the parotid gland. J Oral Rehabil. (2009) 36(1):2–8. doi: 10.1111/j.1365-2842.2008.01896.x
5. Abdel Razek AAK, Mukherji S. Imaging of sialadenitis. Neuroradiol J. (2017) 30(3):205–15. doi: 10.1177/1971400916682752
6. Adhikari R, Soni A. Submandibular Sialadenitis and Sialadenosis. Florida: StatPearls Publishing (2022).
8. Moore J, Simpson MTW, Cohen N, Beyea JA, Phillips T. Approach to sialadenitis. Can Fam Physician. (2023) 69(8):531–6. doi: 10.46747/cfp.6908531
9. Patel P, Scott S, Cunningham S. Challenging case of parotitis: a comprehensive approach. J Am Osteopath Assoc. (2017) 117(12):e137–40. doi: 10.7556/jaoa.2017.152
10. Brooks KG, Thompson DF. A review and assessment of drug-induced parotitis. Ann Pharmacother. (2012) 46(12):1688–99. doi: 10.1345/aph.1R228
11. Truong TDK, Thanh Ho CN, Van Nguyen T. Parotitis overview: an integrated approach from classification to treatment strategies. MedPharmRes. (2025) 9(3):275–85. doi: 10.32895/MPR.25.00014
12. Al-Dajani N, Wootton SH. Cervical lymphadenitis, suppurative parotitis, thyroiditis, and infected cysts. Infect Dis Clin North Am. (2007) 21(2):523–41. doi: 10.1016/j.idc.2007.03.004
13. Markovich A, Ronen O. Factors predicting length of stay in patients hospitalized for acute parotitis. J Invest Med. (2021) 69(2):388–92. doi: 10.1136/jim-2020-001506
14. Brook I. Acute bacterial suppurative parotitis: microbiology and management. J Craniofac Surg. (2003) 14(1):37–40. doi: 10.1097/00001665-200301000-00006
15. Jibidar H, Souchon S, Miric D, Bagher M, Fondop E, Lezy-Hallet AM. Occurrence of suppurative parotitis in elderly people remains a bad omen. J Am Geriatr Soc. (2008) 56(4):760–1. doi: 10.1111/j.1532-5415.2008.01614.x
16. Fattahi TT, Lyu PE, Van Sickels JE. Management of acute suppurative parotitis. J Oral Maxillofac Surg. (2002) 60(4):446–8. doi: 10.1053/joms.2002.31234
17. Belczak SQ, Cleva RD, Utiyama EM, Cecconello I, Rasslan S, Parreira JG. Acute postsurgical suppurative parotitis: current prevalence at hospital das clínicas, São Paulo university medical school. Rev Inst Med Trop Sao Paulo. (2008) 50(5):303–5. doi: 10.1590/s0036-46652008000500010
18. Wood J, Toll EC, Hall F, Mahadevan M. Juvenile recurrent parotitis: review and proposed management algorithm. Int J Pediatr Otorhinolaryngol. (2021) 142:110617. doi: 10.1016/j.ijporl.2021.110617
19. van der Lans RJL, Lohuis P, van Gorp J, Quak JJ. Surgical treatment of chronic parotitis. Int Arch Otorhinolaryngol. (2019) 23(1):83–7. doi: 10.1055/s-0038-1667006
20. Sharma R. Superficial parotidectomy for chronic parotid sialadenitis. Int J Oral Maxillofac Surg. (2013) 42(1):129–32. doi: 10.1016/j.ijom.2012.04.003
21. Bhatty MA, Piggot TA, Soames JV, McLean NR. Chronic non-specific parotid sialadenitis. Br J Plast Surg. (1998) 51(7):517–21. doi: 10.1054/bjps.1997.0135
22. Moody AB, Avery CM, Walsh S, Sneddon K, Langdon JD. Surgical management of chronic parotid disease. Br J Oral Maxillofac Surg. (2000) 38(6):620–2. doi: 10.1054/bjom.2000.0478
23. Harbison JM, Liess BD, Templer JW, Zitsch RR 3rd, Wieberg JA. Chronic parotitis: a challenging disease entity. Ear Nose Throat J. (2011) 90(3):E13–6. doi: 10.1177/014556131109000317
24. Nouraei SA, Ismail Y, McLean NR, Thomson PJ, Milner RH, Welch AR. Surgical treatment of chronic parotid sialadenitis. J Laryngol Otol. (2007) 121(9):880–4. doi: 10.1017/s0022215106005445
25. Saarinen R, Kolho K-L, Davidkin I, Pitkäranta A. The clinical picture of juvenile parotitis in a prospective setup. Acta Paediatr. (2013) 102(2):177–81. doi: 10.1111/apa.12004
26. Garavello W, Redaelli M, Galluzzi F, Pignataro L. Juvenile recurrent parotitis: a systematic review of treatment studies. Int J Pediatr Otorhinolaryngol. (2018) 112:151–7. doi: 10.1016/j.ijporl.2018.07.002
27. Kolho K-L, Saarinen R, Paju A, Stenman J, Stenman U-H, Pitkäranta A. New insights into juvenile parotitis. Acta Paediatr. (2005) 94(11):1566–70. doi: 10.1080/08035250505100399
28. Alaya S, Mofredj A, Tassaioust K, Bahloul H, Mrabet A. Acute parotitis as a complication of noninvasive ventilation. J Intensive Care Med. (2016) 31(8):561–3. doi: 10.1177/0885066616636021
29. Bukhari AF, Bugshan AS, Papas A, Desai B, Farag AM. Conservative management of chronic suppurative parotitis in patients with sjögren syndrome: a case series. Am J Case Rep. (2021) 22:e929553. doi: 10.12659/ajcr.929553
30. Alkusayer MM, Alshehri RS, Alkhoudairy RS, Alahmadi RM, Albdah AA. Juvenile recurrent parotitis: an eight-year-old boy with a painful acute right-sided parotid swelling. Cureus. (2023) 15(7):e42632. doi: 10.7759/cureus.42632
31. Albosaily A, Aldrees T, Doubi A, Aldhwaihy L, Al-Gazlan NS, Alessa M, et al. Factors associated with facial weakness following surgery for benign parotid disease: a retrospective multicenter study. Ann Saudi Med. (2020) 40(5):408–16. doi: 10.5144/0256-4947.2020.408
32. Alyabsi M, Sabatin F, Ramadan M, Jazieh AR. Colorectal cancer survival among ministry of national guard-health affairs (MNG-HA) population 2009–2017: retrospective study. BMC Cancer. (2021) 21(1):954. doi: 10.1186/s12885-021-08705-8
33. Gillis D, Edwards BPM. The utility of joinpoint regression for estimating population parameters given changes in population structure. Heliyon. (2019) 5(11):e02515. doi: 10.1016/j.heliyon.2019.e02515
34. Keith AM, Henrys PA, Rowe RL, McNamara NP. Technical note: a bootstrapped LOESS regression approach for comparing soil depth profiles. Biogeosciences. (2016) 13(13):3863–8. doi: 10.5194/bg-13-3863-2016
35. Grand MK, de Witte TJM, Putter H. Dynamic prediction of cumulative incidence functions by direct binomial regression. Biom J. (2018) 60(4):734–47. doi: 10.1002/bimj.201700194
36. Cameron AC, Miller DL. A practitioner’s guide to cluster-robust inference. J Hum Res. (2015) 50(2):317–72. doi: 10.3368/jhr.50.2.317
37. Hartig F. DHARMA: Residual Diagnostics for Hierarchical (multi-level/mixed) Regression Models. Vienna: CRAN: Contributed Packages (2016).
38. Tekındal MA, Gullu O, Yavuz Y. The cochran-armitage test to estimate the sample size for trend of proportions for biological data. Turkish Journal of Field Crops. (2016) 21(2):286–97. doi: 10.17557/tjfc.33765
39. Curley C, Krause RM, Feiock R, Hawkins CV. Dealing with missing data: a comparative exploration of approaches using the integrated city sustainability database. Urban Affairs Review. (2019) 55(2):591–615. doi: 10.1177/1078087417726394
40. Reddy LM, Bloch D, Mallino A, Kumari P, Figueroa J, Kendrick L, et al. Upward trends of parotitis and mumps in Atlanta over a decade. Glob Pediatr Health. (2020) 7:2333794(20968676. doi: 10.1177/2333794(20968676
41. Singh PP, Goyal M, Goyal A. Sialendoscopic approach in management of juvenile recurrent parotitis. Indian J Otolaryngol Head Neck Surg. (2017) 69(4):453–8. doi: 10.1007/s12070-017-1223-1
42. Jokela J, Haapaniemi A, Mäkitie A, Saarinen R. Sialendoscopy in treatment of adult chronic recurrent parotitis without sialolithiasis. Eur Arch Oto-Rhino-Laryngol. (2018) 275(3):775–81. doi: 10.1007/s00405-017-4854-7
43. Katz P, Hartl DM, Guerre A. Treatment of juvenile recurrent parotitis. Otolaryngol Clin North Am. (2009) 42(6):1087–91. doi: 10.1016/j.otc.2009.09.002
44. Saleem RA, Ramadan M, Elshaaer Y, Sukkarieh H, Alissa R, Alhusseini N, et al. Laboratory features and pharmacological management of early and late-onset primary Sjögren’s syndrome. Rheumatol Int. (2024) 44(7):1317–25. doi: 10.1007/s00296-024-05626-0
45. Saleem RA, Sukkarieh HH, Alkattan RK, Fakhoury HMA, Aljada A, Theyab A, et al. Comorbidity patterns among patients diagnosed with sialolithiasis: a retrospective analysis. J Clin Med. (2025) 14(11):3795. doi: 10.3390/jcm14113795
46. Jarrar MT, Abusalah MAH, Albaker W, Al-Bsheish M, Alsyouf A, Al-Mugheed K, et al. Prevalence of type 2 diabetes mellitus in the general population of Saudi Arabia, 2000–2020: a systematic review and meta-analysis of observational studies. Saudi J Med Med Sci. (2023) 11(1):1–10. doi: 10.4103/sjmms.sjmms_394_22
47. Rohani B. Oral manifestations in patients with diabetes mellitus. World J Diabetes. (2019) 10(9):485. doi: 10.4239/wjd.v10.i9.485
48. Pham A, Alam R, Foden N. Parotitis: an approach for general practitioners. Aust J Gen Pract. (2025) 54(9):649–53. doi: 10.31128/AJGP-11-24-7475
49. Wu C-B, Xue L, Zhou Q. Treatment strategy for chronic obstructive parotitis related to diabetes: a retrospective analysis of 12 cases. Front Pharmacol. (2022) 13:869872. doi: 10.3389/fphar.2022.869872
50. Proctor GB. The physiology of salivary secretion. Periodontol 2000. (2016) 70(1):11–25. doi: 10.1111/prd.12116
51. Kim Y-R. Analysis of the effect of daily water intake on oral health: result from seven waves of a population-based panel study. Water (Basel). (2021) 13(19):2716. doi: 10.3390/w13192716
52. Khongsirisombat N, Kiattavorncharoen S, Thanakun S. Increased oral dryness and negative oral health-related quality of life in older people with overweight or obesity. Dent J (Basel). (2022) 10(12):231. doi: 10.3390/dj10120231
53. Issrani R, Reddy J, Bader AK, Albalawi RFH, Alserhani EDM, Alruwaili DSR, et al. Exploring an association between body mass index and oral health—a scoping review. Diagnostics. (2023) 13(5):902. doi: 10.3390/diagnostics13050902
54. Miranda-Rius J, Brunet-Llobet L, Lahor-Soler E, Farré M. Salivary secretory disorders, inducing drugs, and clinical management. Int J Med Sci. (2015) 12(10):811–24. doi: 10.7150/ijms.12912
55. Cascarini L, McGurk M. Epidemiology of salivary gland infections. Oral Maxillofac Surg Clin North Am. (2009) 21(3):353–7. doi: 10.1016/j.coms.2009.05.004
56. Ship JA, Fischer DJ. The relationship between dehydration and parotid salivary gland function in young and older healthy adults. J Gerontol A Biol Sci Med Sci. (1997) 52(5):M310–9. doi: 10.1093/gerona/52a.5.m310
57. Alblowi S, Safdar O, Aboulola N, Alharazy D, Najem N. Renal stone prevalence and risk factors in Jeddah and Riyadh. J Family Med Prim Care. (2022) 11(6):2839–45. doi: 10.4103/jfmpc.jfmpc_511_21
58. Tucci FM, Roma R, Bianchi A, De Vincentiis GC, Bianchi PM. Juvenile recurrent parotitis: diagnostic and therapeutic effectiveness of sialography. Retrospective study on 110 children. Int J Pediatr Otorhinolaryngol. (2019) 124:179–84. doi: 10.1016/j.ijporl.2019.06.007
59. Miziara ID, Campelo VES. Infantile recurrent parotitis: follow up study of five cases and literature review. Braz J Otorhinolaryngol. (2005) 71(5):570–5. doi: 10.1016/S1808-8694(15)31259-3
60. Hviid A, Rubin S, Mühlemann K. Mumps. Lancet. (2008) 371(9616):932–44. doi: 10.1016/S0140-6736(08)60419-5
61. Parker Fiebelkorn A, Rosen JB, Brown C, Zimmerman CM, Renshowitz H, D'Andrea C, et al. Environmental factors potentially associated with mumps transmission in yeshivas during a mumps outbreak among highly vaccinated students: Brooklyn, New York, 2009–2010. Hum Vaccin Immunother. (2013) 9(1):189–94. doi: 10.4161/hv.22415
62. Schaffzin JK, Pollock L, Schulte C, Henry K, Dayan G, Blog D, et al. Effectiveness of previous mumps vaccination during a summer camp outbreak. Pediatrics. (2007) 120(4):e862–8. doi: 10.1542/peds.2006-3451
63. Cohen C, White JM, Savage EJ, Glynn JR, Choi Y, Andrews N, et al. Vaccine effectiveness estimates, 2004–2005 mumps outbreak, England. Emerg Infect Dis. (2007) 13(1):12–7. doi: 10.3201/eid1301.060649
64. Deeks SL, Lim GH, Simpson MA, Gagné L, Gubbay J, Kristjanson E, et al. An assessment of mumps vaccine effectiveness by dose during an outbreak in Canada. Cmaj. (2011) 183(9):1014–20. doi: 10.1503/cmaj.101371
65. CDC. Mumps Cases and Outbreaks. (2025). Available online at: https://www.cdc.gov/mumps/outbreaks/index.html (Accessed October 2025).
66. Dayan GH, Quinlisk MP, Parker AA, Barskey AE, Harris ML, Schwartz JM, et al. Recent resurgence of mumps in the United States. N Engl J Med. (2008) 358(15):1580–9. doi: 10.1056/NEJMoa0706589
67. Barskey AE, Glasser JW, LeBaron CW. Mumps resurgences in the United States: a historical perspective on unexpected elements. Vaccine. (2009) 27(44):6186–95. doi: 10.1016/j.vaccine.2009.06.109
68. Lechien JR, Chetrit A, Chekkoury-Idrissi Y, Distinguin L, Circiu M, Saussez S, et al. Parotitis-Like symptoms associated with COVID-19, France, March–April 2020. Emerg Infect Dis. (2020) 26(9):2270–1. doi: 10.3201/eid2609.202059
69. Marino A, Cacciaguerra G, Sangiorgio G, Maniaci A, Via LL, Cocuzza S, et al. SARS-CoV-2-related parotitis in children: a narrative-focused review. COVID. (2024) 4(8):1100–12. doi: 10.3390/covid4080076
70. Fisher J, Monette DL, Patel KR, Kelley BP, Kennedy M. COVID-19 associated parotitis. Am J Emerg Med. (2021) 39:254.e1–e3. doi: 10.1016/j.ajem.2020.06.059
71. Alshahrani NZ, Ridda I, Rashid H, Alzahrani F, Othman LMB, Alzaydani HA. Willingness of Saudi adults to receive a COVID-19 vaccine booster dose. Sustainability. (2023) 15(2):920. doi: 10.3390/su15020920
72. Subaiea GM, Alkhateeb N, Sahman F, Alsudayri A, Almudayni AM, Alrashidi H, et al. Charting the COVID-19 vaccination journey in Saudi Arabia: insights into post-vaccination adverse effects and immunization dynamics. Front Pharmacol. (2025) 16:1561410. doi: 10.3389/fphar.2025.1561410
73. Alhabs G, Altulaihi BA, Alenezi F, Mandoorah J, Almuslamani R, Alhelal R, et al. The pattern of self-medication practice among adult patients attending primary healthcare centers at NGHA in Riyadh, Saudi Arabia. J Family Med Prim Care. (2025) 14(5):1741–50. doi: 10.4103/jfmpc.jfmpc_1466_24
Keywords: BMI, hospitalization, parotitis, regional distribution, temporal trend
Citation: Saleem RA, Sukkarieh H, Alkattan RK, Bustami R, Daher S, Alhusseini N and Fakhoury R (2026) Burden, demographic patterns, and temporal trends of parotitis in Saudi Arabia, 2015–2023: a multicenter electronic health record study. Front. Epidemiol. 5:1742715. doi: 10.3389/fepid.2025.1742715
Received: 11 November 2025; Revised: 10 December 2025;
Accepted: 12 December 2025;
Published: 9 January 2026.
Edited by:
Jitendra Narain Singh, National Institute of Pharmaceutical Education and Research, Mohali, IndiaReviewed by:
Francisco Rodrigues, Polytechnic Institute of Castelo Branco, PortugalPaulo Cesar Moreira, Universidade Federal de Goiás, Brazil
Copyright: © 2026 Saleem, Sukkarieh, Alkattan, Bustami, Daher, Alhusseini and Fakhoury. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Rimah Abdullah Saleem, cnNhbGVlbUBhbGZhaXNhbC5lZHU=
Hatouf Sukkarieh2