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Does This Child With High Blood Pressure Have Secondary Hypertension?The Rational Clinical Examination Systematic Review

To identify the key insights or developments described in this article
1 Credit CME
Key Points

Question  Which clinical findings differentiate children and adolescents with secondary hypertension from those with primary hypertension?

Findings  The clinical findings associated with secondary hypertension included age of 6 years or younger, history of prematurity at birth, family history of secondary hypertension, low body weight, microalbuminuria, serum uric acid concentration of 5.5 mg/dL or lower, and increased blood pressure load (defined as the percentage of individual blood pressure readings ≥95th percentile for sex and height) using 24-hour ambulatory blood pressure monitoring. The findings that were associated with lower likelihood of secondary hypertension included family history of any hypertension, obesity, and asymptomatic presentation. Hypertension stage, headache, and left ventricular hypertrophy did not predict primary hypertension vs secondary hypertension.

Meaning  Family history of secondary hypertension, younger age, lower body weight, and increased blood pressure load using 24-hour ambulatory blood pressure monitoring were associated with a higher likelihood of secondary hypertension. No individual sign or symptom definitively differentiates secondary hypertension from primary hypertension.

Abstract

Importance  Guidelines recommend that all children and adolescents with hypertension undergo evaluation for secondary causes. Identifying clinical factors associated with secondary hypertension may decrease unnecessary testing for those with primary hypertension.

Objective  To determine the utility of the clinical history, physical examination, and 24-hour ambulatory blood pressure monitoring for differentiating primary hypertension from secondary hypertension in children and adolescents (aged ≤21 years).

Data Sources and Study Selection  The databases of MEDLINE, PubMed Central, Embase, Web of Science, and Cochrane Library were searched from inception to January 2022 without language limits. Two authors identified studies describing clinical characteristics in children and adolescents with primary and secondary hypertension.

Data Extraction and Synthesis  For each clinical finding in each study, a 2 × 2 table was created that included the number of patients with and without the finding who had primary vs secondary hypertension. Risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies tool.

Main Outcomes and Measures  Random-effects modeling was used to calculate sensitivity, specificity, and likelihood ratios (LRs).

Results  Of 3254 unique titles and abstracts screened, 30 studies met inclusion criteria for the meta-analysis and 23 (N = 4210 children and adolescents) were used for pooling in the meta-analysis. In the 3 studies conducted at primary care clinics or school-based screening clinics, the prevalence of secondary hypertension was 9.0% (95% CI, 4.5%-15.0%). In the 20 studies conducted at subspecialty clinics, the prevalence of secondary hypertension was 44% (95% CI, 36%-53%). The demographic findings most strongly associated with secondary hypertension were family history of secondary hypertension (sensitivity, 0.46; specificity, 0.90; LR, 4.7 [95% CI, 2.9-7.6]), weight in the 10th percentile or lower for age and sex (sensitivity, 0.27; specificity, 0.94; LR, 4.5 [95% CI, 1.2-18]), history of prematurity (sensitivity range, 0.17-0.33; specificity range, 0.86-0.94; LR range, 2.3-2.8), and age of 6 years or younger (sensitivity range, 0.25-0.36; specificity range, 0.86-0.88; LR range, 2.2-2.6). Laboratory studies most associated with secondary hypertension were microalbuminuria (sensitivity, 0.13; specificity, 0.99; LR, 13 [95% CI, 3.1-53]) and serum uric acid concentration of 5.5 mg/dL or lower (sensitivity range, 0.70-0.73; specificity range, 0.65-0.89; LR range, 2.1-6.3). Increased daytime diastolic blood pressure load combined with increased nocturnal systolic blood pressure load on 24-hour ambulatory blood pressure monitoring was associated with secondary hypertension (sensitivity, 0.40; specificity, 0.82; LR, 4.8 [95% CI, 1.2-20]). Findings associated with a decreased likelihood of secondary hypertension were asymptomatic presentation (LR range, 0.19-0.36), obesity (LR, 0.34 [95% CI, 0.13-0.90]), and family history of any hypertension (LR, 0.42 [95% CI, 0.30-0.57]). Hypertension stage, headache, and left ventricular hypertrophy did not distinguish secondary from primary hypertension.

Conclusions and Relevance  Family history of secondary hypertension, younger age, lower body weight, and increased blood pressure load using 24-hour ambulatory blood pressure monitoring were associated with a higher likelihood of secondary hypertension. No individual sign or symptom definitively differentiates secondary hypertension from primary hypertension.

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CME Disclosure Statement: Unless noted, all individuals in control of content reported no relevant financial relationships. If applicable, all relevant financial relationships have been mitigated.

Article Information

Corresponding Author: James T. Nugent, MD, MPH, Clinical and Translational Research Accelerator, Temple Medical Center, 60 Temple St, Ste 6C, New Haven, CT 06510 (james.nugent@yale.edu).

Accepted for Publication: February 21, 2023.

Author Contributions: Dr Nugent had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: Nugent, Saran, Wilson, Greenberg.

Acquisition, analysis, or interpretation of data: Nugent, Jiang, Funaro, Saran, Young, Ghazi, Bakhoum, Greenberg.

Drafting of the manuscript: Nugent, Funaro, Greenberg.

Critical revision of the manuscript for important intellectual content: Nugent, Jiang, Saran, Young, Ghazi, Bakhoum, Wilson, Greenberg.

Statistical analysis: Nugent.

Administrative, technical, or material support: Funaro, Saran, Young, Wilson, Greenberg.

Supervision: Bakhoum, Wilson, Greenberg.

Conflict of Interest Disclosures: Dr Wilson reported receiving grants from AstraZeneca, Vifor Pharma, and Whoop Inc. No other disclosures were reported.

AMA CME Accreditation Information

Credit Designation Statement: The American Medical Association designates this Journal-based CME activity activity for a maximum of 1.00  AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to:

  • 1.00 Medical Knowledge MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program;;
  • 1.00 Self-Assessment points in the American Board of Otolaryngology – Head and Neck Surgery’s (ABOHNS) Continuing Certification program;
  • 1.00 MOC points in the American Board of Pediatrics’ (ABP) Maintenance of Certification (MOC) program;
  • 1.00 Lifelong Learning points in the American Board of Pathology’s (ABPath) Continuing Certification program; and
  • 1.00 credit toward the CME [and Self-Assessment requirements] of the American Board of Surgery’s Continuous Certification program

It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting MOC credit.

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