ICD-10: Z87.710

Personal history of (corrected) hypospadias

Additional Information

Clinical Information

ICD-10 code Z87.710 refers to a personal history of corrected hypospadias, a congenital condition affecting the male urethra. Understanding the clinical presentation, signs, symptoms, and patient characteristics associated with this condition is essential for healthcare providers, particularly in the context of patient history and ongoing care.

Clinical Presentation of Hypospadias

Hypospadias is characterized by an abnormal placement of the urethral opening, which can occur anywhere along the ventral side of the penis, from the glans to the perineum. The severity of hypospadias can vary significantly, influencing the clinical presentation:

  • Mild Cases: The urethral opening may be located just below the tip of the penis (distal hypospadias).
  • Moderate to Severe Cases: The opening may be located further down the shaft or even at the base of the penis (proximal hypospadias), which can lead to more complex surgical corrections.

Signs and Symptoms

Patients with a history of corrected hypospadias may present with various signs and symptoms, particularly if they have undergone surgical intervention:

  • Urinary Symptoms: Patients may experience abnormal urinary stream patterns, such as spraying or difficulty directing the urine flow, especially if the correction was not fully successful.
  • Penile Appearance: The penis may have a curvature (chordee) or an abnormal shape, which can be a residual effect of the condition or the surgical correction.
  • Scarring: Surgical sites may show signs of scarring or changes in skin texture, which can be a concern for both function and aesthetics.
  • Psychosocial Impact: There may be psychological effects related to the condition, particularly in older children and adults, including concerns about body image and sexual function.

Patient Characteristics

The characteristics of patients with a history of corrected hypospadias typically include:

  • Age: Hypospadias is usually diagnosed at birth or during early childhood, with surgical correction often performed within the first year of life. Therefore, many patients will be children or young adults.
  • Gender: Hypospadias exclusively affects males, as it is a male-specific congenital condition.
  • Family History: There may be a familial component, as hypospadias can occur more frequently in certain families, suggesting a genetic predisposition.
  • Associated Conditions: Patients may have other congenital anomalies, such as undescended testicles (cryptorchidism) or other urogenital abnormalities, which can influence their overall health status and management needs.

Conclusion

In summary, ICD-10 code Z87.710 captures the personal history of corrected hypospadias, a condition that can have lasting implications for urinary function and psychosocial well-being. Understanding the clinical presentation, signs, symptoms, and patient characteristics is crucial for healthcare providers to offer appropriate follow-up care and support. Regular monitoring and assessment can help address any ongoing issues related to urinary function and psychological health, ensuring a comprehensive approach to patient care.

Description

The ICD-10 code Z87.710 is designated for individuals with a personal history of corrected hypospadias. This code falls under the broader category of Z87, which pertains to personal history of other diseases and conditions. Below is a detailed clinical description and relevant information regarding this condition.

Understanding Hypospadias

Definition

Hypospadias is a congenital condition in which the opening of the urethra is not located at the tip of the penis but rather on the underside. This condition can vary in severity, with the urethral opening potentially located anywhere along the shaft of the penis or even at the base near the scrotum.

Types of Hypospadias

Hypospadias is classified into several types based on the location of the urethral opening:
- Glanular Hypospadias: Opening at the glans (tip of the penis).
- Coronal Hypospadias: Opening at the coronal margin (just below the glans).
- Shaft Hypospadias: Opening located along the shaft of the penis.
- Penoscrotal Hypospadias: Opening located at the junction of the penis and scrotum.

Clinical Presentation

Patients with hypospadias may present with:
- Abnormal urinary stream.
- Difficulty with urination.
- Potential for associated conditions such as undescended testicles or other genital anomalies.

Treatment and Correction

Surgical Intervention

The primary treatment for hypospadias is surgical correction, typically performed during infancy or early childhood. The surgery aims to reposition the urethral opening to its normal location and may also involve reconstructing the penis to ensure proper function and appearance.

Postoperative Care

Post-surgery, patients are monitored for complications such as:
- Infection.
- Urethral stricture (narrowing).
- Fistula formation (abnormal connection between the urethra and skin).

ICD-10 Code Z87.710

Significance of the Code

The code Z87.710 specifically indicates a personal history of corrected hypospadias. This means that the individual has undergone surgical correction for the condition and is now being monitored for any long-term effects or complications that may arise from the condition or its treatment.

Usage in Clinical Settings

This code is essential for:
- Documenting a patient's medical history.
- Ensuring appropriate follow-up care.
- Facilitating communication among healthcare providers regarding the patient's past medical conditions.

The Z87 category includes other codes for personal histories of various conditions, which can be useful for comprehensive patient assessments. For instance, Z87.7 encompasses personal histories of other diseases and conditions, allowing for a broader understanding of a patient's health background.

Conclusion

The ICD-10 code Z87.710 serves as an important marker in a patient's medical record, indicating a history of corrected hypospadias. Understanding this condition, its treatment, and the implications of the code is crucial for ongoing patient care and management. Proper documentation and follow-up can help ensure that any potential complications are addressed promptly, contributing to the overall health and well-being of the patient.

Approximate Synonyms

ICD-10 code Z87.710 refers to the "Personal history of (corrected) hypospadias," which is a medical classification used to indicate a patient's past medical history regarding this specific condition. Hypospadias is a congenital condition in males where the urethra does not open at the tip of the penis but rather on the underside. The term "corrected" implies that surgical intervention has been performed to address the condition.

  1. Hypospadias: This is the primary term for the condition itself, which can be classified into various types based on the location of the urethral opening.

  2. Corrected Hypospadias: This term specifically refers to cases where surgical correction has been performed, making it a direct alternative to the ICD-10 code description.

  3. Congenital Hypospadias: This term emphasizes the congenital nature of the condition, indicating that it is present at birth.

  4. Urethral Anomaly: A broader term that can encompass various conditions affecting the urethra, including hypospadias.

  5. Surgical History of Hypospadias Repair: This phrase describes the surgical intervention that a patient has undergone to correct hypospadias.

  6. Post-Surgical Hypospadias: This term can be used to describe the status of a patient who has undergone surgery for hypospadias.

  7. Urogenital Anomaly: A more general term that includes hypospadias as part of a range of conditions affecting the urogenital system.

  8. History of Urethral Reconstruction: This term may be used in medical records to indicate that a patient has had surgery to correct a urethral defect, such as hypospadias.

  • Q54.0: This code refers to "Hypospadias," which is the primary diagnosis for the condition itself, without the indication of correction.
  • Z87.71: This code indicates a personal history of other congenital malformations, which may be relevant in broader discussions of congenital conditions.

Conclusion

Understanding the alternative names and related terms for ICD-10 code Z87.710 is essential for accurate medical documentation and communication among healthcare providers. These terms not only help in identifying the condition but also in understanding the patient's medical history and the interventions they have undergone. If you need further information or specific details about hypospadias or its management, feel free to ask!

Diagnostic Criteria

The ICD-10 code Z87.710 refers to a personal history of corrected hypospadias, which is a congenital condition affecting the male urethra. Understanding the criteria for diagnosing this condition involves several key aspects, including clinical evaluation, medical history, and the specifics of the surgical correction.

Understanding Hypospadias

Hypospadias is a condition where the urethral opening is not located at the tip of the penis but rather on the underside. This condition can vary in severity, and surgical correction is often performed during infancy or early childhood to reposition the urethral opening and ensure normal urinary function and appearance.

Diagnostic Criteria for Z87.710

1. Medical History

  • Previous Diagnosis: A confirmed diagnosis of hypospadias must be documented in the patient's medical history. This includes any prenatal ultrasounds or postnatal examinations that identified the condition.
  • Surgical Intervention: Documentation of surgical correction is essential. This includes details about the type of surgery performed, the date of the procedure, and any follow-up care.

2. Clinical Evaluation

  • Physical Examination: A thorough physical examination by a healthcare provider is necessary to assess the current state of the genitalia and confirm that the hypospadias has been corrected. This may include evaluating the position of the urethral opening and the overall anatomy of the penis.
  • Assessment of Functionality: Evaluation of urinary function post-surgery is crucial. This includes checking for any complications such as urinary incontinence, stricture, or recurrent infections.

3. Documentation Requirements

  • Surgical Records: Complete surgical records should be available, detailing the procedure and any complications that arose during or after the surgery.
  • Follow-Up Reports: Regular follow-up reports that indicate the patient's recovery and any ongoing issues related to the correction of hypospadias are important for establishing a personal history.

4. Exclusion of Current Conditions

  • The diagnosis of Z87.710 specifically indicates a personal history, meaning that there should be no current manifestations of hypospadias. If there are ongoing issues, a different diagnosis may be more appropriate.

Conclusion

In summary, the criteria for diagnosing the ICD-10 code Z87.710, which denotes a personal history of corrected hypospadias, involve a comprehensive review of the patient's medical history, surgical records, and clinical evaluations. Proper documentation and follow-up care are essential to ensure that the condition has been adequately addressed and that the patient is functioning normally post-correction. This thorough approach not only aids in accurate coding but also ensures that the patient receives appropriate ongoing care.

Treatment Guidelines

When addressing the standard treatment approaches for ICD-10 code Z87.710, which denotes a personal history of corrected hypospadias, it is essential to understand both the condition itself and the implications of having a personal history of it. Hypospadias is a congenital condition where the urethral opening is not located at the tip of the penis, and it is typically corrected through surgical intervention during infancy or early childhood.

Understanding Hypospadias

Hypospadias is classified based on the location of the urethral opening, which can be at the glans (tip of the penis), along the shaft, or at the base near the scrotum. The condition can lead to various complications, including difficulties with urination, sexual function, and psychological impacts due to the appearance of the penis. Surgical correction is the standard treatment, which usually involves repositioning the urethral opening and reconstructing the penis to ensure normal function and appearance.

Treatment Approaches for Z87.710

1. Surgical Correction

For individuals with a history of hypospadias, the primary treatment approach is the surgical correction that was performed during infancy or early childhood. This surgery typically involves:

  • Urethroplasty: Reconstructing the urethra to create a new opening at the tip of the penis.
  • Glandular or Shaft Reconstruction: Depending on the severity and location of the hypospadias, additional procedures may be necessary to ensure proper penile appearance and function.

2. Follow-Up Care

Post-surgical follow-up is crucial for monitoring the outcomes of the correction. This includes:

  • Regular Check-Ups: Pediatric urologists often recommend regular follow-ups to assess urinary function and the cosmetic appearance of the penis.
  • Monitoring for Complications: Patients may need to be monitored for potential complications such as urethral strictures, fistulas, or recurrent hypospadias.

3. Psychosocial Support

Given the potential psychological impact of hypospadias and its correction, especially in older children and adolescents, psychosocial support may be beneficial. This can include:

  • Counseling: Providing support to address any body image issues or anxiety related to the condition.
  • Education: Informing patients and families about the condition, treatment options, and expected outcomes can help alleviate concerns.

4. Management of Associated Conditions

Individuals with a history of hypospadias may also have associated conditions, such as undescended testicles or other urogenital anomalies. Management of these conditions may involve:

  • Additional Surgical Interventions: If other anomalies are present, further surgical procedures may be necessary.
  • Endocrine Evaluation: In some cases, hormonal evaluations may be warranted, especially if there are concerns about sexual development.

5. Long-Term Health Monitoring

Patients with a history of hypospadias should be aware of the need for long-term health monitoring, which may include:

  • Urological Assessments: Regular assessments to ensure normal urinary function and to check for any late-onset complications.
  • Sexual Health Education: As patients reach adolescence, education regarding sexual health and function becomes increasingly important.

Conclusion

In summary, the standard treatment approaches for ICD-10 code Z87.710, which indicates a personal history of corrected hypospadias, primarily involve the surgical correction performed in early life, followed by ongoing monitoring and support. Regular follow-ups, psychosocial support, and management of any associated conditions are essential components of care. By addressing both the physical and emotional aspects of the condition, healthcare providers can help ensure a positive outcome for individuals with a history of hypospadias.

Related Information

Clinical Information

  • Abnormal urethral opening placement
  • Urethral opening located on ventral side
  • Severity varies from mild to severe
  • Urinary symptoms present in some cases
  • Abnormal urinary stream patterns occur
  • Penile curvature or abnormal shape present
  • Scarring at surgical sites common
  • Psychological effects related to condition
  • Condition affects males exclusively
  • Familial component with genetic predisposition
  • Associated conditions like undescended testicles

Description

  • Congenital condition of urethral opening
  • Opening not at tip of penis
  • Varies in severity and location
  • Glanular, coronal, shaft, penoscrotal types
  • Abnormal urinary stream and urination difficulties
  • Potential for undescended testicles or other anomalies
  • Surgical correction during infancy or childhood
  • Monitoring for postoperative complications

Approximate Synonyms

  • Hypospadias
  • Corrected Hypospadias
  • Congenital Hypospadias
  • Urethral Anomaly
  • Surgical History of Hypospadias Repair
  • Post-Surgical Hypospadias
  • Urogenital Anomaly
  • History of Urethral Reconstruction

Diagnostic Criteria

Treatment Guidelines

  • Surgical correction is primary treatment approach
  • Urethroplasty reconstructs urethra in infancy
  • Glandular or shaft reconstruction may be needed
  • Regular follow-up appointments are essential
  • Monitor for complications such as strictures or fistulas
  • Provide psychosocial support for body image issues
  • Counseling and education can alleviate concerns
  • Manage associated conditions like undescended testicles
  • Additional surgical interventions may be necessary
  • Hormonal evaluations may be warranted in some cases
  • Long-term health monitoring is crucial for patients

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It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.