Required material
• 100 IU of botulinum toxin A (BTA) diluted in 6 mL of saline solution, the solution
should be gently mixed to prevent protein denaturation.
• Infiltration needle
• Ultrasound device
• A nerve-stimulator
Botulinum toxin infiltration will be performed under sedation. Once the patient is
sedated, we will conduct an examination to locate the trigger points to be injected.
Internal Obturator Muscle
To examine the internal obturator, the index finger is inserted into the vagina and directed
anterolaterally. Using a pincer movement, the thumb palpates the obturator foramen. At
the level of the clitoris, the muscle can be found.
To insert the needle, it is positioned at the clitoral level, near the inguinal fold, and
directed laterally. The correct needle placement should be verified using both a nerve
stimulator and ultrasound
Ultrasound verification: The transducer is placed in a parasagittal plane at the inguinal
fold, over the anterior pubic ramus.
Nerve-stimulator verification: The power is gradually increased from 0.02 to 1 MHz,
allowing for palpation of muscle excitation during the examination.
Once verified, the botulinum toxine is administered. To ensure effective distribution of
the medication, 1 cc of saline solution can be injected.
Puborectalis Muscle
To examine the puborectalis muscle, the finger is inserted into the vagina and moved
laterally. Posterolateral pressure is applied to locate the trigger points.
For injection, once the muscle is located, the needle is inserted 1 cm lateral to the
perineal body and directed medially towards the vagina. As mentioned earlier, correct
needle placement should be verified using nerve stimulation and ultrasound. In this
case, the transducer should be placed over the vaginal introitus, and with a lateral
sweeping motion, the needle can be located.
After proper verification, the medication will be administered.
Post-Procedure Care
After completing the infiltration, the patient is awakened and remains under observation
for two hours.
One of the most common side effects of the injection is mild pain during the week
following the procedure
Follow-up evaluations will be conducted at one month, three months, and six months to
assess effectiveness and potential improvement using the previously mentioned
questionnaires.