Parturients in Labour Clinical Trial
Official title:
Alteration in Hearing Following Accidental Dural Puncture. A Study in Parturients
Headache following accidental dural punction as during epidural analgesia can be severe and
sometimes very disabling. The incidence of PDPH is 10-40%, most starting within 48 h of
dural puncture. Although spontaneous resolution of headaches is common in most patients
within 7 days, in 20% can they be persistent and in some very disabling. The exact reason
for the characteristic headache is unknown, but it is believed to be the result of leakage
of cerebro-spinal fluid (CSF) from the dural puncture. The greater the leakage of CSF, the
more severe and persistent the headache. This is why larger needles (lower gauge) are known
to have a higher incidence of PDPH. However, the type of needle also seems to play an
important role in the likelihood of PDPH.
Headache following accidental PDPH is very typical as it increases significantly when
sitting or standing and often disappears completely on lying down. It is typically located
in the back of the head, accentuated by light and often decreases with intake of large
quantity of fluids. In many cases, it is self-limiting and most often decreases with time
and bed rest.
Diagnosis of PDPH is clinical and sometimes difficult. It is well known that liquor leakage,
as following spinal anaesthesia, results in partial loss of unilateral or bilateral hearing
that can be detected by oto-acoustic hearing loss. We plan to use this knowledge and test
the hypothesis that measurement of hearing loss may be a diagnostic method for confirmation
of clinical symptoms and signs of accidental PDPH.
Parturients who have received epidural analgesia during labour would be included in this
study and these would comprise of:
1. patients without clinical symptoms of postdural puncture headache
2. patients with clinical symptoms of postdural puncture headache
In addition, a control group of parturients who have not received an epidural analgesia
would constitute the control group.
All patients would have audiometry (oto-acoustic emission - OAE, and auditory steady state
response - ASSR) done following diagnosis of PDPH. Subsequently, the patients would be
observed for 24 h to assess whether the headache resolves spontaneously. A new audiometry
would be done at this stage. Those patients with substantial evidence of PDPH at this stage
would receive an epidural blood patch (EBP) and a new audiometric assessment would be made
after 4 h and 24 h to assess whether any audiometric deficit has resolved or not. All
patients would have a similar measurement of hearing after 3 months when it is believed that
most patients have returned to normal hearing. In addition to audiometric analysis, patients
would be asked to fill out a detailed PDPH questionnaire at the same time periods.
All measurements would be compared with patients who have received an EDA but without PDPH
and those who have not received an EDA.
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Observational Model: Case Control, Time Perspective: Prospective