The Development of Approaches to the Repetition of Dose
in Hahnemann's Homeopathy
The issue of repetition of dose is intimately tied up with the related
issues of dose and potency. This essay is intended to be read alongside its
sister-essay, The
Development of Dose and Potency in the History of Homeopathy.
In the early years of homeopathy, we find little written about the issue of
repetition of dose. Undoubtedly Hahnemann was experimenting widely, and he
likely viewed the issue of repetition similarly to the manner in which he viewed
dose at this time (see the accompanying essay re dose
and potency) - as a variable to be determined individually for each of the
various medicinal substances he employed, guided by an evolving recognition of
the general significance of the minimum dose. It was not until 1825 (year 29*),
with the recognition of the principle of dynamization, that Hahnemann broke from
materialistic perspectives re dose, and began to see dose as an issue that
transcended the physical properties of the particular medicinal substance in
question.
From this early period we have only a few glimpses at Hahnemann's practices
re repetition.
In his booklet Cure and Prevention of Scarlet Fever (1801; year 6*)
(discussing the use of poppy in treating the active acute illness): "It is
unnecessary to repeat these doses oftener than every four or eight hours, in
some cases not more than every twenty-four hours, and that sometimes only a
couple of times throughout the whole fever, for which the more frequent or more
rare occurrence of these symptoms must be our guide". In the treatment of
the desquamation following difficult cases, he dosed chamomilla daily.
In Treatment of the Typhus or Hospital Fever at Present Prevailing
(Allgem. Anzeig. der Deutschen, 1814; year 19) (discussing the use of Bryonia in
the active acute illness): "and as long as the improvement goes on, we give
him no other medicine, nor even repeat the same one; for none of the medicines
here recommended can be used oftener than once (in the dose of a drop) - seldom
can they be given a second time with advantage."
The issue of repetition of dose began to receive understandably greater
attention in the context of treating chronic disease.
It was in 1829 that Hahnemann proposed the standardized use of the 30th centesimal
potency, and this was his preferred preparation when he wrote part 1
of Chronic Diseases in 1828 (year 32). His posology in treating chronic
disease is detailed on pp. 119-129, & p. 137 (in the Jain edition). The
carefully chosen dose & potency (most usually a single 30C pellet, dry or
moistened) was allowed to act until the dose had exhausted its favorable action,
with no other prescription to be considered so long as the improvement
continued. Repetition or change of remedy was considered only when the old
symptoms, which had been eradicated or very much diminished by the previous
dose, commenced to rise again for a few days; discernment of the time to
consider a second prescription required experience and careful observation.
Hahnemann suggested that the "third leading mistake" in treating
chronic disease was in not waiting until the dose had exhausted its action; that
this might require 30, 40, even 50 or more days, but could not be predicted
ahead of clinical observation of the progress of the case. He suggested that practitioners
"scrupulous on the wrong occasion" mitigate their own
and their patients' impatience by giving milk sugar (sac lac) as a placebo
during this period of observant waiting.
The only exception to patient waiting for such extended periods, was when the
initial dose exhausted its action unexpectedly soon. He suggested it was then
best to repeat, but if the same remedy was indicated, to repeat it at an altered
potency. This could involve moving either up or down in the potency scale -
e.g., from 30C to 24C, 18C to 24C, etc.
There is some heralding of his later use of split doses in medicinal
solution, in his advice that to allow the dose to act more strongly, it could be
given in water, divided over 2-3 days (not longer), stirred each time to modify
the potency.
Hahnemann also introduced in this work the administration of remedies by
olfaction, which he elaborated on later in 1832-1833; and he later introduced
administration by application to the (healthy) external skin. As the issues of
dose and repetition of dose are relatively independent of the method of
administration, I will not go into greater detail on these topics now, but will
rather cover them in a separate essay.
The 4th edition of the Organon, published the following year (1829),
similarly advised that a "single dose of a well-selected homoeopathic
medicine should always be allowed first fully to expend its action before a new
medicine is given or the same one repeated".
Constantine Hering left Germany for Surinam in 1827, and was shipwrecked off
Martha's Vineyard on his attempt to return home in 1833. He settled in
Philadelphia well-practiced in the methods of the 4th edition of the Organon
& the 1st edition of Chronic Diseases, and rooted the development of
homeopathy in North America strongly this "wait & watch"
methodology. Kent later provided perhaps the most eloquent and detailed
description of this approach in his Lecture
on the Second Prescription, read before the International Hahnemannian
Association at Niagara Falls in 1888.
Between 1829 and 1833 (years 33-37), Hahnemann's focus was very much on the
treatment of chronic disease, and overcoming the obstacles presented to its most
rapid and gentle cure. He experienced difficulties using the "wait &
watch" approach, which he described in the note to §246 of the 5th edition
of the Organon: "...the vital force dose not quietly adapt itself to
the transition from the natural disease to the similar medicinal disease, but is
usually so violently excited and disturbed by a larger dose, or by smaller doses
of even a homeopathically chosen remedy given rapidly one after the other, that
in most cases its reaction will be anything but salutary and will do more harm
than good". This difficulty led him into exploring the dosing alternatives
described below, introduced to practice between 1833 and 1838 (years 37-42).
When Hahnemann published the 5th edition of the Organon in 1833 (year
37), he introduced an option he felt preferable to this "wait &
watch" approach, suggesting that a more rapid cure could be had by
repeating a dose at "suitable intervals which experience has proved to be
best adapted" , guided by the "nature of the medicinal substance, the
corporeal constitution of the patient, and the magnitude of the disease".
He suggested repeating dry or moistened 30C globules (in Hahnemann's notation,
X, referring to the decillionth dilution) at an unaltered dose & potency.
Dosing frequency might range from every 7 to 14 days in a chronic illness of
slow pace, to every five minutes in an acute illness of rapid pace, guided by
clinical experience and observation of the progress of the case. This approach
often required that an "intercurrent" remedy be given after several
doses; a precaution that was reversed with the later introduction of gradual
ascending potencies. He modified the preparation of his centesimal potencies
when intended to be used in this manner, reducing the number of successions at
each dilution step from 10 to 2.
Four years later, in the Preface to part 3 of Chronic Diseases (1837,
year 41), Hahnemann described a major refinement of this repeated-dose approach,
noting: "Experience has shown me, as it has no doubt also shown to most of
my followers, that it is most useful in diseases of any magnitude (not excepting
even the most acute, and still more so in the half-acute, in the tedious and
most tedious) to give to the patient the powerful homoeopathic pellet or pellets
only in solution, and this solution in divided doses." Repeated doses of
the medicine were considered "indispensable to secure the cure of a
serious, chronic disease". He provides directions to dissolve one or more
pellets (centesimal pellets, usually 30C [X in Hahnemann's notation, for the
decillionth dilution]) in 7-20 tablespoons of water, and to give portions of
this solution (1 tablespoon, or a small part of a tablespoon in more sensitive
patients) in acute illness "every 6, 4 or 2 hours; when very urgent, even
every hour or 1/2 hour", and in chronic diseases, "a dose (e.g., a
spoonful) every two days, more usually every day". Each subsequent dose was
to be modified "only a little in its degree of dynamizaton so the vital
force will calmly receive the same medicine", by shaking the solution 5-6
times. After the solution was used up in this manner, if a subsequent bottle of
the same remedy was required, he suggested either (1)preparing the 2nd bottle
with one or two pellets of the same medicine in a lower potency (e.g.,
30C -> 24C); or, (2)if the same potency were desired, to make it up in the
manner the first bottle, but prior to the first dose, to give it as many shakes
plus a few more as the previous bottle had received during the entire time of
its use.
He described an alternative "small bottle" method of making up the
medicinal solution, using 200, 300 or 400 drops of water & brandy to
half-fill a small vial, into which one or more pellets were dissolved, and
briskly shaken 5-6 times before each dose. According to the vitality &
sensitivity of the patient, 1, 2, 3 or several drops were removed to a cup
containing a spoonful of water, to be stirred, and the contents (or a portion of
the contents) to be taken for a dose.
In 1838 (year 42), Hahnemann developed his new potencies, his
"medicaments au globule" (the LM or Q or 50-millesimal potencies),
which were intended to optimize the medicinal solution dosing approach described
above. He shared his experience with these only with Boenninghausen, and first
wrote about them in the 6th edition of the Organon, the year prior to his death
(1842), but which was only made available to the homoeopathic community 80 years
later, in 1921. Directions for the preparation of LMs are provided in the 6th
edition of the Organon, in §270; and for their use in §s245-248 and 280-282.
Choudhury's book Fifty Millesimal Potency - Theory and Practice is an
excellent resource for this method; the best writings I've seen on this approach
are the series of articles titled Hahnemann's Advanced Methods available
on David Little's website.
I'll outline the basics of this approach below, but refer practitioners to the
resources above (& particularly to David Little's writings) as guides to
actual application of this approach.
In the 6th edition of the Organon, Hahnemann states (§246):
"Every perceptibly progressive and strikingly increasing amelioration in a
transient (acute) or persistent (chronic) disease, is a condition which, as long
as it lasts, completely precludes every repetition of the administration of any
medicine whatsoever, because all the good the medicine taken continues to effect
is new hastening towards its completion. Every new dose of any medicine
whatsoever, even of the one last administered, that has hitherto shown itself to
be salutary, would in this case disturb the work of amelioration".
However, in gradual amelioration, he suggests that one can ensure and hasten
cure if one repeats the dose in medicinal solution with modification of potency
each time by succession. He provided much more explicit instructions for this
approach than for the methods that led up to its development. Most importantly,
it is important that the degree of potency deviate somewhat from the previous
and subsequent ones, in order to avoid the development of accessory symptoms
(symptoms of the similar medicinal disease that are not part of, & therefore
are not homoeopathic to, the original natural disease of the patient). In order
to hasten cure, one may also gradually increase the size of the dose, but not so
aggressively as to result in a homoeopathic aggravation. Repetition of the dose
in this manner was to be carried on until eradication of the disease, or until
the picture of the disease-gestalt changed to one demanding a different remedy (§248)
The actual potency selected to begin treatment, the size of the dose(s)
given, and the frequency of repetition of the dose were variables to be
determined individually for each case. Hahnemann does provide some general
guidelines for consideration, outlined below.
He suggested 2 options for making up the medicinal solution (§ 248, note).
The first involves using one or (rarely) more pellets in 40, 30, 20, 15 or 8
tblsp water (4 - 20 oz), adding alcohol or a piece of charcoal to keep the
solution from spoiling. This would be succussed about 8, 10 or 12 times before
each dose, and a dose would consist of one or several teaspoons.
The second option uses one or (rarely) more pellets in 7-8 tblsp (~4oz)
water, preserved with alcohol or charcoal. After succussing as above, one
tablespoon of this solution would be stirred vigorously into a dilution glass
containing 8-10 tblsp (4-5oz) water, and a portion of this would be given for a
dose. In sensitive patients, a tsp of this dilution would be stirred into a
second dilution glass, and this might be carried through a third or even a
fourth dilution glass to create an appropriately small dose.
Repetition was recommended (§246 & §248) "at intervals that
experience has shown to be the most distinctly appropriate for the best possible
acceleration of treatment"; in chronic diseases of slow pace, this might be
daily or every second day; in acute diseases, it might be every 6, 4, 3, or 2
hrs; in urgent cases, it could be hourly or even more frequently.
If a second or subsequent bottle of the same remedy is required, this should
be made up with a pellet of higher potency. Over the course of treatment, it is
likely that the size of the dose would need to be increased to ensure progress
in the case, but this should be done only gradually to avoid creating
aggravation, and particularly to avoid the production of accessory symptoms by
the repeated doses.
Any "perceptibly progressive and strikingly increasing
amelioration" would preclude continued repetition (§246), as would any
aggravation (§282). As the natural disease of the patient lessens in intensity
towards the end of treatment, symptoms of the medicinal disease resembling those
of the original natural disease of the patient might appear; this would occasion
a reduction in the size of the dose and/or the dosing frequency, or a brief
suspension of dosing to assess the status of the remnants of the natural disease
prior to proceeding (§248 &§s280-281).
Although Hahnemann did share some of his early experiences with giving centesimal
remedies in split dose in medicinal solution in an 1835 letter to
Hering; and although Hahnemann was certainly familiar with the experiences of
Hering (and others) in using high potencies according to the 4th-edition
"wait and watch" methodology (and in fact, as the note to §246 in the
5th edition of the Organon reveals, had made his own observations on this
method); these two approaches to dosing continued to develop rather
independently in the Hahnemannian and Hering-Kentian lineages of 19th century
homeopathy. It is important to recognize that they each have their own set of
safeguards, principally from the risk of producing non-homoeopathic aggravation
or accessory symptoms of medicinal disease that could be obstructive of cure.
These are outlined in the careful methodologies of use, perhaps described best,
respectively, (1)in the 6th edition of the Organon, §s245-248 and
280-282, in Choudhury's book Fifty Millesimal Potency - Theory and Practice,
and in David Little's series of articles on Hahnemann's
Advanced Methods; and (2)in Kent's
Lecture on the Second Prescription.
Perhaps it is a gift that difficulties in trans-Atlantic communication, and
the delayed publication of the 6th edtion of the Organon, permitted these
posologies to each develop to their current fruition. Today we can learn from
both approaches, and select that which appears to be optimal for each case that
sits before us.
*As in previous essays, I've
adopted a chronology dating from Hahnemann's publication of Essay on a New
Principal for Ascertaining the Curative Power of Drugs, establishing 1796 as
the "birth" of homeopathy. This is done purely to simplify the picture
of the developmental chronology of our art. To those who might quibble and ask
that the translation of Cullen's Materia Medica be used as a landmark (1790), I
might suggest that we call this the date of conception, followed by a 6-year
gestation.
© 1998, Will Taylor, MD
may be freely distributed with credit to the author